Leukocyte telomere length and chronic disease burden in an adult community sample: a cross-sectional study.

IF 1
Jerome Alfred Q Tabajonda, Shang-Hsien Yang, Yi-Ling Shen, Flordeluna Z Mesina, Maureen B Sabit, Teresa T Sy Ortin, Carl Lexter B Tan, Cheng-Yoong Pang, Chi-Cheng Li, Liuh-Yow Chen, Pia Marie S P Albano
{"title":"Leukocyte telomere length and chronic disease burden in an adult community sample: a cross-sectional study.","authors":"Jerome Alfred Q Tabajonda, Shang-Hsien Yang, Yi-Ling Shen, Flordeluna Z Mesina, Maureen B Sabit, Teresa T Sy Ortin, Carl Lexter B Tan, Cheng-Yoong Pang, Chi-Cheng Li, Liuh-Yow Chen, Pia Marie S P Albano","doi":"10.1093/labmed/lmag023","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Telomere length is a biomarker of cellular aging and chronic disease risk, but its population-level correlates and disease-specific patterns remain unclear. This study examined telomere length associations and its contribution to disease prediction.</p><p><strong>Methods: </strong>Leukocyte telomere length measured using quantitative polymerase chain reaction was analyzed in 615 Filipino adults. Associations with sociodemographic, lifestyle, and physiologic factors were evaluated among healthy participants using variance-robust methods and Welch tests. Linear support vector classifiers with SHapley Additive exPlanations interpretation predicted cancer, cardiovascular disease (CVD), mental health disorders, allergy, and diabetes using 5-fold cross-validation.</p><p><strong>Results: </strong>Postgraduate participants had shorter telomere lengths than did high school graduates (mean difference, 2.740; P = .02) and college graduates (mean difference, 2.884; P = .01). Telomere length did not differ between individuals without CVD and CVD alone; however, CVD-only cases had shorter telomere lengths than did those with additional comorbidities (mean difference, -3.253; P = .009). Single allergy cases had shorter telomere lengths (P = .03), whereas cancer-only cases had longer telomere lengths (P = .003). Model accuracies ranged from 85.37% to 93.47%, with telomere length contributing mainly to cancer prediction.</p><p><strong>Discussion: </strong>Telomere length showed disease-specific associations and improved cancer prediction but had limited links with measured exposures. Longitudinal studies are needed to clarify causality and refine telomere length-based risk stratification.</p>","PeriodicalId":94124,"journal":{"name":"Laboratory medicine","volume":"57 3","pages":""},"PeriodicalIF":1.0000,"publicationDate":"2026-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Laboratory medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/labmed/lmag023","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

Introduction: Telomere length is a biomarker of cellular aging and chronic disease risk, but its population-level correlates and disease-specific patterns remain unclear. This study examined telomere length associations and its contribution to disease prediction.

Methods: Leukocyte telomere length measured using quantitative polymerase chain reaction was analyzed in 615 Filipino adults. Associations with sociodemographic, lifestyle, and physiologic factors were evaluated among healthy participants using variance-robust methods and Welch tests. Linear support vector classifiers with SHapley Additive exPlanations interpretation predicted cancer, cardiovascular disease (CVD), mental health disorders, allergy, and diabetes using 5-fold cross-validation.

Results: Postgraduate participants had shorter telomere lengths than did high school graduates (mean difference, 2.740; P = .02) and college graduates (mean difference, 2.884; P = .01). Telomere length did not differ between individuals without CVD and CVD alone; however, CVD-only cases had shorter telomere lengths than did those with additional comorbidities (mean difference, -3.253; P = .009). Single allergy cases had shorter telomere lengths (P = .03), whereas cancer-only cases had longer telomere lengths (P = .003). Model accuracies ranged from 85.37% to 93.47%, with telomere length contributing mainly to cancer prediction.

Discussion: Telomere length showed disease-specific associations and improved cancer prediction but had limited links with measured exposures. Longitudinal studies are needed to clarify causality and refine telomere length-based risk stratification.

成人社区样本中的白细胞端粒长度和慢性疾病负担:一项横断面研究。
端粒长度是细胞衰老和慢性疾病风险的生物标志物,但其在人群水平上的相关性和疾病特异性模式尚不清楚。本研究检验了端粒长度关联及其对疾病预测的贡献。方法:采用定量聚合酶链反应测定615例菲律宾成人白细胞端粒长度。使用方差稳健方法和Welch检验评估健康参与者与社会人口统计学、生活方式和生理因素的关联。线性支持向量分类器与SHapley加性解释解释预测癌症,心血管疾病(CVD),精神健康障碍,过敏和糖尿病使用5倍交叉验证。结果:研究生受试者的端粒长度比高中毕业生短(平均差异为2.740;P =。02)和大学毕业生(平均差异为2.884;P = 0.01)。端粒长度在没有CVD和单独CVD的个体之间没有差异;然而,仅cvd患者的端粒长度比其他合并症患者短(平均差异为-3.253;P = 0.009)。单例过敏患者端粒长度较短(P =。03),而只有癌症的患者端粒长度更长(P = 0.003)。模型准确率在85.37% ~ 93.47%之间,端粒长度对癌症预测的贡献最大。讨论:端粒长度显示疾病特异性关联和改进的癌症预测,但与测量暴露的联系有限。需要纵向研究来澄清因果关系和完善基于端粒长度的风险分层。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书