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Chronic diseases, chest computed tomography, and laboratory tests as predictors of severe respiratory failure and death in elderly Brazilian patients hospitalized with COVID-19: a prospective cohort study



The primary risk factors for severe respiratory failure and death in the elderly hospitalized with COVID-19 remain unclear.


To determine the association of chronic diseases, chest computed tomography (CT), and laboratory tests with severe respiratory failure and mortality in older adults hospitalized with COVID-19.


This was a prospective cohort with 201 hospitalized older adults with COVID-19. Chronic diseases, chest CT, laboratory tests, and other data were collected within the first 48 h of hospitalization. Outcomes were progression to severe respiratory failure with the need of mechanical ventilation (SRF/MV) and death.


The mean age was 72.7 ± 9.2 years, and 63.2% were men. SRF/MV occurred in 16.9% (p < 0.001), and death occurred in 8%. In the adjusted regression analyses, lung involvement over 50% [odds ratio (OR): 3.09 (1.03–9.28; 0.043)], C-reactive protein (CRP) > 80 ng/mL [OR: 2.97 (0.99–8.93; 0.052)], Vitamin D < 40 ng/mL [OR: 6.41 (1.21–33.88; 0.029)], and hemoglobin < 12 g/mL [OR: 3.32 (1.20–9.20; 0.020)] were independent predictors for SFR/MV, while chronic atrial fibrillation [OR: 26.72 (3.87–184.11; 0.001)], cancer history [OR:8.32 (1.28–53.91; 0.026)] and IL-6 > 40 pg/mL [OR:10.01 (1.66–60.13; 0.012)] were independent predictors of death.


In hospitalized older adults with COVID-19, tomographic pulmonary involvement > 50%, anemia, vitamin D below 40 ng/mL, and CRP above 80 mg/L were independent risk factors for progression to SRF/MV. The presence of chronic atrial fibrillation, previous cancer, IL-6 > 40 pg/mL, and anemia were independent predictors of death.

Peer Review reports


The COVID-19 pandemic has been characterized by severe impacts on the elderly population, who suffered high hospitalization rates, unfavorable clinical evolution, and substantial mortality [1]. In the United States, older adults accounted for 31% of cases with clinical manifestations, 45% of hospitalizations, and 53% of admissions to intensive care units (ICU). Approximately 80% of fatal cases occurred among people over 65 years old, 46% between 65 and 84 years old, and 34% among those over 85 years old [1].

Acute respiratory distress syndrome is the primary clinical manifestation of severe disease and the strongest predictor of mortality from COVID-19, especially when requiring mechanical ventilation [2]. Age above 65 years is an independent predictor for acute respiratory distress syndrome [3], and this could be caused by the dysfunction of the immune system associated with aging, with exacerbated inflammatory reactions and decreased anti-inflammatory responses (Inflammaging) [4]. Additionally, the elderly have a higher prevalence of chronic diseases, physical frailty, and malnutrition that stimulate the increase in inflammatory interleukins and hypercoagulation states [5, 6]. Laboratory values that can help diagnose these conditions are high levels of neutrophils, C-reactive protein (CRP), troponin, myoglobin, d-dimer, lactate dehydrogenase (LDH), and IL-6; these parameters and low lymphocyte counts predict progression to respiratory failure and death [7,8,9,10].

Nevertheless, the relationship of chronic diseases and imaging and laboratory parameters with the development of respiratory failure and mortality due to COVID-19 in the elderly remains poorly understood [6, 11, 12]. To better understand these associations, we determined the predictive value of chronic comorbidities, pulmonary involvement by chest CT, and laboratory tests at the time of hospitalization, with respiratory failure requiring mechanical ventilation and mortality in an elderly population hospitalized with SARS-Cov-2 infection.


Study design

This was a prospective cohort study of older adults with confirmed SARS-Cov-2 infection hospitalized for COVID-19.

Study sample

We considered 201 participants (Fig. 1). Inclusion criteria were age over 60 years and have a positive RT-PCR for SARS-CoV-2 at the time of hospitalization. Exclusion criteria were previously diagnosed moderate or severe dementia, use of prohibited medications (previous use of corticosteroids > 7.5 mg/day of methyl prednisolone for more than 3 months, use of immunosuppressants, chemotherapeutic agents, biological immunomodulators).

Fig. 1
figure 1

Flowchart of the study design

This study followed the relevant ethical guidelines and regulations as described in the Declaration of Helsinki and was approved by the Ethics Committee of the Hospital Israelita Albert Einstein and of Plataforma Brasil under the numbers: 4.082.096 e 4.186.636.

All participants, caregivers, or family members provided written or electronic consent (after a telephone conversation in the latter’s case). Participants were followed during their entire hospital stay and up to 30 days after hospital discharge. Four inpatients remained at the end of the study, all with more than 60 days in the hospital.


Demographic data, ethnicity, health habits (smoking and drinking), education (years) and marital status, and variables of interest (described below) were evaluated. All information was collected by phone call or from the electronic medical record.

Concomitant medications

Information on chronic medications was obtained. During hospitalization, uses of corticosteroids (oral or intravenous), vitamin D, tocilizumab, oseltamivir, remdesivir, and convalescent plasma were evaluated.

Chronic diseases

Hypertension, diabetes mellitus, heart failure, previous myocardial infarction, atrial fibrillation, history of stroke, asthma, osteoporosis, osteoarthritis, previous bone fracture, Parkinson’s disease, Alzheimer’s disease, chronic kidney disease (CKD) (non-hemodialysis (HD)), end-stage renal disease (on HD), current and previous cancer, falls in the previous 6 months, and physical frailty. Chronic diseases were assessed with a family member or caregiver.

