# The association between the vitamin B1 intake and risk of non-melanoma skin cancer in U.S. adults: a cross-sectional study

**Authors:** Shiyi Huang, Lungang Shi, Yang Ma, Yuebin Zhu, Yingshi Liang, Haofeng Huang

PMC · DOI: 10.3389/fnut.2025.1571991 · Frontiers in Nutrition · 2025-04-30

## TL;DR

This study finds that higher vitamin B1 intake is linked to a higher risk of non-melanoma skin cancer in U.S. adults.

## Contribution

The study is one of the first to explore the association between vitamin B1 consumption and non-melanoma skin cancer risk using a large national dataset.

## Key findings

- Higher vitamin B1 intake was associated with an 11% increased risk of non-melanoma skin cancer per unit increase.
- A linearly positive relationship between vitamin B1 consumption and NMSC risk was confirmed using curve fitting.
- The association remained consistent across various subgroups, suggesting a broad pattern.

## Abstract

The incidence of non-melanoma skin cancer (NMSC) has been steadily increasing in recent years, primarily due to global climate change and heightened exposure to ultraviolet (UV) radiation. This trend is particularly pronounced among Caucasians, whose lack of melanin in skin cells renders them more susceptible to UV-induced damage. Although NMSC is associated with low mortality, its high incidence imposes a significant economic burden on society. Consequently, identifying novel risk factors and predictors has become increasingly important. Growing attention has been directed toward the relationship between diet and diseases, including cancer. While research on dietary factors and NMSC has gained momentum, studies specifically examining the link between vitamin B1 intake and NMSC remain limited. Therefore, this study aims to explore the potential association between vitamin B1 consumption and the risk of developing NMSC.

The authors conducted a cross-sectional study utilizing data from six cycles of the National Health and Nutrition Examination Survey (NHANES) database spanning 2005 to 2016. Out of 60,936 participants initially identified, 30,982 individuals who did not meet the study criteria were excluded, resulting in a final sample of 29,954 participants. In this study, the exposure variable was vitamin B1 intake. This was calculated by counting the amount of vitamin B1 contained in food consumed over a 24-h period. Outcome variable was presence of non-melanoma skin cancer. For the analysis of bivariate variables, multiple linear regression models were primarily employed. Additional analyses included curve fitting and subgroup analysis to further explore the relationships and trends.

The mean age of participants included in the analysis was 49.66 years, with an approximately equal male-to-female ratio. Among these, 499 individuals were diagnosed with NMSC, with a mean age of 68.27 years and a prevalence rate of 1.67%. The probability of having NMSC was positively correlated with vitamin B1 consumption, according to logistic regression analysis. Specifically, an 11% increased incidence of NMSC was linked to every unit increase in vitamin B1 consumption. The risk rose by up to 1.65 times in those with high vitamin B1 consumption, making this link more noticeable. A linearly positive relationship between vitamin B1 consumption and NMSC risk was found using smoothed curve fitting. Subgroup analyses confirmed that this positive association remained consistent across different population subgroups.

This study identified a positive association between vitamin B1 intake and NMSC. However, due to the inherent limitations of cross-sectional studies, further prospective studies are needed to confirm the causal relationship.

## Linked entities

- **Chemicals:** vitamin B1 (PubChem CID 1130)
- **Diseases:** non-melanoma skin cancer (MONDO:0002656)

## Full-text entities

- **Genes:** TKT (transketolase) [NCBI Gene 7086] {aka HEL-S-48, HEL107, SDDHD, TK, TKT1}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, JUNB (JunB proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 3726] {aka AP-1}
- **Diseases:** Scars (MESH:D002921), hemorrhagic (MESH:D006470), SCC (MESH:D002294), hypoxia (MESH:D000860), prostate cancer (MESH:D011471), BCC (MESH:D002280), gastric cancer (MESH:D013274), carcinogenic (MESH:D011230), lactic acidosis (MESH:D000140), NMSC (MESH:D012878), carcinogenesis (MESH:D063646), thiamine deficiency (MESH:D013832), triple-negative breast cancer (MESH:D064726), Tumor (MESH:D009369), hypoxic (MESH:D002534), bladder cancer (MESH:D001749), metastasis (MESH:D009362), melanoma (MESH:D008545), colorectal cancer (MESH:D015179), immune dysregulation (OMIM:614878), deaths (MESH:D003643), inflammation (MESH:D007249), hypertension (MESH:D006973), metabolic abnormalities (MESH:D008659), tumorigenic (MESH:D002471), breast cancer (MESH:D001943), leukemia (MESH:D007938), diabetes (MESH:D003920)
- **Chemicals:** calcium (MESH:D002118), nucleotide (MESH:D009711), tricarboxylic acid (MESH:D014233), oxygen (MESH:D010100), caffeine (MESH:D002110), lactate (MESH:D019344), proanthocyanidins (MESH:D044945), Vitamin A (MESH:D014801), pentose phosphate (MESH:D010428), Grape seed (-), nicotinamide (MESH:D009536), GSH (MESH:D005978), GSP (MESH:C511402), Vitamin D (MESH:D014807), TCA (MESH:D014238), vitamin C (MESH:D001205), Thiamine (MESH:D013831), RNS (MESH:D026361), ROS (MESH:D017382), folate (MESH:D005492), succinyl coenzyme A. (MESH:C012046), acetyl coenzyme A (MESH:D000105), alcohol (MESH:D000438), ribulose-5-phosphate (MESH:C031524), beta-carotene (MESH:D019207), pyruvate (MESH:D019289), TPP (MESH:D013835), beta-cryptoxanthin (MESH:D000072743), erythrose-4-phosphate (MESH:C026959), melanin (MESH:D008543), alpha-ketoglutarate (MESH:D007656)
- **Species:** Homo sapiens (human, species) [taxon 9606], Nicotiana tabacum (American tobacco, species) [taxon 4097], Tetrastichus ennis (species) [taxon 2931463], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12075143/full.md

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Source: https://tomesphere.com/paper/PMC12075143