Literature DB >> 32752589

Association of Comorbidities With Pneumonia and Death Among COVID-19 Patients in Mexico: A Nationwide Cross-sectional Study.

Akram Hernández-Vásquez1, Diego Azañedo2, Rodrigo Vargas-Fernández3, Guido Bendezu-Quispe4.   

Abstract

OBJECTIVES: The goal of this study was to identify chronic conditions and multimorbidity patterns in patients with coronavirus disease 2019 (COVID-19) and to examine their associations with pneumonia and death.
METHODS: This cross-sectional study analyzed the official data of COVID-19 patients in Mexico through May 18, 2020 (released by the Secretaría de Salud de México). Adjusted logistic regression models were applied to assess the associations of comorbidities with pneumonia and death. The marginal effects were estimated, and the probability of pneumonia or death according to the number of comorbidities was graphed for each year of age.
RESULTS: Of the 51 053 COVID-19 patients enrolled in the final analysis, 27 667 (54.2%) had no chronic conditions, while 13 652 (26.7%), 6518 (12.8%) and 3216 (6.3%) were reported to have 1, 2, and 3 or more simultaneous conditions, respectively. Overall, a significant incremental gradient was observed for the association between multimorbidity and pneumonia (p<0.001); for 2 chronic conditions, the adjusted odds ratio (aOR) was 2.07 (95% confidence interval [CI], 1.95 to 2.20), and for ≥3 conditions, the aOR was 2.40 (95% CI, 2.22 to 2.60). A significant incremental gradient was also found for the relationship between multimorbidity and death (p<0.001); an aOR of 2.51 (95% CI, 2.30 to 2.73) was found for 2 chronic conditions and an aOR of 3.49 (95% CI, 3.15 to 3.86) for ≥3 conditions.
CONCLUSIONS: Underlying chronic conditions and multimorbidity are associated with pneumonia and death in Mexican COVID-19 patients. Future investigation is necessary to clarify the pathophysiological processes behind this association, given the high burden of chronic diseases in various countries, including Mexico.

Entities:  

Keywords:  COVID-19; Comorbidity; Mexico; Multimorbidity; Severe acute respiratory syndrome coronavirus 2

Mesh:

Year:  2020        PMID: 32752589      PMCID: PMC7411245          DOI: 10.3961/jpmph.20.186

Source DB:  PubMed          Journal:  J Prev Med Public Health        ISSN: 1975-8375


INTRODUCTION

Coronavirus disease 2019 (COVID-19) is a recently-discovered infectious disease caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus that has quickly become a global pandemic. As of the writing of this report, more than 3 million cases and nearly 250 000 deaths have been documented. However, the epidemiology of the disease is still being studied, and much more information is required to establish adequate measures for its prevention and control, especially among patients vulnerable to severe disease (pneumonia) or death [1]. Several studies have demonstrated higher frequencies of severe cases and mortality among COVID-19 patients with underlying comorbidities, such as diabetes, high blood pressure (HBP), obesity, and cardiovascular disease (CVD), relative to patients without comorbidities [2,3]. Although the causal mechanisms by which chronic conditions increase the risk of COVID-19 severity and mortality are still being studied, it has been postulated that patients with HBP and diabetes have an increased susceptibility of severe SARS-CoV-2 infection [4,5]. It has also been proposed that SARS-CoV-2 infection may cause or worsen endotheliitis, which can further affect the condition of people with previous endothelial dysfunction, such as those with obesity, diabetes, HBP, and other CVDs [5]. This raises the question of how multimorbidity—the presence of 2 or more chronic comorbidities—may influence disease severity and mortality in patients with SARS-CoV-2 infection. Mexico has one of the highest COVID-19 mortality rates among Latin American countries. As of May 18, 2020, more than 20 000 confirmed cases and 2154 deaths attributed to COVID-19 had been reported in Mexico [1]. The potential associations of multimorbidity with disease severity and mortality in COVID-19 patients have received special attention in Mexico, as it is one of the Latin American countries with the highest prevalence of chronic conditions; 19.0-25.5% of Mexican adults have HBP, 10.0% have diabetes, and 28.0% are obese [6,7]. To date, only 1 peer-reviewed study, conducted in China, has reported a higher combined risk of admission to intensive care, intubation, or death in patients with multimorbidity compared to those without multimorbidity [8]. However, this association has not been studied in Latin America, and pneumonia and death have not been considered as separate outcomes. The epidemiological surveillance system of the Secretaría de Salud de México collects information regarding the characteristics and comorbidities of diagnosed COVID-19 cases, as well as their clinical course and outcomes. The government of Mexico has released these data. In this study, we aimed to identify the chronic conditions and multimorbidity patterns present among COVID-19 patients and to examine their associations with pneumonia and death. Our results could help facilitate better understanding and decision-making regarding the identification of groups at relatively high risk of severe illness and death due to COVID-19 and the implementation of preventative measures affecting these groups.

