The Association of Body Mass Index with COVID-19 Complications and Survival Rate at a Tertiary Hospital
by
, , , , ,
Salma AlBahrani
1,2,
Thekra N. Al-Maqati
3,*,
Yaser A. Al Naam
3,
Jaber S. Alqahtani
4
,
Abdullah S. Alqahtani
4,
Saad AlRabeeah
4,
Abdulelah M. Aldhahir
5,
Faisal Alkhalaf
3,
Hind R. Alzuraiq
6,
Maryam Hamad Alenezi
7,
Amal Alzahrani
8,
Mohanad Bakkar
1,
Zainab Albahrani
9 and
Rawan M. Maawadh
3 1
Internal Medicine Department, King Fahad Military Medical Complex, Dammam 34313, Saudi Arabia
2
Department of Internal Medicine, College of Medicine, Imam Abdulrahman Bin Faisal University, Dammam 34313, Saudi Arabia
3
Department of Clinical Laboratory Sciences, Prince Sultan Military College of Health Sciences, Dammam 31448, Saudi Arabia
4
Department of Respiratory Care, Prince Sultan Military College of Health Sciences, Dammam 31448, Saudi Arabia
5
Respiratory Therapy Department, Faculty of Applied Medical Sciences, Jazan University, Jazan 45142, Saudi Arabia
6
Pharmacy Department, King Fahad Military Medical Complex, Dammam 34313, Saudi Arabia
7
Medical Administration Department, King Fahad Military Medical Complex, Dammam 34313, Saudi Arabia
8
Training Department, King Fahad Military Medical Complex, Dammam 34313, Saudi Arabia
9
Internal Medicine Department, National Guard Hospital, Alhassa 31982, Saudi Arabia
*
Author to whom correspondence should be addressed.
Life 2023, 13(7), 1572; https://doi.org/10.3390/life13071572
Submission received: 8 May 2023
/
Revised: 14 June 2023
/
Accepted: 7 July 2023
/
Published: 16 July 2023
(This article belongs to the Special Issue Epidemiology, Virology, and Prevention of Infectious Diseases in Human)
Abstract
:A high body mass index (BMI) is a known risk factor for coronavirus infection in hospitalized patients. Our study examined the association between BMI and complications and the survival rate among COVID-19 patients. This retrospective analysis used data from a tertiary hospital in the Eastern Region of Saudi Arabia during two waves of the COVID-19 pandemic. The study included 600 participants, with the majority being between 41 and 60 years old (41.3%) and men comprising 63.5% of the sample. Approximately 42.5% of patients were obese, and 31.3% were overweight. The results showed that BMI was significantly linked to respiratory diseases (p = 0.013); end-stage renal disease (p = 0.021); and cardiovascular disease (p = 0.003) but not diabetes mellitus (p = 0.064). Death occurred in 10.8% of patients; 33.8% were admitted to the ICU; 13.8% needed mechanical ventilation; and 60.7% had lung infiltration. Obese patients with oxygen saturation levels below 93% were 2.45 times more likely to require mechanical ventilation than those in the normal-weight group. Overweight and obese patients were also more likely to require mechanical ventilation than normal-weight patients, with odds ratios of 3.66 and 2.81, respectively. The BMI categorized was not associated with survival rate in COVID-19-hospitalized patients using Kaplan-Meier survival plots (p = 0.061). However, the BMI categorized was associated with survival rate in COVID-19 ICU patients (p < 0.001). In addition, the overweight showed a statistically significant higher hazard ratio of 2.22 (p = 0.01) compared to normal-weight patients using a Cox regression model. A high BMI was identified as an independent risk factor for reduced oxygen saturation (<93%), the need for mechanical ventilation, lung infiltration, mortality, and longer ICU stays in COVID-19 patients.
1. Introduction
Obesity and overweight have been identified as risk factors contributing to the development of severe illnesses that lead to hospitalization for COVID-19 infection [1]. However, the association may be subject to index event bias, a form of collider bias. Most existing research investigating this potential link has compared the outcomes of both obese and non-obese patients in the intensive care unit (ICU) [2]. Since severe COVID-19 cases and obesity might result in hospitalization, a link between the two may not reveal the full picture. A large population-based investigation that controlled for collider bias found that people with a body mass index of 30 kg/m2 and above had a greater risk of COVID-19 death than those with a BMI of 30 kg/m2 or lower [3]. In Saudi Arabia, the latest survey shows that 33.7% of the adult population is obese, while 68.2% are overweight [4]. The high prevalence of overweight and obesity in the country indicates a lack of or ineffective preventive measures. Early results from single or oligo-center studies suggest that obesity may be a major reason why COVID-19 patients require hospitalization and are at higher risk of mortality [5] as the COVID-19 pandemic continues to spread [6].
In addition, being overweight increases the risk of contracting respiratory illnesses such as the flu. Conversely, individuals with a normal weight are less likely to experience complications from influenza, such as hospitalization, mortality, extended stays, or the need for mechanical ventilation, compared to those with a higher body mass index (BMI) [7]. A study investigated the risk of death among patients admitted to the ICU and found that a high BMI was associated with an increased risk of death [8]. However, a recent study with 193 COVID-19 patients showed that BMI was unrelated to the survival rate [9]. Currently, few studies on large, diverse patient populations are widely generalizable concerning hospitalization due to COVID-19. Thus, it is unclear how body mass index (BMI) affects clinical outcomes for COVID-19 patients’ cardiovascular, respiratory, and other systems [10].
Older people are less likely to develop a critical case of COVID-19 than younger people, but it is unclear whether being overweight benefits from the purported protective impact of youth [11]. Preliminary research suggests that young COVID-19 hospital patients who are overweight are at an increased risk of poor outcomes [12], but it has not been thoroughly investigated whether obesity and age might interact in a way that varies by age. Ignoring this possibility could have negative consequences for overweight young people and COVID-19 prevention measures [10]. Meanwhile, numerous meta-analyses and comprehensive reviews have found that severe acute respiratory infection outcomes appear to be worse in obese individuals [13]. However, most subjects in these studies were hospitalized after experiencing severe COVID-19 symptoms [14], which could indicate collider bias.
In a previous population study, researchers focused on the effects of obesity (defined as a BMI of 30 kg/m2 or more). However, little research has been conducted on how being overweight (defined as a BMI of >25 kg/m2) affects most people who do not have obesity [14]. Currently, no recent studies have firmly examined the association between BMI and complications and survival rate among hospitalized COVID-19 patients during two waves of the COVID-19 pandemic.
2. Materials and Methods
2.1. Study Design
The data related to demographic characteristics, health outcomes, and comorbidities used in this retrospective study were extracted from existing medical records of patients treated during the first two waves of the COVID-19 pandemic at a tertiary hospital in the Kingdom of Saudi Arabia from March 2020 to December 2021. Before conducting this research, approval was obtained from the Institutional Review Board of the Armed Forces hospitals in the Eastern Province (IRB #AFHER-IRB-2020-034). The data gathered from medical records consisted of 813 patients who tested positive for SARS-CoV-2 using RT-PCR procedures and were admitted to healthcare facilities. From the collected sample, 213 patients were excluded because 189 were missing data related to demographic characteristics, health outcomes, or comorbidities; ten were under 18 years old; and 14 were not included due to being underweight according to their BMI.
2.2. BMI Calculation
BMI is calculated by dividing a person’s weight in kilograms by the square of their height in meters. This measurement is critical for identifying obesity and overweight trends within the population, as it measures body fat. The formula for calculating BMI is as follows: BMI (in kilograms per square meter) = weight (in kilograms) / height2 (in meters).
2.3. Statistical Analyses
The raw data extracted from medical records were first compiled and organized in Microsoft Excel. Missing values were removed, and the data were then exported to SPSS v.26 for analysis. Descriptive and inferential statistical analyses were conducted to understand trends in the dataset. Nonparametric Kruskal-Wallis and Chi-square tests were used for independent continuous and categorical variables, respectively, to determine their relationship with BMI unadjusted data and COVID-19 outcomes, as well as other comorbidities. Covariates included in the multivariate logistic regression model were adjusted after being found statistically significant (p < 0.05) in the univariate analysis. The World Health Organization (WHO) BMI guidelines were followed in this study to facilitate comparison with previous research. The standard BMI grouping categorized normal weight as 18.5–24.9 kg/m2, overweight as 25–29.9 kg/m2, and obese as ≥30 kg/m2, with normal weight as the reference group.
The Kaplan-Meier estimate compared survival rates in three BMI categories: 18.5–24.9 kg/m2 for normal weight, 25–29.9 kg/m2 for overweight, and ≥30 kg/m2 for obese. Data were analyzed using the Cox regression model, adjusting for age, gender, cardiovascular disease (CVD), renal disease (RD), and end-stage renal disease (ESRD) to assess the hazard ratio (HR). The main outcome variable was death, and BMI was considered independent.
3. Results
3.1. Demographic Characteristics of the Study Sample
The demographic characteristics of the study sample showed that most participants (41.3%) were in the age range of 41–60 years, and 63.5% were male. The BMI distribution revealed that 42.5% of the participants were obese, 31.3% were overweight, and 26.16% had a normal weight. Regarding comorbidities, 47.5% of the participants had diabetes mellitus, 18.3% had cardiovascular disease, and 12% had respiratory diseases. Among patient admissions, 10.8% resulted in deaths, 33.8% were ICU admissions, 51.2% of patients had an oxygen saturation of 95% or less, 13.8% were on mechanical ventilation, and 60.7% had lung infiltration. The findings suggest that the data sample was diverse, enabling comparisons between different BMI groups to understand COVID-19 outcomes, including categorical data on age, gender, and various comorbidities, which reduced bias in the statistical analysis. Additionally, continuous data on the length of hospital stay (with a mean of 29 days) helped in understanding how BMI affects the severity of COVID-19 illness.
3.2. Assessing the Relationship between Demographics, Comorbidities, COVID-19 Outcomes, and BMI Category
Table 1 summarizes the relationship between demographic characteristics, comorbidities, COVID-19 outcomes, and BMI categories. The Chi-square test results indicate that age group and gender were significantly associated with BMI categories, with p-values of <0.001 and 0.005, respectively. Specifically, 44.3% of patients in the 41–60 age group were obese, and significantly more men (56.5%) than women (43.5%) were obese. No significant association was found between diabetes mellitus and BMI categories (p = 0.064). However, the results show significant associations between BMI categories and respiratory, cardiovascular, and ESRDs, with p-values of 0.013, 0.003, and 0.021, respectively.
Regarding COVID-19 outcomes, obesity was associated with several adverse outcomes, as the category shows significantly lower oxygen saturation (<93%) (p = 0.002), significantly higher cases of lung infiltrate (p < 0.001), significantly higher demand for mechanical ventilation (p < 0.001), and significantly higher death rates (p < 0.001). However, there were no significant associations between BMI categories and ICU admissions (p = 0.418). The Kruskal-Wallis test for investigating the differences in the length of hospital stay between BMI categories shows statistically significant differences (χ2(2) = 19.79, p < 0.001). A post hoc test using the Dunn-Bonferroni method revealed that patients with normal weight had significantly shorter hospital stays than those with obesity (p < 0.001). However, there were no significant differences between the other BMI categories and the normal or underweight group regarding the length of hospital stay (Table 2).
3.3. Estimated Relationship between BMI Categories as The independent Variable with COVID-19 Complication Outcomes and Mortality in Hospitalized and ICU Patients
Table 3 presents the logistic regression model for BMI categories adjusted for age, gender, RD, ESRD, and cardiovascular disease to estimate the relationship between COVID-19 complications and weight-related categories, namely obese and overweight, with normal weight as the reference group. The findings show that obese patients were more likely to have low oxygen saturation (<93%) than the normal weight group (OR = 2.450; p < 0.001). Additionally, significantly higher rates of obese (OR = 2.815; p = 0.012) and overweight (OR = 3.666; p = 0.001) patients required mechanical ventilation compared to those in the normal weight category. There was no statistically significant difference in lung infiltrate cases between the overweight and normal weight groups (OR = 0.894; p = 0.664). However, a statistically significant correlation was found between the obese group and lung infiltrate cases compared to the normal weight group (OR = 3.384; p < 0.001).
Figure 1 illustrates the impact of BMI levels (18.5–24.9, 25–30, and >30) on the survival rate of hospitalized COVID-19 patients using Kaplan-Meier survival plots. The results indicate that the survival rate among these three BMI levels was not statistically significant (p = 0.061). However, for ICU COVID-19 patients, the survival rate was statistically significant (p < 0.001). The Cox regression model was used to estimate the hazard ratio (HR) for death as the main outcome variable. BMI was considered an independent variable, adjusting for age, gender, CVD, RD, and ESRD (Figure 2, Table 4). The model shows no statistical significance for the obese (HR = 1.175; p = 0.662) and overweight (OR = 1.535; p = 0.202) compared to the reference group among hospitalized patients. For ICU patients with COVID-19, the Cox regression model shows no statistical significance for the obese (HR = 0.675; p = 0.263), while the overweight group was statistically significant (OR = 2.222; p = 0.011) compared to the reference group (normal weight) (Figure 2, Table 4).
4. Discussion
A key finding was that among the patients admitted with COVID-19, 42.5% were obese and 31.3% were overweight. This result aligns with previous studies, including WHO [4], which reported that during the COVID-19 period, there was a prevalence rate of 68.2% for overweight and 33.7% for obesity in Saudi Arabia. Furthermore, other literature supports these findings, showing a high prevalence of obesity and overweight among COVID-19 patients in other countries, such as South Korea [5]. The finding can be explained by Lindgren et al., who indicate that obesity and overweight limit the respiratory capacity of individuals by reducing resting lung volumes [15]. In this respect, since COVID-19 is primarily a respiratory failure condition, patients who were overweight or obese were more likely to be affected. The high rates of obesity noted among COVID-19 patients were also linked to reduced access to healthy food and removed work environments and movement restrictions, which limited physical activity patterns [16,17]. In this respect, it was realized that increased obesity trends during the pandemic combined systemic challenges and poor personal decisions related to diet and physical exercise.
The results also revealed that BMI categories are not significantly linked to diabetes mellitus compared to ESRD, respiratory diseases, and cardiovascular disease, among the comorbidities. This finding suggests that obesity is unlikely to trigger insulin resistance and affect blood glucose absorption in cells. In keeping with our study, similar results were reported: no significant associations between BMI categories and diabetes [2]. The result contrasts with wider literature showing that there is a strong link between diabetes mellitus and obesity [18,19]. Essentially, studies have shown that obesity increases the development of insulin resistance by releasing more pro-inflammatory substances, thereby accelerating diabetes development [16]. The inconsistency between the obtained results and the literature needs further investigation. Therefore, addressing obesity should involve educating individuals on healthy nutrition as the primary strategy for avoiding unhealthy food intake, such as artificial sugars, which not only cause obesity but also contribute to diabetes mellitus.
When analyzing the relationship between BMI groups and COVID-19 outcomes, the study found a significant difference in mortality rates among the groups. Those with obesity also showed a significantly higher demand for mechanical ventilation, higher cases of lung infiltrate, and lower oxygen saturation compared to those in the normal weight categories. This finding suggests that obesity increases distress in patients due to its numerous comorbidities, which is consistent with Rietman et al.’s study [20], which found that obesity is strongly associated with physical frailty and negatively affects a patient’s ability to perform certain tasks. The study also reveals that a higher BMI increases the risk of adverse COVID-19 treatment outcomes because affected patients must deal with many health issues that weaken the immune system.
The current study also found that BMI categories were associated with age group and gender with p-values of <0.001 and 0.005, respectively. Similarly, a recent study in Saudi Arabia reported p-values of <0.0001 and 0.021 for age group and gender, respectively [21]. Since these p-values are less than 0.05, it can be inferred that age group and gender were statistically significant in demonstrating the association of COVID-19 with the patient’s BMI.
Furthermore, the study found p-values of 0.003 for cardiovascular disease, 0.013 for respiratory diseases, and 0.021 for ESRD, while noting 0.064 for diabetes mellitus. The results suggested that except for diabetes mellitus, BMI significantly affected most comorbidities noted during COVID-19 and adversely affected the health of the patients. The result is consistent with that of Townsend et al., showing that during COVID-19, there were higher rates of hospitalization for patients who were obese and had comorbidities such as cardiovascular diseases [22]. Similarly, the finding can be explained by Reitman et al., who showed that BMI was significantly related to physical frailty since obese individuals are more likely to suffer from damage to most body organs that are overworked [20]. The views explain the significant relationships with cardiovascular, respiratory, and ESRD diseases that are linked to specific organs but not diabetes mellitus.
