Alopecia Areata, patchy hair loss which may progress to total scalp or body hair loss, affects 1-2 percent of the population. We hypothesize that Alopecia Areata is an HLA (histocompatibility locus antigens) restricted, T cell mediated autoimmune reaction to hair follicle antigens or viral infection resulting from the interactions of multiple genes of immune response which may result in the production of specific antibodies to the hair follicle. Alopecia Areata occurs with other autoimmune diseases, in identical twins and in families. It is associated with HLA alleles and with other immune related genes that may interact to determine susceptibility, resistance, and persistence. Possible viral infection and antibodies to hair follicle, melanocytes, keratinocytes, and endothelial cells are of unknown significance. Our goal is to investigate the genetic mechanism of Alopecia Areata in families of the purpose of disease prevention, early intervention, and development of specific therapies. We propose: a) to identify and collect DNA from AA families; b) to determine the genetic models for Alopecia Areata by using the simultaneous information on both the aggregation and association of the HLA marker with the disease and also on the risk of being affected for some relatives of a patient; c) to identify disease-predisposing amino acids in the HLA region involved in the Alopecia Areata process; d) to identify polymorphic markers for genetic loci that are associated with Alopecia Areata in families. To accomplish aim a we will collect families from several dermatology clinics in Houston.
For aims b and c we will apply MASC and haplotype methods.
For aim d, we will use parametric and nonparametric linkage methods.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Small Research Grants (R03)
Project #
1R03AR045789-01
Application #
2793460
Study Section
Special Emphasis Panel (ZAR1-JRL-A (O1))
Project Start
1998-09-30
Project End
2001-08-31
Budget Start
1998-09-30
Budget End
1999-08-31
Support Year
1
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Texas MD Anderson Cancer Center
Department
Public Health & Prev Medicine
Type
Other Domestic Higher Education
DUNS #
001910777
City
Houston
State
TX
Country
United States
Zip Code
77030
Barahmani, Nazila; de Andrade, Mariza; Slusser, Joshua P et al. (2008) Human leukocyte antigen class II alleles are associated with risk of alopecia areata. J Invest Dermatol 128:240-3
Barahmani, Nazila; de Andrade, Mariza; Slusser, Joshua P et al. (2006) Major histocompatibility complex class I chain-related gene A polymorphisms and extended haplotypes are associated with familial alopecia areata. J Invest Dermatol 126:74-8
Barahmani, Nazila; Barahamani, Nazila; de Andrade, Mariza et al. (2002) Interleukin-1 receptor antagonist allele 2 and familial alopecia areata. J Invest Dermatol 118:335-7
de Andrade, M; Jackow, C M; Dahm, N et al. (1999) Alopecia areata in families: association with the HLA locus. J Investig Dermatol Symp Proc 4:220-3