METHODS

Study Design and Data Source

A cross-sectional study was performed to analyze the publicly available data of patients with COVID-19 diagnosed via reverse transcription-polymerase chain reaction (RT-PCR). These data were released by the Secretaría de Salud de México and covered the period ending on May 18, 2020. Socio-demographic and medical data (regarding date of disease onset, disease duration, epidemiological profile, presence of chronic conditions, molecular diagnostic test result, and vital status), were collected by physicians using an epidemiological COVID-19 case report form in suspected COVID-19 patients. These data were systematized using an epidemiological surveillance system and are available at https://www.gob.mx/salud/documentos/datos-abiertos-152127.

Study Variables

The dependent variables were pneumonia and death in patients with COVID-19. Eight comorbidities were included as independent variables: HBP, diabetes, obesity, asthma, immunosuppression, other CVDs, chronic obstructive pulmonary disease (COPD), and chronic kidney disease. The chronic conditions included in the analysis corresponded to the conditions reported as associated with COVID-19 in the literature [9-15] and the availability of the relevant information in the patient data. A simple count of the 8 comorbidities was used to classify participants into 4 categories: no comorbidity, 1 comorbidity, 2 comorbidities, or 3 or more comorbidities. Likewise, the 3 most frequent comorbidities (HBP, diabetes, and obesity) were classified into dyads. The presence of ≥2 of the 8 reported comorbidities was considered to indicate multimorbidity.

Statistical Analysis

The variables of interest were presented as frequencies and percentages for the categorical variables and as means and standard deviations for the continuous variables. The frequencies of pneumonia and death were presented according to the characteristics and comorbidities evaluated and stratified by sex. Simple logistic regression models were applied to measure the associations of the independent variables with pneumonia and death in patients with COVID-19. The chronic conditions that were found to be associated with pneumonia or death (p<0.05) in the simple logistic regression analysis were included in two adjusted logistic regression models. The covariables included in the adjusted models were age (continuous), gender (men/women), and smoking status (yes/no). The results were expressed as odds ratios (ORs) and adjusted odds ratios (aORs) with 95% confidence intervals (CIs) for both models. Based on the adjusted models, the marginal effects were estimated along with their 95% CI, and the probabilities of pneumonia and death according to the number of comorbidities for each year of age were graphed. Statistical analysis was performed using Stata version 14 (StataCorp., College Station, TX, USA). For all analyses, a p-value <0.05 was considered statistically significant.

Ethics Statement

As an analysis of secondary data, this study did not require the approval of an institutional ethics committee. The data are publicly available on the platform of the Secretaría de Salud de México under the Mexican open data policy intended to facilitate the access, use, reuse, and redistribution of information.

RESULTS

Complete data regarding the study variables were available for 51 053 patients with COVID-19, and these patients were included in the analysis. A total of 580 patients were excluded due to incomplete data. Of the included patients, 29 422 were men (57.6%). The overall mean age was 46.6±15.8 years (men, 47.1±15.7 years; women, 45.8±16.0 years). The mean disease duration was 4.2±3.3 days. A total of 14 684 (28.8%) patients presented with pneumonia (men, 32.5%; women, 23.7%). Regarding the presence of chronic conditions, 27 667 (54.2%) of the participants had no comorbidities, while 13 652 (26.7%) presented 1 chronic condition. Multimorbidity was present in 9734 (19.1%) of the patients, with the presence of 2 (n=6518, 12.8%) and 3 (n=2490, 4.9%) comorbidities being the most common. The largest number of simultaneous chronic conditions was 8 (14 patients) (Table 1).
Table 1.

Characteristics of the Mexican population with coronavirus disease 2019 (COVID-19)

