Prevalence of filaggrin loss-of-function variants in Chilean population with and without atopic dermatitis

dc.contributor.authorCárdenas, Geovanna
dc.contributor.authorIturriaga, Carolina
dc.contributor.authorHernández, Carol
dc.contributor.authorTejos-Bravo, Macarena
dc.contributor.authorPérez-Matelina, Guillermo
dc.contributor.authorCabalin, Carolina
dc.contributor.authorUrzúa, Marcela
dc.contributor.authorVenegas-Salas, Luis
dc.contributor.authorFraga, Juan P.
dc.contributor.authorRebolledo-Jaramillo, Boris
dc.contributor.authorPoli, Cecilia
dc.contributor.authorRepetto, Gabriela
dc.contributor.authorCasanello, Paola
dc.contributor.authorCastro-Rodriguez, José
dc.contributor.authorBorzutzky, Arturo
dc.date.accessioned2021-11-26T21:01:34Z
dc.date.available2021-11-26T21:01:34Z
dc.date.issued2021
dc.description.abstractBackground Filaggrin (FLG) loss-of-function variants are major genetic risk factors for atopic dermatitis (AD), but these have not been studied in Latin American populations with and without AD. Methods FLG variants R501X and 2282del4 were genotyped in 275 Chilean adults with and without AD from the “Early origins of allergy and asthma” (ARIES) cohort and in 227 patients from an AD cohort based in Santiago, Chile. Results Among adults in the ARIES cohort, 3.3% were carriers of R501X and 2.9% of 2282del4 variants, all heterozygotes. In this cohort, 6.2% were FLG variant carriers: 11.1% of subjects reporting AD were carriers of FLG variants vs. 5.2% in those without AD (P = 0.13). In this first cohort, FLG variants were not significantly associated with asthma, allergic rhinitis, or food allergy. In the AD cohort, the prevalence of FLG variants was 7% for R501X, 2.2% for the 2282del4 variant, and 9.3% for the combined genotype. In this cohort, FLG variants were present in 15.5% of severe AD vs. 7.1% of mild-to-moderate AD subjects (P = 0.056). Evaluation of Chilean population from both cohorts combined (n = 502) revealed that FLG variants were not significantly associated with AD (OR = 1.92 [95% CI 0.95–3.9], P = 0.067) but were associated with asthma (OR = 2.16 [95% CI 1.02– 4.56], P = 0.039). Conclusions This is the first study to evaluate FLG loss-of-function variants R501X and 2282del4 in Latin American population, revealing a similar prevalence of these FLG variant carriers to that of European populations. Among Chileans, FLG variants were significantly associated with asthma but not AD.es
dc.identifier.citationCárdenas, G.V., Iturriaga, C., Hernández, C.D., Tejos-Bravo, M., Pérez-Mateluna, G., Cabalin, C., Urzúa, M., Venegas-Salas, L.F., Fraga, J.P., Rebolledo, B., Poli, M.C., Repetto, G.M., Casanello, P., Castro-Rodríguez, J.A. and Borzutzky, A. (2021), Prevalence of filaggrin loss-of-function variants in Chilean population with and without atopic dermatitis. Int J Dermatoles
dc.identifier.urihttps://doi.org/10.1111/ijd.15887es
dc.identifier.urihttp://hdl.handle.net/11447/5129
dc.language.isoenes
dc.sourceInternational journal of dermatology
dc.titlePrevalence of filaggrin loss-of-function variants in Chilean population with and without atopic dermatitises
dc.typeArticlees

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