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Predictors for quality of life in older adults: network analysis on cognitive and neuropsychiatric symptoms

Abstract

Background

Quality of life (QoL) of older adults has become a pivotal concern of the public and health system. Previous studies found that both cognitive decline and neuropsychiatric symptoms (NPS) can affect QoL in older adults. However, it remains unclear how these symptoms are related to each other and impact on QoL. Our aim is to investigate the complex network relationship between cognitive and NPS symptoms in older adults, and to further explore their association with QoL.

Methods

A cross-sectional study was conducted in a sample of 389 older individuals with complaints of memory decline. The instruments included the Neuropsychiatric Inventory, the Mini Mental State Examination, and the 36-item Short Form Health Survey. Data was analyzed using network analysis and mediation analysis.

Results

We found that attention and agitation were the variables with the highest centrality in cognitive and NPS symptoms, respectively. In an exploratory mediation analysis, agitation was significantly associated with poor attention (β = -0.214, P < 0.001) and reduced QoL (β = -0.137, P = 0.005). The indirect effect of agitation on the QoL through attention was significant (95% confidence interval (CI) [-0.119, -0.035]). Furthermore, attention served as a mediator between agitation and QoL, accounting for 35.09% of the total effect.

Conclusions

By elucidating the NPS-cognition-QoL relationship, the current study provides insights for developing rehabilitation programs among older adults to ensure their QoL.

Peer Review reports

Introduction

Rapid population ageing is a global trend, with the number of people aged 60 years and older will be increased to 1.4 billion by 2030 and 2.1 billion by 2050 [1]. Driven by recent declines in fertility/mortality and increases in life expectancy, China is now home to the largest population of older people in the world [2]. The ageing fact raises significant concerns about the well-being of older adults bringing about various challenges involving socio-economic, medical security, and family relationships [1]. Quality of life (QoL) has been recognized by the World Health Organization (WHO) as a key construct to be measured in the older adult population [3], that is an important indicator for successful or poor ageing process [4]. A recent study proposed that the focus of research needs to shift from the treatment of chronic diseases to QoL improvement of the elderly [5]. The QoL could be preserved in older population, provided they remain independence and active, and fulfill social roles [4]. How to ensure QoL has become a pivotal concern of the public and health system. Accumulating evidence of research has identified a variety of predictors for QoL in the ageing group, such as age [6], gender [7], chronic health conditions [8, 9], depression [10, 11], anxiety [12], and functional status [8, 13].

The existing literature suggested that QoL may be used as an outcome measure in aging research across multiple domains, including cognitive disorders, neuropsychiatric conditions, chronic illnesses, physical disabilities, and geriatric interventions [14, 15]. For example, previous studies have used QoL to evaluate the impacts of Alzheimer’s disease on daily function and well-being [16, 17]. In neuropsychiatric research, QoL serves to evaluate symptom severity and treatment effects [18]. Beyond mental health, QoL has also been employed as an indicator of functional status in older adults with chronic diseases [19]. Assessing QoL provides a comprehensive evaluation of how various age-related conditions affect overall well-being and satisfaction with life [20]. The multidimensional nature of QoL makes it a relevant and informative outcome measure in gerontological research.

As people grow older, their cognitive functions gradually decline [21]. The prevalence of cognitive impairment among older adults was substantial. In China, the prevalence of mild cognitive impairment (MCI) and dementia in adults aged 60 years or older was estimated to be 15.5% and 6%, respectively [22]. In the United States, the prevalence of MCI and dementia was 22% and 10%, respectively [23]. Cognitive functions can be divided into several specific domains, including attention, memory, executive function, language, and visuospatial abilities. These different cognitive domains are interrelated and decline with normal ageing [24]. For instance, deficits in attention may impair memory encoding and retrieval processes, limiting an individual’s ability to effectively acquire and recall information [25], while executive function difficulties can affect problem-solving abilities and task switching, making it challenging for individuals to adapt to new situations and effectively handle complex tasks [26]. Meanwhile, cognitive training on one specific cognitive domain showed significant transfer effects on untrained domains [27, 28]. A series of studies showed that cognitive problems can negatively impact on QoL of older people, such as reduced self-care ability in daily life [29], limited social activities and engagement [30], and impaired crucial aspects of daily life [31]. Addressing the cognitive difficulties through appropriate interventions can significantly improve the QoL in older population.

In addition, the older adults is also susceptible to experiencing various neuropsychiatric symptoms (NPS) that can further diminish their QoL [32]. The most common NPS included depression, anxiety, apathy, aggression, and sleep disorder [33,34,35]. NPS often accompanies cognitive impairment [36]. Indeed, the occurrence of NPS increases in frequency and severity with cognitive decline [37], which is associated with a 3-fold increased risk of dementia and a 2-fold increased risk of MCI [38]. A study has shown that approximately 79.5% of patients with MCI and 91.2% of patients with dementia experience NPS [39]. The NPS not only have a negative impact on QoL of patients, but also impose a great burden on their families and the society [40]. Therefore, effective treatment and management of NPS are also crucial [41].

Easterbrook’s theory proposes that emotional arousal leads to a narrowing of attention and subsequently affects an individual’s perception and experience [42]. According to this theory, when individuals are in an emotionally agitated or highly aroused state, their cognitive resources are restricted and their attention is narrowed. Additionally, previous studies have shown that NPS could have a direct impact on cognitive functions. For example, NPS such as anxiety and depression affect a variety of cognitive functions including working memory [43]. Another study found that hallucinations in MCI individuals were associated with poorer attention, suggesting that NPS may precede cognitive impairment [36]. Other research found that agitation affects the QoL of older people [44]. The existing theory and studies have suggested a path between agitation and attention, which gives us a direction for the exploratory mediation effect. Therefore, an exploratory mediation analysis was performed to test Easterbrook’s theory. We hypothesized that attention mediates the relationship between NPS and QoL.