CharacteristicsOverall (n = 51 053)Men (n = 29 422)Women (n = 21 631)
Age (y)46.6±15.847.1±15.745.8±16.0
Duration of illness4.2±3.34.2±3.34.1±3.3
HBP
 No39 963 (78.3)23 147 (78.7)16 816 (77.7)
 Yes11 090 (21.7)6275 (21.3)4815 (22.3)
Diabetes
 No41 667 (81.6)23 976 (81.5)17 691 (81.8)
 Yes9386 (18.4)5446 (18.5)3940 (18.2)
Obesity
 No40 412 (79.2)23 625 (80.3)16 787 (77.6)
 Yes10 641 (20.8)5797 (19.7)4844 (22.4)
Asthma
 No49 463 (96.9)28 752 (97.7)20 711 (95.7)
 Yes1590 (3.1)670 (2.3)920 (4.3)
Immunosuppression
 No50 212 (98.4)28 987 (98.5)21 225 (98.1)
 Yes841 (1.6)435 (1.5)406 (1.9)
Other CVD
 No49 682 (97.3)28 628 (97.3)21 054 (97.3)
 Yes1371 (2.7)794 (2.7)577 (2.7)
COPD
 No49 934 (97.8)28 815 (97.9)21 119 (97.6)
 Yes1119 (2.2)607 (2.1)512 (2.4)
Chronic kidney disease
 No49 795 (97.5)28 662 (97.4)21 133 (97.7)
 Yes1258 (2.5)760 (2.6)498 (2.3)
HBP and diabetes
 No35 519 (69.6)20 435 (69.5)15 084 (69.7)
 Yes15 534 (30.4)8987 (30.5)6547 (30.3)
HBP and obesity
 No32 874 (64.4)19 187 (65.2)13 687 (63.3)
 Yes18 179 (35.6)10 235 (34.8)7944 (36.7)
Diabetes and obesity
 No33 769 (66.1)19 546 (66.4)14 223 (65.8)
 Yes17 284 (33.9)9876 (33.6)7408 (34.2)
Smoking
 No46 715 (91.5)26 232 (89.2)20 483 (94.7)
 Yes4338 (8.5)3190 (10.8)1148 (5.3)
Pneumonia
 No36 369 (71.2)19 857 (67.5)16 512 (76.3)
 Yes14 684 (28.8)9565 (32.5)5119 (23.7)
Death
 No45 820 (89.7)25 862 (87.9)19 958 (92.3)
 Yes5233 (10.3)3560 (12.1)1673 (7.7)
Time from disease onset to death10.6±6.510.8±6.510.2±6.5
Comorbidities
 027 667 (54.2)16 068 (54.6)11 599 (53.6)
 113 652 (26.7)7993 (27.2)5659 (26.2)
 26518 (12.8)3725 (12.7)2793 (12.9)
 32490 (4.9)1305 (4.4)1185 (5.5)
 4572 (1.1)263 (0.9)309 (1.4)
 5109 (0.2)49 (0.2)60 (0.3)
 624 (0.0)9 (0.0)15 (0.1)
 77 (0.0)5 (0.0)2 (0.0)
 814 (0.0)5 (0.0)9 (0.0)
Multimorbidity
 027 667 (54.2)16 068 (54.6)11 599 (53.6)
 113 652 (26.7)7993 (27.2)5659 (26.2)
 26518 (12.8)3725 (12.7)2793 (12.9)
 ≥33216 (6.3)1636 (5.6)1580 (7.3)

Values are presented as number (%) or mean±standard deviation.

HBP, high blood pressure; CVD, cardiovascular disease; COPD, chronic obstructive pulmonary disease.

The results included 5233 (10.3%) deaths (men, 12.1%; women, 7.7%), with a mean time from disease onset to death of 10.6±6.5 days (Table 1). Regarding age group, pneumonia was reported in more than 50% of the people in the 65-74 (50.3%), 75-84 (53.7%), and 85 or older (51.4%) age groups, while the greatest frequencies of death were found in the 65- 74 (27.1%), 75-84 (29.1%), and 85 or older (31.3%) age groups (Table 2). In the adjusted logistic regression model, across the entire study population, it was found that chronic conditions such as HBP, diabetes, obesity, immunosuppression, other CVDs, COPD, and chronic kidney disease were associated with an increased risk of pneumonia. In men, other CVDs and COPD were not found to be associated with pneumonia. Likewise, across the study population, chronic conditions such as HBP, diabetes, obesity, immunosuppression, other CVDs, COPD, and chronic kidney disease were associated with an increased probability of death (Table 3).
Table 2.

Frequencies of pneumonia and death in the Mexican population with coronavirus disease 2019 (COVID-19) according to age group

CharacteristicsOverallMenWomen
Pneumonia
 Total (n)14 68495655119
 0-19115 (9.5)70 (11.1)45 (7.7)
 20-443727 (16.3)2477 (19.5)1250 (12.4)
 45-543733 (32.2)2537 (37.0)1196 (25.2)
 55-643496 (41.9)2250 (45.3)1246 (37.0)
 65-742242 (50.3)1425 (52.0)817 (47.6)
 75-841087 (53.7)647 (54.5)440 (52.5)
 ≥ 85284 (51.4)159 (54.3)125 (48.1)
Deaths
 Total (n)523335601673
 0-1920 (1.6)13 (2.1)7 (1.2)
 20-44708 (3.1)512 (4.0)196 (1.9)
 45-541161 (10.0)845 (12.3)316 (6.7)
 55-641374 (16.5)928 (18.7)446 (13.3)
 65-741207 (27.1)798 (29.1)409 (23.8)
 75-84590 (29.1)357 (30.1)233 (27.8)
 ≥85173 (31.3)107 (36.5)66 (25.4)

Values are presented as number (% of the row).

Table 3.

