Association between telomere length and erectile dysfunction: a cross-sectional study.


Journal

Frontiers in endocrinology
ISSN: 1664-2392
Titre abrégé: Front Endocrinol (Lausanne)
Pays: Switzerland
ID NLM: 101555782

Informations de publication

Date de publication:
2024
Historique:
received: 24 02 2024
accepted: 27 06 2024
medline: 26 7 2024
pubmed: 26 7 2024
entrez: 26 7 2024
Statut: epublish

Résumé

Leukocyte telomere length (LTL) serves as a significant biomarker of aging. Erectile dysfunction (ED) is a commonly observed condition among middle-aged and older men. The objective of this study is to explore the potential association between LTL and ED. We utilized data from the National Health and Nutrition Examination Survey (NHANES) to examine the association between LTL and ED. Weighted multivariate regression analyses were performed as the primary statistical method. Subgroup analyses were conducted to investigate specific population subsets, and restricted cubic spline (RCS) analyses were employed to assess the non-linear relationship between LTL and ED. The results of weighted multivariate regression analyses revealed a negative correlation between LTL and the risk of ED. Individuals with ED exhibited shorter LTL compared to those without ED. For each unit increase in LTL, there was a 54% reduction in the risk of ED (odds ratios[OR] 0.46, 95% confidence intervals[CI] 0.25-0.85). When LTL was considered as a categorical variable, the group with the longest LTL (Q5) had a 44% lower risk of ED compared to the group with the shortest LTL(Q1) (OR 0.56, 95% CI 0.39-0.81). A non-linear relationship was observed between TL and ED. Various sensitivity analyses were conducted to validate the stability of the results, and consistent findings were obtained. The negative association between leukocyte LTL and ED suggests that delaying the shortening of LTL may decrease the risk of ED.

Sections du résumé

Background UNASSIGNED
Leukocyte telomere length (LTL) serves as a significant biomarker of aging. Erectile dysfunction (ED) is a commonly observed condition among middle-aged and older men. The objective of this study is to explore the potential association between LTL and ED.
Methods UNASSIGNED
We utilized data from the National Health and Nutrition Examination Survey (NHANES) to examine the association between LTL and ED. Weighted multivariate regression analyses were performed as the primary statistical method. Subgroup analyses were conducted to investigate specific population subsets, and restricted cubic spline (RCS) analyses were employed to assess the non-linear relationship between LTL and ED.
Results UNASSIGNED
The results of weighted multivariate regression analyses revealed a negative correlation between LTL and the risk of ED. Individuals with ED exhibited shorter LTL compared to those without ED. For each unit increase in LTL, there was a 54% reduction in the risk of ED (odds ratios[OR] 0.46, 95% confidence intervals[CI] 0.25-0.85). When LTL was considered as a categorical variable, the group with the longest LTL (Q5) had a 44% lower risk of ED compared to the group with the shortest LTL(Q1) (OR 0.56, 95% CI 0.39-0.81). A non-linear relationship was observed between TL and ED. Various sensitivity analyses were conducted to validate the stability of the results, and consistent findings were obtained.
Conclusion UNASSIGNED
The negative association between leukocyte LTL and ED suggests that delaying the shortening of LTL may decrease the risk of ED.

Identifiants

pubmed: 39055058
doi: 10.3389/fendo.2024.1391013
pmc: PMC11269092
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1391013

Informations de copyright

Copyright © 2024 Chen, Liu, Zhou, Lin, Jiang and Xie.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Xiaobao Chen (X)

Department of Urology, Fujian Medical University Union Hospital, Fuzhou, China.

Binhong Liu (B)

Department of Urology, Fujian Medical University Union Hospital, Fuzhou, China.

Junkai Zhou (J)

Department of Urology, Fujian Medical University Union Hospital, Fuzhou, China.

Junwei Lin (J)

Department of Urology, Fujian Medical University Union Hospital, Fuzhou, China.

Wei Jiang (W)

Department of Urology, Fujian Medical University Union Hospital, Fuzhou, China.

Ruoyun Xie (R)

Department of Urology, Fujian Medical University Union Hospital, Fuzhou, China.

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