To assess the presence of physical frailty, the FRAIL questionnaire [13] was used as it does not involve any physical performance activities to avoid the risk of staff contamination and recognizing the limits of the participants’ clinical conditions. A final score of 3 or more was considered frail, while 1 or 2 indicated pre-frail, and zero indicated robust.

Laboratory tests

Complete blood count (hemoglobin (Hb), total leucocytes (TLeuc), total lymphocytes (TLymp), 25-hydroxyvitamin D (25(OH)D), alanine transaminase (ALT), aspartate aminotransferase (AST), CRP, interleukin 6 (IL-6), D-dimer, creatinine (Creat), myoglobin (Myo) were collected during the first 48 h of hospitalization. Laboratory tests were assessed as categorical variables in the form of quartiles.

The following quartiles were used in the analyses of the association with clinical outcomes:

  • Lower quartiles:

    • Hemoglobin (< 11.7 g/mL, approximated to 12 g/ml, was defined as anemia)

    • Total lymphocytes (< 597/μL, approximated to 600/μL)

  • Higher quartiles:

    • D-dimer (> 1046 ng/mL, approximated to 1000 ng/mL)

    • CRP (> 80.8 mg/L, approximated to 80 mg/L)

    • IL-6 (> 39.7 pg/mL, approximated to 40 pg/mL)

    • Creatinine (> 1.13 mg/dL, approximated to 1.1 mg/dL)

    • Myoglobin (> 63.34 ng/mL, approximated to 65 ng/mL)

    • TLeuc (> 9570/μL, approximated to 10,000/μL)

    • 25(OH)D (> 38 ng/dL, approximated to 40 ng/dL)

    • ALT (> 42 U/mL, approximated to 40 U/mL)

    • AST (> 48 U/mL, approximated to 50 U/mL)

Pulmonary involvement as assessed by chest CT

Pulmonary involvement was based on the chest CT performed 48 h pre- or post-hospitalization. All patients were scanned in the supine position from the lung apex to the diaphragm during end-inspiration using a 64-slice CT scanner. We recorded the presence of typical factors such as ground-glass reticular opacities, with or without consolidations, were quantified, and the pulmonary involvement, in percentages.

For this study, chest CT involvement was classified as:

  1. I-

    No involvement (no affected area)

  2. II-

    Mild impairment (affected area up to 24%)

  3. III-

    Moderate impairment (affected area 25–49%)

  4. IV-

    Severe impairment (affected area > 50%)


The clinical outcomes evaluated were severe respiratory failure with the need for mechanical ventilation (SRF/MV), death during the hospital stay, and up to 30 days after discharge. These outcomes were assessed by daily monitoring of the electronic medical record by a study team member. Vital status was confirmed by each subject’s physician or by the hospital’s medical team.

Statistical analyses

The sample size was based on previous literature [14,15,16,17] and an estimate of the number of participants admitted to the hospital with a confirmed SARS-CoV-2 infection.

For the analyses, the four participants who remained hospitalized on the final day of the follow-up were included; however, their data were truncated at the end of the study.

To compare groups, the chi-square test and the analysis of variance were used for qualitative and quantitative variables, respectively.

To determine which factors predicted outcomes, we initially evaluated those that showed significance in the correlation test with p < 0.09. Then, a logistic regression analysis was performed for each factor in a univariate form; factors that remained significant were then evaluated in an adjusted analysis. In the end, only factors with p < 0.05 were considered statistically significant. Statistical software SPSS version 22.0 (SPSS, Inc., Chicago, IL, USA) was used for all analyses. Statistical significance was set at p < 0.05.


The mean age was 72.7 years (± 9.2 years), with 44 (21.9%) aged ≥80 years (Table 1). The vast majority were Caucasian (n = 187, 93%) and 127 (63.2%) were men. Our sample was composed of highly educated people (average of 13.9 years of study, 61.5% of whom had more than 13 years of formal education) compared to the average in the population (9.4 years) [18]. At the end of the study, 181 (90%) were discharged, 15 of whom were readmitted within 30 days (Fig. 1).

Table 1 Demographic characteristics according to clinical outcomes

Thirty-four (16.9%) participants progressed to respiratory failure with the need of mechanical ventilation, and 16 (8%) died (15 in-hospital and one during the 30-day follow-up after discharge) (Table 2).

Table 2 Laboratory results according to clinical outcomes


The patients who died were older (> 80 years), had a higher prevalence of chronic atrial fibrillation, CKD, and a tendency to have had a history of cancer. There was no gender predominance, and all were Caucasian. Severe pulmonary involvement at the beginning of the study was not statistically associated with death during hospitalization. The laboratory characteristics of the elderly who died were high levels of CRP, IL-6, D-dimer, leukocytes, and creatinine, and low hemoglobin levels.

Most deceased patients had hospital stays beyond 18 days (n = 12; 75%; p < 0.001), were transferred to the ICU (n = 13; 81.3%; p < 0.001), and almost all required mechanical ventilation (n = 14, 87.5%; p < 0.001). Higher leucocytes lost statistical significance in the univariate logistic regression analysis, and history of cancer remained borderline (Table 2), while the others remained significant. On adjusted logistic regression analysis, atrial fibrillation, history of cancer, and high IL-6 levels remained significant, while anemia remained borderline (Fig. 2).