Associations of chronic conditions with pneumonia and death in the Mexican population with coronavirus disease 2019 (COVID-19)

Chronic conditionsPneumonia
Death
OR (95% CI)aOR (95% CI)[1]OR (95% CI)aOR (95% CI)[1]
Overall
 HBP2.41 (2.31, 2.52)[*]1.47 (1.40, 1.54)[*]3.15 (2.97, 3.34)[*]1.67 (1.57, 1.79)[*]
 Diabetes2.93 (2.79, 3.06)[*]1.94 (1.84, 2.04)[*]3.34 (3.14, 3.55)[*]2.00 (1.87, 2.13)[*]
 Obesity1.47 (1.40, 1.54)[*]1.49 (1.42, 1.56)[*]1.49 (1.40, 1.59)[*]1.62 (1.52, 1.74)[*]
 Asthma0.74 (0.66, 0.83)[*]0.91 (0.80, 1.03)0.75 (0.63, 0.91)[*]1.02 (0.84, 1.23)
 Immunosuppression1.91 (1.67, 2.20)[*]1.71 (1.48, 1.98)[*]2.35 (1.98, 2.78)[*]1.99 (1.66, 2.38)[*]
 Other CVD2.08 (1.87, 2.32)[*]1.23 (1.10, 1.38)[*]2.64 (2.32, 3.01)[*]1.34 (1.17, 1.55)[*]
 COPD2.62 (2.32, 2.95)[*]1.30 (1.15, 1.48)[*]3.81 (3.34, 4.34)[*]1.62 (1.40, 1.87)[*]
 Chronic kidney disease2.75 (2.46, 3.08)[*]2.01 (1.78, 2.26)[*]4.37 (3.87, 4.94)[*]3.08 (2.70, 3.51)[*]
 HBP and diabetes2.91 (2.80, 3.03)[*]1.84 (1.76, 1.92)[*]3.69 (3.48, 3.92)[*]2.00 (1.87, 2.13)[*]
 HBP and obesity2.11 (2.03, 2.20)[*]1.57 (1.50, 1.64)[*]2.68 (2.53, 2.84)[*]1.83 (1.72, 1.95)[*]
 Diabetes and obesity2.30 (2.21, 2.39)[*]1.83 (1.75, 1.91)[*]2.71 (2.56, 2.88)[*]2.08 (1.96, 2.21)[*]
Men
 HBP2.13 (2.01. 2.25)[*]1.34 (1.26, 1.43)[*]2.67 (2.47, 2.87)[*]1.48 (1.37, 1.61)[*]
 Diabetes2.59 (2.44, 2.75)[*]1.76 (1.65, 1.88)[*]2.84 (2.63, 3.07)[*]1.76 (1.62, 1.91)[*]
 Obesity1.36 (1.28, 1.44)[*]1.42 (1.34, 1.51)[*]1.36 (1.26, 1.48)[*]1.55 (1.42, 1.69)[*]
 Asthma0.74 (0.62, 0.88)[*]0.91 (0.76, 1.09)0.72 (0.55, 0.94)[*]0.96 (0.73, 1.27)
 Immunosuppression1.73 (1.43, 2.10)[*]1.48 (1.21, 1.81)[*]2.29 (1.83, 2.87)[*]1.85 (1.46, 2.36)[*]
 Other CVDs1.82 (1.58, 2.09)[*]1.11 (0.95, 1.29)2.32 (1.97, 2.75)[*]1.23 (1.03, 1.47)[*]
 COPD2.12 (1.80, 2.49)[*]1.09 (0.92, 1.29)3.28 (2.75, 3.91)[*]1.46 (1.20, 1.76)[*]
 Chronic kidney disease2.43 (2.10, 2.81)[*]1.84 (1.58, 2.15)[*]3.80 (3.26, 4.44)[*]2.79 (2.36, 3.29)[*]
 HBP and diabetes2.52 (2.39, 2.66)[*]1.64 (1.55, 1.74)[*]3.04 (2.83, 3.26)[*]1.72 (1.59, 1.86)[*]
 HBP and obesity1.89 (1.80, 1.99)[*]1.46 (1.38, 1.54)[*]2.34 (2.18, 2.51)[*]1.68 (1.55, 1.81)[*]
 Diabetes and obesity2.06 (1.96, 2.17)[*]1.69 (1.60, 1.78)[*]2.35 (2.19, 2.52)[*]1.88 (1.74, 2.02)[*]
Women
 HBP3.03 (2.83, 3.25)[*]1.67 (1.54, 1.80)[*][*][*]4.51 (4.07, 4.99)[*]2.11 (1.88, 2.36)[*]
 Diabetes3.60 (3.34, 3.87)[*]2.23 (2.06, 2.41)[*]4.60 (4.15, 5.11)[*]2.52 (2.25, 2.81)[*]
 Obesity1.74 (1.62, 1.86)[*]1.57 (1.46, 1.70)[*]1.86 (1.67, 2.07)[*]1.73 (1.55, 1.94)[*]
 Asthma0.84 (0.72, 0.99)[*]0.91 (0.77, 1.08)0.92 (0.71, 1.19)Not include
 Immunosuppression2.30 (1.88, 2.81)[*]2.01 (1.62, 2.49)[*]2.73 (2.43, 3.07)[*]1.99 (1.76, 2.24)[*]
 Other CVDs2.56 (2.16, 3.03)[*]1.42 (1.19, 1.71)[*]3.33 (2.71, 4.10)[*]1.53 (1.23, 1.92)[*]
 COPD3.57 (2.99, 4.25)[*]1.58 (1.31, 1.91)[*]5.01 (4.11, 6.12)[*]1.83 (1.47, 2.27)[*]
 Chronic kidney disease3.31 (2.77, 3.96)[*]2.28 (1.89, 2.76)[*]5.55 (4.55, 6.77)[*]3.63 (2.93, 4.49)[*]
 HBP and diabetes3.75 (3.52, 4.01)[*]2.21 (2.05, 2.38)[*]5.72 (5.14, 6.37)[*]2.77 (2.47, 3.12)[*]
 HBP and obesity2.64 (2.47, 2.81)[*]1.75 (1.64, 1.88)[*]3.78 (3.40, 4.20)[*]2.19 (1.96, 2.45)[*]
 Diabetes and obesity2.82 (2.65, 3.01)[*]2.07 (1.93, 2.21)[*]3.79 (3.42, 4.21)[*]2.57 (2.31, 2.87)[*]

