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Clinical Research

A higher BMI is not associated with a different immune response and disease course in critically ill COVID-19 patients



Obesity appears to be an independent risk factor for ICU admission and a severe disease course in COVID-19 patients. An aberrant inflammatory response and impaired respiratory function have been suggested as underlying mechanisms. We investigated whether obesity is associated with differences in inflammatory, respiratory, and clinical outcome parameters in critically ill COVID-19 patients.


Sixty-seven COVID-19 ICU patients were divided into obese (BMI ≥ 30 kg/m2, n = 18, 72% class I obesity, 28% class II obesity) and non-obese (BMI < 30 kg/m2, n = 49) groups. Concentrations of circulating interleukin (IL)-6, IL-8, IL-10, tumor necrosis factor alpha (TNF-α), interferon gamma (IFN-γ), interferon gamma-induced protein (IP)-10, monocyte chemoattractant protein (MCP)-1, and IL-1 receptor antagonist (RA) were determined from ICU admission until 10 days afterward, and routine laboratory and clinical parameters were collected.


BMI was 32.6 [31.2–34.5] and 26.0 [24.4–27.7] kg/m2 in the obese and non-obese group, respectively. Apart from temperature, which was significantly lower in obese patients (38.1 [36.9–38.9] vs. 38.7 [38.0 −39.5] °C, p = 0.02), there were no between-group differences on ICU admission. Plasma cytokine concentrations declined over time (p < 0.05 for all), but no differences between obese and non-obese patients were observed. Also, BMI did not correlate with the cytokine response (IL-6 r = 0.09, p = 0.61, TNF-α r = 0.03, p = 0.99, IP-10 r = 0.28, p = 0.11). The kinetics of clinical inflammatory parameters and respiratory mechanics were also similar in both groups. Finally, no differences in time on ventilator, ICU length of stay or 40-day mortality between obese and non-obese patients were apparent.


In COVID-19 patients requiring mechanical ventilation in the ICU, a higher BMI is not related to a different immunological response, unfavorable respiratory mechanics, or impaired outcome.


The Coronavirus Disease 2019 (COVID-19) pandemic currently sweeps across the globe, leading to high morbidity and mortality. This infection, caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), can cause acute respiratory distress syndrome (ARDS) requiring mechanical ventilation in the intensive care unit (ICU). Age, male sex, and multiple comorbidities, including type 2 diabetes, hypertension, and coronary artery disease, were identified as risk factors related to severity of COVID-19 disease [1,2,3,4]. These comorbidities are more prevalent in the obese population than in patients with a normal body weight [5]. Also, the prevalence of obesity among COVID-19 patients requiring mechanical ventilation was shown to be higher than expected when compared to controls with non COVID-19-related acute pulmonary diseases, and the need for mechanical ventilation increased with increasing body mass index (BMI) [6, 7]. Finally, mortality was shown to be significantly higher in overweight/obese COVID-19 patients compared to normal-weight patients [7]. Of interest, obesity itself is also recognized as an independent risk factor of severe pulmonary H1N1 influenza infection and mortality [8].

The underlying mechanisms of obesity as a factor contributing to COVID-19 disease severity are currently poorly understood, but various possible explanations have been proposed. For instance, in obese patients, pulmonary function may be restricted because of decreased functional residual capacity, resulting in lower blood oxygen levels [9]. In addition, the angiotensin converting enzyme 2 receptor, which is utilized by SARS-CoV-2 to enter cells, is highly expressed by adipocytes and expression levels were shown to be higher in adipocytes of patients with obesity and type 2 diabetes [10]. Therefore, it appears plausible that adipose tissue may serve as a reservoir for the virus, leading to more pronounced and sustained viral shedding, resulting in a perpetual inflammatory response and impaired outcome.

To date, it is not known whether obesity is only a risk factor for COVID-19 susceptibility and for the need of intensive care, or whether it also influences the outcome of the patients once admitted on ICUs. Previous studies in critically ill COVID-19 patients have yielded ambiguous results, with some reporting associations between lower BMI and mortality [11], whereas others showed increased mortality in (severely) obese patients [12, 13]. In the present study, we investigated associations between obesity and the immune response as well as the clinical course of SARS-CoV-2 infection in critically ill patients on the ICU of a tertiary university hospital. Elucidating these mechanisms may pave the way for the development of new treatment strategies for obese COVID-19 patients.


