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PLoS One. 2018 Jun 6;13(6):e0196517. doi: 10.1371/journal.pone.0196517. eCollection 2018.

Development and pilot-testing of the Alopecia Areata Assessment Tool (ALTO).

Author information

1
Department of Dermatology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, United States of America.
2
Loyola University, Chicago, Illinois, United States of America.
3
Department of Dermatology, Alpert Medical School of Brown University, Providence, Rhode Island, United States of America.

Abstract

BACKGROUND:

Alopecia areata (AA) is an autoimmune disease characterized by non-scarring hair loss. The lack of a definitive biomarker or formal diagnostic criteria for AA limits our ability to define the epidemiology of the disease. In this study, we developed and tested the Alopecia Areata Assessment Tool (ALTO) in an academic medical center to validate the ability of this questionnaire in identifying AA cases.

METHODS:

The ALTO is a novel, self-administered questionnaire consisting of 8 closed-ended questions derived by the Delphi method. This prospective pilot study was administered during a 1-year period in outpatient dermatology clinics. Eligible patients (18 years or older with chief concern of hair loss) were recruited consecutively. No patients declined to participate. The patient's hair loss diagnosis was determined by a board-certified dermatologist. Nine scoring algorithms were created and used to evaluate the accuracy of the ALTO in identifying AA.

RESULTS:

239 patients (59 AA cases and 180 non-AA cases) completed the ALTO and were included for analysis. Algorithm 5 demonstrated the highest sensitivity (89.8%) while algorithm 3 demonstrated the highest specificity (97.8%). Select questions were also effective in clarifying disease phenotype.

CONCLUSION:

In this study. we have successfully demonstrated that ALTO is a simple tool capable of discriminating AA from other types of hair loss. The ALTO may be useful to identify individuals with AA within large populations.

PMID:
29874239
PMCID:
PMC5991373
DOI:
10.1371/journal.pone.0196517
[Indexed for MEDLINE]
Free PMC Article

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