Lv Ying, Cao Xiaodi, Yu Kai, Pu Jie, Tang Zhiguo, Wei Na, Wang Junkui, Liu Fuqiang, Li Shangjian
Department of Cardiology, Shaanxi Provincial People's Hospital, Xi'an, Shaanxi, China.
Department of Cardiology, Jiangsu Provincial People's Hospital and The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Front Cardiovasc Med. 2024 Feb 14;11:1283132. doi: 10.3389/fcvm.2024.1283132. eCollection 2024.
Gender disparities in mortality have drawn great interest, with previous studies identifying various biological, social, and behavioral factors contributing to the observed gender differences. This study aims to identify the sources of gender disparities in mortality rates and quantify the extent to which these factors mediate the gender differences in all-cause mortality.
Data from the National Health and Nutrition Examination Survey (NHANES) conducted between 2005 and 2018 were analyzed. A total of 38,924 participants were included in the study. Gender information, socioeconomic status, lifestyle factors, and baseline disease status were obtained through questionnaires. Blood samples were collected to assess serological indicators. All-cause and cardiovascular mortality were considered as primary and secondary outcomes, respectively.
The study with an average age of 50.1 ± 17.9 years. Among the participants, 50.7% were women, and 41.8% were non-Hispanic White. The median follow-up length was 87 months [Inter-Quartile Range (IQR): 47-128]. Men showed higher rates of all-cause and cardiovascular mortality compared to women in both the general population and the population with cardiovascular disease. After adjustment for potential confounders (age, race, marital status, socioeconomic status, lifestyle level, smoking status, cardiovascular disease, hypertension, diabetes and cancer), the men: women hazard ratios (HRs) for all-cause and cardiovascular mortality were 1.58 [95% Confidence Interval (CI): 1.48-1.68] and 1.60 (95%CI:1.43-1.80) in the general population. Among individuals with cardiovascular disease, the fully adjusted HR for all-cause mortality was 1.34 (95% CI: 1.20 to 1.51), and for cardiovascular mortality, the fully adjusted HRs was 1.52 (95% CI: 1.26 to 1.83). Mediation analysis revealed that uric acid levels significantly mediated the association between gender and all-cause mortality, accounting for 17.53% (95% CI: 11.0% to 23.7%) in the general population and 27.47% (95% CI: 9.0% to 13.6%) in the population with cardiovascular disease.
The study highlights the complex interplay of biological and social factors contributing to gender disparities in mortality. Uric acid was identified as key mediators of the gender-mortality association. These findings can inform targeted interventions aimed at reducing gender disparities in mortality and promoting better public health outcomes.
死亡率方面的性别差异引起了极大关注,以往研究确定了导致观察到的性别差异的各种生物、社会和行为因素。本研究旨在确定死亡率性别差异的来源,并量化这些因素在全因死亡率性别差异中所起的中介作用程度。
分析了2005年至2018年期间进行的美国国家健康与营养检查调查(NHANES)的数据。共有38924名参与者纳入本研究。通过问卷调查获取性别信息、社会经济地位、生活方式因素和基线疾病状况。采集血样以评估血清学指标。全因死亡率和心血管死亡率分别被视为主要和次要结局。
该研究的平均年龄为50.1±17.9岁。参与者中,50.7%为女性,41.8%为非西班牙裔白人。中位随访时长为87个月[四分位间距(IQR):47 - 128]。在一般人群和患有心血管疾病的人群中,男性的全因死亡率和心血管死亡率均高于女性。在对潜在混杂因素(年龄、种族、婚姻状况、社会经济地位、生活方式水平、吸烟状况、心血管疾病、高血压、糖尿病和癌症)进行调整后,一般人群中男性与女性的全因死亡率和心血管死亡率风险比(HRs)分别为1.58[95%置信区间(CI):1.48 - 1.68]和1.60(95%CI:1.43 - 1.80)。在患有心血管疾病的个体中,全因死亡率的完全调整后HR为1.34(95%CI:1.20至1.51),心血管死亡率的完全调整后HR为1.52(95%CI:1.26至1.83)。中介分析显示,尿酸水平显著介导了性别与全因死亡率之间的关联,在一般人群中占17.53%(95%CI:11.0%至23.7%),在患有心血管疾病的人群中占27.47%(95%CI:9.0%至13.6%)。
该研究强调了生物和社会因素在死亡率性别差异中复杂的相互作用。尿酸被确定为性别 - 死亡率关联的关键中介因素。这些发现可为旨在减少死亡率性别差异和促进更好公共卫生结果的针对性干预提供参考。