Study design and participants

In this prospective observational cohort study, all consecutive COVID-19 patients admitted to the ICU in the Radboud University Medical Center (Nijmegen, The Netherlands) between March 11 and April 27 were included. COVID-19 was diagnosed by a positive SARS-CoV-2 RT-PCR test in nasopharyngeal and throat swabs and/or by typical chest CT-scan findings. Patients with a pre-existing immunosuppressed status or other comorbidities that strongly influence prognosis were excluded. Patients were divided into an obese (BMI ≥ 30 kg/m2) and non-obese (BMI < 30 kg/m2) group, according to the classification of obesity by the World Health Organisation [14]. Also, individual BMI values were correlated with circulating cytokine concentrations. The study was carried out in the Netherlands in accordance with the applicable rules concerning the review of research ethics committees and informed consent. All patients or legal representatives were informed about the study details and could decline to participate.

Data collection

Data were collected from the electronic patient files (EPIC, EPIC Systems Corporation, Verona, Wisconsin, USA) and recorded in the good clinical practice-compliant data management system Castor (Castor EDC, Amsterdam, the Netherlands). ICU admission day was designated as day 1, and serial data were obtained for 10 consecutive days. Clinical outcomes (time on mechanical ventilation, ICU length of stay (LOS), and mortality) were recorded for 40 consecutive days. Serial values of mean arterial pressure, body temperature, and leukocyte differentiation as well as circulating levels of C-reactive protein (CRP), procalcitonin (PCT), D-dimer, ferritin, and cytokines (see below) were used to assess the inflammatory response to SARS-CoV-2 infection. Patients were actively cooled when they had a fever of >40 °C. In these cases, body temperature was imputed as 40 °C. Positive end expiratory pressure (PEEP), tidal volume per kilograms ideal body weight (TVIBW) and PaO2/FiO2 ratio were used to assess the level of respiratory support required. Tidal volume was only recorded in patients on volume-controlled mechanical ventilation. Because the vast majority of patients were switched to pressure support ventilation after 4 days of ICU admission, TVIBW data were analyzed until this timepoint. Ideal body weight was calculated based on sex and height, using the formulas provided by the ARDS Network [15].

Cytokine concentration measurements

A baseline blood sample was obtained within the first 48 h following ICU admission and serial samples were collected every other day. Ethylenediaminetetraacetic acid-anticoagulated blood was centrifuged (2000 × g, 10 min, 4 °C), after which plasma was stored at −80 °C until analysis. Concentrations of interleukin (IL)-6, IL-8, IL-10, tumor necrosis factor (TNF)-α, interferon gamma (IFN-γ), IFN-γ-induced protein (IP)-10, monocyte chemoattractant protein (MCP)-1, and IL-1 receptor antagonist (IL-1RA) were determined in one batch using a Luminex assay (Milliplex, Millipore, Billerica, USA). The lower detection limit was 3.2 pg/mL for all cytokines.

Statistical analysis

Statistical analysis was performed using SPSS 25 (IBM) and Graphpad Prism 8 software (GraphPad Software). Several variables were not measured daily; therefore, depending on the frequency of measurements, data were binned into 2 or 3 days using a custom script made in R-studio v3.6.2 ( Because of the relatively small group size, normality was not assumed and all data are displayed as median with interquartile range [IQR] or geometric mean with 95% confidence interval. Baseline characteristics were analyzed using chi-square tests and Mann–Whitney U tests. Between-group differences over time were analyzed using linear mixed effects model analysis on log-transformed data followed by post-hoc analyses using Sidak’s multiple comparisons tests in all serially measured variables. Relationships between BMI and cytokines were analyzed using Spearman’s correlation. Time on mechanical ventilation, ICU LOS, and mortality were analyzed using log-rank and chi-square tests. Patients who died in the hospital or those who were still in the ICU and/or receiving mechanical ventilation on day 40 were censored at day 41 for the analysis of time on mechanical ventilation and ICU LOS. For the mortality analysis, patients who were discharged alive from the hospital or were still in the ICU or hospital on day 40 were censored at day 41.


Patient characteristics

All 77 patients with proven COVID-19 consecutively admitted to the ICU of Radboud University Medical Center were assessed for study inclusion. Patients with a pre-existing immunosuppressed status were excluded (n = 9, see Supplementary Fig. 1), and one patient refused participation. The remaining study population (n = 67) was divided in obese (n = 18, of which 72% with class I obesity and 28% with class II obesity) and non-obese (n = 49) groups (Fig. 1a). BMI of the entire study population was 27.7 [24.9–30.8] kg/m2 (Fig. 1), with BMI’s of 32.6 [31.2–34.5] and 26.0 [24.4–27.7] kg/m2 in the in the obese and non-obese groups, respectively (p < 0.0001, Table 1). All patients were mechanically ventilated. Temperature at ICU admission was 38.1 [36.9–38.9] °C in the obese group and 38.7 [38.0–39.5] °C in the non-obese group (p = 0.007). No significant differences in age, sex, APACHE II score, medical history, and other clinical or laboratory parameters between the two groups were observed at ICU admission (Table 1).

Fig. 1: Body mass index distribution and plasma cytokine levels.
figure 1

a Histogram depicting body mass index (BMI) frequencies. Kinetics of concentrations of circulating b interleukin (IL)-6, c IL-8, d IL-10, e tumor necrosis factor alpha (TNF-α), f interferon gamma (IFN-γ), g interferon gamma-induced protein (IP)-10, h monocyte chemoattractant protein (MCP)-1 and i IL-1 receptor antagonist (RA). Data are presented as geometric mean with 95% confidence interval. *p < 0.05, calculated using Sidak’s post-hoc multiple comparisons tests on individual timepoints.

Table 1 Patient characteristics at the time of ICU admission.

Inflammation and respiration

Plasma concentrations of all measured pro-inflammatory cytokines were highest at ICU admission and decreased over time both in the obese and non-obese groups (p < 0.05 for all cytokines, Fig. 1b–i). Except for slightly higher IP-10 levels in obese vs. non-obese patients at days 9–10, no between-group differences in any of the measured cytokines on any timepoints were observed (Fig. 1b–i). Furthermore, BMI did not correlate with concentrations of IL-6, TNF-α, and IP-10 at ICU admission (r = −0.09 p = 0.61, r = 0.03 p = 0.99 and r = 0.28 p = 0.11, respectively, Fig. 2) or any other cytokine measured (r values ranging from −0.11 to 0.06, p values all >0.50, see Supplementary Fig 2). Despite a trend toward less pronounced leucocytosis in obese patients, no significant differences were present between both groups at any of the timepoints (Fig. 3a). The baseline difference in temperature (i.e., higher in non-obese patients) persisted at later timepoints, but did not attain statistical significance (Fig. 3b). No differences were observed in CRP levels between the obese and non-obese groups (Fig. 3c). Also, no significant differences in plasma concentrations of PCT, ferritin and d-dimer were observed between both groups (Supplementary Fig. 3). Finally, no between-group differences in any of the ventilation parameters were observed (Supplementary Fig. 4).

Fig. 2: Relationship between BMI and concentrations of circulating cytokines on day of admission to the intensive care unit.
figure 2

a Interleukin (IL)-6, b tumor necrosis factor alpha (TNF-α) and c interferon gamma-induced protein (IP)-10. r- and p values were calculated using Spearman’s correlation. See supplementary Fig. 2 for the relationships between BMI and the other measured circulating cytokine concentrations.

Fig. 3: Routine laboratory and clinical inflammatory parameters.
figure 3

a White blood cell counts (WBC), b temperature, c circulating C-reactive protein (CRP). Data are represented as geometric mean (a) or geometric mean with 95% confidence interval (b, c). No significant differences on any of the individual timepoints were observed according to Sidak’s post-hoc multiple comparisons tests.

Clinical outcomes

On day 40 of ICU admission, 11% (n = 2) of the patients of the obese group was still mechanically ventilated and 17% (n = 3) was still in the ICU, while 16% (n = 8) of patients of the non-obese group were still mechanically ventilated and in the ICU (p = 0.60 and p = 0.97, respectively). Time on ventilator was 22 (16–40) days in the obese group and 27 (14–40) days in the non-obese group (p = 0.41). ICU length of stay was 25 (17–40) and 29 (15–40) days in the obese and non-obese group, respectively (p = 0.53). Forty-day ICU mortality was 17% (n = 3) in the obese group and 24% (n = 12) in the non-obese group (p = 0.50). The Kaplan–Meier curves for time on mechanical ventilation, ICU LOS and mortality are presented in Fig. 4.

Fig. 4: Clinical outcome data.
figure 4

a Time on mechanical ventilation, b ICU length-of-stay, c ICU mortality. p values depicted in the panels were calculated using log-rank tests. Dotted lines indicate 95% confidence intervals.


In this observational study in critically ill COVID-19 patients, we observed that, while disease severity and other baseline covariates were similar, temperature at ICU admission was lower in obese compared to non-obese patients. This observation may suggest that the endogenous immune-hypothalamus axis responsible for the induction of fever (IL-1-IL-6-PGE2 pathway) is less pronounced in obese compared to non-obese patients. However, no significant differences in plasma concentrations of various inflammatory markers and cytokines (most importantly IL-6) were observed between both groups. To gain sensitivity to detect a possible relationship between BMI and the cytokine response we performed correlation analyses that confirmed lack of such a relationship. Also, no significant difference in duration of mechanical ventilation, ICU length of stay, or mortality was observed between the obese and non-obese group. Taken together, these data indicate that once a COVID-19 patient becomes critically ill, the immune response and clinical course of the disease is not relevantly influenced by the patients’ BMI.