OR, odds ratio; CI, confidence interval; aOR, adjusted odds ratio; HBP, high blood pressure; CVD, cardiovascular disease; COPD, chronic obstructive pulmonary disease.

Adjusted analysis by age, sex, and smoking status in overall population (by age and smoking status in men and women).

p<0.05.

A significant incremental gradient was observed for the association between multimorbidity and pneumonia in the general population (p<0.001), with the presence of 1 (aOR, 1.68; 95% CI, 1.60 to 1.77), 2 (aOR, 2.07; 95% CI, 1.95 to 2.20), and 3 or more chronic conditions (aOR, 2.40; 95% CI, 2.22 to 2.60) associated with a progressively increasing probability of this outcome. Likewise, across the study population, a significant incremental gradient (p<0.001) was found for the relationship between multimorbidity and death, in which the presence of 1 (aOR, 1.89; 95% CI, 1.75 to 2.04), 2 (aOR, 2.51; 95% CI, 2.30 to 2.73), and 3 or more chronic conditions (aOR, 3.49; 95% CI, 3.15 to 3.86) were associated with an increased probability of death among the patients. These gradients demonstrating higher probabilities of pneumonia and death in patients with more chronic conditions were also present in both men and women and were statistically significant (Table 4).
Table 4.

Associations of multimorbidity with pneumonia and death in the Mexican population with coronavirus disease 2019 (COVID-19)

Pneumonia
Death
OR (95% CI)aOR (95% CI)OR (95% CI)aOR (95% CI)
Overall[1]
 01.00 (reference)1.00 (reference)1.00 (reference)1.00 (reference)
 12.10 (2.01, 2.20)1.68 (1.60, 1.77)2.57 (2.39, 2.77)1.89 (1.75, 2.04)
 23.18 (3.01, 3.37)2.07 (1.95, 2.20)4.40 (4.06, 4.77)2.51 (2.30, 2.73)
 ≥33.95 (3.66, 4.26)2.40 (2.22, 2.60)6.56 (5.96, 7.21)3.49 (3.15, 3.86)
p-trend[2]<0.001<0.001<0.001<0.001
Men[3]
 01.00 (reference)1.00 (reference)1.00 (reference)1.00 (reference)
 11.95 (1.84, 2.07)1.59 (1.50, 1.69)2.30 (2.11, 2.51)1.74 (1.59, 1.91)
 22.74 (2.54, 2.95)1.83 (1.69, 1.98)3.58 (3.24, 3.95)2.12 (1.91, 2.35)
 ≥33.29 (2.96, 3.65)2.00 (1.80, 2.23)5.13 (4.54, 5.81)2.75 (2.42, 3.14)
p-trend[2]<0.001<0.001<0.001<0.001
Women[3]
 01.00 (reference)1.00 (reference)1.00 (reference)1.00 (reference)
 12.46 (2.28, 2.66)1.88 (1.73, 2.04)3.57 (3.09, 4.13)2.43 (2.09, 2.83)
 24.28 (3.90, 4.69)2.55 (2.31, 2.81)7.50 (6.45, 8.72)3.72 (3.17, 4.36)
 ≥35.67 (5.07, 6.34)3.04 (2.70, 3.43)12.14 (10.33, 14.26)5.42 (4.57, 6.44)
p-trend[2]<0.001<0.001<0.001<0.001

OR, odds ratio; CI, confidence interval; aOR, adjusted odds ratio.

