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Nutritional determinants of frailty in older adults: A systematic review

Abstract

Background

Frailty is a geriatric syndrome that affects multiple domains of human functioning. A variety of problems contributes to the development of this syndrome; poor nutritional status is an important determinant of this condition. The purpose of this systematic review was to examine recent evidence regarding the association between nutritional status and frailty syndrome in older adults.

Methods

PubMed, Web of Science, and Scopus electronic databases were searched using specific key words, for observational papers that were published during the period from 2005 to February 2017 and that studied the association or relationship between nutritional status and frailty in older adults. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) Statement was followed to assess the quality of the included articles.

Results

Of the 2042 studies found, nineteen met the inclusion criteria. Of these studies, five provided data on micronutrients and frailty, and reported that frailty syndrome is associated with low intakes of specific micronutrients. Five studies provided data on macronutrients and frailty, and among those studies, four revealed that a higher protein intake was associated with a lower risk of frailty. Three studies examined the relationship between diet quality and frailty, and showed that the quality of the diet is inversely associated with the risk of being frail. Two studies provided data on the antioxidant capacity of the diet and frailty, and reported that a high dietary antioxidant capacity is associated with a lower risk of developing frailty. Finally, seven studies evaluated the relationship between scores on both the Mini Nutritional Assessment (MNA) and the MNA-SF (Short Form) and frailty, and revealed an association between malnutrition and/or the risk of malnutrition and frailty.

Conclusions

This systematic review confirms the importance of both quantitative (energy intake) and qualitative (nutrient quality) factors of nutrition in the development of frailty syndrome in older adults. However, more longitudinal studies on this topic are required to further understand the potential role of nutrition in the prevention, postponement, or even reversion of frailty syndrome.

Peer Review reports

Background

One of the populations with the most serious shifts in demographics is the world’s aging population. According to current estimations, the number of people aged 60 years or over is projected to grow from 901 million to 1.4 billion globally between 2015 and 2030 and will reach nearly 2.1 billion by 2050 [1]. The main reason that people are living longer is a reduction in mortality due to advances in health services, medicine, wealth and income, nutrition, behavior, and education [2]. However, living longer is not equivalent to being healthy, and increasing age is commonly related to different levels of frailty [3, 4].

The study of frailty has attracted enormous scientific interest in recent years because it affects multiple domains of human functioning, including gait, mobility, balance, muscle strength, motor processing, cognition, endurance, physical activity, and nutrition [5]. The decline across these multiple physiological systems triggers increased utilization of medical and social resources [3] with consequent economic expenditures.

Fried et al. [3] defined the presence of the frailty phenotype based on the presence of three or more of the following physical criteria: weight loss, exhaustion, physical activity, walking time, and grip strength. People are classified as frail if they meet three or more of these features, pre-frail if they meet one or two, and non-frail if they do not meet any of the criteria. Frailty is considered an early stage of disability, and as such it is characterized the potential for reversibility [6], meaning that appropriate interventions at the proper time can be used to prevent, postpone or even reverse this phenomenon [7].

A variety of problems contribute to the development of frailty and include, environmental factors such as physical activity [8] or a poorer nutritional status [9,10,11], both of which are important determinants in the development of frailty syndrome. Inadequate dietary intake has been associated with many conditions, such as an increased risk of chronic diseases [12], decreased antioxidant defenses [13], impaired immune responses [14], an increased risk of osteoporotic fractures [15], peripheral arterial disease [16], and frailty [10, 17]. Optimal nutrition is important for not only the prevention and treatment of different diseases [18], but also the facilitation of independence throughout the life cycle, which improves the quality of life of our elders, and ultimately promotes healthy aging [19]. In fact, the importance of nutrition as a means for postponing frailty in elderly people is a well-established phenomenon [20]. Nevertheless, a major obstacle to the success of nutritional interventions that is discussed in the literature has been the difficulty in comparing studies due to the use of multiple and different methods to measure nutritional status. To evaluate malnutrition, healthcare professionals and researchers rely on body mass index, anthropometry, biochemical markers, as well as a variety of nutritional screening tools [21]. Considering this difficulty and assuming that good nutritional interventions may play a role in the postponement or even reversion of frailty in the elderly, the aim of this systematic review was to critically appraise recent evidence pertaining to the association between nutritional status and frailty syndrome in older adults.

Methods

Data sources and search strategy

A systematic review of recent literature, published from January 2005 to February 2017 was performed. Three computerized electronic databases (PubMed, Web of Science, and Scopus) were searched using the following key search words: (“nutritional status” OR “nutrient deficiency” OR “nutrient deficiencies “OR “nutrient deficient” OR “nutrient intake” OR “nutritional intake” OR “food intake” OR “dietary intake” OR “dietary adequacy” OR “nutrition assessment” OR “nutritional assessment “OR “malnutrition” OR “undernutrition” OR “malnourishment”) AND (“frail” OR “frailty” OR “frail elderly”) AND (“elderly” OR “older adults” OR “older people” OR “geriatric”). All possible articles were merged into a single file, and duplicate records were removed after they were checked manually. Two independent reviewers evaluated the appropriateness of inclusion, and any conflicts that arose were discussed until a consensus was reached. In cases where a consensus was not reached, a third reviewer was included in the discussion.

Inclusion and exclusion criteria

We included original scientific articles that met the following predefined criteria:

Setting: Community-dwelling or institutionalized frail elderly people who were aged 65 years or older were included. As a condition, frailty should be defined with a clear operational definition/measurement. The study was excluded if it defined frailty according to disabilities, comorbidities, nutritional status, or cognitive impairment. Outcomes: Only studies that examined the association or relationship between nutritional status and frailty as a primary outcome were included. Articles should have a record of micronutrient and/or macronutrient status and/or a clear operational definition/measurement of nutritional status; Language: Only full-text articles published in either English or Spanish were considered. It is important to note that we focused the search on undernutrition, malnutrition and nutritional deficiencies and that any research on overnutrition or obesity was not included.

Exclusion criteria: Abstracts, reviews, books, book chapters, letters, conference abstracts, short surveys, studies based on the description of a protocol, and interventional studies, as well as studies based on the perspective of the authors, and comments on an article were excluded.

Data extraction

Studies were synthesized according to the following characteristics: authors and year, study design, country and sample characteristics (age and sex), setting, operational definition of frailty, nutritional measurement tools, prevalence/incidence of frailty and nutritional status, and main findings. This was a systematic review that did not require the ethics approval of an ethics committee. Because of the heterogeneity of the study designs, a narrative synthesis approach, rather than a meta-analysis, was utilized to examine the results. Different estimators of effect size (ES) were calculated according to the data to be compared. Cohen’s d values were reported as indicators of effect size (ES) for comparing the mean values. We interpreted the importance of the ES using the benchmarks for “small ES” (d = 0.2), “medium ES” (d = 0.5) and “large ES” (d = 0.8) as defined by Cohen [22]. The ES of the difference between two proportions was estimated according to the arcsine transformation by Cohen [22], and a Cohen’s h value was obtained. We interpreted the importance of these ES using the benchmarks for “small ES” (h = 0.2), “medium ES” (h = 0.5) and “large ES” (h = 0.8). Finally, odds ratios were converted into ES using a method proposed by Hasselblad & Hedges [23].

Results

The review procedure is described in Fig. 1. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) Statement was followed [24, 25] to assess the quality of the included articles (see Additional file 1). As shown in the figure, a total of 2042 studies were identified: After the removal of duplicates, 1121 were considered potentially relevant and were screened for pertinent content. From these studies, 1062 were excluded based on the title and abstract, while 59 were retrieved for full-text assessment. In the next phase, 40 articles were excluded based on the inclusion criteria (see Additional file 2): 19 were excluded for not meeting the setting characteristics, and 21 were excluded for not meeting the review objective. Ultimately, 19 studies met the criteria and were included in this review (see Figure 1).

Fig. 1
figure 1

Flow diagram of study selection

Participants and study characteristics

The included articles encompassed a sample of 22,270 older adults (63.2% women), with a mean age of 74.5 ± 7.0 years (extracted whenever possible). A total of 21,033 participants were community-dwelling elders, 111 lived in residential care facilities, and one study [26] recruited 1126 participants from both settings (community-dwelling people living either on their own or in a family house and those who were living in a nursing home). Eight studies were conducted in Europe [9, 26,27,28,29,30,31,32], seven in Asia [11, 33,34,35,36,37,38], and four in the United States of America [10, 17, 39, 40].

The identification of frail older people was based on the frailty phenotype [10, 17, 26,27,28,29, 33, 40] described by Fried et al. [3], on modifications of the frailty phenotype [9, 30, 32, 37, 38, 40], on the Study of Osteoporotic Fractures (SOF) Frailty Index [11, 33, 35, 36], and on the FRAIL scale [35]. Specific nutritional measurement tools employed in each paper are described in Table 1.

