SwePub
Sök i LIBRIS databas

  Utökad sökning

L773:1872 9711 OR L773:0161 813X
 

Sökning: L773:1872 9711 OR L773:0161 813X > Modification by the...

Modification by the genes ALAD and VDR of lead-induced cognitive effects in children

Pawlas, Natalia (författare)
Broberg Palmgren, Karin (författare)
Lund University,Lunds universitet,Avdelningen för arbets- och miljömedicin,Institutionen för laboratoriemedicin,Medicinska fakulteten,Division of Occupational and Environmental Medicine, Lund University,Department of Laboratory Medicine,Faculty of Medicine
Olewinska, Elzbieta (författare)
visa fler...
Prokopowicz, Adam (författare)
Skerfving, Staffan (författare)
Lund University,Lunds universitet,Avdelningen för arbets- och miljömedicin,Institutionen för laboratoriemedicin,Medicinska fakulteten,Division of Occupational and Environmental Medicine, Lund University,Department of Laboratory Medicine,Faculty of Medicine
Pawlas, Krystyna (författare)
visa färre...
 (creator_code:org_t)
Elsevier BV, 2012
2012
Engelska.
Ingår i: NeuroToxicology. - : Elsevier BV. - 1872-9711 .- 0161-813X. ; 33:1, s. 37-43
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Lead has negative effect on cognitive functions in children. However, individuals differ in susceptibility. One possible explanation is a genetic predisposition. Polymorphisms in the B-aminolevulinic acid dehydratase (ALAD) and the vitamin D receptor (VDR) genes may modify lead metabolism and neurotoxicity, but information regarding the central nervous system is very limited. The aim of the study was to determine whether ALAD and VDR polymorphisms modify blood lead (B-Pb), and the association between B-Pb and cognitive function (IQ) in children. In 2007-2010 a cohort of 175 children (age 6-10 years, mean 7.8) was recruited in Southern Poland, tested for IQ (Wechsler intelligence scale) and analyzed for B-Pb (range 9.0-221; mean 46.6 mu g/L), ALAD (Rsal, Mspl) and VDR (Fokl, Bsml, Taql) polymorphisms. ALAD or VDR genotypes were not associated with B-Pb. B-Pb was non-significantly negatively associated with full scale IQ (r(S) = -0.11; P = 0.14), and significantly with performance subscale results (r(S) = -0.19; P = 0.01). The ALAD Rsal polymorphism modified the relationship between full scale IQ and B-Pb: Rsal T carriers had a steeper slope compared to CC homozygote carriers (beta coefficient -0.06 vs 0.32, respectively, P for interaction < 0.001, adjusted for the child's age, mother's education and family income). This means that with increasing B-Pb with 1 mu g/L,T carriers demonstrate 0.06 score lower IQ. For the VDR Bsml, B carriers had a steeper slope than the bb homozygotes carriers (beta coefficient -0.08 vs 0.16, respectively, P for interaction = 0.001), and similar effect was found for Taql t carriers vs TT homozygotes (P for interaction = 0.02). For ALAD Mspl and VDR Fokl there was no significant modification. The ALAD Rsal, VDR Bsml and Taql polymorphisms modified the relationship between IQ and B-Pb. Hence, there is a fraction of the population, which is particularly sensitive to lead neurotoxicity. (C) 2011 Elsevier Inc. All rights reserved.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Arbetsmedicin och miljömedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Occupational Health and Environmental Health (hsv//eng)

Nyckelord

Central nervous system
Neurotoxicity
Polymorphism
Lead
IQ
Gene-environment interaction

Publikations- och innehållstyp

art (ämneskategori)
ref (ämneskategori)

Hitta via bibliotek

Till lärosätets databas

Sök utanför SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy