Skip to main content
Top
Published in: BMC Cancer 1/2023

Open Access 01-12-2023 | Obesity | Research

Is obesity a risk factor for melanoma?

Authors: Yuval Arbel, Yifat Arbel, Amichai Kerner, Miryam Kerner

Published in: BMC Cancer | Issue 1/2023

Login to get access

Abstract

Objectives

Are twofold: 1) to estimate the relationship between obesity (BMI ≥30) and the prevalence of melanoma in different US states and 2) to examine the possibility of defining a new risk group. This might enhance the possibility of detection, which in turn, might increase the survival rates of patients.

Study design

A cohort Study, based on data at the US statewide level in 2011–2017, where the dependent variable (the annual new melanoma cases per 100,000 persons) is adjusted for age.

Method

Quadratic regression analysis. This model permits a non-monotonic variation of obesity with new melanoma cases adjusted for age, where the control variable is the level of UV radiation.

Results

Demonstrate a negative correlation between obesity and incidence of melanoma. This outcome is further corroborated for Caucasians.

Conclusions

We should continue to establish primary prevention of melanoma by raising photo protection awareness and secondary prevention by promoting skin screening (by physician or self) among the entire population group in all BMI ranges. Advanced secondary melanoma prevention including noninvasive diagnosis strategies including total body photography, confocal microscopy, AI strategies should focus the high-risk sub group of Caucasians with BMI < 30.
Appendix
Available only for authorised users
Footnotes
1
As McQuade et al. [18] suggest: “Although the impact of obesity associated inflammation on carcinogenesis has been well studied, the impact of energy balance on anti-tumor immune response has not been examined to date and should be investigated as a potential explanation underlying the observed interaction between BMI and both targeted and immune therapy.” (page 320).
 
2
This calculation transforms the variable to percentage points, so that obesity prevalence of X percent in the population (0 ≤ X ≤ 100) equals X%.
 
3
The information was obtained from Center for Disease Control and Prevention (CDC) [6]: United States Cancer Statistics, available at: https://​www.​cdc.​gov/​cancer/​uscs/​ [last accessed on December 22, 2022]. The reason for the white-black choice is our findings these groups have the most extreme differences in terms of melanoma prevalence. In this context, see the graph at Additional file 1: Appendix S1.
 
4
Incorporation of the time variable (Year − 2011) addresses the possibility of spurious or nonsense correlation in time series analysis. According to Johnston and Dinardo [14], series, responding to unrelated mechanisms, such as, death rates in England and Wales and the proportion of all marriages solemnized in the Church of England from 1866 to 1911 [29], may display contemporaneous upward or downward movement. This problem may be addressed by fitting trends to such series. Regression outcomes reported in Table 6, demonstrate that while melanoma prevalence rises by 0.336−0.384% per annum only for the white population, obesity prevalence increases by 0.382−0.465% per annum only for the black population.
 
5
Calculations of the figures were carried out in Stata software package version 16 via the following commands:
• margins White, at(Obesity_prevalence==(10(1)55))
• marginsplot, noci
• margins White, at(Obesity_prevalence==(10(1)55)) contrast
• marginsplot
The “margins” and “marginsplot” commands come after the corresponding regression analysis.
 
Literature
4.
go back to reference Baldwin J, Janitz AE, Erb-Alvarez J, Snider C, Campbell JE. Prevalence and mortality of melanoma in Oklahoma among racial groups, 2000-2008. J Oklahoma State Med Assoc. 2016;109(7–8):311–6. Baldwin J, Janitz AE, Erb-Alvarez J, Snider C, Campbell JE. Prevalence and mortality of melanoma in Oklahoma among racial groups, 2000-2008. J Oklahoma State Med Assoc. 2016;109(7–8):311–6.
14.
go back to reference Johnston J, Dinardo J. Econometric Methods. 4th ed; 1997. Johnston J, Dinardo J. Econometric Methods. 4th ed; 1997.
22.
go back to reference Pollack LA, Li J, Berkowitz Z, Weir HK, Wu X-C, Ajani UA, et al. Melanoma survival in the United States, 1992 to 2005. J Am Acad Dermatol. 2011;65(5):S78.CrossRefPubMedPubMedCentral Pollack LA, Li J, Berkowitz Z, Weir HK, Wu X-C, Ajani UA, et al. Melanoma survival in the United States, 1992 to 2005. J Am Acad Dermatol. 2011;65(5):S78.CrossRefPubMedPubMedCentral
25.
go back to reference Sergentanis TN, Antoniadis AG, Gogas HJ, et al. Obesity and risk of malignant melanoma: a meta-analysis of cohort and case-control studies. Eur J Cancer. 2013;49:642–57.CrossRefPubMed Sergentanis TN, Antoniadis AG, Gogas HJ, et al. Obesity and risk of malignant melanoma: a meta-analysis of cohort and case-control studies. Eur J Cancer. 2013;49:642–57.CrossRefPubMed
30.
go back to reference Zhang M, Li P, Zhu Y, Chang H, Wang X, Liu W, et al. Higher visceral fat area increases the risk of vitamin D insufficiency and deficiency in Chinese adults Nutr. Metab. 2015;12(2015):015–0046. Zhang M, Li P, Zhu Y, Chang H, Wang X, Liu W, et al. Higher visceral fat area increases the risk of vitamin D insufficiency and deficiency in Chinese adults Nutr. Metab. 2015;12(2015):015–0046.
Metadata
Title
Is obesity a risk factor for melanoma?
Authors
Yuval Arbel
Yifat Arbel
Amichai Kerner
Miryam Kerner
Publication date
01-12-2023
Publisher
BioMed Central
Published in
BMC Cancer / Issue 1/2023
Electronic ISSN: 1471-2407
DOI
https://doi.org/10.1186/s12885-023-10560-8

Other articles of this Issue 1/2023

BMC Cancer 1/2023 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine