Evidence map›Paper›PMID 28212612›Full record

ArticleBMC medical genetics2017

African ancestry is associated with facial melasma in women: a cross-sectional study.

Maria Paula Barbieri D'Elia, Marcela Calixto Brandão, Bruna Ribeiro de Andrade Ramos, Márcia Guimarães da Silva, Luciane Donida Bartoli Miot, Sidney Emanuel Batista Dos Santos, Hélio Amante Miot

Open access · goldAbstract read
In one paragraph

Article in BMC medical genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. The Effect of Melasma on the Quality of Life in People with Darker Skin Types Living in Durban, South Africa.International journal of environmental research and public health · 2023
    Article
  6. Article
  7. New Mechanistic Insights of Melasma.Clinical, cosmetic and investigational dermatology · 2023
    Review
  8. Update on Melasma-Part I: Pathogenesis.Dermatology and therapy · 2022
    Review
  9. Article
  10. Article
  11. Article
  12. The potential European genetic predisposition for non-contact anterior cruciate ligament injury.Knee surgery, sports traumatology, arthroscopy : official journal of the ESSKA · 2018
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Impact of environmental changes on Dermatology.Anais brasileiros de dermatologia
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Maria Paula Barbieri D'EliaDepartment of Dermatology, FMB-Unesp, Botucatu, SP, Brazil.
Marcela Calixto BrandãoDepartment of Pathology, FMB-Unesp, Botucatu, SP, Brazil.
Bruna Ribeiro de Andrade RamosDepartment of Pathology, FMB-Unesp, Botucatu, SP, Brazil.
Márcia Guimarães da SilvaDepartment of Pathology, FMB-Unesp, Botucatu, SP, Brazil.
Luciane Donida Bartoli MiotDepartment of Dermatology, FMB-Unesp, Botucatu, SP, Brazil.
Sidney Emanuel Batista Dos SantosInstitute of Biological Sciences, UFPA, Belém, PA, Brazil.
Hélio Amante MiotDepartment of Dermatology, FMB-Unesp, Botucatu, SP, Brazil. heliomiot@fmb.unesp.br.
Universidade Estadual Paulista (Unesp) · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMelasma is a chronic acquired focal hypermelanosis affecting photoexposed areas, especially for women during fertile age. Several factors contribute to its development: sun exposure, sex steroids, medicines, and family history. Melanic pigmentation pathway discloses several SNPs in different populations. Here, we evaluated the association between genetic ancestry and facial melasma.

methodsA cross-sectional study involving women with melasma and an age-matched control group from outpatients at FMB-Unesp, Botucatu-SP, Brazil was performed. DNA was extracted from oral mucosa swabs and ancestry determined by studying 61 INDELs. The genetic ancestry components were adjusted by other known risk factors by multiple logistic regression.

resultsWe evaluated 119 women with facial melasma and 119 controls. Mean age was 39 ± 9 years. Mean age at beginning of disease was 27 ± 8 years. Pregnancy (40%), sun exposure (37%), and hormonal oral contraception (22%) were the most frequently reported melasma triggers. All subjects presented admixed ancestry, African and European genetic contributions were significantly different between cases and controls (respectively 10% vs 6%; 77% vs 82%; p < 0.05). African ancestry (OR = 1.04; 95% CI 1.01 to 1.07), first generation family history (OR = 3.04; 95% CI 1.56 to 5.94), low education level (OR = 4.04; 95% CI 1.56 to 5.94), and use of antidepressants by individuals with affected family members (OR = 6.15; 95% CI 1.13 to 33.37) were associated with melasma, independently of other known risk factors.

conclusionsFacial melasma was independently associated with African ancestry in a highly admixed population.

Indexed as

AdultBlack PeopleBrazilCase-Control StudiesContraceptives, OralCross-Sectional StudiesDNAFemaleHumansINDEL MutationLogistic ModelsMelanosisMiddle AgedMouth MucosaOdds RatioPregnancyContraceptives, OralDNAAncestryContraceptivesGonadal steroid hormonesHormonesINDELMelanosisMelasmaOral contraceptivesPigmentationPigmentation disordersPregnancySkin pigmentationUltraviolet rays

Identifiers

PMID28212612
PMCPMC5316149
OpenAlexW2588746987

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.