Relation of circulating estrogens with hair relaxer and skin lightener use among postmenopausal women in Ghana.

Endogenous estrogens Ghana Hair relaxer use Postmenopausal women Skin lightener use

Journal

Journal of exposure science & environmental epidemiology
ISSN: 1559-064X
Titre abrégé: J Expo Sci Environ Epidemiol
Pays: United States
ID NLM: 101262796

Informations de publication

Date de publication:
03 2023
Historique:
received: 06 08 2021
accepted: 16 12 2021
revised: 09 12 2021
pubmed: 8 1 2022
medline: 15 3 2023
entrez: 7 1 2022
Statut: ppublish

Résumé

Hair relaxers and skin lighteners have been commonly used by African women, with suggestions that they may have hormonal activity. To investigate the relationship of hair relaxer and skin lightener use to serum estrogen/estrogen metabolite levels. We utilized the postmenopausal population-based controls of the Ghana Breast Health Study to estimate adjusted geometric means (GM) and 95% confidence intervals of individual circulating estrogen levels by hair relaxer/skin lightener exposure categories. Of the 585 postmenopausal women included in our analysis, 80.2% reported hair relaxer use and 29.4% skin lightener use. Ever hair relaxer use was positively associated with estriol (adjusted GM 95.4 pmol/L vs. never 74.5, p value = 0.02) and 16-epiestriol (20.4 vs. 16.8, p value = 0.05) particularly among users of lye-based hair relaxers. Positive associations between scalp burns and unconjugated estrogens were observed (e.g., unconjugated estrone: 5+ scalp burns 76.9 [59.6-99.2] vs. no burns 64.0 [53.7-76.3], p-trend = 0.03). No association was observed between use of skin lighteners and circulating estrogens. This study presents evidence that circulating 16-pathway estrogens (i.e., estriol and 16-epiestriol) may be increased in users of lye-based hair relaxer products. Among hair relaxer users, unconjugated estrogen levels were elevated in women with a greater number of scalp burns. In this population-based study of hair relaxer and skin lightener use among postmenopausal women in Ghana, altered estrogen metabolism was observed with hair relaxer use, particularly among women using lye-based products or with a greater number of scalp burns. In contrast, skin lightener use was not associated with differences in estrogen metabolism in this population. Continued investigation of the potential biological impact on breast cancer risk of hair relaxer use is warranted.

Sections du résumé

BACKGROUND
Hair relaxers and skin lighteners have been commonly used by African women, with suggestions that they may have hormonal activity.
OBJECTIVES
To investigate the relationship of hair relaxer and skin lightener use to serum estrogen/estrogen metabolite levels.
METHODS
We utilized the postmenopausal population-based controls of the Ghana Breast Health Study to estimate adjusted geometric means (GM) and 95% confidence intervals of individual circulating estrogen levels by hair relaxer/skin lightener exposure categories.
RESULTS
Of the 585 postmenopausal women included in our analysis, 80.2% reported hair relaxer use and 29.4% skin lightener use. Ever hair relaxer use was positively associated with estriol (adjusted GM 95.4 pmol/L vs. never 74.5, p value = 0.02) and 16-epiestriol (20.4 vs. 16.8, p value = 0.05) particularly among users of lye-based hair relaxers. Positive associations between scalp burns and unconjugated estrogens were observed (e.g., unconjugated estrone: 5+ scalp burns 76.9 [59.6-99.2] vs. no burns 64.0 [53.7-76.3], p-trend = 0.03). No association was observed between use of skin lighteners and circulating estrogens.
SIGNIFICANCE
This study presents evidence that circulating 16-pathway estrogens (i.e., estriol and 16-epiestriol) may be increased in users of lye-based hair relaxer products. Among hair relaxer users, unconjugated estrogen levels were elevated in women with a greater number of scalp burns.
IMPACT STATEMENT
In this population-based study of hair relaxer and skin lightener use among postmenopausal women in Ghana, altered estrogen metabolism was observed with hair relaxer use, particularly among women using lye-based products or with a greater number of scalp burns. In contrast, skin lightener use was not associated with differences in estrogen metabolism in this population. Continued investigation of the potential biological impact on breast cancer risk of hair relaxer use is warranted.

Identifiants

pubmed: 34992224
doi: 10.1038/s41370-021-00407-4
pii: 10.1038/s41370-021-00407-4
pmc: PMC9256865
mid: NIHMS1765322
doi:

Substances chimiques

Estrogens 0
Lye 0
Estriol FB33469R8E

Types de publication

Journal Article Research Support, N.I.H., Intramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

301-310

Subventions

Organisme : Intramural NIH HHS
ID : ZIA CP010167
Pays : United States

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2022. This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply.

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Auteurs

Ashley M Geczik (AM)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Roni T Falk (RT)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Xia Xu (X)

Protein Characterization Laboratory, Leidos-Frederick, Inc, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.

Beatrice Wiafe-Addai (B)

Peace and Love Hospital, Kumasi, Ghana.

Joel Yarney (J)

Korle Bu Teaching Hospital, Accra, Ghana.

Baffour Awuah (B)

Komfo Anokye Teaching Hospital, Kumasi, Ghana.

Richard Biritwum (R)

University of Ghana, Accra, Ghana.

Verna Vanderpuye (V)

Korle Bu Teaching Hospital, Accra, Ghana.

Florence Dedey (F)

Korle Bu Teaching Hospital, Accra, Ghana.

Ernest Adjei (E)

Komfo Anokye Teaching Hospital, Kumasi, Ghana.

Francis Aitpillah (F)

Komfo Anokye Teaching Hospital, Kumasi, Ghana.

Ernest Osei-Bonsu (E)

Komfo Anokye Teaching Hospital, Kumasi, Ghana.

Joseph Oppong (J)

Komfo Anokye Teaching Hospital, Kumasi, Ghana.

Nicholas Titiloye (N)

Komfo Anokye Teaching Hospital, Kumasi, Ghana.

Lawrence Edusei (L)

Korle Bu Teaching Hospital, Accra, Ghana.

Kofi Nyarko (K)

University of Ghana, Accra, Ghana.

Joe-Nat Clegg-Lamptey (JN)

Korle Bu Teaching Hospital, Accra, Ghana.

Seth Wiafe (S)

Loma Linda University, School of Public Health, Loma Linda, CA, USA.

Daniel Ansong (D)

Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

Thomas U Ahearn (TU)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Jonine Figueroa (J)

The University of Edinburgh, Cancer Research UK Edinburgh Center, Edinburgh, UK.

Montserrat Garcia-Closas (M)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Louise A Brinton (LA)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Britton Trabert (B)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA. britton.trabert@nih.gov.

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