Fig. 2
figure 2

Odds ratio graph for death (non-adjusted and adjusted). Legend: dotted line (−-----): non-adjusted logistic regression analyses; continuous line ( ): adjusted logistic regression analyses for all significant variables. Variables evaluated without adjustment: Age > 80 = individuals aged 80 years or more; CKD = chronic kidney disease; Prior cancer, Atrial Fib = prior atrial fibrillation, IL-6 = interleukin 6 > 40 pg/mL, CRP = C-reactive protein> 80 mg/L; D dimer = d dimer> 1000 ng/ml, Hemoglobin = hemoglobin< 12 g/mL; Leucocytes = leucocytes > 10.000 μL; Creatinine = creatinine > 1.1 mg/dL; Myoglobin = myoglobin> 65 ng/mL). Variables evaluated with adjustment: Age > 80 Adj = individuals aged 80 years or more; CKD Adj = chronic kidney disease; Prior cancer Adj, Atrial Fib Adj = prior atrial fibrillation, IL-6 Adj = interleukin 6 > 40 pg/mL; CRP Adj = C-reactive protein> 80 mg/L; D dimer Adj = d dimer> 1000 ng/ml, Hemoglobin Adj = hemoglobin< 12 g/mL; Creatinine Adj = creatinine > 1.1 mg/dL; Myoglobin Adj = myoglobin> 65 ng/mL)

Severe respiratory failure and mechanical ventilation

Elderly patients who progressed to SSRF/MV were characterized by a higher prevalence of chronic atrial fibrillation, chronic kidney disease (non-HD), and end-stage renal disease (on HD). Severe pulmonary involvement and higher levels of CRP, IL-6, D-dimer, AST, creatinine, myoglobin, and lower levels of Tlymp, Hb, and 25(OH)D were associated with respiratory failure (Table 1). 14 (41.2%) died among these patients, and 30 (88.2%) stayed in the hospital for a prolonged period.

In the analyses with all statistically significant variables in the univariate logistic regression, severe pulmonary involvement, high CRP, low hemoglobin, and vitamin D predicted respiratory failure with the need for mechanical ventilation (Fig. 3).

Fig. 3
figure 3

Odds ratio graphs for severe respiratory failure (non-adjusted and adjusted). Legend: dotted line (------): non-adjusted logistic regression analyses. Continuous line ( ): adjusted logistic regression analyses for all significant variables. Variables evaluated without adjustment: Age > 80 = individuals aged 80 years or more; CKD = chronic kidney disease; CT scan = thomographic lung involvement over 50%; Marital status; Atrial Fib = prior atrial fibrillation, Vitamin D = vitamin D < 40 ng/dl; IL-6 = interleukin 6 > 40 pg/mL, CRP = C-reactive protein> 80 mg/L; D dimer = d dimer> 1000 ng/ml, Hemoglobin = hemoglobin< 12 g/mL; Leucocytes = leucocytes > 10.000 μL; Lymphocytes = lymphocytes < 600/μL; AST = aspartate aminotransferase > 50 U/mL; Creatinine = creatinine > 1.1 mg/dL; Myoglobin = myoglobin> 65 ng/mL). Variables evaluated with adjustment: Age > 80 Adj = individuals aged 80 years or more; CKD Adj = chronic kidney disease; CT scan Adj = lung involvement over 50%; Marital status Adj; Atrial Fib Adj = prior atrial fibrillation, Vitamin D Adj = vitamin D < 40 ng/dl; IL-6 Adj = interleukin 6 > 40 pg/mL, CRP Adj = C-reactive protein> 80 mg/L; D dimer Adj = d dimer> 1000 ng/ml, Hemoglobin Adj = hemoglobin< 12 g/mL; AST Adj = aspartate aminotransferase > 50 U/mL; Creatinine Adj = creatinine > 1.1 mg/dL; Myoglobin Adj = myoglobin> 65 ng/mL)

Concomitant medications

During hospitalization, 182 (90.5%) participants received oral or intravenous corticosteroids, (1.99%) convalescent plasma, 3 (1.49%) received tocilizumab, 4 (1.99%) received oseltamivir and 1 (0.49%) participant received remdesevir. These medications did not influence the outcomes.


The main contribution of this study was our demonstration that there were significant associations between clinical, radiological, and laboratory parameters with the risk of progression to SRF/MV and death during hospital stays due to COVID-19 in an elderly population.

Anemia as an independent predictor of SRF/MV and mortality remains controversial. A meta-analysis [19] regarding hematologic parameters showed no significant difference between the hemoglobin levels of those who progressed to severe disease or death and patients who did not present these outcomes. Nevertheless, Tao et al. found results similar to ours; they observed that anemia diagnosed in the first 24 h of hospitalization significantly increased the risk of evolution o severe COVID-19 [20]. Wang et al. also found that hemoglobin levels were significantly lower among patients who needed ICU than those who did not [21]. Lower hemoglobin levels have been reported in COVID-19 patients [22, 23] and this may be associated with the intensity of the inflammatory process that interferes with the iron metabolism mediated by the increase in IL-6 and by the direct action of pro-inflammatory cytokines such as interferon-γ, IL-1, IL-33, and tumor necrosis factor (TNF)-α on erythropoiesis, characterized by decreased erythrocyte synthesis [24,25,26].