Traditional analytic approaches rely on total scale scores to describe symptom severity, which may obscure meaningful associations between individual symptoms [45]. In contrast, network analysis has emerged as a novel approach to investigate the interactions among multiple variables and to reveal their complex interrelationships comprehensively [46]. Network model is also useful for understanding the mechanisms of comorbidities [47]. Particularly, network approach has wide applications to understand psychopathology in the field of psychology and psychiatry [48]. In the network, nodes represent symptoms and edges represent correlations between symptoms. The width of the edge indicates the strength of the association between nodes [49]. By applying network analysis, the central symptoms can be identified. The central symptoms have significant clinical value and great practical implication, because the central symptoms are more likely to activate and influence other symptoms, and they are important targets for clinical intervention and treatment [50]. However, network analysis cannot establish causality or directional interconnections among nodes, which can be supplemented by mediation analyses. Mediation analysis can provide an insight into what path of connections among nodes (predictors and mediators) leads to the outcome variables. By exploring NPS-cognition interaction, we can reveal the specific processes that lead to impact on QoL. In addition, mediation analysis can provide preliminary explanations and speculations about the relationships between variables. It can also provide valuable insights for further research and practice. It is noted that network analysis and mediation analysis have different strengths that can complement each other [51]. The combining approach of network and mediation analysis has been widely used in the literature [52,53,54,55,56]. For instance, network and moderator analysis were used to identify what path determines stigma in mental health professionals, considering personality traits, burnout, and professional variables [54].

To this end, our study aims to investigate the relationship between cognitive symptoms, NPS, and QoL in older people with complaints of memory loss using network analysis and mediation analysis. Specifically, we used network analysis to examine the relationship between cognition and NPS, and to identify the most core symptoms. Next, we used an exploratory mediation analysis to investigate the relationship between these core symptoms and QoL. We hypothesized that cognitive symptoms are closely related to NPS, and the core symptom of cognition mediate the relationship between the core NPS and QoL. By elucidating the NPS-cognition-QoL relationship, we hope to provide insights for developing effective interventions and rehabilitation programs for older adults to ensure their QoL.

Methods

Participants

We recruited 389 older participants (220 female, mean age = 73.85 years, SD = 8.43) from nursing homes in Nanchang and the psychiatric department of China-Japan Union Hospital in Jilin, China. They were selected based on the following criteria. The inclusion criteria were as follows: (1) aged 60 years and above; (2) self-reported memory decline; (3) native Chinese speaker. The exclusion criteria were as follows: (1) severe visual, auditory, or language impairment that prevented adequate response to assessment questions; (2) severe brain injury or mental illness, such as head injury, tumor, or schizophrenia; (3) history of alcohol or drug dependence or abuse; (4) history of vascular or traumatic brain injury or event that may affect cognitive function; (5) unable to cooperate with the investigation. Sociodemographic indicators, such as age, gender and level of education of the participants, were obtained through self-report. The current study was reviewed and approved by the Ethics Committee of China-Japan Union Hospital (Ethics number: 20,221,020,028), and all participants were asked to provide written consent before initiating the survey. During the data collection process, approximately 20% of the older adults contacted indicated that they did not want to participate in the questionnaire assessment. They were therefore not included in this study.

Measurements

The Neuropsychiatric Inventory (NPI) [57] was used to assess an individual’s NPS. Previous literature has extensively utilized the NPI scale for evaluating NPS in the general older population [36, 58]. It is a 12-item questionnaire that evaluates both the frequency and severity of the patient’s symptoms and the caregiver’s stress. The 12 items included delusions, hallucinations, agitation, depression/dysphoria, anxiety, apathy, irritability, euphoria, disinhibition, aberrant motor behavior, sleep and nighttime behavior disorders, appetite and eating disorders. The total NPI score is the sum of intensity scores for all 12 items (0 to 144), with higher scores indicating more NPS in patients and greater stress in carers. The Chinese version of the NPI demonstrated good reliability in assessing NPS in dementia patients with Cronbach alpha being 0.84 [59]. The Mini Mental State Examination (MMSE) [60] was used to evaluate an individual’s cognitive functions, including orientation (10 points), memory (6 points), attention (5 points), and language (9 points). Its score ranges from 0 to 30, with lower scores indicating worse cognitive functions. The Chinese version of MMSE has been extensively validated and applied in clinical assessment [61]. We used the 36-item Short-Form Health Survey (SF-36) [62] to assess QoL. The scale has been widely used and is a valid tool for evaluating the health status and QoL of the older adults [63]. The scale consists of 36 items reflecting changes in the patient’s health status over the past year, which included eight dimensions: physical functioning, role physical, bodily pain, general health perception, vitality, social functioning, role emotional, and mental health. Each dimension has a score ranging from 0 to 100, with higher scores indicating better QoL. The Chinese version of the SF-36 scale demonstrates good reliability among older population, making it a suitable tool for assessing their QoL [64, 65].

Statistical analysis

SPSS 23.0 software was used to conduct descriptive statistical analyses, with means and standard deviations used for continuous variables and frequencies and percentages used for categorical variables. Use Pearson’s correlation for continuous, normally distributed variables, and Spearman’s correlation for ordinal or non-normally distributed data. The prevalence plot of NPS was generated by the R software.

Network analysis

We conducted a network analysis to investigate the relationship between NPS and cognitive functions using the qgraph, mgm, bootnet, and huge packages in R [66]. To improve the interpretability of the results, we regularized the network using the Least Absolute Shrinkage and Selection Operator method [67]. This method allows the coefficients of non-significant variables to be shrunk to zero, thus achieving the purpose of variable selection. The centrality indices of node strength, closeness, betweenness, and expected influence were calculated using the qgraph package [68]. To determine whether highly central nodes were significantly different from other nodes, we performed a test of differences in node centrality using the bootnet package [66]. Comparison with other nodes allowed us to identify critical symptoms in the network [49]. The mgm package [69] was used to calculate the predictability of each node, which allowed us to assess the extent to which each node could be predicted by its neighboring nodes. In addition, we calculated correlation coefficients between all items in network analysis and QoL.

To ensure the accuracy and replicability of our results, we conducted stability and accuracy tests using the R package bootnet. We assessed the accuracy of network connections and tested whether the centrality estimates differed across variables. We also tested the stability of edge weights and the order of nodes in terms of centrality. To evaluate the stability of centrality indices, we performed bootstrapping test [66] and calculated the correlation stability coefficient. If the stability coefficient exceeded 0.5, centrality was indicated as stable [66].

Exploratory mediation analysis

We conducted an exploratory mediation analysis [70] to examine the path relationships between variables. It was hypothesized that the core cognitive function mediated the relationship between the core NPS and QoL. A bootstrap mediation analysis was conducted using the PROCESS procedure to test this hypothesis. The data were standardized prior to the mediation analysis. Furthermore, the participants’ gender, age and level of education were included in the analysis as control variables.

Results

Descriptive result

Among the participants, 151 (38.80%) had subjective cognitive decline (SCD), 75 (19.20%) had MCI, and 163 (41.9%) had dementia. The average age of the participants was 73.85 (SD = 8.43), with 56.56% were female. In this study, 77.12% of the participants experienced at least one NPS. The NPS symptoms with a prevalence exceeding 10% were selected for network analysis, which included sleep and nighttime behavior disorders (42.16%), anxiety (39.59%), irritability (25.19%), appetite and eating disorders (23.91%), depression (17.74%), agitation (13.88%), and apathy (10.54%) (Fig. 1). These symptoms were selected based on previous research and clinical significance [71,72,73,74,75]. They are the most prevalent and clinically worrisome neuropsychiatric symptoms among older adults and have received the attention of numerous researchers [35, 76]. The four cognitive domains, including orientation, memory, attention, and language, were selected for network analysis. Demographic information about the participants was listed in Table 1.

Fig. 1
figure 1

The prevalence of different NPS scores ≥ 1 (n = 389). Note: NPS = Neuropsychiatric symptoms; SLE = Sleep and Nighttime Behavior Disorders; APP = Appetite and Eating Disorders; ABE = Aberrant Motor Behavior

Table 1 Clinical and demographics data (n = 389)

Network analysis result

As shown in Fig. 2, the relationship between NPS and cognitive function involved several dimensions. The centrality estimates of the network nodes were presented in Fig. 3. “Attention” was the variable with the highest centrality in cognitive functions (strength = 1.79, closeness = 1.30, betweenness = 2.08). In addition, “Attention” demonstrated high predictability (predictability = 0.427), ranking second only to “Orientation” (predictability = 0.429). “Agitation” had the highest centrality and predictability in NPS (strength = 0.54, closeness = 0.79, expected influence = 0.87, predictability = 0.30). Although we did not find connections between the “Language” node and any of the NPS nodes, the “Language” node was strongly associated with the other three cognitive functions (Orientation (r = 0.437, P < 0.001), Memory (r = 0.496, P < 0.001), and Attention (r = 0.508, P < 0.001). The highest correlation between the variables in the network analysis was 0.63 and between the variables in the network analysis and QoL was 0.40 (Table 2). The results of the network analysis revealed good stability with a stability coefficient of 0.67. The stability analysis of the edge weights reliably estimated the strength of the ties within the network. Further, we found that even though up to 50% of the nodes in each network were discarded, their order of centrality remained stable.

Fig. 2
figure 2

Network of cognition and NPS (n = 389). Note: Nodes represent evaluated variables, and edges represent connections between variables, with the edge width corresponding to the strength of the connections; blue (red) edges represent positive (negative) connections; the circle surrounding each node represents the predictability estimate, which indicates the level to which neighboring nodes can predict a node (similar to R2)

Fig. 3
figure 3

Centrality plot of the cognition and NPS network. Note: The plot is standardized, with higher scores indicating greater centrality. SLE = Sleep and Nighttime Behavior Disorders; ORI = Orientation; MEM = Memory; LAN = Language; IRR = Irritability; DEP = Depression; ATT = Attention; APP = Appetite and Eating Disorders; APA = Apathy; ANX = Anxiety; AGI = Agitation.

Table 2 Correlation coefficient of cognitive functions, NPS and QoL

Exploratory mediation analysis result

Based on network analysis results, we further examined the relationship between agitation, attention, and QoL. The findings revealed significant correlations among agitation, attention, and QoL. Specifically, agitation showed a significant negative correlation with attention (r = -0.256, P < 0.001) and QoL (r = -0.249, P < 0.001). Furthermore, attention exhibited a significant positive correlation with QoL (r = 0.340, P < 0.001) (Table 2).

Mediation analysis is a statistical method for testing causality [77], but its interpretation of causality is only valid if the direction of influence between variables is clear and all other potentially confounding variables are considered. In the exploratory mediation analysis of the present study, we hypothesized that agitation influences attention rather than attention affects agitation. It is worth noting that the latter hypothesis may also be plausible, and we have therefore taken it into account in interpreting the results of this study (see Discussion).

The exploratory mediation model (Table 3; Fig. 4) aims to clarify the relationship between agitation as the independent variable and QoL as the dependent variable, by adding a third theoretical variable (attention) as a mediator. The findings showed that attention partially mediated the relationship between the QoL and the agitation. Agitation was a negative predictor of attention (β = -0.214, P < 0.001), indicating that older people with higher agitation levels were associated with poorer attention. The direct effect of agitation on QoL was negatively significant after controlling for the effect of attention (β = -0.137, P = 0.005). The indirect effect of agitation on the QoL through attention was significant (95% CI [-0.119, -0.035]). The mediation analysis revealed that attention mediated the relationship between agitation and QoL, accounting for 35.09% of the total effect.

Table 3 Exploratory mediation of attention in the relationship between agitation and QoL (n = 389)
Fig. 4
figure 4

Mediating effect of attention in the relationship between agitation and QoL (n = 389). Note: Quality of life (QoL) was assessed as the dependent variable using the 36-item Short-Form Health Survey (SF-36). The numbers next to the arrows demonstrate the standardized path coefficients. The solid arrows represent the statistically significant paths

Discussion

To our knowledge, this is the first study to use network analysis and mediation analysis to investigate the relationship among NPS, cognitive function, and QoL in older population. Our findings revealed that NPS had a prevalence of 77.12% among the participants. Furthermore, the occurrence and severity of NPS increased as cognitive decline worsened, while the QoL decreased. These results are in line with previous research findings [78, 79].

The network analysis in this study visualized the complex network of relationships between different NPS and cognition, providing important insights into their interaction. We observed that “Attention” had the highest values in three centrality measures (strength, closeness, and betweenness) among cognitive functions, indicating its crucial role in the network. The importance of attention in cognition has been widely reported in the literature [80, 81]. It reflects an individual’s ability to select, focus, and sustain attention to external stimuli. Whatever its severity, attention disorders have an impact on other cognitive functions (such as memory and learning). Most importantly, it has the potential to perturb execution of daily activities and skills [82].

In NPS, “Agitation” has the highest values in the centrality measures of strength, closeness, and expected influence, indicating that it is the most important in the network. Moreover, there is a strong correlation between agitation and symptoms such as irritability and apathy, which increases its centrality in the network. On the other hand, the higher centrality of agitation aligns with its significance in psychology and neuroscience. For example, studies have shown the widespread presence of agitation and aggressive behavior NPS [83]. Therefore, it is reasonable for the “Agitation” to have higher centrality in the network. Interestingly, the “Language” node was not directly linked to the NPS node, but it exhibited a robust and meaningful relationship with the other three cognitive functions. These results suggested that language function may indirectly affect NPS by influencing other cognitive functions, which provides clues for further exploration of the role of language function in the development of NPS.

The results of the network analysis revealed the importance of variables within the network and provided clues to further understanding of the relationship between cognitive function and NPS. Exploratory mediation analysis revealed the mediating role of attention between agitation and QoL, suggesting that agitation indirectly affects QoL by influencing attention. This finding supports Easterbrook’s theory, which believes that emotional arousal leads to a narrowing of attention and affects an individual’s perceptions and experiences [42]. Agitation may impact various aspects of attention. First, agitation can make it difficult for individuals to concentrate because they become emotionally agitated and their attention is disrupted. Second, it may cause individuals to focus excessively on potential threats or conflicts, leading to a bias towards negative or hostile stimuli while ignoring other important information [84]. Additionally, agitation can interfere with the regulation of attention in social interactions, making it difficult to recognize and understand the emotions and intentions of others [85]. Furthermore, limited attention has a negative impact on individuals’ QoL [86]. These attention difficulties can manifest across various domains of daily life, including work, learning, social interactions, and emotional regulation, consequently reducing overall life quality. In individuals with Attention-Deficit/Hyperactivity Disorder (ADHD) [87, 88], Post-Traumatic Stress Disorder (PTSD) [89], and Autism Spectrum Disorder (ASD) [90, 91], it is commonly observed that attention problems, impulse control difficulties, agitation/aggressive, and anger-related issues coexist, indicating a link between agitation and attention. It is necessary to mention that the mechanisms of influence in these areas are not fully understood from the intervention point of view. Our findings are consistent with previous studies [92], indicating that a significant portion of the shared variance between agitation and cognition can be explained by attention. Therefore, it may be possible to attempt to alleviate the effects of agitation on QoL by intervening on attention. For instance, cognitive training may be used to help older adults learn how to better regulate their attention, focusing on the positive and reducing the concern for negative agitation. Psychological and social support may also be provided to older adults to help them deal effectively with agitation and change the way agitation is perceived. Strengthening social support for older adults and providing more social resources and emotional support can help to distract attention and reduce the impact of agitation on QoL. It is important to emphasize that the results of this study only provide preliminary basis for the development of possible interventions, and the design and implementation of specific interventions need to be considered in conjunction with the results of further studies and practical situations.

It is worth noting that the mediation analysis in this study were conducted based on cross-sectional data, so it is possible that alterations in attention in older adults may also affect agitation. Actually, in another set of exploratory mediation analysis, we found that agitation mediated the relationship between attention and QoL, although this mediating effect was only 8.30%. These findings suggest that inferring causal direction from mediation analysis in cross-sectional studies is difficult. In addition, unmeasured other variables related to attention and QoL may influence the observed mediating effects. Longitudinal studies that measure data at multiple time points are the only way to derive causal associations. However, our findings suggest an important role for attention in the effects of agitation on QoL.

Limitations and future directions

This study has several limitations. First, the use of a cross-sectional design prevents us from establishing causal relationships. Future studies could be conducted longitudinally to track changes in cognitive function and NPS over time in older adults, which could help us to investigate trends in the dynamics of cognitive decline and its predictive factors at different stages, and reveal causal relationships between variables. Second, the cognitive assessment dimension includes only four measures from the MMSE scale and does not encompass other cognitive dimensions such as executive function and visuospatial abilities. Future research could consider incorporating these cognitive dimensions into analysis as well. Third, we adjusted for a limited set of covariates in the mediation analysis, including gender, age, and education level, while ignoring other potential confounders, such as marital status and living area. These potential confounders were not controlled for due to data unavailability. Future research could collect data on more covariates and perform more comprehensive analyses. Fourth, participants in this study were recruited from a nursing home and an outpatient clinic in two regions, which may not be representative of the older population across different regions of China. Therefore, the generalizability and applicability of our findings need to be further examined in more diverse older populations. Fifth, the network analysis found that there may be various other mediations going through attention which is picked up in the high betweenness score, but exploring the associations among these variables was beyond the scope of our study. Future studies could further explore this interesting issue. The last but not the least, the sample in this study was population specific and future researches could use network analysis to explore the relationship between NPS and cognitive function in groups with normal/SCD, MCI and dementia. These different groups may have different symptom networks related to the severity and subgroups of cognitive impairment.

Conclusions

In conclusion, a network model of the relationship between NPS and cognitive functions was developed in this study. We identified the crucial roles of agitation and attention in the network, and their impact on QoL. We found that attention mediated the relationship between agitation and QoL, accounting for 35.09% of the total effect. This suggests that attention plays a critical role in the mechanism of how agitation affects QoL. These findings provide valuable insights into understanding the associations among NPS, cognition, and QoL in older adults, with significant clinical implications.

Data Availability

The data may be available from the corresponding author on reasonable request.

Abbreviations

QoL:

Quality of Life

WHO:

World Health Organization

NPS:

Neuropsychiatric Symptoms

NPI:

Neuropsychiatric Inventory

MMSE:

Mini Mental State Examination

MCI:

Mild Cognitive Impairment

SCD:

Subjective Cognitive Decline

SF-36:

36-item Short-Form Health Survey

SD:

Standard Deviation

ADHD:

Attention-Deficit/Hyperactivity Disorder

PTSD:

Post-Traumatic Stress Disorder

ASD:

Autism Spectrum Disorder

LL:

Lower Limit

UL:

Upper Limit

CI:

Confidence Interval

ABE:

Aberrant Motor Behavior

SLE:

Sleep and Nighttime Behavior Disorders

ORI:

Orientation

MEM:

Memory

LAN:

Language

IRR:

Irritability

DEP:

Depression

ATT:

Attention

APP:

Appetite and Eating Disorders

APA:

Apathy

ANX:

Anxiety

AGI:

Agitation

References

  1. WHO. Ageing and health. World Health Organization. 2022. https://www.who.int/news-room/fact-sheets/detail/ageing-and-health. Accessed 29 June 2023.

  2. The L. Population ageing in China: crisis or opportunity? Lancet. 2022;400(10366):1821.

    Article  Google Scholar 

  3. World Health Organization. (1998). Programme on mental health: WHOQOL user manual. 2012 revision. World Health Organization. https://apps.who.int/iris/handle/10665/77932. Accessed 29 June 2023.

  4. Bowling A. Quality of life in older age: what older people say. In: Mollenkopf H, Walker A, editors. Quality of life in Old Age: International and Multi-disciplinary perspectives. Netherlands: Springer; 2007. pp. 15–30.

    Chapter  Google Scholar 

  5. Dogra S, Dunstan DW, Sugiyama T, Stathi A, Gardiner PA, Owen N. Active aging and Public Health: evidence, implications, and opportunities. Annu Rev Public Health. 2022;43:439–59.

    Article  PubMed  Google Scholar 

  6. Brett CE, Dykiert D, Starr JM, Deary IJ. Predicting change in quality of life from age 79 to 90 in the Lothian Birth Cohort 1921. Qual Life Res. 2019;28(3):737–49.

    Article  PubMed  Google Scholar 

  7. Campos AC, Ferreira e Ferreira E, Vargas AM, Albala C, Aging. Gender and quality of life (AGEQOL) study: factors associated with good quality of life in older Brazilian community-dwelling adults. Health Qual Life Outcomes. 2014;12:166.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Bowling A, Banister D, Sutton S, Evans O, Windsor J. A multidimensional model of the quality of life in older age. Aging Ment Health. 2002;6(4):355–71.

    Article  CAS  PubMed  Google Scholar 

  9. Chan SW, Chiu HF, Chien WT, Goggins W, Thompson D, Hong B. Predictors of change in health-related quality of life among older people with depression: a longitudinal study. Int Psychogeriatr. 2009;21(6):1171–9.

    Article  PubMed  Google Scholar 

  10. Stone AA, Schwartz JE, Broderick JE, Deaton A. A snapshot of the age distribution of psychological well-being in the United States. Proc Natl Acad Sci U S A. 2010;107(22):9985–90.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Lapid MI, Rummans TA, Boeve BF, McCormick JK, Pankratz VS, Cha RH, et al. What is the quality of life in the oldest old? Int Psychogeriatr. 2011;23(6):1003–10.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Shrestha S, Stanley MA, Wilson NL, Cully JA, Kunik ME, Novy DM, et al. Predictors of change in quality of life in older adults with generalized anxiety disorder. Int Psychogeriatr. 2015;27(7):1207–15.

    Article  PubMed  Google Scholar 

  13. Davis JC, Bryan S, Best JR, Li LC, Hsu CL, Gomez C, et al. Mobility predicts change in older adults’ health-related quality of life: evidence from a Vancouver falls prevention prospective cohort study. Health Qual Life Outcomes. 2015;13:101.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Haraldstad K, Wahl A, Andenæs R, Andersen JR, Andersen MH, Beisland E, et al. A systematic review of quality of life research in medicine and health sciences. Qual Life Res. 2019;28(10):2641–50.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Băjenaru L, Balog A, Dobre C, Drăghici R, Prada GI. Latent profile analysis for quality of life in older patients. BMC Geriatr. 2022;22(1):848.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Ashizawa T, Igarashi A, Sakata Y, Azuma M, Fujimoto K, Kobayashi T, et al. Impact of the severity of Alzheimer’s Disease on the quality of life, activities of Daily Living, and Caregiving costs for institutionalized patients on Anti-alzheimer medications in Japan. J Alzheimers Dis. 2021;81(1):367–74.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Boada M, López OL, Olazarán J, Núñez L, Pfeffer M, Puente O, et al. Neuropsychological, neuropsychiatric, and quality-of-life assessments in Alzheimer’s Disease patients treated with plasma exchange with albumin replacement from the randomized AMBAR study. Alzheimers Dement. 2022;18(7):1314–24.

    Article  CAS  PubMed  Google Scholar 

  18. Shin IS, Carter M, Masterman D, Fairbanks L, Cummings JL. Neuropsychiatric symptoms and quality of life in Alzheimer Disease. Am J Geriatr Psychiatry. 2005;13(6):469–74.

    Article  PubMed  Google Scholar 

  19. Megari K. Quality of life in Chronic Disease patients. Health Psychol Res. 2013;1(3):e27.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Institute of Medicine (US) Council on Health Care Technology; Mosteller F, Falotico-Taylor J, editors. Quality of Life and Technology Assessment: Monograph of the Council on Health Care Technology. Washington (DC): National Academies Press (US). ; 1989. 6, Assessing Quality of Life: Measures and Utility. Available from: https://www.ncbi.nlm.nih.gov/books/NBK235120/ Copyright © National Academy of Sciences.; 1989.

  21. Murman DL. The impact of age on Cognition. Semin Hear. 2015;36(3):111–21.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Jia L, Du Y, Chu L, Zhang Z, Li F, Lyu D, et al. Prevalence, risk factors, and management of Dementia and mild cognitive impairment in adults aged 60 years or older in China: a cross-sectional study. The Lancet Public Health. 2020;5(12):e661–71.

    Article  PubMed  Google Scholar 

  23. Manly JJ, Jones RN, Langa KM, Ryan LH, Levine DA, McCammon R, et al. Estimating the prevalence of Dementia and mild cognitive impairment in the US: the 2016 Health and Retirement Study Harmonized Cognitive Assessment Protocol Project. JAMA Neurol. 2022;79(12):1242–9.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Kirova AM, Bays RB, Lagalwar S. Working memory and executive function decline across normal aging, mild cognitive impairment, and Alzheimer’s Disease. Biomed Res Int. 2015;2015:748212.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Ortega R, López V, Carrasco X, Escobar MJ, García AM, Parra MA, et al. Neurocognitive mechanisms underlying working memory encoding and retrieval in Attention-Deficit/Hyperactivity disorder. Sci Rep. 2020;10(1):7771.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Perry RJ, Hodges JR. Attention and executive deficits in Alzheimer’s Disease. A critical review. Brain. 1999;122(Pt 3):383–404.