Adjusted analysis by age, sex, and smoking status.

Test for trend of OR.

Adjusted analysis by age and smoking status.

Figure 1 shows the marginal effects of age and number of comorbidities on the probabilities of pneumonia and death. The probabilities of both pneumonia and death increased with the number of comorbidities and age.
Figure. 1.

Marginal effects of age (in years) and number of comorbidities on the probabilities of (A) pneumonia or (B) death in the Mexican population with coronavirus disease 2019 (COVID-19).

DISCUSSION

In this study, we sought to identify patterns of chronic conditions and multimorbidity and to evaluate their associations with pneumonia and death in Mexican patients with COVID-19. Chronic conditions such as HBP, diabetes, obesity, other CVDs, and chronic kidney disease were found to increase the likelihood of pneumonia. Likewise, HBP, diabetes, obesity, immunosuppression, COPD, and chronic kidney disease increased the probability of death in patients with COVID-19. Regarding multimorbidity, a greater number of chronic conditions was found to be associated with an increased probability of death or pneumonia among the study sample. In the present study, an association was found between chronic conditions and pneumonia in patients with COVID-19. An early report from Wuhan, China, noted that about half of a sample of patients who were hospitalized for SARS-CoV-2 pneumonia had an additional medical condition. The most common comorbidities were HBP, diabetes, CVDs, and malignancies, which (except for malignancies) coincide with the most frequent conditions found in the Mexican population with COVID-19. Likewise, in the study from Wuhan, these conditions were associated with the presence of pneumonia [2]. Furthermore, the Centers for Disease Control and Prevention in the United States reported that people with serious medical conditions such as asthma (moderate to severe), COPD, diabetes, CVDs, kidney diseases, severe obesity, immunosuppression, and liver diseases have a greater probability of developing severe forms of COVID-19, including pneumonia [15]. It has been postulated that the development and severity of pneumonia may be influenced by the use of antihypertensive medication, commonly prescribed to patients with HBP and diabetes. These medications may lead to elevated lung tissue concentrations of angiotensin-converting enzyme 2, which acts as the receptor for the entry of SARS-CoV-2 [16,17]. However, other authors have reported that elevated angiotensinconverting enzyme 2 levels are not associated with an increased risk of pneumonia [18]. This suggests the need for further study of the influence of chronic conditions on the development of COVID-19. Regarding multimorbidity and pneumonia in patients with COVID-19, the probability of developing pneumonia was found to increase as the number of chronic conditions increased. COVID-19 patients with comorbidities have been reported to exhibit a worse response to treatment than patients without comorbidities [19]. HBP and respiratory and CVDs are associated with a relatively severe presentation of COVID-19, including the development of pneumonia [20-22]. Likewise, greater patient age is associated with the development of pneumonia and the severe presentation of COVID-19 [23]. The presence of multimorbidity among adults (particularly older adults) impacts the physical and mental health of this group, particularly in lowincome and middle-income countries [24]. This affects the response capacity to treatment in these patients. An association was found between the presence of chronic conditions and death in patients with COVID-19. In China, a higher frequency of COVID-19 infection and a greater lethality of the disease have been reported among patients with HBP [4,13,20,24]. Diabetes has also been described as one of the most common chronic conditions in patients with COVID-19, especially among those in the intensive care unit or with severe forms of the disease [12,19,25]. Obesity is another chronic condition associated with increased mortality risk due to challenges in the management of obese patients in relation to positioning, mobilization, and intubation [26,27]. Regarding immunosuppression, the host immunological response to SARSCoV-2 infection and its relationship with the pathophysiology and prognosis of the disease is still under study [28,29]. It has been reported that patients with COPD have an increased risk of developing severe forms of illness, possibly due to alterations in the inflammatory response, immunological and microbiome imbalances, and the use of corticosteroids, among other factors [30]. Chronic kidney disease has also been described as a chronic condition associated with a greater risk of severe manifestation of COVID-19 and death [8,31,32]. With respect to the relationship between multimorbidity and death in patients with COVID-19, an incrementally higher probability of death was observed among patients with more chronic conditions. The prevalence of multimorbidity increases with age [33]. In addition, it has been reported that older adults who have 2 or more comorbidities have a higher mortality rate than adults who do not [33,34]. The case series on COVID-19 published to date describe greater disease severity and a higher risk of death among older patients, particularly the most elderly [11,14]. In Mexico, the presence of multimorbidity in adults has been described as a predictor of quality of life and all-cause mortality [35]. Mexico has a significant burden of disease due to chronic diseases; in 2016, 80% of deaths were attributable to chronic conditions [6]. This high rate of deaths due to chronic diseases corresponds to the high prevalence of chronic conditions in the Mexican population, among which 25.5% of individuals have HBP [7], and 28% of adults are obese [6]. Given that multimorbidity can increase the risk of death due to COVID-19, in countries like Mexico, which have a high burden of disease due to these conditions, it is necessary to develop strategies to mitigate the spread of this disease in these population subgroups to decrease the impact of COVID-19 on health systems. This study was not without limitations. The data analyzed were secondary in nature, and the accuracy of the data therefore, cannot be guaranteed. Additionally, the cases analyzed included only patients diagnosed with COVID-19 via RT-PCR, and thus, false-negative results of the RT-PCR test would not have been included in the analysis. In addition, bias may have been introduced insofar as the process of obtaining and handling of the sample influenced the results of the diagnostic test. Another possible source of bias stems from the fact that patients with asymptomatic or mildly symptomatic COVID-19 who did not seek medical attention would not have been included among the cases analyzed. Despite the limitations inherent to the information source, the use of a large dataset that includes all COVID-19 cases identified with molecular diagnostic tests and collected officially by the government of Mexico is useful for the initial study of the relationship between multimorbidity and COVID-19, bearing in mind the high burden of disease due to chronic conditions in Mexico. In conclusion, several chronic conditions are associated with the development of pneumonia and death in Mexican patients with COVID-19. Additionally, an increase in the number of simultaneous chronic conditions was found to be associated with increased risk of pneumonia and death among these patients. These findings may be useful in the effort by decisionmakers to develop strategies to prevent COVID-19 in vulnerable subgroups, such as people with comorbidities. According to reports from different sources, patients with chronic conditions have a greater risk of COVID-19 than patients without such conditions. Hence, additional research is necessary to understand and deepen the study of the pathophysiological processes that determine this association, and this research is particularly important due to the high burden of chronic disease in various Latin American countries, including Mexico.
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1.  Clinical Characteristics of 138 Hospitalized Patients With 2019 Novel Coronavirus-Infected Pneumonia in Wuhan, China.