Additionally, the study found a p-value of 0.418 for ICU admissions, p = 0.002 for oxygen saturation of 95% or less, <0.001 for mechanical ventilation, <0.001 for lung infiltrate, <0.001 for the length of hospital stay, and 0.004 for deaths. In comparison, other studies have reported p-values of <0.0001 for ICU admissions, <0.010 for oxygen saturation of 95% or less, 0.35 for mechanical ventilation, <0.0001 for lung infiltrate, 0.001 for the length of hospital stay, and 0.05 for deaths [22]. Since the p-values for these outcomes are less than 0.05, it is clear that patients’ BMIs are statistically significantly associated with COVID-19 outcomes in hospitalized patients. The study’s findings on deaths demonstrate the influence of patients’ BMI since the p-value is greater than 0.05.
The study also used a logistic regression model that adjusted for age, gender, RD, CVD, and ESRD to estimate the relationship between outcomes and weight-related categories, with normal weight as the reference group. The p-value for ICU admissions attributed to overweight and obesity was not significant, in contrast to other studies that found a p-value of 0.014 for ICU admissions attributed to overweight and <0.0001 for obesity [23]. Comparing these findings reveals that ICU admissions are an appropriate intervention for overweight and obese patients since their frequency in these groups is higher than in the reference group.
We found that the p-value for oxygen saturation of 95% or less attributed to being overweight was not significant, while the p-value for obesity was <0.001 with an OR of 2.450. A comparable study reported that oxygen saturation is less than 95% and statistically significant for overweight and obese COVID-19 patients, with p-values of <0.0001 and <0.0123, respectively [24]. The study’s findings estimated that overweight and obese patients were 3.666 and 2.815 times more likely to require mechanical ventilation than normal-weight patients, respectively. Wider literature has shown p-values of <0.019 for overweight and <0.0001 for obesity for mechanical ventilation [25,26,27,28,29,30].
Furthermore, we found that the p-value for lung infiltrate was not statistically significant for overweight compared to normal weight. In contrast, the p-value for lung infiltrate attributed to obesity was statistically significant, with a p-value of <0.001 and an OR of 3.384. Lung infiltrate attributed to overweight was 0.601, while it was <0.0001 for obesity [31,32,33]. These findings suggest lung infiltration is ineffective for overweight patients since its p-value is greater than 0.05. However, lung infiltration is 3.4 times more likely in obese patients than in the reference group.
We found that the survival rate of COVID-19 patients admitted to the hospital was not statistically significant (p = 0.71) based on different levels of BMI. However, the survival rate between BMI categories (p < 0.001) for those admitted to the ICU was statistically significant. These findings were similar to that of a large cohort study of Swedish ICU patients with COVID-19, where a high BMI was associated with an increased risk of death and a prolonged length of stay in the ICU [8]. In contrast, other studies have revealed that BMI is unrelated to the survival rate in COVID-19 patients admitted to the ICU [9].
5. Conclusions
This retrospective study was conducted during the first two waves of the COVID-19 pandemic, and a high BMI was identified as an independent risk factor associated with an increased risk of lower oxygen saturation (<93%), requiring mechanical ventilation, lung infiltrate, death, and prolonged length of stay in the ICU. Based on these findings, it is suggested that individuals with obesity should be closely monitored when hospitalized for COVID-19.
Author Contributions
Conceptualisation, S.A. (Salma AlBahrani) and J.S.A.; Methodology, S.A. (Salma AlBahrani), T.N.A.-M., Y.A.A.N., A.S.A., A.M.A., A.A. and M.H.A.; Software, R.M.M., F.A. and Z.A.; Formal Analysis, T.N.A.-M., S.A. (Saad AlRabeeah) and R.M.M.; Investigation, A.M.A. and H.R.A.; Resources, M.B., A.A., S.A. (Saad AlRabeeah) and H.R.A.; Data Curation, F.A., J.S.A. and A.S.A.; Writing—Original Draft Preparation, S.A. (Salma AlBahrani), T.N.A.-M., Y.A.A.N. and Z.A.; Writing—Review and Editing, S.A. (Salma AlBahrani), T.N.A.-M., Y.A.A.N., R.M.M., A.S.A. and S.A. (Saad AlRabeeah), A.M.A., F.A., M.H.A., M.B., H.R.A. and J.S.A.; Supervision, J.S.A.; Project Administration, S.A. All authors have read and agreed to the published version of the manuscript.
Funding
This research received no external funding.
Institutional Review Board Statement
The study was conducted in accordance with the Declaration of Helsinki and approved by the Institutional Review Board of the Armed Forces hospitals located in Eastern Province (IRB #AFHER-IRB-2020-034).
Informed Consent Statement
Not applicable.
Data Availability Statement
The data presented in this study are available upon reasonable request from the corresponding author.
Acknowledgments
The authors would like to thank the Department of Internal Medicine for sourcing and organizing the data and KFMMC and Osama Al. Titi for helping us in arranging and finalizing the raw data.
Conflicts of Interest
The authors declare no conflict of interest.
