Genome-Wide Association Analysis of Pancreatic Beta-Cell Glucose Sensitivity

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Genome-Wide Association Analysis of Pancreatic Beta-Cell Glucose Sensitivity. / Deshmukh, Harshal A; Madsen, Anne Lundager; Viñuela, Ana; Have, Christian Theil; Grarup, Niels; Tura, Andrea; Mahajan, Anubha; Heggie, Alison J; Koivula, Robert W; De Masi, Federico; Tsirigos, Konstantinos K; Linneberg, Allan; Drivsholm, Thomas; Pedersen, Oluf; Sørensen, Thorkild I A; Astrup, Arne; Gjesing, Anette A P; Pavo, Imre; Wood, Andrew R; Ruetten, Hartmut; Jones, Angus G; Koopman, Anitra D M; Cederberg, Henna; Rutters, Femke; Ridderstrale, Martin; Laakso, Markku; McCarthy, Mark I; Frayling, Tim M; Ferrannini, Ele; Franks, Paul W; Pearson, Ewan R; Mari, Andrea; Hansen, Torban; Walker, Mark.

In: Journal of Clinical Endocrinology and Metabolism, Vol. 106, No. 1, 2021, p. 80-90.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Deshmukh, HA, Madsen, AL, Viñuela, A, Have, CT, Grarup, N, Tura, A, Mahajan, A, Heggie, AJ, Koivula, RW, De Masi, F, Tsirigos, KK, Linneberg, A, Drivsholm, T, Pedersen, O, Sørensen, TIA, Astrup, A, Gjesing, AAP, Pavo, I, Wood, AR, Ruetten, H, Jones, AG, Koopman, ADM, Cederberg, H, Rutters, F, Ridderstrale, M, Laakso, M, McCarthy, MI, Frayling, TM, Ferrannini, E, Franks, PW, Pearson, ER, Mari, A, Hansen, T & Walker, M 2021, 'Genome-Wide Association Analysis of Pancreatic Beta-Cell Glucose Sensitivity', Journal of Clinical Endocrinology and Metabolism, vol. 106, no. 1, pp. 80-90. https://doi.org/10.1210/clinem/dgaa653

APA

Deshmukh, H. A., Madsen, A. L., Viñuela, A., Have, C. T., Grarup, N., Tura, A., Mahajan, A., Heggie, A. J., Koivula, R. W., De Masi, F., Tsirigos, K. K., Linneberg, A., Drivsholm, T., Pedersen, O., Sørensen, T. I. A., Astrup, A., Gjesing, A. A. P., Pavo, I., Wood, A. R., ... Walker, M. (2021). Genome-Wide Association Analysis of Pancreatic Beta-Cell Glucose Sensitivity. Journal of Clinical Endocrinology and Metabolism, 106(1), 80-90. https://doi.org/10.1210/clinem/dgaa653

Vancouver

Deshmukh HA, Madsen AL, Viñuela A, Have CT, Grarup N, Tura A et al. Genome-Wide Association Analysis of Pancreatic Beta-Cell Glucose Sensitivity. Journal of Clinical Endocrinology and Metabolism. 2021;106(1):80-90. https://doi.org/10.1210/clinem/dgaa653

Author

Deshmukh, Harshal A ; Madsen, Anne Lundager ; Viñuela, Ana ; Have, Christian Theil ; Grarup, Niels ; Tura, Andrea ; Mahajan, Anubha ; Heggie, Alison J ; Koivula, Robert W ; De Masi, Federico ; Tsirigos, Konstantinos K ; Linneberg, Allan ; Drivsholm, Thomas ; Pedersen, Oluf ; Sørensen, Thorkild I A ; Astrup, Arne ; Gjesing, Anette A P ; Pavo, Imre ; Wood, Andrew R ; Ruetten, Hartmut ; Jones, Angus G ; Koopman, Anitra D M ; Cederberg, Henna ; Rutters, Femke ; Ridderstrale, Martin ; Laakso, Markku ; McCarthy, Mark I ; Frayling, Tim M ; Ferrannini, Ele ; Franks, Paul W ; Pearson, Ewan R ; Mari, Andrea ; Hansen, Torban ; Walker, Mark. / Genome-Wide Association Analysis of Pancreatic Beta-Cell Glucose Sensitivity. In: Journal of Clinical Endocrinology and Metabolism. 2021 ; Vol. 106, No. 1. pp. 80-90.

