Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels Article Swipe

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Wei‐Min Chen , Michael R. Erdos , Anne Jackson , Richa Saxena , Serena Sanna , Kristi D. Silver , Nicholas J. Timpson , Torben Hansen , Marco Orrù , Maria Grazia Piras , Lori L. Bonnycastle , Cristen J. Willer , Valeriya Lyssenko , Haiqing Shen , Johanna Kuusisto , Shah Ebrahim , Natascia Sestu , William L. Duren , Maria Cristina Spada , Heather M. Stringham , Laura J. Scott , Nazario Olla , Amy J. Swift , Samer S. Najjar , Braxton D. Mitchell , Debbie A. Lawlor , George Davey Smith , Yoav Ben‐Shlomo , Gary L. Andersen , Knut Borch‐Johnsen , Torben Jørgensen , Jouko Saramies ·

YOU? · · 2020 · Open Access · · DOI: https://doi.org/10.17615/sgy6-c717

Identifying the genetic variants that regulate fasting glucose concentrations may further our understanding of the pathogenesis of diabetes. We therefore investigated the association of fasting glucose levels with SNPs in 2 genome-wide scans including a total of 5,088 nondiabetic individuals from Finland and Sardinia. We found a significant association between the SNP rs563694 and fasting glucose concentrations (P = 3.5 × 10–7). This association was further investigated in an additional 18,436 nondiabetic individuals of mixed European descent from 7 different studies. The combined P value for association in these follow-up samples was 6.9 × 10–26, and combining results from all studies resulted in an overall P value for association of 6.4 × 10–33. Across these studies, fasting glucose concentrations increased 0.01–0.16 mM with each copy of the major allele, accounting for approximately 1% of the total variation in fasting glucose. The rs563694 SNP is located between the genes glucose-6-phosphatase catalytic subunit 2 (G6PC2) and ATP-binding cassette, subfamily B (MDR/TAP), member 11 (ABCB11). Our results in combination with data reported in the literature suggest that G6PC2, a glucose-6-phosphatase almost exclusively expressed in pancreatic islet cells, may underlie variation in fasting glucose, though it is possible that ABCB11, which is expressed primarily in liver, may also contribute to such variation.

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Impaired fasting glucose Internal medicine Biology Medicine Endocrinology Type 2 diabetes Diabetes mellitus Impaired glucose tolerance

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Type: article
Language: en
Landing Page: https://doi.org/10.17615/sgy6-c717
OA Status: green
Cited By: 8
Related Works: 10
OpenAlex ID: https://openalex.org/W4299305824

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DOI: https://doi.org/10.17615/sgy6-c717

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Title: Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels

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Type: article

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Language: en

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Publication year: 2020

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Publication date: 2020-11-04

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Authors: Wei‐Min Chen, Michael R. Erdos, Anne Jackson, Richa Saxena, Serena Sanna, Kristi D. Silver, Nicholas J. Timpson, Torben Hansen, Marco Orrù, Maria Grazia Piras, Lori L. Bonnycastle, Cristen J. Willer, Valeriya Lyssenko, Haiqing Shen, Johanna Kuusisto, Shah Ebrahim, Natascia Sestu, William L. Duren, Maria Cristina Spada, Heather M. Stringham, Laura J. Scott, Nazario Olla, Amy J. Swift, Samer S. Najjar, Braxton D. Mitchell, Debbie A. Lawlor, George Davey Smith, Yoav Ben‐Shlomo, Gary L. Andersen, Knut Borch‐Johnsen, Torben Jørgensen, Jouko Saramies

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Landing page: https://doi.org/10.17615/sgy6-c717

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Concepts: Impaired fasting glucose, Internal medicine, Biology, Medicine, Endocrinology, Type 2 diabetes, Diabetes mellitus, Impaired glucose tolerance

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Cited by: 8

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Citations by year (recent): 2023: 1, 2019: 1, 2017: 1, 2015: 1, 2014: 1

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