When evaluating the outcomes separately, lung involvement above 50%, CRP > 80 mg/L, and vitamin D < 40 ng/mL remained independent risk factors for SRF/MV. The prognostic value of lung involvement evaluated by chest CT scan varied substantially according to the type of population and period of disease [27]. Colombi et al. [28] showed that, in patients in the emergency room, radiological compromise appeared to predict progression to respiratory failure, need for ICU admission, and death, even among those with mild clinical symptoms. Cereser et al. evaluated high-resolution chest CTs of 77 hospitalized patients and observed that, after adjusting for age and comorbidity, severe pulmonary impairment increased the risk for respiratory failure by approximately eight times [29]. Turcato et al. demonstrated an inverse relationship between arterial oxygen pressure and pulmonary impairment, indicating that lung involvement can be a marker of functional impairment resulting from the inflammatory process [30]. Zhang et al. observed a significant difference between the average of inflammatory markers in patients with severe pulmonary involvement compared to those with less radiological involvement [31].

Our findings corroborate these previous findings; the mean of inflammatory markers (CRP and IL 6) in our study was about twice as high among those who progressed to SRF/MV (Table 2). Other factors related to the aging process, such as a decrease in the number of type II pneumocytes, alveolar stiffening, decreased exchange of carbon dioxide and oxygen, lower vital capacity, and respiratory muscle weakness resulting from sarcopenia, may also contribute to early respiratory failure in the elderly [32]. In our view, and that of others, the inflammatory process appears to play a decisive role in the evolution of these patients to SRF/MV and death, even more so among the elderly that might already suffer from Inflammaging [4].

One of the laboratory parameters that surprised us was that serum vitamin D < 40 ng/dl was an independent risk factor for SRF/MV, even after adjusting for all other factors established in the literature [15,16,17, 26, 28, 30, 31]. In our study, low vitamin D was a significant predictor of SRF/MV but not for death, and this could be due to the participation of vitamin D in the immune system through several pathways. It stimulates macrophages to produce 1,25 (OH)-2-vitamin-D that acts as an anti-inflammatory, inhibiting the activation of B-cells and immunoglobulin synthesis [33], and as an anti-infectious agent by inducing the production of IL-10 in Treg cells. It also promotes Th2 cells that limit the inflammatory process and decreases the production of tumor necrosis factor α [34,35,36]. It is worth mentioning that the critical inverse relationship between serum vitamin D levels and IL-6 levels is considered one of the principal factors of the inflammatory storm [37]. Another factor related to the lower vitamin D effect can be attributed to its influence on the renin-angiotensin system, and ACE2 receptors found in various organs [38] and decrease with aging [39]. The decrease in ACE2 receptors has been associated with higher mortality by COVID-19, whereas the higher expression, mainly in the lungs, was related to a better outcome and a lower incidence of acute lung injury [40]. Vitamin D increases the expression of ACE2 receptors but also modulates the genetic expression of renin, resulting in a smaller effect of renin on its receptor; that is, there is less chance of pulmonary vasoconstriction and myocardial injury, less renal perfusion, pulmonary edema, and renal and myocardial failure seen in severe COVID-19 [41,42,43,44]. The protective effect of vitamin D by the renin-angiotensin system concerning COVID-19 remains unclear. The use of prior vitamin D supplementation was high (56%); however, this fact did not significantly modify outcomes. Nevertheless, the significant differences among quartiles in the percentage of participants using vitamin D demonstrated that the lower risk of poor outcomes observed in the upper quartile might be related to the previous use of vitamin D. Although this may suggest that vitamin D supplementation may act as a protective factor, studies of vitamin D supplementation and its protective effect remain controversial [45,46,47]. Recently, a study evaluated high doses of vitamin D versus placebo and found no significant changes in the length of hospital stay and mortality from COVID-19 [48].; on the other hand, another study found that vitamin D supplementation was associated with a trend toward higher mortality [49], and yet another study found a significant reduction in the need for ICU care [50].

Our study’s overall mortality rate was 8%, with a higher rate in participants aged ≥80 years (17.8%). Bonanad et al. showed a mortality rate in people over 60 years of 12.1, and 29.6% among those over 80 years old with COVID-19 [51]. Contrary to other studies, age above 80 years did not remain a significant factor after adjustment for several variables, suggesting that the clinical vulnerability determined by chronic diseases and the intensity of the inflammatory process may surpass age as a determinant of death. In our study, atrial fibrillation and previous cancer history remained significant after adjusting for inflammatory variables. The influence of these comorbidities with factors independent of death suggests that a phenotype of physical frailty may be present. However, we did not detect a significant correlation between the diagnosis of frailty and death when using the adapted FRAIL scale. This was also noted by Baktashet et al. that showed that frailty, diagnosed by the Rockwood questionnaire [52], did not change the mortality rate or the risk of a more extended hospital stay [16]. Some factors may explain this finding, including the type of instrument used to diagnose frailty, as both the FRAIL [13] and the Rockwood [52] questionnaires are subjective. In our study, the subjectivity bias may have been even greater, since in about 50% of the cases, information was collected from the caregiver, who may under or overestimate the frailty criteria. We opted not to use instruments as the one described by Fried et al. [53] as they involve objective measures of physical performance, and this could pose a risk of COVID-19 transmission to the research team, and the clinical condition of the participant with respiratory difficulty could modify the physical performance tests.

