Background: The unfavorable clinical outcome (higher rates of severity/morbidity/mortality) of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has a disproportionate bias towards the male sex despite no sex-based difference noted in the risk for the infection. These outcomes have widely been hinged on dysregulated systemic inflammation. Hence, this study was aimed to evaluate the influence of systemic inflammation on sex-based bias in SARS-CoV-2 infection among indigenes of Nigerian Methods: Patients’ data with positive real-time polymerase chain reaction (RT-PCR) test for coronavirus disease 2019 (COVID-19), who were admitted/managed at the Eleme treatment center in Port Harcourt, southern Nigeria, were enrolled for this study. All relevant data was acquired from archived case notes, medical review charts, nurses’ charts, and laboratory records by trained research assistants using validated data collection templates. All the collated/abstracted data were analyzed/compared between the male and female patients using both descriptive and comparative statistical tools. Results A total of eligible 598 patients were included in the analysis among them 373 (62.4%) and 225 (37.6%) males and females, respectively. The males were much older (43.63±5.93 vs. 41.15±6.09; p<0.036) with higher mean body mass index and body temperature at presentation. Significant differences were observed in terms of the age distribution, occupational, educational, marital, residential status, cigarette smoking, alcohol consumption, body mass index, comorbid, severity, and clinical outcomes between the males and females (<0.05). In addition, the males had significantly higher mean levels of creatinine, C-reactive protein (CRP), Glasgow Prognostic Score (GPS), D-dimer, total WBC, neutrophil counts, composite neutrophil/lymphocyte ratio (NLR) but lower levels of albumin, total protein, isolated platelet count, and isolated lymphocyte count (p<0.05). The males maintained a significant linear relationship with the CRP (β: 0.61; SE: 0.13; p<0.001), composite GPS (β: 0.59; SE: 0.01; p<0.001), D-dimer (β: 0.52; SE: 0.09; p<0.001), and the composite NLR (β: 0.38; SE: 0.10; p<0.001) compare to their female counterparts. Additionally, CRP (OR: 8.86; 95%CI: 7.34-9.78; p<0.001), the composite GPS (OR: 7.41; 95%CI: 6.36-8.79; p<0.001), D-dimer (OR: 5.4; 95%CI: 4.32-6.65), and the composite NLR (OR: 4.23; 95%CI: 3.44-5.69; p<0.001) all had significant and robust associations with unfavorable clinical outcomes among the males compared to the females. Conclusion: Exaggerated systemic inflammatory markers/indices were more pronounced among the males in association with unfavorable clinical outcomes. These sex-based characteristics should be factored in during the management of SARS-CoV-2 infection. However, further studies are recommended to evaluate conclusions from the current study.
Published in | European Journal of Clinical and Biomedical Sciences (Volume 8, Issue 1) |
DOI | 10.11648/j.ejcbs.20220801.11 |
Page(s) | 1-8 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
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Copyright © The Author(s), 2022. Published by Science Publishing Group |
SARS-CoV-2, COVID-19, Sex-based Inflammatory Markers/Indices
[1] | Mallah SI, Ghorab OK, Al-Salmi S, Abdellatif OS, Tharmaratnam T, Iskandar MA, et al. COVID-19: breaking down a global health crisis. Ann Clin Microbiol Antimicrob. 2021; 20 (1): 35. DOI: 10.1186/s12941-021-00438-7. |
[2] | Bchetnia M, Girard C, Duchaine C, Laprise C. The outbreak of the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2): A review of the current global status. J Infect Public Health. 2020; 13 (11): 1601-10. |
