Yu-Wei Fang, Hsuan-Cheng Lin, Chikang Wang, Chien-Yu Lin
{"title":"Serum human epididymis protein 4 and long-term mortality in U.S. women: a nationally representative cohort study.","authors":"Yu-Wei Fang, Hsuan-Cheng Lin, Chikang Wang, Chien-Yu Lin","doi":"10.1016/j.clinsp.2026.101133","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Serum Human Epididymal secretory protein E4 (HE4) is a biomarker in gynecologic oncology and is increasingly linked to fibrosis and adverse outcomes across organ systems; however, its population-level prognostic value beyond cancer and advanced organ failure remains unclear.</p><p><strong>Patients and methods: </strong>We analyzed women aged ≥ 20-years in the National Health and Nutrition Examination Survey (NHANES) 2001-2002 cycle with serum HE4 (unweighted n = 2200; weighted population ≈46.9 million) linked to mortality outcomes through 2019.</p><p><strong>Results: </strong>Over a median 199.3-months of follow-up, 466 deaths occurred. Higher ln-HE4 levels were strongly associated with Chronic Kidney Disease (CKD) (Odds Ratio [OR = 2.07], 95% CI: 1.38-3.12) and history of lung disease (OR = 1.34, 95% CI: 1.06-1.71). In fully adjusted models, higher ln-HE4 was associated with all-cause mortality (Hazard Ratio [HR = 1.29], 95% CI: 1.03-1.63) and cancer mortality (HR = 1.60, 95% CI: 1.02-2.49). Chronic lower respiratory disease mortality showed a positive but imprecise association because of limited events (n = 25; HR = 3.16, 95% CI: 1.26-7.91). For diabetes mortality, the estimate was also imprecise and not statistically significant (n = 18; HR = 3.84, 95% CI: 0.92-16.00). Trends across quartiles were significant for all-cause (p for trend = 0.001) and cancer mortality (p for trend = 0.006). Sensitivity analyses were broadly consistent, although estimates for outcomes with few events should be interpreted cautiously.</p><p><strong>Conclusions: </strong>In a nationally representative cohort of U.S. women, higher serum HE4 was associated with increased risks of all-cause and cancer mortality. Associations with chronic lower respiratory disease and diabetes mortality were based on few events and should be interpreted cautiously. These results support HE4 as a potential population-level prognostic biomarker beyond oncology, warranting validation in other cohorts and mechanistic studies.</p>","PeriodicalId":520594,"journal":{"name":"Clinics (Sao Paulo, Brazil)","volume":"81 ","pages":"101133"},"PeriodicalIF":2.4000,"publicationDate":"2026-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13586584/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinics (Sao Paulo, Brazil)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.clinsp.2026.101133","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose: Serum Human Epididymal secretory protein E4 (HE4) is a biomarker in gynecologic oncology and is increasingly linked to fibrosis and adverse outcomes across organ systems; however, its population-level prognostic value beyond cancer and advanced organ failure remains unclear.
Patients and methods: We analyzed women aged ≥ 20-years in the National Health and Nutrition Examination Survey (NHANES) 2001-2002 cycle with serum HE4 (unweighted n = 2200; weighted population ≈46.9 million) linked to mortality outcomes through 2019.
Results: Over a median 199.3-months of follow-up, 466 deaths occurred. Higher ln-HE4 levels were strongly associated with Chronic Kidney Disease (CKD) (Odds Ratio [OR = 2.07], 95% CI: 1.38-3.12) and history of lung disease (OR = 1.34, 95% CI: 1.06-1.71). In fully adjusted models, higher ln-HE4 was associated with all-cause mortality (Hazard Ratio [HR = 1.29], 95% CI: 1.03-1.63) and cancer mortality (HR = 1.60, 95% CI: 1.02-2.49). Chronic lower respiratory disease mortality showed a positive but imprecise association because of limited events (n = 25; HR = 3.16, 95% CI: 1.26-7.91). For diabetes mortality, the estimate was also imprecise and not statistically significant (n = 18; HR = 3.84, 95% CI: 0.92-16.00). Trends across quartiles were significant for all-cause (p for trend = 0.001) and cancer mortality (p for trend = 0.006). Sensitivity analyses were broadly consistent, although estimates for outcomes with few events should be interpreted cautiously.
Conclusions: In a nationally representative cohort of U.S. women, higher serum HE4 was associated with increased risks of all-cause and cancer mortality. Associations with chronic lower respiratory disease and diabetes mortality were based on few events and should be interpreted cautiously. These results support HE4 as a potential population-level prognostic biomarker beyond oncology, warranting validation in other cohorts and mechanistic studies.