Table 1 Observational studies on nutrition and frailty (associations)

Nutritional outcomes

Association between micronutrients and frailty

Five studies provided data on micronutrients and frailty [9, 10, 17, 38, 39] and used some specific micronutrients as a measure of nutrient intake. In all five studies, frailty syndrome was independently associated with a low intake of specific micronutrients. In a cross-sectional analysis of the InCHIANTI study, Bartali et al. [9] found that a low intake of certain micronutrients (vitamins D, E, and C, and folate) was significantly related to frailty independent of energy intake. In a cross-sectional multicenter study among three generations (dietetic students, their mothers, and their grandmothers), Kobayashi et al. [38] found that 10 of 12 micronutrients studied (vitamin A, α-carotene, β-carotene, β-carotene equivalent, cryptoxanthin, vitamin D, α-tocopherol, vitamin B6, folate, and vitamin C) were associated with a lower prevalence of frailty. By using a sample of community-dwelling women from the Women’s Health and Aging Studies (WHAS) I and II, Matteini et al. [39] showed that older women with increased concentrations of methylmalonic acid (MMA: a marker of vitamin B12 tissue deficiency) had 40%–60% greater odds of being pre-frail (p-values <0.07) and 1.66–2.33 times greater odds of being frail (p-values <0.02) compared to patients who were not frail. By using the same sample, Michelon et al. [17] reported that the age-adjusted odds ratios of being frail were higher for older women with lower levels of micronutrients: such as serum total carotenoids, α-tocopherol, 25-hydroxyvitamin D, and vitamin B6. Importantly, after adjusting for age, sociodemographic status, smoking status, and body mass index, the association between micronutrients and frailty was strongest for total carotenoids, β-carotene, and lutein/zeaxanthin. Finally, Semba et al. [10], also used data from the WHAS-I study, and showed that women in the lowest quartile of serum carotenoids and α-tocopherol had a significantly increased risk of becoming frail over a 3-year period. By applying a multivariate grouped-time Cox proportional hazards model, the number of nutrient deficiencies was also related to an increased risk of becoming frail.

The role of macronutrient intake in frailty

Five studies reported data on the relationships between macronutrients and frailty [9, 28, 32, 37, 40]. Three of the studies found that a higher protein intake was associated with a lower risk of frailty [9, 32, 37], whereas two studies reported that the amount of protein intake was not associated with frailty [28, 40]. In particular, Bartali et al. [9] found an association between low protein intake (lowest quintile; energy intake of ≤21 kcal/kg/day) and frailty after adjusting for energy intake. In a community-dwelling elder population from France, Rahi et al. [32] found that a 1 g/kg protein intake was associated with a lower prevalence of frailty, after adjusting for sociodemographic and clinical factors. In a multicenter cross-sectional study that explored the association between protein or amino acid intake and frailty, Kobayashi et al. [37] showed that a higher intake of total protein was significantly associated with a lower prevalence of frailty among older Japanese women, regardless of the protein source (animal sources: fish and shellfish, meat, eggs, and dairy products; plant sources: cereals, pulses, potatoes, confectionaries, fruits and vegetables), or the amino acid that composed the protein (leucine, isoleucine, valine, methionine, cysteine, branched chain amino acids, sulfur amino acids, and essential amino acids). Although amino acid consumption was inversely associated with frailty, the association of total protein intake was stronger than those of any individual amino acids. The authors concluded that neither the protein sources nor the type of amino acids were particularly relevant in the prevention of frailty. In another cross-sectional study that investigated the association between the amount and distribution of protein intake throughout the day (morning, noon, evening) and frailty in older German community-dwelling seniors, Bollwein et al. [28] found that the amount of protein intake was not associated with frailty or any of its individual criteria (the authors only found a significant trend concerning low physical activity). However, the distribution of protein intake throughout the day was significantly associated with frailty. Specifically, frail older adults showed a more uneven distribution of protein intake throughout the day with a lower morning intake and a higher midday intake than pre-frail and non-frail participants. In a longitudinal study that examined the association between baseline dietary variables and baseline frailty status, Shikany et al. [40] found that while a higher intake of fiber and carbohydrates significantly decreased the risk of intermediate or frail status relative to a robust status, a higher fat intake significantly increased the risk of being frail relative to a robust status. Notably, protein intake was not associated with the risk of frailty relative to a robust status [40].

