Association between a rare SNP in the second intron of human Agouti related protein gene and increased BMI

<p>Abstract</p> <p>Background</p> <p>The agouti related protein (AGRP) is an endogenous antagonist of the melanocortin 4 receptor and is one of the most potent orexigenic factors. The aim of the present study was to assess the genetic variability of <it>AGRP </...

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Main Authors: Ignatovica Vita (Author), Pirags Valdis (Author), Kapa Ivo (Author), Kalnina Ineta (Author), Schiöth Helgi B (Author), Klovins Janis (Author)
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Published: BMC, 2009-07-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Ignatovica Vita  |e author 
700 1 0 |a Pirags Valdis  |e author 
700 1 0 |a Kapa Ivo  |e author 
700 1 0 |a Kalnina Ineta  |e author 
700 1 0 |a Schiöth Helgi B  |e author 
700 1 0 |a Klovins Janis  |e author 
245 0 0 |a Association between a rare SNP in the second intron of human Agouti related protein gene and increased BMI 
260 |b BMC,   |c 2009-07-01T00:00:00Z. 
500 |a 10.1186/1471-2350-10-63 
500 |a 1471-2350 
520 |a <p>Abstract</p> <p>Background</p> <p>The agouti related protein (AGRP) is an endogenous antagonist of the melanocortin 4 receptor and is one of the most potent orexigenic factors. The aim of the present study was to assess the genetic variability of <it>AGRP </it>gene and investigate whether the previously reported SNP rs5030980 and the rs11575892, a SNP that so far has not been studied with respect to obesity is associated with increased body mass index (BMI).</p> <p>Methods</p> <p>We determined the complete sequence of the <it>AGRP </it>gene and upstream promoter region in 95 patients with severe obesity (BMI > 35 kg/m<sup>2</sup>). Three polymorphisms were identified: silent mutation c.123G>A (rs34123523) in the second exon, non-synonymous mutation c.199G>A (rs5030980) and c.131-42C>T (rs11575892) located in the second intron. We further screened rs11575892 in a selected group of 1135 and rs5030980 in group of 789 participants from the Genome Database of Latvian Population and Latvian State Research Program Database.</p> <p>Results</p> <p>The CT heterozygotes of rs11575892 had significantly higher mean BMI value (p = 0.027). After adjustment for age, gender and other significant non-genetic factors (presence of diseases), the BMI levels remained significantly higher in carriers of the rs11575892 T allele (p = 0.001). The adjusted mean BMI value of CC genotype was 27.92 ± 1.01 kg/m<sup>2 </sup>(mean, SE) as compared to 30.97 ± 1.03 kg/m<sup>2 </sup>for the CT genotype. No association was found between rs5030980 and BMI.</p> <p>Conclusion</p> <p>This study presents an association of rare allele of <it>AGRP </it>polymorphism in heterozygous state with increased BMI. The possible functional effects of this polymorphism are unclear but may relate to splicing defects.</p> 
546 |a EN 
690 |a Internal medicine 
690 |a RC31-1245 
690 |a Genetics 
690 |a QH426-470 
655 7 |a article  |2 local 
786 0 |n BMC Medical Genetics, Vol 10, Iss 1, p 63 (2009) 
787 0 |n http://www.biomedcentral.com/1471-2350/10/63 
787 0 |n https://doaj.org/toc/1471-2350 
856 4 1 |u https://doaj.org/article/6c1278f1b9874f70beb39bf3e91f48f7  |z Connect to this object online.