References
- Watanabe, M.; Caruso, D.; Tuccinardi, D.; Risi, R.; Zerunian, M.; Polici, M.; Pucciarelli, F.; Tarallo, M.; Strigari, L.; Manfrini, S.; et al. Visceral fat shows the strongest association with the need of intensive care in patients with COVID-19. Metabolism 2020, 111, 154319. [Google Scholar] [CrossRef]
- AlKhafaji, D.; Al Argan, R.; Albahrani, S.; Al Elq, A.; Albaker, W.; Al-Hariri, M.; Alwaheed, A.; Alqatari, S.; Alzaki, A.; Alsaid, A.; et al. The impact of obesity on hospitalized patients with COVID-19 infection in the Eastern Province of Saudi Arabia. J. Med. Life 2022, 15, 425–432. [Google Scholar] [CrossRef] [PubMed]
- Williamson, E.J.; Walker, A.J.; Bhaskaran, K.; Bacon, S.; Bates, C.; Morton, C.E.; Curtis, H.J.; Mehrkar, A.; Evans, D.; Inglesby, P.; et al. Factors associated with COVID-19-related death using OpenSAFELY. Nature 2020, 584, 430–436. [Google Scholar] [CrossRef] [PubMed]
- World Health Organization, WHO. World Health Organisation Diabetes Country Profiles: Saudi Arabia. 2016. Available online: https://www.who.int/diabetes/country-profiles/sau_en.pdf (accessed on 31 May 2021).
- Cho, Y.; Cho, Y.; Choi, H.J.; Lee, H.; Lim, T.H.; Kang, H.; Ko, B.S.; Oh, J. The effect of BMI on COVID-19 outcomes among older patients in South Korea: A nationwide retrospective cohort study. Ann. Med. 2021, 53, 1293–1302. [Google Scholar] [CrossRef] [PubMed]
- Peng, Y.D.; Meng, K.; Guan, H.Q.; Leng, L.; Zhu, R.R.; Wang, B.Y.; He, M.A.; Cheng, L.X.; Huang, K.; Zeng, Q.T. Clinical characteristics and outcomes of 112 cardiovascular disease patients infected by 2019-nCoV. Zhonghua Xin Xue Guan Bing Za Zhi 2020, 48, E004. [Google Scholar]
- Földi, M.; Farkas, N.; Kiss, S.; Zádori, N.; Váncsa, S.; Szakó, L.; Dembrovszky, F.; Solymár, M.; Bartalis, E.; Szakács, Z.; et al. Obesity is a risk factor for developing critical condition in COVID-19 patients: A systematic review and meta-analysis. Obes. Rev. 2020, 21, e13095. [Google Scholar] [CrossRef]
- Sjögren, L.; Stenberg, E.; Thuccani, M.; Martikainen, J.; Rylander, C.; Wallenius, V.; Olbers, T.; Kindblom, J.M. Impact of obesity on intensive care outcomes in patients with COVID-19 in Sweden—A cohort study. PLoS ONE 2021, 16, e0257891. [Google Scholar] [CrossRef]
- Zangeneh, M.; Valeh, T.; Sharifi, A. Survival analysis based on body mass index in patients with COVID-19 admitted to the intensive care unit of Amir Al-Momenin Hospital in Arak–2021. Obes. Med. 2022, 32, 100420. [Google Scholar] [CrossRef]
- Chandarana, H.; Dane, B.; Mikheev, A.; Taffel, M.; Feng, Y.; Rusinek, H. Visceral adipose tissue in patients with COVID-19: Risk stratification for severity. Abdom. Radiol. 2021, 46, 818–825. [Google Scholar] [CrossRef]
- Wu, J.; Li, W.; Shi, X. Early antiviral treatment contributes to alleviate the severity and improve the prognosis of patients with novel coronavirus disease (COVID-19). J. Intern. Med. 2020, 288, 128–138. [Google Scholar] [CrossRef] [Green Version]
- Huang, Y.; Lu, Y.; Huang, Y.-M. Obesity in patients with COVID-19: A systematic review and meta-analysis. Metabolism 2020, 113, 154378. [Google Scholar] [CrossRef] [PubMed]
- Barron, E.; Bakhai, C.; Kar, P.; Weaver, A.; Bradley, D.; Ismail, H.; Knighton, P.; Holman, N.; Khunti, K.; Sattar, N.; et al. Associations of type 1 and type 2 diabetes with COVID-19-related mortality in England: A whole-population study. Lancet Diabetes Endocrinol. 2020, 8, 813–822. [Google Scholar] [CrossRef] [PubMed]
- O’brien, J.M.; Phillips, G.S.; Ali, N.A.; Lucarelli, M.; Marsh, C.B.; Lemeshow, S. Body mass index is independently associated with hospital mortality in mechanically ventilated adults with acute lung injury. Crit. Care Med. 2006, 34, 738–744. [Google Scholar] [CrossRef]
- Lindgren, M.; Toska, T.; Alex, C.; Lundberg, C.E.; Cronie, O.; Rosengren, A.; Adiels, M.; Sjöland, H. BMI, sex and outcomes in hospitalised patients in western Sweden during the COVID-19 pandemic. Sci. Rep. 2022, 12, 4918. [Google Scholar] [CrossRef]
- Popkin, B.M.; Du, S.; Green, W.D.; Beck, M.A.; Algaith, T.; Herbst, C.H.; Alsukait, R.F.; Alluhidan, M.; Alazemi, N.; Shekar, M. Individuals with obesity and COVID-19: A global perspective on the epidemiology and biological relationships. Obes. Rev. 2020, 21, e13128. [Google Scholar] [CrossRef]
- Griffith, G.J.; Morris, T.T.; Tudball, M.J.; Herbert, A.; Mancano, G.; Pike, L.; Sharp, G.C.; Sterne, J.; Palmer, T.M.; Smith, G.D.; et al. Collider bias undermines our understanding of COVID-19 disease risk and severity. Nat. Commun. 2020, 11, 5749. [Google Scholar] [CrossRef] [PubMed]