Relationship between dietary patterns and frailty

One longitudinal study explored the relationship between dietary patterns and the four-year risk of frailty [34]. In a sample of Chinese community-dwelling older adults, Chan et al. [34] found that a higher score of “snacks-drinks-milk products” patterns decreased the risk of being frail. This association disappeared when the model was adjusted for age and sex, or for other demographic and lifestyle factors. No association with the incidence of frailty was found for “vegetables-fruits products” or “meat-fish products” patterns.

Relationship between diet quality and frailty

Three studies examined the relationship between diet quality and frailty [27, 34, 40], and showed that the overall quality of the diet was inversely associated with the risk of being frail. With the use of a Mediterranean-Diet Score (MDS) to evaluate a priori-defined dietary patterns, Bollwein et al. [27] found that compared to a less healthy diet, community-dwelling older adults who had the healthiest diet had a significantly decreased risk of being frail. The effect of the diet was graded, as manifested by the linear trend in the odds ratios (OR). Considering the singular frailty criteria, there was a significant and inverse association between “weight loss,” “low physical activity,” and “low walking speed” and the MDS. With the use of the Diet Quality Index-International (DQI-I) and the MDS, Chan et al. [34] explored the associations between dietary patterns and four-year incident frailty in older Chinese adults and found that participants with a higher DQI-I score (which represents a balanced diet in terms of energy and nutrient intake) had a reduced risk of frailty in both sex- and age-adjusted models. However, the authors did not find any association between MDS and frailty. Finally, in an analysis of the Osteoporotic Fractures in Men (MrOS) longitudinal study that used the Diet Quality Index Revised (DQI-R), Shikany et al. [40] found, that the DQI-R score in a cohort of older men was inversely associated with frailty status relative to a robust status at both a baseline and second clinic visit (a mean of 4.6 years later).

Antioxidant capacity of the diet and frailty

Two studies reported data on the antioxidant capacity of a diet compared to frailty [31, 38]. Both studies showed that a higher dietary antioxidant capacity is associated with frailty status. Specifically, in a cross-sectional multicenter study, Kobayashi et al. [38] found that a higher intake of dietary total antioxidant capacity (TAC) measured with four assays (ferric reducing ability of plasma (FRAP), oxygen radical absorbance capacity (ORAC), Trolox equivalent antioxidant capacity (TEAC), and total radical-trapping antioxidant parameters (TRAP)) was inversely associated with frailty. The intake of green tea, coffee, vegetables, and fruits which contributes to dietary TAC was also associated with lower odds of frailty, since the odds ratios were less pronounced than those for dietary TAC. Rabassa et al. [31] designed a longitudinal study that investigated the association of habitual dietary resveratrol exposure (measured by total dietary resveratrol (TDR), total urinary resveratrol (TUR), and the combination of both measures (TDR + TUR) with frailty syndrome and each of its 5 criteria at baseline and at 3-, 6-, and 9-year follow-up periods. The authors found that high habitual dietary resveratrol exposure was associated with a lower risk of developing frailty syndrome in older adults during the first 3 years of follow-up but not after 6- and 9-years follow-up periods, despite results that trended in the same direction. Considering individual frailty criteria during the 3-year follow-up period, and after adjusting for baseline frailty syndrome and for potential covariates (including energy intake), participants in the highest tertile of TDR + TUR had a lower risk of feeling exhausted than did those participants in the lowest tertile. No associations were observed for other frailty criteria. Considering TDR exposure, raw models identified a significant inverse association between this measure and low levels of physical activity at the 3, 6, and 9-year follow-up periods, although this relationship was not present in the adjusted models.

Relationships between the mini nutritional assessment (MNA®) and the mini nutritional assessment shot form (MNA-SF®) scores and frailty

Six studies evaluated the relationship between MNA and MNA-SF [41] scores and frailty [11, 26, 29, 30, 33, 35, 36], and revealed a significant association between malnutrition, the risk of malnutrition, and frailty status. Specifically, Chang [11] found that frail Taiwanese community-dwelling elders had a particularly high risk of malnutrition. Bollwein et al. [29] reported a significant association between frailty status and the three dimensions of the MNA score: MNA total scores, MNA-subscores, and 12 of the 18 MNA single items. Boulos et al. [33] reported a strong association between 14 of the 18 MNA items and frailty status. In addition, by applying a multivariate analysis, the authors found a strong and independent relationship between frailty and both malnutrition and the risk of malnutrition. In a pioneer study carried out in Asian pre-frail elders, Chang and Lin [35] revealed a relationship between pre-frail status and the total MNA score. Similarly, El Zoghbi et al. [36] showed that frailty was inversely correlated with the nutritional status of 111 institutionalized elders. In a multicenter study, Eyigor et al. [26] found that several socio-demographic factors, lifestyle variables, and clinical characteristics (such as malnutrition) were related to frailty. Specifically, the authors found that being malnourished increased the risk of being frail. Finally, in a sample of 640 community-dwelling Spanish elders, Jürschik et al. [30] found a significant association between the 5 frailty criteria and malnourishment, as identified by the MNA and the MNA-SF, and argued that both tests could be used to identify frail elders.