Obesity has been identified as a risk factor for severe disease and ICU admission in COVID-19 patients admitted to non-intensive care hospital wards [16, 17]. This is not necessarily in contrast with our findings, as obese individuals may be more susceptible to infection, might have a different immune response prior to becoming critically ill, and/or may require more respiratory support [6]. Although several studies have assessed associations between BMI and clinical outcomes/mortality in critically ill COVID-19 patients, conflicting findings have been reported [11,12,13]. As such, the relationship between obesity and mortality in these critically ill patients remains unclear. What our study adds pertaining to the role of BMI in critically ill COVID-19 patients are data of inflammatory/immunological markers. Of interest, a paradoxical relationship between obesity and mortality has been described in the general ICU population, as well as in critically ill patients suffering from different infectious diseases, such as pneumonia and bacterial sepsis [18, 19]. Overall, obese patients demonstrate a better survival compared to non-obese individuals, even when corrected for several covariates. This phenomenon has been coined the obesity paradox [20]. Our study was underpowered to demonstrate statistically significant differences in mortality between obese and non-obese patients, and therefore we are unable to confirm or reject the presence of the obesity paradox in COVID-19 patients.

The present study has several limitations. First, because of the observational nature of the study, no direct link between cause and effect can be deduced. Second, because of the relatively small group of (especially obese) patients, a type 2 error is possible, and our findings should be regarded as indicative, not conclusive. Nevertheless, there were also no nonsignificant trends in inflammatory parameters or correlations between BMI and any of the circulating cytokines, which would be expected in case BMI would play an crucial role in the immune response in critically ill COVID-19 patients. Third, the present study was conducted in a single center in the Netherlands, where (morbid) obesity may be less widespread compared to other countries. Accordingly, the obese group consisted largely of mildly obese patients and no patients with a BMI above 40 kg/m2 were present in our cohort. Fourth, because patients in our cohort were all included after ICU admission and received mechanical ventilation, no statements can be made about the relationship between obesity and the risk of ICU admission or requirement of mechanical ventilation. Finally, we focused on innate immunity, so possible differences between obese and non-obese COVID-19 patients in adaptive immune response remain to be explored.

In conclusion, the results of this study indicate that, in critically ill COVID-19 patients requiring mechanical ventilation, the patients’ BMI is not related to a different innate immune response, unfavorable respiratory mechanics, or impaired outcome. A larger multi-center study with a more expansive BMI distribution is warranted to confirm our findings.

Data availability

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


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The RCI-COVID-19 study group

Pleun Hemelaar2, Remi Beunders2, Tim Frenzel2, Jeroen Schouten2, Sjef van der Velde2, Hetty van der Eng2, Noortje Roovers2, Margreet Klop-Riehl2, Jelle Gerretsen2, Nicole Waalders2, Hidde Heesakkers2, Tirsa van Schaik2, Leonie Buijsse2, Leo Joosten2, Quirijn de Mast2, Martin Jaeger2, Ilse Kouijzer2, Helga Dijkstra2, Heidi Lemmers2, Reinout van Crevel2, Josephine van de Maat2, Gerine Nijman2, Simone Moorlag2, Esther Taks2, Priya Debisarun2, Heiman Wertheim2, Joost Hopman2, Janette Rahamat-Langendoen2, Chantal Bleeker-Rovers2, Hans Koenen2, Esther Fasse2, Esther van Rijssen2, Manon Kolkman2, Bram van Cranenbroek2, Ruben Smeets2, Irma Joosten2


The study was internally funded by the participating departments. EJK was funded by a Radboudumc COVID-19 grant. MGN was supported by an ERC Advanced Grant (#833247) and a Spinoza Grant of the Netherlands Organization for Scientific Research.

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Authors and Affiliations




EJK, AHdN, WJC, MK and PP designed the study. AHdN, IG, and NAFJ were responsible for sample collection and laboratory processing. EJK, WJC, and MK were responsible for data collection and management. EJK and WJC performed the statistical analysis and drafted the manuscript. AHdN, IG, NAFJ, MGN, FLvdV, JGvdH, MK and PP critically revised the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Peter Pickkers.

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The authors declare that they have no conflict of interest.

Ethical approval

The study was carried out in the Netherlands in accordance with the applicable rules concerning the review of research ethics committees and informed consent. All patients or legal representatives were informed about the study details and could decline to participate.

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Members of the RCI-COVID-19 study group are listed above Author contributions.

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Kooistra, E.J., de Nooijer, A.H., Claassen, W.J. et al. A higher BMI is not associated with a different immune response and disease course in critically ill COVID-19 patients. Int J Obes 45, 687–694 (2021).

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