[3] | Hozhabri H, Piceci Sparascio F, Sohrabi H, Mousavifar L, Roy R, Scribano D, et al. The Global Emergency of Novel Coronavirus (SARS-CoV-2): An Update of the Current Status and Forecasting. Int J Environ Res Public Health. 2020; 17 (16): 5648. DOI: 10.3390/ijerph17165648. |
[4] | Wang Y, Wang Y, Chen Y, Qin Q. Unique epidemiological and clinical features of the emerging 2019 novel coronavirus pneumonia (COVID-19) implicate special control measures. J Med Virol. 2020; 92 (6): 568-76. |
[5] | Chen W, Lin Y, Huang H, Cai M, Lin D, Su M, et al. A Retrospective Study of the Epidemiologic and Clinical Characteristics of COVID-19 Among Hospitalized Patients in Quanzhou, China. Infect Microbes Dis. 2021; 3 (1): 32-40. DOI: 10.1097/IM9.0000000000000048. |
[6] | Lau ES, McNeill JN, Paniagua SM, Liu EE, Wang JK, Bassett IV, et al. Sex differences in inflammatory markers in patients hospitalized with COVID-19 infection: Insights from the MGH COVID-19 patient registry. PLoS One. 2021; 16 (4): e0250774. DOI: 10.1371/journal.pone.0250774. |
[7] | Guerson-Gil A, Palaiodimos L, Assa A, Karamanis D, Kokkinidis D, Chamorro-Pareja N, et al. Sex-specific impact of severe obesity in the outcomes of hospitalized patients with COVID-19: a large retrospective study from the Bronx, New York. Eur J Clin Microbiol Infect Dis. 2021; 40 (9): 1963-74. |
[8] | Ten-Caten F, Gonzalez-Dias P, Castro Í, Ogava RLT, Giddaluru J, Silva JCS, et al. In-depth analysis of laboratory parameters reveals the interplay between sex, age, and systemic inflammation in individuals with COVID-19. Int J Infect Dis. 2021; 105: 579-87. |
[9] | Kelada M, Anto A, Dave K, Saleh SN. The Role of Sex in the Risk of Mortality from COVID-19 Amongst Adult Patients: A Systematic Review. Cureus. 2020; 12 (8): e10114. DOI: 10.7759/cureus.10114. |
[10] | Haitao T, Vermunt JV, Abeykoon J, Ghamrawi R, Gunaratne M, Jayachandran M, et al. COVID-19 and Sex Differences: Mechanisms and Biomarkers. Mayo Clin Proc. 2020; 95 (10): 2189-203. |
[11] | Ya'qoub L, Elgendy IY, Pepine CJ. Sex and gender differences in COVID-19: More to be learned! Am Heart J Plus. 2021; 3: 100011. DOI: 10.1016/j.ahjo.2021.100011. |
[12] | Naing L, Winn T, Rusli BN. Practical issues in calculating the sample size for prevalence studies. Arch Orofac Sci. 2006; 1: 9–14. |
[13] | Nigerian Centre for Disease Control (NCDC) National Interim Guidelines for Clinical Management of COVID-19. Accessed 30th December 2021. |
[14] | Kuluöztürk M, Deveci F, Turgut T, Öner Ö. The Glasgow Prognostic Score and fibrinogen to albumin ratio as prognostic factors in hospitalized patients with COVID-19. Expert Rev Respir Med. 2021; 15 (8): 1061-68. |
[15] | Physical status: the use and interpretation of anthropometry. Report of a WHO Expert Committee. World Health Organ Tech Rep Ser. 1995; 854: 1-452. |
[16] | Gebhard C., Regitz-Zagrosek V., Neuhauser H. K., Morgan R., Klein S. L. Impact of sex and gender on COVID-19 outcomes in Europe. Biol Sex Differ. 2020; 11 (1): 29. |
[17] | Pivonello R, Auriemma RS, Pivonello C, Isidori AM, Corona G, Colao A, Millar RP. Sex disparities in COVID-19 severity and outcome: are men weaker or women stronger? Neuroendocrinology. 2021; 111 (11): 1066-85. |
[18] | Falahi S, Kenarkoohi A. Sex and gender differences in the outcome of patients with COVID-19. J Med Virol. 2021; 93 (1): 151-52. |
[19] | Capuano A, Rossi F, Paolisso G. COVID-19 kills more men than women: an overview of possible reasons. Front Cardiovasc Med. 2020; 7: 131. DOI: 10.3389/fcvm.2020.00131. |
APA Style