Our study has limitations. The study population may have a selection bias as the refusal by some physicians and participants/family members could be related to the severity of the clinical condition; consequently, we may have underrepresented the number of individuals with a higher chance of death. In our study, it was not possible to distinguish whether the anemia was acute or chronic, since we did not specifically ask about previous anemia nor did we have access to previous laboratory tests. During hospitalization we did not follow D dimer levels of the patients, nor did we evaluate whether the physicians prescribed new AC drugs or changed old ones. This did not enable us to assess whether AC significantly modified the rate of death and respiratory failure. We did not assess respiratory parameters such as respiratory rate, oxygen pressure, and arterial CO2 values, which are significant predictors of severe outcomes.


In hospitalized older adults with COVID-19, tomographic pulmonary involvement > 50%, anemia, vitamin D below 40 ng/mL, and CRP above 80 mg/L are independent factors for progression to severe respiratory failure and the need for mechanical ventilation. The presence of chronic atrial fibrillation, previous cancer, IL-6 > 40 pg/mL, and anemia were independent predictors of death.


Studies are still needed to better understand the etiology of anemia in the older adults hospitalized for COVID-19, as well as whether its correction may result in modification of severe outcomes. The identification of the risk factors described above may be of great importance for early adoption of therapies in these patients. Vitamin D supplementation to achieve levels equivalent to or greater than 40 ng/ml may be useful in elderly patients, with the goal of improving immunity and achieving better control of the inflammatory response. However, randomized controlled studies in elderly patients are still needed to confirm this possibility.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.





alanine transaminase


aspartate aminotransferase


chronic kidney disease (non-hemodialysis)




C-reactive protein


computed tomography


end-stage renal disease (on HD)






intensive care units




lactate dehydrogenase




severe respiratory failure with the need of mechanical ventilation


total leucocytes


total lymphocytes


tumor necrosis factor


  1. CDC COVID-19 Response Team. Severe Outcomes Among Patients with Coronavirus Disease 2019 (COVID-19) — United States, February 12–March 16, 2020. MMWR Morb Mortal Wkly Rep. 2020;69:343–346. DOI:

  2. Guan W, Ni Z, Hu Y, Liang W, Ou C, He J, et al. Clinical characteristics of coronavirus disease 2019 in China. N Engl J Med. 2020;382(18):1708–20 Available from:

    CAS  Article  Google Scholar 

  3. Xu X-W, Wu X-X, Jiang X-G, Xu K-J, Ying L-J, Ma C-L, et al. Clinical findings in a group of patients infected with the 2019 novel coronavirus (SARS-Cov-2) outside of Wuhan, China: retrospective case series. BMJ. 2020;27;368:m792.

  4. Franceschi C, Capri M, Monti D, Giunta S, Olivieri F, Sevini F, et al. Inflammaging and anti-inflammaging: a systemic perspective on aging and longevity emerged from studies in humans. Mech Ageing Dev. 2007;128(1):92–105 Available from:

    CAS  Article  Google Scholar 

  5. Ye Q, Wang B, Mao J. The pathogenesis and treatment of the `cytokine storm’ in COVID-19. J Infect. 2020;80(6):607–13 Available from:

    CAS  Article  Google Scholar 

  6. Rizzo P, Vieceli Dalla Sega F, Fortini F, Marracino L, Rapezzi C, Ferrari R. COVID-19 in the heart and the lungs: could we “Notch” the inflammatory storm? Basic Res Cardiol. 2020;115(3):31. Available from:

  7. Laguna-Goya R, Utrero-Rico A, Talayero P, Lasa-Lazaro M, Ramirez-Fernandez A, Naranjo L, et al. IL-6–based mortality risk model for hospitalized patients with COVID-19. J Allergy Clin Immunol. 2020;146(4):799-807.e9.

  8. Blanco-Melo D, Nilsson-Payant BE, Liu W-C, Uhl S, Hoagland D, Møller R, et al. Imbalanced Host Response to SARS-CoV-2 Drives Development of COVID-19. Cell. 2020;181(5).

  9. Chen G, Wu D, Guo W, Cao Y, Huang D, Wang H, et al. Clinical and immunological features of severe and moderate coronavirus disease 2019. J Clin Invest. 2020;130(5):2620–9 Available from:

    CAS  Article  Google Scholar 

  10. Huang C, Wang Y, Li X, Ren L, Zhao J, Hu Y, et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet. 2020;395(10223).

  11. Prietl B, Treiber G, Pieber T, Amrein K. Vitamin D and immune function. Nutrients. 2013;5(7):2502–21 Available from:

    CAS  Article  Google Scholar 

  12. Biesalski HK. Vitamin D deficiency and co-morbidities in COVID-19 patients – A fatal relationship? NFS J. 2020;20:10–21. Available from:

  13. Morley JE, Malmstrom TK, Miller DK. A simple frailty questionnaire (FRAIL) predicts outcomes in middle aged African Americans. J Nutr Health Aging. 2012;16(7):601–8 Available from:

    CAS  Article  Google Scholar 

  14. Carpagnano GE, Di Lecce V, Quaranta VN, Zito A, Buonamico E, Capozza E, et al. Vitamin D deficiency as a predictor of poor prognosis in patients with acute respiratory failure due to COVID-19. J Endocrinol Invest. 2021;44(4):765–71 Available from:

    CAS  Article  Google Scholar 

  15. De Smet D, De Smet K, Herroelen P, Gryspeerdt S, Martens GA. Serum 25(OH)D level on hospital admission associated with COVID-19 stage and mortality. Am J Clin Pathol. 2021;155(3):381–8 Available from:

