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[JAMA Intern Med发表论文]: CKD 5期成年患者病死率及接受肾脏替代治疗的性别差异
2026年01月20日 时讯速递, 进展交流 [JAMA Intern Med发表论文]: CKD 5期成年患者病死率及接受肾脏替代治疗的性别差异已关闭评论

Original Investigation 

Women's Health 

Sex Differences in Mortality and Receipt of Kidney Replacement Therapy Among Adults With Stage 5 Chronic Kidney Disease

Christian Chan, Simon Sawhney, Sofia B. Ahmed, et al

JAMA Intern Med Published Online: November 17, 2025

doi: 10.1001/jamainternmed.2025.5979

Key Points

Question  Does the female survival advantage observed in the general population persist among adults with stage 5 chronic kidney disease (CKD)?

Findings  In this cohort study of 7506 adults with incident stage 5 CKD in Alberta, Canada, female individuals were older at disease onset than male individuals. In analyses stratified by age and comorbidities, female individuals younger than 55 years were less likely to survive or receive a kidney transplant than male individuals; female individuals older than 65 years had similar survival but were less likely to receive dialysis.

Meaning  Female individuals may no longer outlive male individuals after developing stage 5 CKD, and their worse outcomes at younger ages warrant further investigation.

Abstract

Importance  Female individuals typically outlive male individuals in the general population. Whether this survival advantage persists among adults with stage 5 chronic kidney disease (CKD) is unknown.

Objective  To examine sex differences in mortality and treatment with kidney replacement therapy (KRT; including dialysis and transplant) among adults with incident stage 5 CKD.

Design, Setting, and Participants  This population-based cohort study used linked administrative and kidney care program data from Alberta, Canada. Adults 18 years and older with incident non–KRT-dependent stage 5 CKD were identified between April 2005 and March 2019 and observed from study entry until death, out-migration, or March 2021. Data were analyzed from January to August 2025.

Main Outcomes and Measures  Sex-specific, age-stratified standardized mortality ratios were calculated using general population mortality data. Five-year probabilities of all-cause death, receipt of maintenance dialysis, and kidney transplant were estimated in incident stage 5 CKD cases using multistate models, stratified by age and presence of diabetes or cardiovascular disease.

Results  Among 7506 cohort members, 4121 (54.9%) were male (median [IQR] age, 70 [58-80] years), and 3385 (45.1%) were female (median [IQR] age, 74 [61-83] years). The median (IQR) follow-up was 7.9 (4.7-11.5) years. Compared with the general population, female individuals experienced greater excess mortality than male individuals, particularly at younger ages (eg, among adults younger than 55 years: standardized mortality ratio, 40.9 [95% CI, 34.6-47.3] in female individuals vs 15.9 [95% CI, 13.5-18.2] in male individuals); this difference narrowed with increasing age. Within the stage 5 CKD cohort, 5-year all-cause mortality risks were higher in younger female individuals than male individuals (younger than 55 years: 20.7% vs 14.6%) and similar between sexes at older ages. Irrespective of comorbidity, female individuals younger than 65 years were substantially less likely to receive a kidney transplant, and female individuals 65 years and older were less likely to receive dialysis or a transplant.

Conclusions and Relevance  In this cohort study using data from a universal health care system, across all ages, the female survival advantage observed in the general population was absent or even reversed after developing stage 5 CKD. Fewer female individuals transitioned to KRT treatment, independent of their comorbidities. Younger female individuals experienced the greatest survival disadvantage and were less likely to receive a transplant. These findings suggest that differences in treatment decision-making or inequities in access to KRT may contribute to poorer outcomes in female individuals, especially at younger ages. Further investigations are warranted to understand the potential underlying structural, social, and biological mechanisms.

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