Discussion

This systematic review regarding the relationship between nutrition measurements (micronutrients, macronutrients/protein intake, diet quality, antioxidant capacity, MNA or MNA-SF scores) and frailty in elderly people, provides current evidence of an association between many of these outcomes and frailty syndrome. The focus on malnutrition, at both the micro- and macronutrient levels is relevant because nutrition was identified in a recent systematic review as a means for delaying the onset of the negative consequences of frailty in older adults [20] as well as for the slowing the development and progression of frailty in elderly people [9]. Similar to a previous article [8], we required rigorous criteria to perform this review and to define frailty in older people; thus, trials that included the word “frail” in the title or in the abstract, and studies that did not rigorously define the word “frail”, were not included.

Five of the articles studied the association between micronutrients and frailty, and reported that low intake of specific micronutrients increased the risk of being frail [9, 10, 17, 38, 39]. Among the micronutrients that were studied, most of them had sequentially decreasing levels in non-frail, pre-frail, and frail older people. One important implication of the inverse association between micronutrients and frailty is that the intake of specific nutrients affect the health of older people and may lead to the development of frailty, among other important conditions. Indeed, different types of cancer are related to deficiencies of carotenoids and vitamins C and E [42]; cardiovascular disease is related to the impaired antioxidant capacity of vitamin E, β-carotene, and vitamin C [43], and sarcopenia is related to low serum concentrations of carotenoids and vitamin E [44]. A rich dietary intake of carotenoids and vitamins could be a potentially modifiable factor for preventing all these conditions. Therefore, it is important to teach our elders about foods that contain specific micronutrients. The goal could be to present specific dietary programs aimed at the avoidance of malnutrition while increasing the intake of foods that are rich in carotenoids and vitamins (such as vegetable foods) depending on the needs of each elder. Based on these findings, Bartali et al. [9] suggested that the quality of the diet, expressed by the intake of specific nutrients, should be included as part of frailty screening, diagnostic and treatment processes, because nutrition is a relevant factor that significantly affect the health of older adults.

Five studies [9, 27, 32, 36, 40] included in this review considered the role of macronutrient and protein intake in frail patients. Three of those studies [9, 32, 37] found that higher protein intake was associated with lower frailty risk, while only one study [28] found that it was actually the overall distribution of the protein throughout daily meals that was significantly associated with frailty. Specifically, Bollwein et al. [28] found greater uniformity in the pattern of protein intake in non-frail elders than in frail or pre-frail older adults. This result occurred with other findings and signaled the importance of ingesting a sufficient amount of protein with each meal, which is recommended at 25–30 g of high-quality protein per meal or approximately 1–1.2 g/kg per day [45].

In addition, the three studies that examined the relationship between overall diet quality and frailty [27, 34, 40] revealed that the quality of the diet is inversely associated with the risk of being frail, thus providing convergent evidence that a potentially modifiable factor, such as dietary intake, may play a crucial role in frailty status. As already suggested [27] and as proposed by the MDS, this effect could be mediated by a low intake of animal products and a high intake of fruits and vegetables. This result coincides with the previously mentioned micronutrient studies that indicated that the main nutritional sources of carotenoids and vitamin C were vegetable foods. Consistent with these results, this review found two studies [31, 38] that showed that a high intake of foods with high dietary antioxidant capacity, such as vegetables, fruits, coffee, and green tea, was associated with a lower risk of developing frailty. In summary, this and the previous findings indicate that a high-quality diet with satisfactory energy intake, the optimal intake of quality protein that is evenly distributed throughout all meals, and meals that are rich in antioxidants, are important factors for preventing and postponing the onset of frailty in older adults.

In is important to note that all the reviewed papers highlighted the importance of different nutritional factors in frailty, regardless of the type of study, the studied sample, or the instruments used to measure frailty and nutritional status.