    Article  Google Scholar 

  16. Baktash V, Hosack T, Patel N, Shah S, Kandiah P, Van den Abbeele K, et al. Vitamin D status and outcomes for hospitalised older patients with COVID-19. Postgrad Med J. 2020;postgradmedj-2020-138712. Available from:

  17. Radujkovic A, Hippchen T, Tiwari-Heckler S, Dreher S, Boxberger M, Merle U. Vitamin D Deficiency and Outcome of COVID-19 Patients. Nutrients. 2020;12(9):2757. Available from:

  18. Villas Bôas B. IBGE: População sem instrução cai e tempo médio de estudo atinge 9,4 anos. Valor Econômico. 2020 [cited 2021 May 8]. Available from:

  19. Henry BM, de Oliveira MHS, Benoit S, Plebani M, Lippi G. Hematologic, biochemical and immune biomarker abnormalities associated with severe illness and mortality in coronavirus disease 2019 (COVID-19): a meta-analysis. Clin Chem Lab Med. 2020;58(7):1021–8 Available from:

    CAS  Article  Google Scholar 

  20. Tao Z, Xu J, Chen W, Yang Z, Xu X, Liu L, et al. Anemia is associated with severe illness in COVID-19: a retrospective cohort study. J Med Virol. 2021;93(3):1478–88 Available from:

    CAS  Article  Google Scholar 

  21. Wang C, Deng R, Gou L, Fu Z, Zhang X, Shao F, et al. Preliminary study to identify severe from moderate cases of COVID-19 using combined hematology parameters. Ann Transl Med. 2020;8(9):593 Available from:

    CAS  Article  Google Scholar 

  22. Taneri PE, Gómez-Ochoa SA, Llanaj E, Raguindin PF, Rojas LZ, Roa-Díaz ZM, et al. Anemia and iron metabolism in COVID-19: a systematic review and meta-analysis. Eur J Epidemiol. 2020;35(8):763–73 Available from:

    CAS  Article  Google Scholar 

  23. Bellmann-Weiler R, Lanser L, Barket R, Rangger L, Schapfl A, Schaber M, et al. Prevalence and Predictive Value of Anemia and Dysregulated Iron Homeostasis in Patients with COVID-19 Infection. J Clin Med. 2020;9(8):2429. Available from:

  24. Weiss G, Goodnough LT. Anemia of chronic disease. N Engl J Med. 2005;352(10):1011–23 Available from:

    CAS  Article  Google Scholar 

  25. Ganz T. Anemia of Inflammation. Longo DL, editor. N Engl J Med. 2019;381(12):1148–57. Available from:

  26. Bergamaschi G, Borrelli de Andreis F, Aronico N, Lenti MV, Barteselli C, Merli S, et al. Anemia in patients with Covid-19: pathogenesis and clinical significance. Clin Exp Med. 2021;21(2):239–46. Available from:

  27. Safiabadi Tali SH, LeBlanc JJ, Sadiq Z, Oyewunmi OD, Camargo C, Nikpour B, et al. Tools and Techniques for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2)/COVID-19 Detection. Clin Microbiol Rev. 2021;34(3). Available from:

  28. Colombi D, Bodini FC, Petrini M, Maffi G, Morelli N, Milanese G, et al. Well-aerated lung on admitting chest CT to predict adverse outcome in COVID-19 pneumonia. Radiology. 2020;296(2):E86–96 Available from:

    Article  Google Scholar 

  29. Cereser L, Da Re J, Zuiani C, Girometti R. Chest high-resolution computed tomography is associated to short-time progression to severe disease in patients with COVID-19 pneumonia. Clin Imaging. 2021;70:61–6. Available from:

  30. Turcato G, Panebianco L, Zaboli A, Scheurer C, Ausserhofer D, Wieser A, et al. Correlation between arterial blood gas and CT volumetry in patients with SARS-CoV-2 in the emergency department. Int J Infect Dis. 2020;97:233–5 Available from:

    CAS  Article  Google Scholar 

  31. Zhang N, Xu X, Zhou L-Y, Chen G, Li Y, Yin H, et al. Clinical characteristics and chest CT imaging features of critically ill COVID-19 patients. Eur Radiol. 2020;30(11):6151–60 Available from:

    CAS  Article  Google Scholar 

  32. Cho SJ, Stout-Delgado HW. Aging and Lung Disease. Annu Rev Physiol. 2020;82(1):433–59 Available from:

    CAS  Article  Google Scholar 

  33. Li H, Liu L, Zhang D, Xu J, Dai H, Tang N, et al. SARS-CoV-2 and viral sepsis: observations and hypotheses. Lancet. 2020;395(10235):1517–20 Available from:

    CAS  Article  Google Scholar 

  34. Meftahi GH, Jangravi Z, Sahraei H, Bahari Z. The possible pathophysiology mechanism of cytokine storm in elderly adults with COVID-19 infection: the contribution of “inflame-aging.” Inflamm Res 2020;69(9):825–839. Available from:

  35. Park MD. Macrophages: a Trojan horse in COVID-19? Nat Rev Immunol. 2020;20(6):351 Available from:

    CAS  Article  Google Scholar 

  36. Zheng M, Gao Y, Wang G, Song G, Liu S, Sun D, et al. Functional exhaustion of antiviral lymphocytes in COVID-19 patients. Cell Mol Immunol. 2020;17(5):533–5 Available from:

    CAS  Article  Google Scholar 

  37. De Vita F, Lauretani F, Bauer J, Bautmans I, Shardell M, Cherubini A, et al. Relationship between vitamin D and inflammatory markers in older individuals. Age (Omaha). 2014;36(4):9694. Available from:

  38. loganathan S, Kuppusamy M, Wankhar W, Gurugubelli KR, Mahadevappa VH, Lepcha L, et al. Angiotensin-converting enzyme 2 (ACE2): COVID 19 gate way to multiple organ failure syndromes. Respir Physiol Neurobiol. 2021;283:103548. Available from:

  39. Xudong X, Junzhu C, Xingxiang W, Furong Z, Yanrong L. Age- and gender-related difference of ACE2 expression in rat lung. Life Sci. 2006;78(19):2166–71 Available from:

    Article  Google Scholar 

  40. Kuba K, Imai Y, Penninger J. Angiotensin-converting enzyme 2 in lung diseases. Curr Opin Pharmacol. 2006;6(3):271–6 Available from:

    CAS  Article  Google Scholar 

  41. Easty DJ, Farr CJ, Hennessy BT. New Roles for Vitamin D Superagonists: From COVID to Cancer. Front Endocrinol (Lausanne). 2021;12. Available from:

  42. Hamming I, Timens W, Bulthuis M, Lely A, Navis G, van Goor H. Tissue distribution of ACE2 protein, the functional receptor for SARS coronavirus. A first step in understanding SARS pathogenesis. J Pathol. 2004;203(2):631–7. Available from:

  43. Li YC, Kong J, Wei M, Chen Z-F, Liu SQ, Cao L-P. 1,25-Dihydroxyvitamin D3 is a negative endocrine regulator of the renin-angiotensin system. J Clin Invest. 2002;110(2):229–38 Available from:

    CAS  Article  Google Scholar 

  44. Yuan W, Pan W, Kong J, Zheng W, Szeto FL, Wong KE, et al. 1,25-Dihydroxyvitamin D3 suppresses renin gene transcription by blocking the activity of the cyclic AMP response element in the renin gene promoter. J Biol Chem. 2007;282(41):29821–30 Available from:

    CAS  Article  Google Scholar 

  45. Turrubiates-Hernández F, Sánchez-Zuno G, González-Estevez G, Hernández-Bello J, Macedo-Ojeda G, Muñoz-Valle J. Potential immunomodulatory effects of vitamin D in the prevention of severe coronavirus disease 2019: An ally for Latin America (Review). Int J Mol Med. 2021;47(4):32. Available from:

  46. Subedi L, Tchen S, Gaire BP, Hu B, Hu K. Adjunctive Nutraceutical Therapies for COVID-19. Int J Mol Sci. 2021;22(4):1963. Available from:

  47. Lotfi M, Hamblin MR, Rezaei N. COVID-19: transmission, prevention, and potential therapeutic opportunities. Clin Chim Acta. 2020;508:254–66. Available from:

  48. Murai IH, Fernandes AL, Sales LP, Pinto AJ, Goessler KF, Duran CSC, et al. Effect of a Single High Dose of Vitamin D 3 on Hospital Length of Stay in Patients With Moderate to Severe COVID-19. JAMA. 2021 ;325(11):1053. Available from:

  49. Cereda E, Bogliolo L, Lobascio F, Barichella M, Zecchinelli AL, Pezzoli G, et al. Vitamin D supplementation and outcomes in coronavirus disease 2019 (COVID-19) patients from the outbreak area of Lombardy, Italy. Nutrition 2021;82:111055. Available from:

  50. Entrenas Castillo M, Entrenas Costa LM, Vaquero Barrios JM, Alcalá Díaz JF, López Miranda J, Bouillon R, et al. “Effect of calcifediol treatment and best available therapy versus best available therapy on intensive care unit admission and mortality among patients hospitalized for COVID-19: A pilot randomized clinical study.” J Steroid Biochem Mol Biol. 2020;203:105751. Available from:

  51. Bonanad C, García-Blas S, Tarazona-Santabalbina F, Sanchis J, Bertomeu-González V, Fácila L, et al. The effect of age on mortality in patients with COVID-19: a Meta-analysis with 611,583 subjects. J Am Med Dir Assoc. 2020;21(7):915–8 Available from:

    Article  Google Scholar 

  52. Rockwood K. A global clinical measure of fitness and frailty in elderly people. Can Med Assoc J. 2005;173(5):489–95 Available from:

    Article  Google Scholar 

  53. Fried LP, Tangen CM, Walston J, Newman AB, Hirsch C, Gottdiener J, et al. Frailty in older adults: Evidence for a phenotype. Journals Gerontol - Ser A Biol Sci Med Sci. 2001;56(3):M146--56. Available from:

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We would like to thank Sandra Carvalho and Fernanda Ferraz Assis for help with all the administrative work in this study.

