COVID-19感染住院患者睾酮水平低与死亡率增加有关

Q3 Medicine
Mark Livingston, S. Ramachandran, Andrew J. Hartland, Aiden Plant, Michael Kirby, Geoffrey Hackett
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No patient was on testosterone therapy (TTh). Results: No significant difference (p = 0.12, rank-sum test) in serum TT between men positive [median TT (IQR) = 3.9 (1.9-7.22) nmol/L, 0 days (median) postadmission] and negative [median TT (IQR) = 5.9 (2.69-10.1) nmol/L, 2 days (median) postadmission] for SARS-CoV-2 was observed. Serum TT was lower (p = 0.0011, rank-sum test) in men with COVID-19 who died [median TT (IQR) = 2.0 (1.5-3.6) nmol/L] compared with survivors [median TT (IQR) = 5.0 (2.6-9.4) nmol/L]. Comorbidities obtained via medication history were not associated with mortality. Mortality (logistic regression) was associated with only age and serum TT (odds ratio: 0.77, 95% confidence intervals [CI]: 0.64-0.91). Survival (Cox regression) was inversely associated with serum TT (continuous variable, hazard ratio [HR]: 0.85) (95% CI: 0.74-0.98), stratified by median, TT ≥3.9 nmol/L (reference, TT <3.9 nmol/L), HR: 0.24 (95% CI: 0.089-0.63). 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引用次数: 2

摘要

目的:尽管男性对COVID-19的易感性与性别相同,但男性出现不良临床结果和死亡的风险更大。这表明血清睾酮可能是一个中介。本回顾性研究的目的是评估COVID-19男性患者血清总睾酮(TT)、其他预后指标与死亡率之间的关系。方法:在沃尔索尔庄园医院连续收治的110例有COVID-19相关症状的男性患者中,85例呈SARS-CoV-2阳性,其中27例死亡。比较了SARS-CoV-2阴性和阳性男性的血清TT(秩和检验),随后确定了后者组中与死亡率相关的因素(秩和、logistic、Cox回归分析)。无患者接受睾酮治疗(TTh)。结果:SARS-CoV-2阳性男性[入院后0天(中位)TT (IQR) = 3.9 (1.9-7.22) nmol/L]与阴性男性[入院后2天(中位)TT (IQR) = 5.9 (2.69-10.1) nmol/L]血清TT差异无统计学意义(p = 0.12,秩和检验)。死亡男性COVID-19患者的血清TT[中位TT (IQR) = 2.0 (1.5-3.6) nmol/L]低于幸存者[中位TT (IQR) = 5.0 (2.6-9.4) nmol/L] (p = 0.0011,秩和检验)。通过用药史获得的合并症与死亡率无关。死亡率(logistic回归)仅与年龄和血清TT相关(优势比:0.77,95%可信区间[CI]: 0.64-0.91)。生存率(Cox回归)与血清TT呈负相关(连续变量,风险比[HR]: 0.85) (95% CI: 0.74-0.98),按中位数分层,TT≥3.9 nmol/L(参考,TT <3.9 nmol/L), HR: 0.24 (95% CI: 0.089-0.63)。结论:血清TT与COVID-19男性患者的死亡率呈负相关,需要在入院时和长期治疗期间进行测量。未来的研究应该确定低血清TT(可能与急性期反应阴性相关)是否会导致较差的预后以及TTh的作用。©Mark Livingston等人,2022;Mary Ann Liebert, Inc.出版。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low Testosterone on Hospital Admission with COVID-19 Infection Is Associated with Increased Mortality
Objective: Males, despite equal sex-related susceptibility to COVID-19, appear at a greater risk of poor clinical outcomes and death. This suggests that serum testosterone could be a mediator. The aim of this retrospective study was to evaluate the association between serum total testosterone (TT), other prognostic indicators, and mortality in men with COVID-19. Methods: Of the 110 men consecutively admitted to Walsall Manor Hospital (with COVID-19 related symptoms) tested for SARS-CoV-2, 85 were positive and 27 of these men died. Serum TT was compared (rank-sum test) between men negative and positive for SARS-CoV-2, and this was followed by establishing factors associated with mortality in the latter group (rank-sum, logistic, Cox regression analyses). No patient was on testosterone therapy (TTh). Results: No significant difference (p = 0.12, rank-sum test) in serum TT between men positive [median TT (IQR) = 3.9 (1.9-7.22) nmol/L, 0 days (median) postadmission] and negative [median TT (IQR) = 5.9 (2.69-10.1) nmol/L, 2 days (median) postadmission] for SARS-CoV-2 was observed. Serum TT was lower (p = 0.0011, rank-sum test) in men with COVID-19 who died [median TT (IQR) = 2.0 (1.5-3.6) nmol/L] compared with survivors [median TT (IQR) = 5.0 (2.6-9.4) nmol/L]. Comorbidities obtained via medication history were not associated with mortality. Mortality (logistic regression) was associated with only age and serum TT (odds ratio: 0.77, 95% confidence intervals [CI]: 0.64-0.91). Survival (Cox regression) was inversely associated with serum TT (continuous variable, hazard ratio [HR]: 0.85) (95% CI: 0.74-0.98), stratified by median, TT ≥3.9 nmol/L (reference, TT <3.9 nmol/L), HR: 0.24 (95% CI: 0.089-0.63). Conclusions: Serum TT was inversely associated with mortality in men with COVID-19 and requires measurement at admission and while managing long COVID. Future research should establish whether low serum TT, possibly associated with negative acute phase response, contributes to poorer prognosis and a role for TTh. © Mark Livingston et al., 2022;Published by Mary Ann Liebert, Inc. 2022.
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CiteScore
2.70
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