Regarding the gap in the literature, future longitudinal studies with larger sample sizes and clinical trials are needed to further improve our knowledge regarding the associations between nutritional status and frailty. Specifically, future studies that examine the relationships between micro- and macronutrients concentrations and frailty are needed. It would also be interesting to determine whether different components of frailty are associated with the quality of the diet, independent of major confounders, in future studies.

This review has several limitations that should be mentioned. The main limitation is that most of the included studies were of a cross-sectional design, and as such, no statements can be made about causal relationships. Indeed, poor nutrition or malnutrition might contribute to frailty, or conversely, frailty might contribute to poor nutrition or malnutrition. Additionally, it is possible that some other mediating factors, such as poor dentition and swallowing problems, reduced smell and taste, or a deteriorated functional capacity that was associated with the need for feeding assistance, might have contributed to the relationship between both variables. Our review has limitations resulting from the search terms and years included. It would be really interesting, in future reviews on the topic, to include articles with malnutrition or frailty as secondary outcomes and more specific terms (protein, carbohydrate, fat, vitamin D, diet quality, dietary pattern, antioxidant, MNA, fruit or vegetable), with no limit of search years. An additional limitation is that only two studies were performed with institutionalized older adults, while seventeen were performed in community-dwelling populations, which limits significant comparisons among settings. Finally, the heterogeneity of the outcome measurements could have limited the strength of the conclusions. Nevertheless, there were also strengths that deserve to be highlighted. The main strength is that this review gives a beneficial outlook on how nutrition is linked to frailty in different elderly populations throughout the world. Thus, the results allow cross-country comparisons. In addition, we required strict criteria to define frailty, nutrition, and malnutrition in older people, and we presented a well-defined question and explicit inclusion criteria.

Establishing an optimal nutrition-based plan for the aging population should be of concern for governments for the judicious allocation of resources and for policy makers who want to add life to years and not years to life [46].

Conclusion

This systematic review analyzes recent evidence that nutrition or nutritional intake is associated with frailty in older adults. However, a straightforward conclusion about the efficacy of nutrition on frailty cannot be established due mainly to the cross-sectional design of many of the included studies. In summary, more prospective cohort studies in older adults are needed to further understand the potential role of nutrition in the prevention, postponement, or the reversal of frailty syndrome.

Abbreviations

BDHQ:

Brief-type Diet History Questionnaire

CI:

Confidence interval

DHQ:

Diet history questionnaire

DQI-I:

Diet Quality Index-International

DQI-R:

Diet Quality Index Revised

EPIC:

European Prospective Investigation into Cancer and Nutrition

FFQ:

Food Frequency Questionnaire

FRAIL:

Fatigue, Resistance, Ambulation, Illness, Low Weight

FRALLE:

Frailty Lleida

FRAP:

Ferric reducing ability of plasma

InCHIANTI:

Invecchiare in Chianti, ageing in the Chianti area

MDS:

Mediterranean-Diet Score

MMA:

Methylmalonic acid

MNA:

Mini Nutritional Assessment

MNA-SF:

Mini nutritional assessment short form

MrOS:

Osteoporotic Fractures in Men

OR:

Odds ratio

ORAC:

Oxygen Radical Absorbance Capacity

RIA:

Radioimmunoassay

SOF:

Study of Osteoporotic Fractures

TAC:

Total antioxidant capacity

TDR:

Total dietary resveratrol

TEAC:

Trolox equivalent antioxidant capacity

tHcy:

Homocysteine

TRAP:

Total radical-trapping antioxidant parameters

TUR:

Total urinary resveratrol

WHAS:

Women’s Health and Aging Study

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This work was supported by the Xunta de Galicia, FrailNet network IN607C, 2016/08.

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CDL, JCMC and LRF contributed to the conception and design of the study. AM and LLL prepared the revised version of the manuscript according to the reviewer’ suggestions. CDL, JCMC, LLL and AM critically reviewed the manuscript before the final submission. CDL, LRF and JLRV performed the search and analyzed the articles. CDL, LLL and AM contributed to the analysis and interpretation of the data, along with drafting the manuscript. All the authors revised the final version of the manuscript and approved its submission for publication.

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Quality assessment of the included papers (n = 19). (DOCX 22 kb)

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Reasons for the exclusion of full-text articles based on the application of inclusion criteria (n = 40). (DOCX 21 kb)

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Lorenzo-López, L., Maseda, A., de Labra, C. et al. Nutritional determinants of frailty in older adults: A systematic review. BMC Geriatr 17, 108 (2017). https://doi.org/10.1186/s12877-017-0496-2

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