- Alyami, M.H.; Naser, A.Y.; Orabi, M.A.A.; Alwafi, H.; Alyami, H.S. Epidemiology of COVID-19 in the Kingdom of Saudi Arabia: An Ecological Study. Front. Public Health 2020, 8, 506. [Google Scholar] [CrossRef]
- Denova-Gutiérrez, E.; Lopez-Gatell, H.; Alomia-Zegarra, J.L.; López-Ridaura, R.; Zaragoza-Jimenez, C.A.; Dyer-Leal, D.D.; Cortés-Alcala, R.; Villa-Reyes, T.; Gutiérrez-Vargas, R.; Rodríguez-González, K.; et al. The Association of Obesity, Type 2 Diabetes, and Hypertension with Severe Coronavirus Disease 2019 on Admission Among Mexican Patients. Obesity 2020, 28, 1826–1832. [Google Scholar] [CrossRef]
- Rietman, M.L.; Van Der A, D.L.; Van Oostrom, S.H.; Picavet, H.S.J.; Dollé, M.E.T.; Van Steeg, H.; Verschuren, W.M.M.; Spijkerman, A.M.W. The association between BMI and different frailty domains: A U-shaped curve? J. Nutr. Health Aging 2018, 22, 8–15. [Google Scholar] [CrossRef]
- Owen, W.F.; Carmona, R.; Pomeroy, C. Failing Another National Stress Test on Health Disparities. JAMA 2020, 323, 1905–1906. [Google Scholar] [CrossRef] [Green Version]
- Townsend, M.J.; Kyle, T.K.; Stanford, F.C. Outcomes of COVID-19: Disparities in obesity and by ethnicity/race. Int. J. Obes. 2020, 44, 1807–1809. [Google Scholar] [CrossRef]
- Clift, A.K.; Coupland, C.A.C.; Keogh, R.H.; Diaz-Ordaz, K.; Williamson, E.; Harrison, E.M.; Hayward, A.; Hemingway, H.; Horby, P.; Mehta, N.; et al. Living risk prediction algorithm (QCOVID) for risk of hospital admission and mortality from coronavirus 19 in adults: National derivation and validation cohort study. BMJ 2020, 371, m3731. [Google Scholar] [CrossRef] [PubMed]
- Sattar, N.; Ho, F.K.; Gill, J.M.; Ghouri, N.; Gray, S.R.; Celis-Morales, C.A.; Katikireddi, S.V.; Berry, C.; Pell, J.P.; McMurray, J.J.; et al. BMI and future risk for COVID-19 infection and death across sex, age and ethnicity: Preliminary findings from UK biobank. Diabetes Metab. Syndr. Clin. Res. Rev. 2020, 14, 1149–1151. [Google Scholar] [CrossRef]
- Hippisley-Cox, J.; Young, D.; Coupland, C.; Channon, K.M.; Tan, P.S.; A Harrison, D.; Rowan, K.; Aveyard, P.; Pavord, I.D.; Watkinson, P.J. Risk of severe COVID-19 disease with ACE inhibitors and angiotensin receptor blockers: Cohort study including 8.3 million people. Heart 2020, 106, 1503–1511. [Google Scholar] [CrossRef] [PubMed]
- Hewitt, J.; Carter, B.; Vilches-Moraga, A.; Quinn, T.J.; Braude, P.; Verduri, A.; Pearce, L.; Stechman, M.; Short, R.; Price, A.; et al. The effect of frailty on survival in patients with COVID-19 (COPE): A multicentre, European, observational cohort study. Lancet Public Health 2020, 5, e444–e451. [Google Scholar] [CrossRef] [PubMed]
- Lockhart, S.M.; O’Rahilly, S. When two pandemics meet: Why is obesity associated with increased COVID-19 mortality? Medicine 2020, 1, 33–42. [Google Scholar] [CrossRef]
- Battisti, S.; Pedone, C.; Napoli, N.; Russo, E.; Agnoletti, V.; Nigra, S.G.; Dengo, C.; Mughetti, M.; Conte, C.; Pozzilli, P.; et al. Computed Tomography Highlights Increased Visceral Adiposity Associated With Critical Illness in COVID-19. Diabetes Care 2020, 43, e129–e130. [Google Scholar] [CrossRef]
- Umbrello, M.; Fumagalli, J.; Pesenti, A.; Chiumello, D. Pathophysiology and Management of Acute Respiratory Distress Syndrome in Obese Patients. Semin. Respir. Crit. Care Med. 2019, 40, 40–56. [Google Scholar] [CrossRef]
- Ni, Y.-N.; Luo, J.; Yu, H.; Wang, Y.-W.; Hu, Y.-H.; Liu, D.; Liang, B.-M.; Liang, Z.-A. Can body mass index predict clinical outcomes for patients with acute lung injury/acute respiratory distress syndrome? A meta-analysis. Crit. Care 2017, 21, 36. [Google Scholar] [CrossRef] [Green Version]
- Dietz, W.; Santos-Burgoa, C. Obesity and its Implications for COVID-19 Mortality. Obesity 2020, 28, 1005. [Google Scholar] [CrossRef] [Green Version]
- Melebari, S.; ElBahrawy, A.; Aljahdali, A.; Hussain, N.; Bahwaireth, L.; Alahmadi, G.; Alharbi, R.; Alghamdi, J.; Alzahrani, O. The prevalence of obesity in hospitalized COVID-19 patients at King Abdullah Medical City, Makkah, Saudi Arabia. Int. J. Med. Dev. Ctries. 2020, 5, 1579–1582. [Google Scholar] [CrossRef]
- Gao, F.; Zheng, K.I.; Wang, X.-B.; Sun, Q.-F.; Pan, K.-H.; Wang, T.-Y.; Chen, Y.-P.; Targher, G.; Byrne, C.D.; George, J.; et al. Obesity Is a Risk Factor for Greater COVID-19 Severity. Diabetes Care 2020, 43, e72–e74. [Google Scholar] [CrossRef] [PubMed]
Figure 1.
