Male-pattern baldness susceptibility locus at 20p11.

We conducted a genome-wide association study for androgenic alopecia in 1,125 men and identified a newly associated locus at chromosome 20p11.22, confirmed in three independent cohorts (n = 1,650; OR = 1.60, P = 1.1 x 10(-14) for rs1160312). The one man in seven who harbors risk alleles at both 20p11.22 and AR (encoding the androgen receptor) has a sevenfold-increased odds of androgenic alopecia (OR = 7.12, P = 3.7 x 10(-15)).

Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology.

The pathogenesis of androgenetic alopecia (AGA, male-pattern baldness) is driven by androgens, and genetic predisposition is the major prerequisite. Candidate gene and genome-wide association studies have reported that single-nucleotide polymorphisms (SNPs) at eight different genomic loci are associated with AGA development. However, a significant fraction of the overall heritable risk still awaits identification. Furthermore, the understanding of the pathophysiology of AGA is incomplete, and each newly associated locus may provide novel insights into contributing biological pathways. The aim of this study was to identify unknown AGA risk loci by replicating SNPs at the 12 genomic loci that showed suggestive association (5 × 10(-8)<P<10(-5)) with AGA in a recent meta-analysis. We analyzed a replication set comprising 2,759 cases and 2,661 controls of European descent to confirm the association with AGA at these loci. Combined analysis of the replication and the meta-analysis data identified four genome-wide significant risk loci for AGA on chromosomes 2q35, 3q25.1, 5q33.3, and 12p12.1. The strongest association signal was obtained for rs7349332 (P=3.55 × 10(-15)) on chr2q35, which is located intronically in WNT10A. Expression studies in human hair follicle tissue suggest that WNT10A has a functional role in AGA etiology. Thus, our study provides genetic evidence supporting an involvement of WNT signaling in AGA development.

Pèls a la llengua

Si sou calbs i voleu deixar de ser-ho, o si la vostra parella és calba i enyoreu aquells cabells llargs i espessos que lluïa a l'època hippie, esteu de sort. Però aneu alerta, perquè si sou d'aquelles persones que els agrada dir que no té pèls a la llengua, potser ara us en sortiran. O almenys això és el que hom pot pensar després de sentir una de les darreres notícies de ciència de gran ressò mediàtic: s'ha aconseguit que a un ratolí modificat genèticament per no tenir cap pèl li'n creixin. Els artífexs han estat els membres d'un equip de recerca de l'Institut Kennedy Krieger de la Johns Hopkins University, dels EUA, encapçalat per Catherine Thompson. I esclar, molts ja s'imaginen lluint llargues i espesses cabelleres on ara només tenen lluentors [...].