Bibtex

@article{9c6caf5aab8744f8b03d1f7b96477e7a,

title = "Genome-Wide Association Analysis of Pancreatic Beta-Cell Glucose Sensitivity",

abstract = "Context: Pancreatic beta-cell glucose sensitivity is the slope of the plasma glucose-insulin secretion relationship and is a key predictor of deteriorating glucose tolerance and development of type 2 diabetes. However, there are no large-scale studies looking at the genetic determinants of beta cell glucose sensitivity.Objective: To understand the genetic determinants of pancreatic beta-cell glucose sensitivity using genome-wide meta-analysis and candidate gene studies.Design: We performed a genome-wide meta-analysis for beta-cell glucose sensitivity in subjects with type 2 diabetes and non-diabetic subjects from 6 independent cohorts (n=5,706). Beta-cell glucose sensitivity was calculated from mixed-meal and oral glucose tolerance tests, and its associations between known glycaemia related SNPS and GWAS SNPs were estimated using linear regression models.Results: Beta-cell glucose sensitivity was moderately heritable (h2 ranged between 34 to 55%) using SNP and family-based analyses. GWAS meta-analysis identified multiple correlated SNPs in the CDKAL1 gene and GIPR-QPCTL gene loci that reached genome-wide significance, with SNP rs2238691 in GIPR-QPCTL (P-value=2.64x10-9) and rs9368219 in the CDKAL1 (P-value=3.15x10-9) showing the strongest association with beta-cell glucose sensitivity. These loci surpassed genome-wide significance when the GWAS meta-analysis was repeated after exclusion of the diabetic subjects. After correction for multiple testing, glycemia associated SNPs in or near the HHEX and IGF2B2 loci were also associated with beta-cell glucose sensitivity.Conclusion: We show that, variation at the GIPR-QPCTL and CDKAL1 loci are key determinants of pancreatic beta cell glucose sensitivity.",

keywords = "Faculty of Science, Glucose intolerance, Diabetes progression, Beta cell function, Incretin, Mathematical model",

author = "Deshmukh, {Harshal A} and Madsen, {Anne Lundager} and Ana Vi{\~n}uela and Have, {Christian Theil} and Niels Grarup and Andrea Tura and Anubha Mahajan and Heggie, {Alison J} and Koivula, {Robert W} and {De Masi}, Federico and Tsirigos, {Konstantinos K} and Allan Linneberg and Thomas Drivsholm and Oluf Pedersen and S{\o}rensen, {Thorkild I A} and Arne Astrup and Gjesing, {Anette A P} and Imre Pavo and Wood, {Andrew R} and Hartmut Ruetten and Jones, {Angus G} and Koopman, {Anitra D M} and Henna Cederberg and Femke Rutters and Martin Ridderstrale and Markku Laakso and McCarthy, {Mark I} and Frayling, {Tim M} and Ele Ferrannini and Franks, {Paul W} and Pearson, {Ewan R} and Andrea Mari and Torban Hansen and Mark Walker",

note = "{\textcopyright} Endocrine Society 2020.",

year = "2021",

doi = "10.1210/clinem/dgaa653",

language = "English",

volume = "106",

pages = "80--90",

journal = "Journal of Clinical Endocrinology and Metabolism",

issn = "0021-972X",

publisher = "Oxford University Press",

number = "1",

}

RIS

TY - JOUR

T1 - Genome-Wide Association Analysis of Pancreatic Beta-Cell Glucose Sensitivity

AU - Deshmukh, Harshal A

AU - Madsen, Anne Lundager

AU - Viñuela, Ana

AU - Have, Christian Theil

AU - Grarup, Niels

AU - Tura, Andrea

AU - Mahajan, Anubha

AU - Heggie, Alison J

AU - Koivula, Robert W

AU - De Masi, Federico

AU - Tsirigos, Konstantinos K

AU - Linneberg, Allan

AU - Drivsholm, Thomas

AU - Pedersen, Oluf

AU - Sørensen, Thorkild I A

AU - Astrup, Arne

AU - Gjesing, Anette A P

AU - Pavo, Imre

AU - Wood, Andrew R

AU - Ruetten, Hartmut

AU - Jones, Angus G

AU - Koopman, Anitra D M

AU - Cederberg, Henna

AU - Rutters, Femke

AU - Ridderstrale, Martin

AU - Laakso, Markku

AU - McCarthy, Mark I

AU - Frayling, Tim M

AU - Ferrannini, Ele

AU - Franks, Paul W

AU - Pearson, Ewan R

AU - Mari, Andrea

AU - Hansen, Torban

AU - Walker, Mark

PY - 2021

Y1 - 2021

N2 - Context: Pancreatic beta-cell glucose sensitivity is the slope of the plasma glucose-insulin secretion relationship and is a key predictor of deteriorating glucose tolerance and development of type 2 diabetes. However, there are no large-scale studies looking at the genetic determinants of beta cell glucose sensitivity.Objective: To understand the genetic determinants of pancreatic beta-cell glucose sensitivity using genome-wide meta-analysis and candidate gene studies.Design: We performed a genome-wide meta-analysis for beta-cell glucose sensitivity in subjects with type 2 diabetes and non-diabetic subjects from 6 independent cohorts (n=5,706). Beta-cell glucose sensitivity was calculated from mixed-meal and oral glucose tolerance tests, and its associations between known glycaemia related SNPS and GWAS SNPs were estimated using linear regression models.Results: Beta-cell glucose sensitivity was moderately heritable (h2 ranged between 34 to 55%) using SNP and family-based analyses. GWAS meta-analysis identified multiple correlated SNPs in the CDKAL1 gene and GIPR-QPCTL gene loci that reached genome-wide significance, with SNP rs2238691 in GIPR-QPCTL (P-value=2.64x10-9) and rs9368219 in the CDKAL1 (P-value=3.15x10-9) showing the strongest association with beta-cell glucose sensitivity. These loci surpassed genome-wide significance when the GWAS meta-analysis was repeated after exclusion of the diabetic subjects. After correction for multiple testing, glycemia associated SNPs in or near the HHEX and IGF2B2 loci were also associated with beta-cell glucose sensitivity.Conclusion: We show that, variation at the GIPR-QPCTL and CDKAL1 loci are key determinants of pancreatic beta cell glucose sensitivity.

AB - Context: Pancreatic beta-cell glucose sensitivity is the slope of the plasma glucose-insulin secretion relationship and is a key predictor of deteriorating glucose tolerance and development of type 2 diabetes. However, there are no large-scale studies looking at the genetic determinants of beta cell glucose sensitivity.Objective: To understand the genetic determinants of pancreatic beta-cell glucose sensitivity using genome-wide meta-analysis and candidate gene studies.Design: We performed a genome-wide meta-analysis for beta-cell glucose sensitivity in subjects with type 2 diabetes and non-diabetic subjects from 6 independent cohorts (n=5,706). Beta-cell glucose sensitivity was calculated from mixed-meal and oral glucose tolerance tests, and its associations between known glycaemia related SNPS and GWAS SNPs were estimated using linear regression models.Results: Beta-cell glucose sensitivity was moderately heritable (h2 ranged between 34 to 55%) using SNP and family-based analyses. GWAS meta-analysis identified multiple correlated SNPs in the CDKAL1 gene and GIPR-QPCTL gene loci that reached genome-wide significance, with SNP rs2238691 in GIPR-QPCTL (P-value=2.64x10-9) and rs9368219 in the CDKAL1 (P-value=3.15x10-9) showing the strongest association with beta-cell glucose sensitivity. These loci surpassed genome-wide significance when the GWAS meta-analysis was repeated after exclusion of the diabetic subjects. After correction for multiple testing, glycemia associated SNPs in or near the HHEX and IGF2B2 loci were also associated with beta-cell glucose sensitivity.Conclusion: We show that, variation at the GIPR-QPCTL and CDKAL1 loci are key determinants of pancreatic beta cell glucose sensitivity.

KW - Faculty of Science

KW - Glucose intolerance

KW - Diabetes progression

KW - Beta cell function

KW - Incretin

KW - Mathematical model

U2 - 10.1210/clinem/dgaa653

DO - 10.1210/clinem/dgaa653

M3 - Journal article

C2 - 32944759

VL - 106

SP - 80

EP - 90

JO - Journal of Clinical Endocrinology and Metabolism

JF - Journal of Clinical Endocrinology and Metabolism

SN - 0021-972X

IS - 1

ER -

ID: 249059625