    Article  PubMed  Google Scholar 

  27. Weng W, Liang J, Xue J, Zhu T, Jiang Y, Wang J, et al. The transfer effects of Cognitive Training on Working Memory among Chinese older adults with mild cognitive impairment: a Randomized Controlled Trial. Front Aging Neurosci. 2019;11:212.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Sala G, Aksayli ND, Tatlidil KS, Tatsumi T, Gondo Y, Gobet FRJCP. Near and Far Transfer in Cognitive Training: A Second-Order Meta-Analysis. 2019.

  29. Hartmann J, Roßmeier C, Riedl L, Dorn B, Fischer J, Slawik T, et al. Quality of life in Advanced Dementia with Late Onset, Young Onset, and very young onset. J Alzheimers Dis. 2021;80(1):283–97.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Shuduo Z, Suhang S, Yinzi J, Zhi-Jie Z. Prospective association between social engagement and cognitive impairment among middle-aged and older adults: evidence from the China Health and Retirement Longitudinal Study. BMJ Open. 2020;10(11):e040936.

    Article  Google Scholar 

  31. Livingston G, Huntley J, Sommerlad A, Ames D, Ballard C, Banerjee S, et al. Dementia prevention, intervention, and care: 2020 report of the Lancet Commission. Lancet. 2020;396(10248):413–46.

    Article  PubMed  PubMed Central  Google Scholar 

  32. Saari T, Hallikainen I, Hintsa T, Koivisto AM. Neuropsychiatric symptoms and activities of daily living in Alzheimer’s Disease: ALSOVA 5-year follow-up study. Int Psychogeriatr. 2020;32(6):741–51.

    Article  PubMed  Google Scholar 

  33. Collins JD, Henley SMD, Suárez-González A. A systematic review of the prevalence of depression, anxiety, and apathy in frontotemporal dementia, atypical and young-onset Alzheimer’s disease, and inherited dementia. Int Psychogeriatr. 2020:1–20.

  34. Johansson M, Stomrud E, Johansson PM, Svenningsson A, Palmqvist S, Janelidze S, et al. Development of apathy, anxiety, and Depression in cognitively unimpaired older adults: effects of Alzheimer’s Disease Pathology and Cognitive decline. Biol Psychiatry. 2022;92(1):34–43.

    Article  PubMed  Google Scholar 

  35. Zhao QF, Tan L, Wang HF, Jiang T, Tan MS, Tan L, et al. The prevalence of neuropsychiatric symptoms in Alzheimer’s Disease: systematic review and meta-analysis. J Affect Disord. 2016;190:264–71.

    Article  PubMed  Google Scholar 

  36. Eikelboom WS, van den Berg E, Singleton EH, Baart SJ, Coesmans M, Leeuwis AE, et al. Neuropsychiatric and cognitive symptoms across the Alzheimer Disease Clinical Spectrum: cross-sectional and longitudinal associations. Neurology. 2021;97(13):e1276–87.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  37. Gonzales MM, Garbarino VR, Pollet E, Palavicini JP, Kellogg DL Jr., Kraig E et al. Biological aging processes underlying cognitive decline and neurodegenerative Disease. J Clin Invest. 2022;132(10).

  38. Mallo SC, Patten SB, Ismail Z, Pereiro AX, Facal D, Otero C, et al. Does the neuropsychiatric inventory predict progression from mild cognitive impairment to Dementia? A systematic review and meta-analysis. Ageing Res Rev. 2020;58:101004.

    Article  PubMed  Google Scholar 

  39. Siafarikas N, Selbaek G, Fladby T, Šaltytė Benth J, Auning E, Aarsland D. Frequency and subgroups of neuropsychiatric symptoms in mild cognitive impairment and different stages of Dementia in Alzheimer’s Disease. Int Psychogeriatr. 2018;30(1):103–13.

    Article  CAS  PubMed  Google Scholar 

  40. Conde-Sala JL, Turró-Garriga O, Piñán-Hernández S, Portellano-Ortiz C, Viñas-Diez V, Gascón-Bayarri J, et al. Effects of anosognosia and neuropsychiatric symptoms on the quality of life of patients with Alzheimer’s Disease: a 24-month follow-up study. Int J Geriatr Psychiatry. 2016;31(2):109–19.

    Article  PubMed  Google Scholar 

  41. Politis AM, Alexopoulos P, Vorvolakos T. May neuropsychiatric symptoms be a potential intervention target to delay functional impairment in Alzheimer’s Disease? Int Psychogeriatr. 2020;32(6):689–91.

    Article  PubMed  Google Scholar 

  42. Easterbrook JA. The effect of emotion on cue utilization and the organization of behavior. Psychol Rev. 1959;66(3):183–201.

    Article  CAS  PubMed  Google Scholar 

  43. Koppel J, Goldberg TE, Gordon ML, Huey E, Davies P, Keehlisen L, et al. Relationships between behavioral syndromes and cognitive domains in Alzheimer Disease: the impact of mood and psychosis. Am J Geriatr Psychiatry. 2012;20(11):994–1000.

    Article  PubMed  Google Scholar 

  44. Schmüdderich K, Holle D, Ströbel A, Holle B, Palm R. Relationship between the severity of agitation and quality of life in residents with Dementia living in German nursing homes - a secondary data analysis. BMC Psychiatry. 2021;21(1):191.

    Article  PubMed  PubMed Central  Google Scholar 

  45. Cai H, Bai W, Liu H, Chen X, Qi H, Liu R, et al. Network analysis of depressive and anxiety symptoms in adolescents during the later stage of the COVID-19 pandemic. Transl Psychiatry. 2022;12(1):98.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  46. Hevey D. Network analysis: a brief overview and tutorial. Health Psychol Behav Med. 2018;6(1):301–28.

    Article  PubMed  PubMed Central  Google Scholar 

  47. Jones PJ, Ma R, McNally RJ. Bridge centrality: A Network Approach to understanding Comorbidity. Multivar Behav Res. 2021;56(2):353–67.

    Article  Google Scholar 

  48. Robinaugh DJ, Hoekstra RHA, Toner ER, Borsboom D. The network approach to psychopathology: a review of the literature 2008–2018 and an agenda for future research. Psychol Med. 2020;50(3):353–66.

    Article  PubMed  Google Scholar 

  49. Costantini G, Epskamp S, Borsboom D, Perugini M, Mõttus R, Waldorp L, et al. State of the aRt personality research: a tutorial on network analysis of personality data in R. J Res Pers. 2015;54:13–29.