Authors:  Dawei Wang; Bo Hu; Chang Hu; Fangfang Zhu; Xing Liu; Jing Zhang; Binbin Wang; Hui Xiang; Zhenshun Cheng; Yong Xiong; Yan Zhao; Yirong Li; Xinghuan Wang; Zhiyong Peng
Journal:  JAMA       Date:  2020-03-17       Impact factor: 56.272

2.  Hypothesis: angiotensin-converting enzyme inhibitors and angiotensin receptor blockers may increase the risk of severe COVID-19.

Authors:  James H Diaz
Journal:  J Travel Med       Date:  2020-05-18       Impact factor: 8.490

3.  Risk Factors Associated With Acute Respiratory Distress Syndrome and Death in Patients With Coronavirus Disease 2019 Pneumonia in Wuhan, China.

Authors:  Chaomin Wu; Xiaoyan Chen; Yanping Cai; Jia'an Xia; Xing Zhou; Sha Xu; Hanping Huang; Li Zhang; Xia Zhou; Chunling Du; Yuye Zhang; Juan Song; Sijiao Wang; Yencheng Chao; Zeyong Yang; Jie Xu; Xin Zhou; Dechang Chen; Weining Xiong; Lei Xu; Feng Zhou; Jinjun Jiang; Chunxue Bai; Junhua Zheng; Yuanlin Song
Journal:  JAMA Intern Med       Date:  2020-07-01       Impact factor: 21.873

4.  Clinical course and outcomes of critically ill patients with SARS-CoV-2 pneumonia in Wuhan, China: a single-centered, retrospective, observational study.

Authors:  Xiaobo Yang; Yuan Yu; Jiqian Xu; Huaqing Shu; Jia'an Xia; Hong Liu; Yongran Wu; Lu Zhang; Zhui Yu; Minghao Fang; Ting Yu; Yaxin Wang; Shangwen Pan; Xiaojing Zou; Shiying Yuan; You Shang
Journal:  Lancet Respir Med       Date:  2020-02-24       Impact factor: 30.700

5.  [Hypertension in Mexican adults: prevalence, diagnosis and type of treatment. Ensanut MC 2016.]

Authors:  Ismael Campos-Nonato; Lucía Hernández-Barrera; Andrea Pedroza-Tobías; Catalina Medina; Simón Barquera
Journal:  Salud Publica Mex       Date:  2018 May-Jun

6.  Chronic obstructive pulmonary disease is associated with severe coronavirus disease 2019 (COVID-19).

Authors:  Giuseppe Lippi; Brandon Michael Henry
Journal:  Respir Med       Date:  2020-03-24       Impact factor: 4.582

7.  Prevalence of comorbidities and its effects in patients infected with SARS-CoV-2: a systematic review and meta-analysis.