Collins Amadi, Stephenson Lawson. (2022). The Impact of Systemic Inflammation on Sex-based Bias Following SARS-CoV-2 Infection. European Journal of Clinical and Biomedical Sciences, 8(1), 1-8. https://doi.org/10.11648/j.ejcbs.20220801.11
ACS Style
Collins Amadi; Stephenson Lawson. The Impact of Systemic Inflammation on Sex-based Bias Following SARS-CoV-2 Infection. Eur. J. Clin. Biomed. Sci. 2022, 8(1), 1-8. doi: 10.11648/j.ejcbs.20220801.11
AMA Style
Collins Amadi, Stephenson Lawson. The Impact of Systemic Inflammation on Sex-based Bias Following SARS-CoV-2 Infection. Eur J Clin Biomed Sci. 2022;8(1):1-8. doi: 10.11648/j.ejcbs.20220801.11
@article{10.11648/j.ejcbs.20220801.11, author = {Collins Amadi and Stephenson Lawson}, title = {The Impact of Systemic Inflammation on Sex-based Bias Following SARS-CoV-2 Infection}, journal = {European Journal of Clinical and Biomedical Sciences}, volume = {8}, number = {1}, pages = {1-8}, doi = {10.11648/j.ejcbs.20220801.11}, url = {https://doi.org/10.11648/j.ejcbs.20220801.11}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ejcbs.20220801.11}, abstract = {Background: The unfavorable clinical outcome (higher rates of severity/morbidity/mortality) of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has a disproportionate bias towards the male sex despite no sex-based difference noted in the risk for the infection. These outcomes have widely been hinged on dysregulated systemic inflammation. Hence, this study was aimed to evaluate the influence of systemic inflammation on sex-based bias in SARS-CoV-2 infection among indigenes of Nigerian Methods: Patients’ data with positive real-time polymerase chain reaction (RT-PCR) test for coronavirus disease 2019 (COVID-19), who were admitted/managed at the Eleme treatment center in Port Harcourt, southern Nigeria, were enrolled for this study. All relevant data was acquired from archived case notes, medical review charts, nurses’ charts, and laboratory records by trained research assistants using validated data collection templates. All the collated/abstracted data were analyzed/compared between the male and female patients using both descriptive and comparative statistical tools. Results A total of eligible 598 patients were included in the analysis among them 373 (62.4%) and 225 (37.6%) males and females, respectively. The males were much older (43.63±5.93 vs. 41.15±6.09; p<0.036) with higher mean body mass index and body temperature at presentation. Significant differences were observed in terms of the age distribution, occupational, educational, marital, residential status, cigarette smoking, alcohol consumption, body mass index, comorbid, severity, and clinical outcomes between the males and females (<0.05). In addition, the males had significantly higher mean levels of creatinine, C-reactive protein (CRP), Glasgow Prognostic Score (GPS), D-dimer, total WBC, neutrophil counts, composite neutrophil/lymphocyte ratio (NLR) but lower levels of albumin, total protein, isolated platelet count, and isolated lymphocyte count (p<0.05). The males maintained a significant linear relationship with the CRP (β: 0.61; SE: 0.13; p<0.001), composite GPS (β: 0.59; SE: 0.01; p<0.001), D-dimer (β: 0.52; SE: 0.09; p<0.001), and the composite NLR (β: 0.38; SE: 0.10; p<0.001) compare to their female counterparts. Additionally, CRP (OR: 8.86; 95%CI: 7.34-9.78; p<0.001), the composite GPS (OR: 7.41; 95%CI: 6.36-8.79; p<0.001), D-dimer (OR: 5.4; 95%CI: 4.32-6.65), and the composite NLR (OR: 4.23; 95%CI: 3.44-5.69; p<0.001) all had significant and robust associations with unfavorable clinical outcomes among the males compared to the females. Conclusion: Exaggerated systemic inflammatory markers/indices were more pronounced among the males in association with unfavorable clinical outcomes. These sex-based characteristics should be factored in during the management of SARS-CoV-2 infection. However, further studies are recommended to evaluate conclusions from the current study.}, year = {2022} }