    Article  Google Scholar 

  50. Fried EI, Cramer AOJ. Moving forward: challenges and directions for psychopathological network theory and methodology. Perspect Psychol Sci. 2017;12(6):999–1020.

    Article  CAS  PubMed  Google Scholar 

  51. Epskamp S, Rhemtulla M, Borsboom D. Generalized Network Psychometrics: Combining Network and Latent Variable models. Psychometrika. 2017;82(4):904–27.

    Article  PubMed  Google Scholar 

  52. Solmi M, Granziol U, Boldrini T, Zaninotto L, Salcuni S. Stigma and attitudes towards restrictive practices in psychiatry among psychology students: a network and path analysis study in an Italian sample. J Ment Health. 2022;31(1):66–74.

    Article  PubMed  Google Scholar 

  53. Dughi T, Rad D, Runcan R, Chiș R, Vancu G, Maier R et al. A Network Analysis-Driven Sequential Mediation Analysis of Students’ Perceived Classroom Comfort and Perceived Faculty Support on the Relationship between Teachers’ Cognitive Presence and Students’ Grit-A Holistic Learning Approach. Behav Sci (Basel). 2023;13(2).

  54. Solmi M, Granziol U, Danieli A, Frasson A, Meneghetti L, Ferranti R, et al. Predictors of stigma in a sample of mental health professionals: Network and moderator analysis on gender, years of experience, personality traits, and levels of burnout. Eur Psychiatry. 2020;63(1):e4.

    Article  PubMed  PubMed Central  Google Scholar 

  55. Wang X, Xia Y, Yan R, Wang H, Sun H, Huang Y, et al. The relationship between disrupted anhedonia-related circuitry and suicidal ideation in major depressive disorder: a network-based analysis. Neuroimage Clin. 2023;40:103512.

    Article  PubMed  PubMed Central  Google Scholar 

  56. Liu X, Yang H, Becker B, Huang X, Luo C, Meng C, et al. Disentangling age- and disease-related alterations in schizophrenia brain network using structural equation modeling: a graph theoretical study based on minimum spanning tree. Hum Brain Mapp. 2021;42(10):3023–41.

    Article  PubMed  PubMed Central  Google Scholar 

  57. Cummings JL. The neuropsychiatric inventory: assessing psychopathology in Dementia patients. Neurology. 1997;48(5 Suppl 6):10–6.

    Google Scholar 

  58. Okura T, Plassman BL, Steffens DC, Llewellyn DJ, Potter GG, Langa KM. Prevalence of neuropsychiatric symptoms and their association with functional limitations in older adults in the United States: the aging, demographics, and memory study. J Am Geriatr Soc. 2010;58(2):330–7.

    Article  PubMed  PubMed Central  Google Scholar 

  59. Leung VP, Lam LC, Chiu HF, Cummings JL, Chen QL. Validation study of the Chinese version of the neuropsychiatric inventory (CNPI). Int J Geriatr Psychiatry. 2001;16(8):789–93.

    Article  CAS  PubMed  Google Scholar 

  60. Folstein MF, Folstein SE, McHugh PR. Mini-mental state. A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res. 1975;12(3):189–98.

    Article  CAS  PubMed  Google Scholar 

  61. Jia X, Wang Z, Huang F, Su C, Du W, Jiang H, et al. A comparison of the Mini-mental State Examination (MMSE) with the Montreal Cognitive Assessment (MoCA) for mild cognitive impairment screening in Chinese middle-aged and older population: a cross-sectional study. BMC Psychiatry. 2021;21(1):485.

    Article  PubMed  PubMed Central  Google Scholar 

  62. Ware JE Jr., Sherbourne CD. The MOS 36-item short-form health survey (SF-36). I. conceptual framework and item selection. Med Care. 1992;30(6):473–83.

    Article  PubMed  Google Scholar 

  63. Lyons RA, Perry HM, Littlepage BN. Evidence for the validity of the short-form 36 Questionnaire (SF-36) in an elderly population. Age Ageing. 1994;23(3):182–4.

    Article  CAS  PubMed  Google Scholar 

  64. Zhou B, Chen K, Wang JF, Wu YY, Zheng WJ, Wang H. [Reliability and validity of a short-Form Health Survey Scale (SF-36), Chinese version used in an elderly population of Zhejiang province in China]. Zhonghua Liu Xing Bing Xue Za Zhi. 2008;29(12):1193–8.

    PubMed  Google Scholar 

  65. Li L, Wang HM, Shen Y. Chinese SF-36 health survey: translation, cultural adaptation, validation, and normalisation. J Epidemiol Community Health. 2003;57(4):259–63.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  66. Epskamp S, Borsboom D, Fried EI. Estimating psychological networks and their accuracy: a tutorial paper. Behav Res Methods. 2018;50(1):195–212.

    Article  PubMed  Google Scholar 

  67. Tibshirani R. Regression shrinkage and selection via the Lasso. J Royal Stat Soc Ser B (Methodological). 1996;58(1):267–88.

    Google Scholar 

  68. McNally RJ. Can network analysis transform psychopathology? Behav Res Ther. 2016;86:95–104.

    Article  PubMed  Google Scholar 

  69. Haslbeck J, Waldorp L. Mgm: estimating time-varying mixed graphical models in high-dimensional data. J Stat Softw. 2020;93.

  70. Erickson KI, Prakash RS, Voss MW, Chaddock L, Heo S, McLaren M, et al. Brain-derived neurotrophic factor is associated with age-related decline in hippocampal volume. J Neurosci. 2010;30(15):5368–75.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  71. Devanand DP, Lee S, Huey ED, Goldberg TE. Associations between neuropsychiatric symptoms and neuropathological diagnoses of Alzheimer Disease and related Dementias. JAMA Psychiatry. 2022;79(4):359–67.

    Article  PubMed  PubMed Central  Google Scholar 

  72. Milani SA, Cantu PA, Berenson AB, Kuo YF, Markides KS, Raji MA. Gender differences in neuropsychiatric symptoms among Community-Dwelling Mexican americans aged 80 and older. Am J Alzheimers Dis Other Demen. 2021;36:15333175211042958.

