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Articles by T. D Dyer
Total Records ( 2 ) for T. D Dyer
  N Franceschini , K. M Rose , K. L Storti , S Rutherford , V. S Voruganti , S Laston , H. H.H Goring , T. D Dyer , J. G Umans , E. T Lee , L. G Best , R. R Fabsitz , S. A Cole , J. W MacCluer and K. E. North
 

Background— Population studies have demonstrated an important role of social, behavioral, and environmental factors in blood pressure (BP) levels. Accounting for the genetic interaction of these factors may help to identify common BP susceptibility alleles.

Methods and Results— We studied the interaction of additive genetic effects and behavioral (physical activity, smoking, alcohol use) and socioeconomic (education) factors on BP in 3600 American Indian participants of the Strong Heart Family Study, using variance component models. The mean and SD of resting systolic and diastolic BPs were 123±17 and 76±11 mm Hg, respectively. We detected evidence for distinct genetic effects on diastolic BP among ever smokers compared with never smokers (P=0.01). For alcohol intake, we observed significant genotype-by-environment interactions on diastolic (g=0.10, P=0.0003) and on systolic BPs (g=0.59, P=0.0008) among current drinkers compared with former or never drinkers. We also detected genotype-by-physical activity interactions on diastolic BP (g=0.35, P=0.0004). Finally, there was evidence for distinct genetic effects on diastolic BP among individuals with less than high school education compared with those with 12 or more years of education (g=0.41, P=0.02).

Conclusions— Our findings suggest that behavioral and socioeconomic factors can modify the genetic effects on BP phenotypes. Accounting for context dependent factors may help us to better understand the complexities of the gene effects on BP and other complex phenotypes with high levels of genetic heterogeneity.

  M. H Fenstad , M. P Johnson , M Loset , S. B Mundal , L. T Roten , I. P Eide , L Bjorge , R. K Sande , A. K Johansson , T. D Dyer , S Forsmo , J Blangero , E. K Moses and R. Austgulen
 

Variation in the Storkhead box-1 (STOX1) gene has previously been associated with pre-eclampsia. In this study, we assess candidate single nucleotide polymorphisms (SNPs) in STOX1 in an independent population cohort of pre-eclamptic (n = 1.139) and non-pre-eclamptic (n = 2.269) women (the HUNT2 study). We also compare gene expression levels of STOX1 and its paralogue, Storkhead box-2 (STOX2) in decidual tissue from pregnancies complicated by pre-eclampsia and/or fetal growth restriction (FGR) (n = 40) to expression levels in decidual tissue from uncomplicated pregnancies (n = 59). We cannot confirm association of the candidate SNPs to pre-eclampsia (P > 0.05). For STOX1, no differential gene expression was observed in any of the case groups, whereas STOX2 showed significantly lower expression in deciduas from pregnancies complicated by both pre-eclampsia and FGR as compared with controls (P = 0.01). We further report a strong correlation between transcriptional alterations reported previously in choriocarcinoma cells over expressing STOX1A and alterations observed in decidual tissue of pre-eclamptic women with FGR.

 
 
 
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