Pulse Brain · Growing Health Evidence Index
Tier 2 — RCT, large cohort or strong causal designPeer-reviewed

Investigating the causal association between liver condition and melanoma: evidence from the National Health and Nutrition Examination Survey and Mendelian randomization.

Bendian Song; Shitong Guo; Qiuchen Li; Zhiyu Li; Jianhai Bi

Melanoma research · 2026

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Summary

This study combined cross-sectional analysis of NHANES data (2001–2004) with Mendelian randomization to investigate a potential causal relationship between liver condition and melanoma risk. In the observational cohort (7,144 participants, 49 melanoma cases), liver condition was associated with a 4.31-fold increased odds of melanoma. Mendelian randomization using genetic instruments confirmed a causal relationship, with sensitivity analyses ruling out horizontal pleiotropy, suggesting liver condition may be a genuine aetiological risk factor for melanoma.

Regional applicability

This study uses United States population data (NHANES) and genetic instruments typically derived from European ancestry populations; findings may have limited direct applicability to United Kingdom populations without validation in UK cohorts. The association between liver condition and melanoma warrants investigation in UK primary care and dermatology settings to inform prevention and screening strategies.

Key measures

Odds ratios (OR) with 95% confidence intervals for melanoma risk; cross-sectional analysis using multivariable logistic regression; inverse variance weighted method for causal inference; Steiger test for direction of causality validation

Outcomes reported

The study examined the association between liver condition and melanoma risk using cross-sectional analysis of NHANES data and Mendelian randomization to infer causality. Primary outcomes were odds ratios for melanoma risk stratified by liver condition status.

Theme
Nutrition & health
Subject
Out of scope / non-food
Study type
Research
Study design
Mendelian randomisation
Source type
Peer-reviewed study
Status
Published
Geography
United States
System type
Human clinical
DOI
10.1097/cmr.0000000000001125
Catalogue ID
NRmu7146f2-024

Topic tags

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