Gender-specific associations of metabolic and circadian syndromes with melanoma risk: insights from NHANES 2007–2018

Melanoma incidence is increasing worldwide, prompting exploration into novel risk factors beyond traditional exposures like ultraviolet radiation. Recent studies suggest that metabolic and circadian disruptions may also contribute to melanoma development, yet their influence is poorly understood. This study examines the relationships between metabolic syndrome (MetS), circadian syndrome (CircS) and melanoma risk, emphasizing differences between different genders. Using National Health and Nutrition Examination Survey (NHANES) data (2007-2018), this cross-sectional study applied logistic regression to assess MetS and CircS associations with melanoma risk, adjusting for demographic and lifestyle factors. Receiver operating characteristic curves evaluated predictive ability, and restricted cubic spline models examined dose-response patterns. Among 29,132 participants, 209 reported a melanoma diagnosis. Individuals with MetS or CircS showed a higher melanoma risk. Analysis by gender revealed stronger associations in males than in females. In males, melanoma risk rose sharply when more than two MetS components were present, indicating a dose-response pattern. Additionally, the triglyceride glucose index levels showed more notable predictive value in females than males. MetS and CircS are associated with a higher melanoma risk, with a greater effect of MetS components in males. These findings highlight the potential relevance of metabolic and circadian health in understanding melanoma risk patterns.

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Publication Details

Journal
Scientific Reports
Published
2025-08-18
DOI
https://doi.org/10.1038/s41598-025-15461-3
Citations
2
Primary Topic
Circadian rhythm and melatonin
Type
article
Field-Weighted Citation Impact
1.83

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article

Gender-specific associations of metabolic and circadian syndromes with melanoma risk: insights from NHANES 2007–2018

Yiru Chen, Wenjing Qi, Feng Niu, Chang Liu et al.
2 citations
Scientific Reports
Circadian rhythm and melatonin
1.83
article

Gender-specific associations of metabolic and circadian syndromes with melanoma risk: insights from NHANES 2007–2018

Yiru Chen, Wenjing Qi, Feng Niu, Chang Liu, Zhenghao Wang
article en
2 citations

Abstract

Melanoma incidence is increasing worldwide, prompting exploration into novel risk factors beyond traditional exposures like ultraviolet radiation. Recent studies suggest that metabolic and circadian disruptions may also contribute to melanoma development, yet their influence is poorly understood. This study examines the relationships between metabolic syndrome (MetS), circadian syndrome (CircS) and melanoma risk, emphasizing differences between different genders. Using National Health and Nutrition Examination Survey (NHANES) data (2007-2018), this cross-sectional study applied logistic regression to assess MetS and CircS associations with melanoma risk, adjusting for demographic and lifestyle factors. Receiver operating characteristic curves evaluated predictive ability, and restricted cubic spline models examined dose-response patterns. Among 29,132 participants, 209 reported a melanoma diagnosis. Individuals with MetS or CircS showed a higher melanoma risk. Analysis by gender revealed stronger associations in males than in females. In males, melanoma risk rose sharply when more than two MetS components were present, indicating a dose-response pattern. Additionally, the triglyceride glucose index levels showed more notable predictive value in females than males. MetS and CircS are associated with a higher melanoma risk, with a greater effect of MetS components in males. These findings highlight the potential relevance of metabolic and circadian health in understanding melanoma risk patterns.

Scientific ReportsVol. 15(1)
Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Peking Union Medical College Hospital (CN)
Chinese Academy of Medical Sciences
Gender equality
Openalex Percentile: Top 14%
Circadian rhythm and melatonin
1.83
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