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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Clinical Endocrinolo...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Clinical Endocrinology
Article . 2009 . Peer-reviewed
License: Wiley Online Library User Agreement
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LRP5 in premature adrenarche and in metabolic characteristics of prepubertal children

Authors: Anne Saarinen; Pauliina Utriainen; Outi Mäkitie; Saila Lappalainen; Raimo Voutilainen; Jarmo Jääskeläinen;

LRP5 in premature adrenarche and in metabolic characteristics of prepubertal children

Abstract

SummaryObjective  Premature adrenarche (PA) is associated with unfavourable metabolic characteristics. We hypothesized that genetic variation in low density lipoprotein (LDL) receptor‐related protein 5 (LRP5), which is involved in Wnt signalling in the adrenal cortex and in cholesterol metabolism, plays a role in the pathogenesis of PA.Design and patients  We performed a cross‐sectional association study in 73 Finnish children with PA and 97 age‐ and gender‐matched healthy controls.Measurements  LRP5 genotypes were determined by direct sequencing. Single‐marker associations with clinical‐metabolic characteristics, including adrenocortical function, glucose tolerance and lipid profile, were examined with age and gender as covariates.Results  Nineteen single nucleotide polymorphisms (SNPs) in LRP5 were found in the 170 children. No significant differences in the genotype distributions were observed between the PA and control groups. SNPs A1330V and N740N were associated with higher serum dehydroepiandrosterone sulphate (DHEAS) levels in the control subjects (A/A vs. A/a; mean 0·8 vs. 1·4 µmol/l, P = 0·01). They were also associated with higher plasma levels of total (4·2 vs. 4·7 mmol/l, P = 0·02) and LDL cholesterol (2·4 vs. 2·9 mmol/l, P = 0·02) in the control group, as was SNP V1119V (P = 0·04 and P = 0·03, respectively). SNPs F549F and V1119V were associated with higher systolic blood pressure (P = 0·04 and P = 0·02, respectively). There were no differences in the parameters of glucose metabolism between the genotype groups.Conclusions  Genetic variation in LRP5 did not predispose to PA but was associated with metabolic characteristics, especially lipid profile, in healthy prepubertal children.

Keywords

Male, Metabolic Syndrome, Genotype, Genetic Variation, Lipids, Polymorphism, Single Nucleotide, Cross-Sectional Studies, Low Density Lipoprotein Receptor-Related Protein-5, Phenotype, Gene Frequency, Case-Control Studies, Humans, Adrenarche, Female, Genetic Predisposition to Disease, Child, Alleles, Finland, LDL-Receptor Related Proteins, Signal Transduction

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
13
Average
Average
Average