lunes, 5 de mayo de 2014

Unaffected family members report improvements in d... [Genet Med. 2014] - PubMed - NCBI

Unaffected family members report improvements in d... [Genet Med. 2014] - PubMed - NCBI



 2014 Apr 24. doi: 10.1038/gim.2014.37. [Epub ahead of print]

Unaffected family members report improvements in daily routine sun protection 2 years following melanoma genetic testing.

Abstract

Purpose:Reducing ultraviolet radiation exposure may decrease melanoma risk in the hereditary melanoma setting. It is unknown whether genetic counseling and test reporting of CDKN2A/p16 mutation status promote long-term compliance with photoprotection recommendations, especially in unaffected mutation carriers.Methods:This study evaluated changes 2 years following melanoma genetic testing in self-reported practice of sun protection (sunscreen, photoprotective clothing, and ultraviolet radiation avoidance) among 37 members of two CDKN2A/p16 kindreds (10 unaffected carriers, 11 affected carriers, and 16 unaffected noncarriers; response rate = 64.9% of eligible participants).Results:Multivariate profile analysis indicated that all three participant groups reported increased daily routine practice of sun protection 2 years following melanoma genetic testing (P < 0.02), with 96.9% reporting that at least one sun protection behavior was part of their daily routine, up from 78.1% at baseline (P < 0.015). Unaffected carriers (P < 0.024) and unaffected noncarriers (P < 0.027) reported significantly more frequent use of photoprotective clothing. Affected carriers maintained adherence to all sun protection behaviors. Reported sunburns in the past 6 months decreased significantly (P < 0.018).Conclusion:Members of high-risk families reported increased daily routine sun protection and decreased sunburns 2 years following melanoma genetic testing, with no net decline in sun protection following negative test results. Thus, genetic testing and counseling may motivate sustained improvements in prevention behaviors.Genet Med advance online publication 24 April 2014Genetics in Medicine (2014); doi:10.1038/gim.2014.37.

PMID:
 
24763292
 
[PubMed - as supplied by publisher]

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