We would also like to thank the physicians that cared for each participant enrolled in this study: Adriano Oliveira Seixas; Alexandre Segre; Alvaro José Federihi; Alvaro Pacheco e Silva Filho; Amit Nussbacher; Antonio Carlos Bacelar Nunes Filho; Antonio Eduardo Pereira Pesaro; Antonio Sergio de Santos Andrade Lopes; Artur Malzyner; Arthur Rothman; Artur Malzyner; Bernardino Thanchesi Junior; Bruno de Arruda Bravim; Caio de Assis Moura Tavares; Carlos Alberto Franchin Neto; Carlos David Carvalho Nascimento; Carlos Vicente Serrano Junior; Carmen Silvia Valente Barbas; Christian Wilhem Gerner de Albuquerque; Clederson Henry Dina; Clineu de Mello Almada; Cristiane Hoelz; Cristiano Rabello Nogueira; Dan Oizerovici; Daniel Sigulem; David Salomão Lewi; Dirceu Hamilton Cordeiro Campleo; Donato Callegaro Filho; Eduardo Correa Meyer; Elcio Pfeferman; Elias Knobel; Erika Maria do Nascimento Kalmar; Fabio Grunspun Pitta; Fabricio Rodrigues Torres de Carvalho; Fabrício Torres de Carvalho; Fabiana Hanna Rachea; Fernando Bacal; Fabio Nasri; Felix Martiniano de Magalhães; Fernando Bacal; Fernando Gatti de Menezes; Fernando Maluf; Flavio Tarasoutchi; Guilherme Benfatti Olivato; Guilherme Linhares Bub; Gustavo Faissol Janot de Matos; Gustavo Henrique Johanson; Helio Arthur Bacha; Helio Romaldini; Humberto Bassit Bogossian; Italo Menezes Andteam; Jairo Tabacon Hidal; Jeancarlo Gorinchteyn; José Campos Filho; José Antonio Domingos C. Longo; José Augusto Marcondes de Souza; José Campos Filho; José Luiz Bonamigo Filho; José Eduardo Afonso Junior; José Renato Martines Martins; Laercio Antonio da Silva; Leandro Santini Echenique; Leonardo José Rolim Ferraz; Luis Fernando Aranha Camargo; Luis Otavio Sales Ferreira Caboclo; Luiz Antonio Massa; Luiz Antonio Raio Granja; Manes Roberto Erlichman; Marcela Costa Batista; Marcelo Dratcu; Marcelo Franken; Marcelo Hisato Kuwakino; Marcelo Nobrega Litvoc; Marcos Knobel; Maria Candida Faria Rizzo; Maria do Carmo Sitta; Mario Claudio Ghefter; Mario Luiz Brusque Severo de Lima; Mauricio Bernstein; Mauricio Pegaro; Mauricio Wajngarten; Milton Rodrigues Junior; Moacyr Silva Jr.; Murillo Santucci Cesar de Assunção; Nelson Hamerschlak; Newton Luiz Russi Callegari; Patricia Tachner Goldenstein; Rafael de Biase; Rafael Medeiros Carraro; Ricardo Borges Magaldi; Ricardo Henrique de Oliveira Braga Teixeira; Ricardo Borges Magaldi; Ricardo Botticini Peres; Riguel Jun Inaoka; Roberto Hirsch; Roberto Sebastian Zeballos; Sandrigo Mangini; Sergio Barsoniti Wey; Sergio do Carmo Jorge; Sergio Flavio Albuquerque Felizola; Silvia Vidal Campos; Sonia Perez Cendon Filha; Telma Antunes; Thiago Zinsly Sampaio Camargo; Zarifa Khoury; Zsuzsanha Ilona Katalin de Jamydi Bella.

Finally, we would like to thank Hypera Pharma Brazil, especially Talita Poli Biasson and Edgar Policelli, for funding this study. The sponsor had no role in the design, methods, subject recruitment, data collections, analysis and preparation of this paper.


This research was funded by Hypera Pharma Group, Brazil.

The sponsor in no way influenced the results of this research; the sponsor did not participate in the study design, data collection, analysis and interpretation or in the manuscript writing process.

We have not signed an agreement with the sponsor that prevents us from publishing both positive and negative results or that forbids us from publishing this research without the prior approval of the sponsor.

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Accordance statement and authors' specific areas of contributions: Statements; All authors confirm authorship and participation in the preparation of the manuscript. This material has not been previously published, is not presently under consideration for publication elsewhere, nor will it be submitted elsewhere while it is under reviewed by your Journal. No other submissions or publications include material that is largely duplicative of that presented in the manuscript or derived from the same subjects. If accepted, the paper will not be published elsewhere in the same form, in English or in any other language, including electronically, without the written consent of the copyright holder. No references were blacked-out. The authors declare that they agree with all the statements presented in this manuscript. This manuscript had been read and approved by all authors. Authors' specific areas of contributions; AFJ, EA, SJMI, JCCG: Study concept and design. EL, EA: Acquisition of data. AFJ, SJMI, ATP, JCCG: Analysis and interpretation of data. AFJ, SJMI, ATP: Drafting of the manuscript. AFJ, SJMI: Critical revision of the manuscript for important intellectual content.

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Correspondence to Alberto Frisoli Junior.

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The authors confirm that all the methodology used in this study was carried out in accordance with the relevant ethical guidelines and regulations described in the Declaration of Helsinky. All participants or caregivers / family members signed the Informed Consent Form (ICF). The signing was performed in person by a member of the study team or through an electronic document sent to the participant, after a phone call in which the ICF was read and explained by a member of the study team. The project and Informed Consent Form (ICF) were approved by the Ethics Committee of the Hospital Israelita Albert Einstein and of Plataforma Brasil under the numbers: 4.082.096 e 4.186.636 .

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Junior, A.F., Azevedo, E., Paes, A.T. et al. Chronic diseases, chest computed tomography, and laboratory tests as predictors of severe respiratory failure and death in elderly Brazilian patients hospitalized with COVID-19: a prospective cohort study. BMC Geriatr 22, 132 (2022).

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  • COVID-19
  • Respiratory failure
  • Elderly
  • Mortality
  • Vitamin D
  • Anemia