Suggestion for linkage of chromosome 1p35.2 and 3q28 to plasma adiponectin concentrations in the GOLDN Study

<p>Abstract</p> <p>Background</p> <p>Adiponectin is inversely associated with obesity, insulin resistance, and atherosclerosis, but little is known about the genetic pathways that regulate the plasma level of this protein. To find novel genes that influence circulating...

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Main Authors: Tsai Michael Y, Hixson James E, Borecki Ingrid B, Peacock James M, Pankow James S, Rasmussen-Torvik Laura J, Kabagambe Edmond K, Arnett Donna K
Format: Article
Language:English
Published: BMC 2009-05-01
Series:BMC Medical Genetics
Online Access:http://www.biomedcentral.com/1471-2350/10/39
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spelling doaj-d598edf0cd75426e87ca2b3af3b42d072021-04-02T03:24:56ZengBMCBMC Medical Genetics1471-23502009-05-011013910.1186/1471-2350-10-39Suggestion for linkage of chromosome 1p35.2 and 3q28 to plasma adiponectin concentrations in the GOLDN StudyTsai Michael YHixson James EBorecki Ingrid BPeacock James MPankow James SRasmussen-Torvik Laura JKabagambe Edmond KArnett Donna K<p>Abstract</p> <p>Background</p> <p>Adiponectin is inversely associated with obesity, insulin resistance, and atherosclerosis, but little is known about the genetic pathways that regulate the plasma level of this protein. To find novel genes that influence circulating levels of adiponectin, a genome-wide linkage scan was performed on plasma adiponectin concentrations before and after 3 weeks of treatment with fenofibrate (160 mg daily) in the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN) Study. We studied Caucasian individuals (n = 1121) from 190 families in Utah and Minnesota. Of these, 859 individuals from 175 families had both baseline and post-fenofibrate treatment measurements for adiponectin. Plasma adiponectin concentrations were measured with an ELISA assay. All participants were typed for microsatellite markers included in the Marshfield Mammalian Genotyping Service marker set 12, which includes 407 markers spaced at approximately 10 cM regions across the genome. Variance components analysis was used to estimate heritability and to perform genome-wide scans. Adiponectin was adjusted for age, sex, and field center. Additional models also included BMI adjustment.</p> <p>Results</p> <p>Baseline and post-fenofibrate adiponectin measurements were highly correlated (r = 0.95). Suggestive (LOD > 2) peaks were found on chromosomes 1p35.2 and 3q28 (near the location of the adiponectin gene).</p> <p>Conclusion</p> <p>Two candidate genes, <it>IL22RA1 </it>and <it>IL28RA</it>, lie under the chromosome 1 peak; further analyses are needed to identify the specific genetic variants in this region that influence circulating adiponectin concentrations.</p> http://www.biomedcentral.com/1471-2350/10/39
collection DOAJ
language English
format Article
sources DOAJ
author Tsai Michael Y
Hixson James E
Borecki Ingrid B
Peacock James M
Pankow James S
Rasmussen-Torvik Laura J
Kabagambe Edmond K
Arnett Donna K
spellingShingle Tsai Michael Y
Hixson James E
Borecki Ingrid B
Peacock James M
Pankow James S
Rasmussen-Torvik Laura J
Kabagambe Edmond K
Arnett Donna K
Suggestion for linkage of chromosome 1p35.2 and 3q28 to plasma adiponectin concentrations in the GOLDN Study
BMC Medical Genetics
author_facet Tsai Michael Y
Hixson James E
Borecki Ingrid B
Peacock James M
Pankow James S
Rasmussen-Torvik Laura J
Kabagambe Edmond K
Arnett Donna K
author_sort Tsai Michael Y
title Suggestion for linkage of chromosome 1p35.2 and 3q28 to plasma adiponectin concentrations in the GOLDN Study
title_short Suggestion for linkage of chromosome 1p35.2 and 3q28 to plasma adiponectin concentrations in the GOLDN Study
title_full Suggestion for linkage of chromosome 1p35.2 and 3q28 to plasma adiponectin concentrations in the GOLDN Study
title_fullStr Suggestion for linkage of chromosome 1p35.2 and 3q28 to plasma adiponectin concentrations in the GOLDN Study
title_full_unstemmed Suggestion for linkage of chromosome 1p35.2 and 3q28 to plasma adiponectin concentrations in the GOLDN Study
title_sort suggestion for linkage of chromosome 1p35.2 and 3q28 to plasma adiponectin concentrations in the goldn study
publisher BMC
series BMC Medical Genetics
issn 1471-2350
publishDate 2009-05-01
description <p>Abstract</p> <p>Background</p> <p>Adiponectin is inversely associated with obesity, insulin resistance, and atherosclerosis, but little is known about the genetic pathways that regulate the plasma level of this protein. To find novel genes that influence circulating levels of adiponectin, a genome-wide linkage scan was performed on plasma adiponectin concentrations before and after 3 weeks of treatment with fenofibrate (160 mg daily) in the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN) Study. We studied Caucasian individuals (n = 1121) from 190 families in Utah and Minnesota. Of these, 859 individuals from 175 families had both baseline and post-fenofibrate treatment measurements for adiponectin. Plasma adiponectin concentrations were measured with an ELISA assay. All participants were typed for microsatellite markers included in the Marshfield Mammalian Genotyping Service marker set 12, which includes 407 markers spaced at approximately 10 cM regions across the genome. Variance components analysis was used to estimate heritability and to perform genome-wide scans. Adiponectin was adjusted for age, sex, and field center. Additional models also included BMI adjustment.</p> <p>Results</p> <p>Baseline and post-fenofibrate adiponectin measurements were highly correlated (r = 0.95). Suggestive (LOD > 2) peaks were found on chromosomes 1p35.2 and 3q28 (near the location of the adiponectin gene).</p> <p>Conclusion</p> <p>Two candidate genes, <it>IL22RA1 </it>and <it>IL28RA</it>, lie under the chromosome 1 peak; further analyses are needed to identify the specific genetic variants in this region that influence circulating adiponectin concentrations.</p>
url http://www.biomedcentral.com/1471-2350/10/39
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