TY - JOUR T1 - The Impact of Systemic Inflammation on Sex-based Bias Following SARS-CoV-2 Infection AU - Collins Amadi AU - Stephenson Lawson Y1 - 2022/02/09 PY - 2022 N1 - https://doi.org/10.11648/j.ejcbs.20220801.11 DO - 10.11648/j.ejcbs.20220801.11 T2 - European Journal of Clinical and Biomedical Sciences JF - European Journal of Clinical and Biomedical Sciences JO - European Journal of Clinical and Biomedical Sciences SP - 1 EP - 8 PB - Science Publishing Group SN - 2575-5005 UR - https://doi.org/10.11648/j.ejcbs.20220801.11 AB - Background: The unfavorable clinical outcome (higher rates of severity/morbidity/mortality) of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has a disproportionate bias towards the male sex despite no sex-based difference noted in the risk for the infection. These outcomes have widely been hinged on dysregulated systemic inflammation. Hence, this study was aimed to evaluate the influence of systemic inflammation on sex-based bias in SARS-CoV-2 infection among indigenes of Nigerian Methods: Patients’ data with positive real-time polymerase chain reaction (RT-PCR) test for coronavirus disease 2019 (COVID-19), who were admitted/managed at the Eleme treatment center in Port Harcourt, southern Nigeria, were enrolled for this study. All relevant data was acquired from archived case notes, medical review charts, nurses’ charts, and laboratory records by trained research assistants using validated data collection templates. All the collated/abstracted data were analyzed/compared between the male and female patients using both descriptive and comparative statistical tools. Results A total of eligible 598 patients were included in the analysis among them 373 (62.4%) and 225 (37.6%) males and females, respectively. The males were much older (43.63±5.93 vs. 41.15±6.09; p<0.036) with higher mean body mass index and body temperature at presentation. Significant differences were observed in terms of the age distribution, occupational, educational, marital, residential status, cigarette smoking, alcohol consumption, body mass index, comorbid, severity, and clinical outcomes between the males and females (<0.05). In addition, the males had significantly higher mean levels of creatinine, C-reactive protein (CRP), Glasgow Prognostic Score (GPS), D-dimer, total WBC, neutrophil counts, composite neutrophil/lymphocyte ratio (NLR) but lower levels of albumin, total protein, isolated platelet count, and isolated lymphocyte count (p<0.05). The males maintained a significant linear relationship with the CRP (β: 0.61; SE: 0.13; p<0.001), composite GPS (β: 0.59; SE: 0.01; p<0.001), D-dimer (β: 0.52; SE: 0.09; p<0.001), and the composite NLR (β: 0.38; SE: 0.10; p<0.001) compare to their female counterparts. Additionally, CRP (OR: 8.86; 95%CI: 7.34-9.78; p<0.001), the composite GPS (OR: 7.41; 95%CI: 6.36-8.79; p<0.001), D-dimer (OR: 5.4; 95%CI: 4.32-6.65), and the composite NLR (OR: 4.23; 95%CI: 3.44-5.69; p<0.001) all had significant and robust associations with unfavorable clinical outcomes among the males compared to the females. Conclusion: Exaggerated systemic inflammatory markers/indices were more pronounced among the males in association with unfavorable clinical outcomes. These sex-based characteristics should be factored in during the management of SARS-CoV-2 infection. However, further studies are recommended to evaluate conclusions from the current study. VL - 8 IS - 1 ER -