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Sökning: id:"swepub:oai:DiVA.org:mdh-52013" > Genotypes Do Not Co...

Genotypes Do Not Confer Risk For Delinquency ut Rather Alter Susceptibility to Positive and Negative Environmental Factors : Gene-Environment Interactions of BDNF Val66Met, 5-HTTLPR, and MAOA-uVNTR

Nilsson, Kent W. (författare)
Uppsala universitet,Centrum för klinisk forskning, Västerås,Uppsala Univ, Cty Hosp, Clin Res Ctr, S-72189 Vasteras, Sweden.
Comasco, Erika (författare)
Uppsala universitet,Institutionen för neurovetenskap,Uppsala Univ, Dept Neurosci, S-75124 Uppsala, Sweden.
Hodgins, Sheilagh (författare)
Karolinska Institutet
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Oreland, Lars (författare)
Uppsala universitet,Neuropsykofarmakologi,Uppsala Univ, Dept Neurosci, S-75124 Uppsala, Sweden.
Åslund, Cecilia (författare)
Uppsala universitet,Centrum för klinisk forskning, Västerås,Uppsala Univ, Cty Hosp, Clin Res Ctr, S-72189 Vasteras, Sweden.
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 (creator_code:org_t)
2015-03-05
2015
Engelska.
Ingår i: International Journal of Neuropsychopharmacology. - : OXFORD UNIV PRESS. - 1461-1457 .- 1469-5111. ; 18:5
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background: Previous evidence of gene-by-environment interactions associated with emotional and behavioral disorders is contradictory. Differences in findings may result from variation in valence and dose of the environmental factor, and/or failure to take account of gene-by-gene interactions. The present study investigated interactions between the brain-derived neurotrophic factor gene (BDNF Val66Met), the serotonin transporter gene-linked polymorphic region (5-HTTLPR), the monoamine oxidase A (MAOA-uVNTR) polymorphisms, family conflict, sexual abuse, the quality of the child-parent relationship, and teenage delinquency. Methods: In 2006, as part of the Survey of Adolescent Life in Vastmanland, Sweden, 1 337 high-school students, aged 1718 years, anonymously completed questionnaires and provided saliva samples for DNA analyses. Results: Teenage delinquency was associated with two-, three-, and four-way interactions of each of the genotypes and the three environmental factors. Significant four-way interactions were found for BDNF Val66Met x 5-HTTLPRxMAOA-uVNTR x family conflicts and for BDNF Val66Met x 5-HTTLPRxMAOA-uVNTR x sexual abuse. Further, the two genotype combinations that differed the most in expression levels (BDNF Val66Met Val, 5-HTTLPR LL, MAOA-uVNTR LL [girls] and L [boys] vs BDNF Val66Met Val/Met, 5-HTTLPR S/LS, MAOA-uVNTR S/SS/LS) in interaction with family conflict and sexual abuse were associated with the highest delinquency scores. The genetic variants previously shown to confer vulnerability for delinquency (BDNF Val66Met Val/Met x 5-HTTLPR S x MAOA-uVNTR S) were associated with the lowest delinquency scores in interaction with a positive child-parent relationship. Conclusions: Functional variants of the MAOA-uVNTR, 5-HTTLPR, and BDNF Val66Met, either alone or in interaction with each other, may be best conceptualized as modifying sensitivity to environmental factors that confer either risk or protection for teenage delinquency.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

Nyckelord

brain-derived neurotrophic factor
gene-environment interaction
juvenile delinquency
monoamine oxidase
serotonin plasma membrane transport proteins

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