Alopecia Areata and malignancies: uncertainties clarified by a large-scale population-based study

The association of AA with malignancies has been a scope of controversy as the current literature is highly inconsistent in this regard. To evaluate the association between AA and hematological malignancies (HMs) and solid malignancies (SMs) using a large-scale, real-life computerized database. A cross-sectional study was conducted to compare the prevalence of HMs and SMs among patients with AA relative to age-, sex-, and ethnicity-matched control subjects. Chi-square and t-tests were used for univariate analysis, and a logistic regression model was used for multivariate analysis. The study included 51,561 patients with AA and 51,410 controls. AA was significantly associated with HMs (adjusted OR, 1.27; 95% CI, 1.07-1.51; P = 0.006). This association was more robust among patients with late-onset AA (≥ 50 years; OR, 1.33; 95% CI, 1.04-1.71; P = 0.025). On the other hand, AA was not found to be significantly associated with SM (adjusted OR, 0.97; 95% CI, 0.88-1.06; P = 0.487), excluding among patients with alopecia totalis and universalis (OR, 2.10; 95% CI, 1.03-4.27; P = 0.036). In a granular analysis including 5 HMs and 18 SMs, non-Hodgkin lymphoma was the only malignancy that proved positively associated with AA (adjusted OR, 1.32; 95% CI, 1.03-1.69; P = 0.028). AA is associated with HMs but not SMs. Further research is warranted to validate our observations in other study cohorts.

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Publication Details

Journal
Archives of Dermatological Research
Published
2024-10-14
DOI
https://doi.org/10.1007/s00403-024-03385-3
Citations
3
Primary Topic
Hair Growth and Disorders
Type
article
Field-Weighted Citation Impact
1.61

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article

Alopecia Areata and malignancies: uncertainties clarified by a large-scale population-based study

Arnon Dov Cohen, Francisco Jiménez Otárola, Khalaf Kridin, Rimma Laufer-Britva et al.
3 citations
Archives of Dermatological Research
Hair Growth and Disorders
1.61
article

Alopecia Areata and malignancies: uncertainties clarified by a large-scale population-based study

Arnon Dov Cohen, Francisco Jiménez Otárola, Khalaf Kridin, Rimma Laufer-Britva, Anna Lyakhovitsky, Baruch Kaplan
article en
3 citations

Abstract

The association of AA with malignancies has been a scope of controversy as the current literature is highly inconsistent in this regard. To evaluate the association between AA and hematological malignancies (HMs) and solid malignancies (SMs) using a large-scale, real-life computerized database. A cross-sectional study was conducted to compare the prevalence of HMs and SMs among patients with AA relative to age-, sex-, and ethnicity-matched control subjects. Chi-square and t-tests were used for univariate analysis, and a logistic regression model was used for multivariate analysis. The study included 51,561 patients with AA and 51,410 controls. AA was significantly associated with HMs (adjusted OR, 1.27; 95% CI, 1.07-1.51; P = 0.006). This association was more robust among patients with late-onset AA (≥ 50 years; OR, 1.33; 95% CI, 1.04-1.71; P = 0.025). On the other hand, AA was not found to be significantly associated with SM (adjusted OR, 0.97; 95% CI, 0.88-1.06; P = 0.487), excluding among patients with alopecia totalis and universalis (OR, 2.10; 95% CI, 1.03-4.27; P = 0.036). In a granular analysis including 5 HMs and 18 SMs, non-Hodgkin lymphoma was the only malignancy that proved positively associated with AA (adjusted OR, 1.32; 95% CI, 1.03-1.69; P = 0.028). AA is associated with HMs but not SMs. Further research is warranted to validate our observations in other study cohorts.

Archives of Dermatological ResearchVol. 316(10)
Ben-Gurion University of the Negev (IL), Bar-Ilan University (IL), Tel Aviv University (IL), Sheba Medical Center (IL), Western Galilee Hospital (IL), Universidad Fernando Pessoa Canarias (ES), Hospital Ruber Internacional (ES), Ariel University (IL), Clalit Health Services (IL), University of Lübeck (DE)
Bar-Ilan University
Openalex Percentile: Top 16%
Hair Growth and Disorders
1.61
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