Authors:  Jing Yang; Ya Zheng; Xi Gou; Ke Pu; Zhaofeng Chen; Qinghong Guo; Rui Ji; Haojia Wang; Yuping Wang; Yongning Zhou
Journal:  Int J Infect Dis       Date:  2020-03-12       Impact factor: 3.623

8.  Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study.

Authors:  Fei Zhou; Ting Yu; Ronghui Du; Guohui Fan; Ying Liu; Zhibo Liu; Jie Xiang; Yeming Wang; Bin Song; Xiaoying Gu; Lulu Guan; Yuan Wei; Hui Li; Xudong Wu; Jiuyang Xu; Shengjin Tu; Yi Zhang; Hua Chen; Bin Cao
Journal:  Lancet       Date:  2020-03-11       Impact factor: 79.321

9.  Host susceptibility to severe COVID-19 and establishment of a host risk score: findings of 487 cases outside Wuhan.

Authors:  Yu Shi; Xia Yu; Hong Zhao; Hao Wang; Ruihong Zhao; Jifang Sheng
Journal:  Crit Care       Date:  2020-03-18       Impact factor: 9.097

10.  The Clinical and Chest CT Features Associated With Severe and Critical COVID-19 Pneumonia.

Authors:  Kunhua Li; Jiong Wu; Faqi Wu; Dajing Guo; Linli Chen; Zheng Fang; Chuanming Li
Journal:  Invest Radiol       Date:  2020-06       Impact factor: 10.065

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  9 in total

1.  Autosomal Dominant Polycystic Kidney Disease Does Not Significantly Alter Major COVID-19 Outcomes among Veterans.

Authors:  Xiangqin Cui; Julia W Gallini; Christine L Jasien; Michal Mrug
Journal:  Kidney360       Date:  2021-04-28

2.  Correlates of In-Hospital COVID-19 Deaths: A Competing Risks Survival Time Analysis of Retrospective Mortality Data.

Authors:  Ashish Goel; Alpana Raizada; Ananya Agrawal; Kamakshi Bansal; Saurabh Uniyal; Pratima Prasad; Anil Yadav; Asha Tyagi; R S Rautela
Journal:  Disaster Med Public Health Prep       Date:  2021-03-25       Impact factor: 1.385

3.  Autosomal Dominant Polycystic Kidney Disease does not significantly alter major COVID-19 outcomes among veterans.

Authors:  Xiangqin Cui; Julia W Gallini; Christine L Jasien; Michal Mrug
Journal:  medRxiv       Date:  2020-11-29

4.  Evaluation of Treatment Outcome for Pneumonia among Pre-Vaccinated COVID-19 Patients with/without Comorbidity in a Public Hospital in Bengkulu, Indonesia.

Authors:  Diana Laila Ramatillah; Siew Hua Gan; Syed Azhar Syed Sulaiman; Dama Puja; Usman Abubakar; Ammar Ali Saleh Jaber; Stefanus Lukas; Nina Jusnita
Journal:  Vaccines (Basel)       Date:  2021-11-30

5.  Association between chronic kidney disease and mortality in patients with a confirmed COVID-19 diagnosis.

Authors:  Jacqueline Betsabe Puicón-Suárez; Sandra Zeña-Ñañez; Virgilio E Failoc-Rojas
Journal:  PeerJ       Date:  2022-06-14       Impact factor: 3.061

6.  Associations of symptom combinations with in-hospital mortality of coronavirus disease-2019 patients using South Korean National data.

Authors:  Suyoung Jo; Hee-Kyoung Nam; Heewon Kang; Sung-Il Cho
Journal:  PLoS One       Date:  2022-08-26       Impact factor: 3.752

7.  Ethnic disparities in COVID-19 mortality in Mexico: A cross-sectional study based on national data.

Authors:  Ismael Ibarra-Nava; Kathia G Flores-Rodriguez; Violeta Ruiz-Herrera; Hilda C Ochoa-Bayona; Alfonso Salinas-Zertuche; Magaly Padilla-Orozco; Raul G Salazar-Montalvo
Journal:  PLoS One       Date:  2021-03-10       Impact factor: 3.240

8.  Trends of COVID-19 Admissions in an Italian Hub during the Pandemic Peak: Large Retrospective Study Focused on Older Subjects.

Authors:  Andrea Ticinesi; Antonio Nouvenne; Nicoletta Cerundolo; Alberto Parise; Beatrice Prati; Angela Guerra; Tiziana Meschi
Journal:  J Clin Med       Date:  2021-03-07       Impact factor: 4.241

9.  COVID-19-related deaths among women of reproductive age in Brazil: The burden of postpartum.

Authors:  Roxana Knobel; Maíra L S Takemoto; Marcos Nakamura-Pereira; Mariane O Menezes; Vicente K Borges; Leila Katz; Melania M R Amorim; Carla B Andreucci
Journal:  Int J Gynaecol Obstet       Date:  2021-07-18       Impact factor: 4.447

  9 in total

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