(a) Kaplan-Meier survival plots show the hospitalized COVID-19 patients’ survival based on different levels of BMI (less than 25, 25 to 30, more than 30) and show that the survival rate in these three levels of body mass index was not statistically significant (p = 0.71). (b) Comparison of ICU COVID-19 patients’ survival based on different levels of BMI was statistically significant. (p < 0.001).
Figure 1.
(a) Kaplan-Meier survival plots show the hospitalized COVID-19 patients’ survival based on different levels of BMI (less than 25, 25 to 30, more than 30) and show that the survival rate in these three levels of body mass index was not statistically significant (p = 0.71). (b) Comparison of ICU COVID-19 patients’ survival based on different levels of BMI was statistically significant. (p < 0.001).
Figure 2.
(a) Cox regression model to estimate HR and 95% CI of the impact of BMI on mortality of hospitalized COVID-19 patients, adjusting for potential confounder variables (age, gender, CD, RD, and ESRD). (b) Cox regression model to estimate HR and 95% CI of the impact of BMI on mortality of ICU COVID-19 patients, adjusting for potential confounder variables (age, gender, CD, RD, and ESRD).
Figure 2.
(a) Cox regression model to estimate HR and 95% CI of the impact of BMI on mortality of hospitalized COVID-19 patients, adjusting for potential confounder variables (age, gender, CD, RD, and ESRD). (b) Cox regression model to estimate HR and 95% CI of the impact of BMI on mortality of ICU COVID-19 patients, adjusting for potential confounder variables (age, gender, CD, RD, and ESRD).
Table 1.
Relationship between demographics, comorbidities, and COVID-19 outcomes with BMI using the Chi-square test for the categorical variables (n = 600).
Table 1.
Relationship between demographics, comorbidities, and COVID-19 outcomes with BMI using the Chi-square test for the categorical variables (n = 600).
| Variable | Total = 600 | Normal Weight = 157 | Overweight = 188 | Obese 255 | (p-Value) |
|---|---|---|---|---|---|
| (1) Demographical | |||||
| (a) Age group | <0.001 * | ||||
| <20 | 26 (4.3%) | 14 (8.9 %) | 9 (4.8%) | 3 (1.2%) | |
| 20–40 | 158 (26.3%) | 44 (28 %) | 42 (22.3%) | 72 (28.2%) | |
| 41–60 | 248 (41.3%) | 53 (33.8 %) | 82 (43.6%) | 113 (44.3%) | |
| 61–80 | 145 (24.2%) | 36 (22.9 %) | 45 (23.9%) | 64 (25.1%) | |
| >80 | 23 (3.8%) | 10 (6.4 %) | 10 (5.3%) | 3 (1.2%) | |
| (b) Gender | 0.005 * | ||||
| Female | 219 (36.5%) | 50 (28%) | 64 (34 %) | 111 (43.5 %) | |
| Male | 381 (63.5%) | 132 (72 %) | 123 (66%) | 144 (56.5 %) | |
| (2) comorbidities | Total =600 | Normal weight =157 | Overweight =188 | Obese 255 | (p-Value) |
| (a) Diabetes mellitus | |||||
| Yes | 285 (47.5%) | 100 (55.4 %) | 82 (43.6 %) | 116 (45.5 %) | |
| No | 315 (52.5%) | 82 (44.6%) | 105 (56.4%) | 139 (54.5 %) | 0.064 |
| (b) Cardiovascular disease | |||||
| Yes | 110 (18.3%) | 26 (16.6 %) | 49 (26.1%) | 35 (13.7%) | |
| No | 490 (81.7%) | 131 (83.4 %) | 139 (73.9%) | 220 (86.3%) | 0.003 * |
| (c)Respiratory Diseases (RD) | 0.013 * | ||||
| Yes | 72 (12%) | 27 (17.2%) | 13 (6.9 %) | 32 (12.5%) | |
| No | 528 (88%) | 130 (82.8 %) | 175 (93.1 %) | 223 (87.5%) | |
| End-Stage Renal Disease (ESRD) | 0.021 * | ||||
| Yes | 33 (5.5%) | 15 (5.1%) | 4 (2.1 %) | 14 (8.9%) | |
| NO | 567 (94.5%) | 240 (94.1 %) | 184 (97.9 %) | 143 (91.1%) | |
| (3) The outcomes | Total = 600 | Normal weight = 157 | Overweight = 188 | Obese 255 | (p-value) |
| (a) Admission to ICU | 0.418 | ||||
| Yes | 203 (33.8%) | 48 (30.6 %) | 70 (37.2 %) | 85 (33.3 %) | |
| No | 397 (66.16%) | 109 (69.4 %) | 118 (62.8%) | 170 (66.7 %) | |
| (b) O2<93% | 0.002 * | ||||
| Yes | 307 (51.2%) | 68 (43.3 %) | 87 (46.3%) | 152 (59.6 %) | |
| NO | 293 (48.8%) | 89 (56.7 %) | 101 (53.7%) | 103 (40.4 %) | |
| (c) Mechanical ventilation | <0.001 * | ||||
| Yes | 83 (13.8%) | 10 (6.4 %) | 39 (20.7 %) | 34 (13.3 %) | |
| No | 517 (86.2%) | 147 (93.6%) | 149 (79.3 %) | 221 (86.7 %) | |
| (d)lung infiltrate | <0.001 * | ||||
| Yes | 364 (60.7%) | 85 (54.1 %) | 90 (47.9%) | 189 (74.1%) | |
| No | 236 (39.3%) | 72 (45.9 %) | 98 (52.1%) | 66 (25.9 %) | |
| (f) Death | 0.004 * | ||||
| Yes | 65 (10.8%) | 23 (14.6 %) | 27 (14.4%) | 15 (5.9%) | |
| No | 535 (89.2%) | 134 (85.4%) | 161 (85.6 %) | 240 (94.1%) |
* significant p-value < 0.05
Table 2.