    Article  PubMed  PubMed Central  Google Scholar 

  73. Liew TM. Neuropsychiatric symptoms in cognitively normal older persons, and the association with Alzheimer’s and Non-alzheimer’s Dementia. Alzheimers Res Ther. 2020;12(1):35.

    Article  PubMed  PubMed Central  Google Scholar 

  74. Cravello L, Palmer K, de Girolamo G, Caltagirone C, Spalletta G. Neuropsychiatric symptoms and syndromes in institutionalized elderly people without Dementia. Int Psychogeriatr. 2011;23(3):425–34.

    Article  PubMed  Google Scholar 

  75. Nunes PV, Schwarzer MC, Leite REP, Ferretti-Rebustini REL, Pasqualucci CA, Nitrini R, et al. Neuropsychiatric inventory in Community-Dwelling older adults with mild cognitive impairment and Dementia. J Alzheimers Dis. 2019;68(2):669–78.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  76. Lyketsos CG, Lopez O, Jones B, Fitzpatrick AL, Breitner J, DeKosky S. Prevalence of neuropsychiatric symptoms in Dementia and mild cognitive impairment: results from the cardiovascular health study. JAMA. 2002;288(12):1475–83.

    Article  PubMed  Google Scholar 

  77. MacKinnon DP, Fairchild AJ, Fritz MS. Mediation analysis. Annu Rev Psychol. 2007;58:593–614.

    Article  PubMed  PubMed Central  Google Scholar 

  78. Janssen N, Handels R, Wimo A, Antikainen R, Laatikainen T, Soininen H, et al. Association between Cognition, Health Related Quality of Life, and costs in a Population at Risk for Cognitive decline. J Alzheimers Dis. 2022;89:1–10.

    Article  Google Scholar 

  79. Mank A, Rijnhart JJM, van Maurik IS, Jönsson L, Handels R, Bakker ED, et al. A longitudinal study on quality of life along the spectrum of Alzheimer’s Disease. Alzheimers Res Ther. 2022;14(1):132.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  80. Stevens C, Bavelier D. The role of selective attention on academic foundations: a cognitive neuroscience perspective. Dev Cogn Neurosci. 2012;2(Suppl 1):30–48.

    Article  Google Scholar 

  81. Lindsay GW. Attention in psychology, Neuroscience, and machine learning. Front Comput Neurosci. 2020;14:29.

    Article  PubMed  PubMed Central  Google Scholar 

  82. Allain H, Akwa Y, Lacomblez L, Lieury A, Bentué-Ferrer D. Impaired cognition and attention in adults: pharmacological management strategies. Neuropsychiatr Dis Treat. 2007;3(1):103–16.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  83. Carrarini C, Russo M, Dono F, Barbone F, Rispoli MG, Ferri L, et al. Agitation and Dementia: Prevention and treatment strategies in Acute and chronic conditions. Front Neurol. 2021;12:644317.

    Article  PubMed  PubMed Central  Google Scholar 

  84. Berenson KR, Gyurak A, Ayduk O, Downey G, Garner MJ, Mogg K, et al. Rejection sensitivity and disruption of attention by social threat cues. J Res Pers. 2009;43(6):1064–72.

    Article  PubMed  PubMed Central  Google Scholar 

  85. Bateman DR, Gill S, Hu S, Foster ED, Ruthirakuhan MT, Sellek AF, et al. Agitation and impulsivity in mid and late life as possible risk markers for incident Dementia. Alzheimers Dement (N Y). 2020;6(1):e12016.

    Article  PubMed  Google Scholar 

  86. Agarwal R, Goldenberg M, Perry R, IsHak WW. The quality of life of adults with attention deficit hyperactivity disorder: a systematic review. Innov Clin Neurosci. 2012;9(5–6):10–21.

    PubMed  PubMed Central  Google Scholar 

  87. Saylor KE, Amann BH. Impulsive aggression as a comorbidity of Attention-Deficit/Hyperactivity disorder in children and adolescents. J Child Adolesc Psychopharmacol. 2016;26(1):19–25.

    Article  PubMed  PubMed Central  Google Scholar 

  88. Tripp G, Wickens JR. Neurobiology of ADHD. Neuropharmacology. 2009;57(7–8):579–89.

    Article  CAS  PubMed  Google Scholar 

  89. Blair KS, Vythilingam M, Crowe SL, McCaffrey DE, Ng P, Wu CC et al. Cognitive control of attention is differentially affected in trauma-exposed individuals with and without post-traumatic stress disorder. Psychol Med. 2013;43(1):85–95.

    Article  PubMed  Google Scholar 

  90. Ridderinkhof A, de Bruin EI, van den Driesschen S, Bögels SM. Attention in children with autism spectrum disorder and the effects of a mindfulness-based program. J Atten Disord. 2020;24(5):681–92.

    Article  Google Scholar 

  91. Hazen EP, Ravichandran C, Rao Hureau A, O'Rourke J, Madva E, McDougle CJ. Agitation in patients with autism spectrum disorder admitted to inpatient pediatric medical units. Pediatrics. 2020;145(Suppl 1):S108–16.

  92. Corrigan JD, Mysiw WJ, Gribble MW, Chock SKJBI. Agitation, cognition and attention during post-traumatic amnesia. 1992;6(2):155–60.

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Acknowledgements

The authors are grateful to the study participants.

Funding

This study was supported by the National Key R&D Program of China under Grant [2020YFC2005800, 2020YFC2005802, 2021ZD0203100, 2021ZD0203103].

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Qian Tao and Qing Zhao contributed to the study concept, design, analysis, interpretation of data, and review and edit the manuscript. Chaoqun He contributed to data analysis, visualization and writing the original draft. Xiangyi Kong, Jinhui Li, Xingyi Wang, Xinqiao Chen, and Yuanyi Wang contributed to the acquisition of data.

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Correspondence to Qing Zhao or Qian Tao.

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This study was conducted in accordance with the principles of the Helsinki Declaration and approved by the Ethics Committee of the China-Japan Union Hospital (Approval No: 20221020028). Prior to the study, all participants were provided with written and oral explanations of the research, and written informed consent was obtained. No personally identifiable information of the participants was disclosed in this manuscript. Therefore, consent for publication is not applicable.

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He, C., Kong, X., Li, J. et al. Predictors for quality of life in older adults: network analysis on cognitive and neuropsychiatric symptoms. BMC Geriatr 23, 850 (2023). https://doi.org/10.1186/s12877-023-04462-4

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