Kruskal-Wallis test investigating the length of hospital stay mean rank between the different BMI categories with post hoc analysis.
Table 2.
Kruskal-Wallis test investigating the length of hospital stay mean rank between the different BMI categories with post hoc analysis.
| BMI | N = 600 | Mean Rank | df | X2 | p-Value | Post Hoc Analysis | p-Value |
|---|---|---|---|---|---|---|---|
| Normal weight 18.5–24.9 | 157 | 345.66 | 2 | 19.79 | <0.001 * | Normal weight vs. Overweight | 0.110 |
| Overweight 25–29.9 | 188 | 306.56 | Normal weight vs. Obese | <0.001 * | |||
| Obese ≥30 Kg/m2 | 255 | 268.23 | Overweight vs. Obese | 0.064 |
* significant p-value < 0.05
Table 3.
Logistic regression model to estimate OR and 95% CI for the association between BMI categories and outcomes with potential confounders.
Table 3.
Logistic regression model to estimate OR and 95% CI for the association between BMI categories and outcomes with potential confounders.
| Model 1. BMI Adjusted for Age, Gender, CVD, RD, and ESRD | ||||||
|---|---|---|---|---|---|---|
| Variable | O2 < 93% | Mechanical Ventilation | Lung Infiltrate | |||
| OR (95% CI) | p-Value | OR (95% CI) | p-Value | OR(95% CI) | p-Value | |
| Normal weight (reference group) | - | - | - | - | - | - |
| Overweight | 1.55 (0.958–2.519) | 0.074 | 3.666 (1.660–8.096) | 0.001 | 0.894 (0.555–1.439) | 0.664 |
| Obese | 2.450 (1.837–4.610) | <0.001 | 2.815 (1.261–6.285) | 0.012 | 3.384 (2.111–5.477) | <0.001 |
Table 4.
Cox regression model to estimate HR and 95% CI of the impact of BMI on mortality of hospitalized COVID-19 patients (A) and ICU patients (B) adjusting for potential confounder variables.
Table 4.
Cox regression model to estimate HR and 95% CI of the impact of BMI on mortality of hospitalized COVID-19 patients (A) and ICU patients (B) adjusting for potential confounder variables.
| Model A. BMI Adjusted for Age, Gender, CVD, RD, and ESRD | Model B. BMI Adjusted for Age, Gender, CVD, RD, and ESRD | |||||
|---|---|---|---|---|---|---|
| Variable | Death | Death | ||||
| HR | (95% CI) | p-Value | HR | (95% CI) | p-Value | |
| Normal weight (reference group) | - | - | - | - | - | - |
| Overweight | 1.535 | (0.794–2.966) | 0.202 | 2.222 | (1.204–4.098) | 0.011 |
| Obese | 1.175 | (0.570–2.421) | 0.662 | 0.675 | (0.339–1.345) | 0.263 |
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content. |
© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
MDPI and ACS Style
AlBahrani, S.; Al-Maqati, T.N.; Al Naam, Y.A.; Alqahtani, J.S.; Alqahtani, A.S.; AlRabeeah, S.; Aldhahir, A.M.; Alkhalaf, F.; Alzuraiq, H.R.; Alenezi, M.H.; et al. The Association of Body Mass Index with COVID-19 Complications and Survival Rate at a Tertiary Hospital. Life 2023, 13, 1572. https://doi.org/10.3390/life13071572
AMA Style
AlBahrani S, Al-Maqati TN, Al Naam YA, Alqahtani JS, Alqahtani AS, AlRabeeah S, Aldhahir AM, Alkhalaf F, Alzuraiq HR, Alenezi MH, et al. The Association of Body Mass Index with COVID-19 Complications and Survival Rate at a Tertiary Hospital. Life. 2023; 13(7):1572. https://doi.org/10.3390/life13071572
Chicago/Turabian StyleAlBahrani, Salma, Thekra N. Al-Maqati, Yaser A. Al Naam, Jaber S. Alqahtani, Abdullah S. Alqahtani, Saad AlRabeeah, Abdulelah M. Aldhahir, Faisal Alkhalaf, Hind R. Alzuraiq, Maryam Hamad Alenezi, and et al. 2023. "The Association of Body Mass Index with COVID-19 Complications and Survival Rate at a Tertiary Hospital" Life 13, no. 7: 1572. https://doi.org/10.3390/life13071572
Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.
