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Mendelian Randomization Studies Do Not Support a Causal Role for Reduced Circulating Adiponectin Levels in Insulin Resistance and Type 2 Diabetes

Adiponectin is strongly inversely associated with insulin resistance and type 2 diabetes, but its causal role remains controversial. We used a Mendelian randomization approach to test the hypothesis that adiponectin causally influences insulin resistance and type 2 diabetes. We used genetic variants...

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Autores principales: Yaghootkar, Hanieh, Lamina, Claudia, Scott, Robert A., Dastani, Zari, Hivert, Marie-France, Warren, Liling L., Stancáková, Alena, Buxbaum, Sarah G., Lyytikäinen, Leo-Pekka, Henneman, Peter, Wu, Ying, Cheung, Chloe Y.Y., Pankow, James S., Jackson, Anne U., Gustafsson, Stefan, Zhao, Jing Hua, Ballantyne, Christie M., Xie, Weijia, Bergman, Richard N., Boehnke, Michael, el Bouazzaoui, Fatiha, Collins, Francis S., Dunn, Sandra H., Dupuis, Josee, Forouhi, Nita G., Gillson, Christopher, Hattersley, Andrew T., Hong, Jaeyoung, Kähönen, Mika, Kuusisto, Johanna, Kedenko, Lyudmyla, Kronenberg, Florian, Doria, Alessandro, Assimes, Themistocles L., Ferrannini, Ele, Hansen, Torben, Hao, Ke, Häring, Hans, Knowles, Joshua W., Lindgren, Cecilia M., Nolan, John J., Paananen, Jussi, Pedersen, Oluf, Quertermous, Thomas, Smith, Ulf, Lehtimäki, Terho, Liu, Ching-Ti, Loos, Ruth J.F., McCarthy, Mark I., Morris, Andrew D., Vasan, Ramachandran S., Spector, Tim D., Teslovich, Tanya M., Tuomilehto, Jaakko, van Dijk, Ko Willems, Viikari, Jorma S., Zhu, Na, Langenberg, Claudia, Ingelsson, Erik, Semple, Robert K., Sinaiko, Alan R., Palmer, Colin N.A., Walker, Mark, Lam, Karen S.L., Paulweber, Bernhard, Mohlke, Karen L., van Duijn, Cornelia, Raitakari, Olli T., Bidulescu, Aurelian, Wareham, Nick J., Laakso, Markku, Waterworth, Dawn M., Lawlor, Debbie A., Meigs, James B., Richards, J. Brent, Frayling, Timothy M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781444/
https://www.ncbi.nlm.nih.gov/pubmed/23835345
http://dx.doi.org/10.2337/db13-0128
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author Yaghootkar, Hanieh
Lamina, Claudia
Scott, Robert A.
Dastani, Zari
Hivert, Marie-France
Warren, Liling L.
Stancáková, Alena
Buxbaum, Sarah G.
Lyytikäinen, Leo-Pekka
Henneman, Peter
Wu, Ying
Cheung, Chloe Y.Y.
Pankow, James S.
Jackson, Anne U.
Gustafsson, Stefan
Zhao, Jing Hua
Ballantyne, Christie M.
Xie, Weijia
Bergman, Richard N.
Boehnke, Michael
el Bouazzaoui, Fatiha
Collins, Francis S.
Dunn, Sandra H.
Dupuis, Josee
Forouhi, Nita G.
Gillson, Christopher
Hattersley, Andrew T.
Hong, Jaeyoung
Kähönen, Mika
Kuusisto, Johanna
Kedenko, Lyudmyla
Kronenberg, Florian
Doria, Alessandro
Assimes, Themistocles L.
Ferrannini, Ele
Hansen, Torben
Hao, Ke
Häring, Hans
Knowles, Joshua W.
Lindgren, Cecilia M.
Nolan, John J.
Paananen, Jussi
Pedersen, Oluf
Quertermous, Thomas
Smith, Ulf
Lehtimäki, Terho
Liu, Ching-Ti
Loos, Ruth J.F.
McCarthy, Mark I.
Morris, Andrew D.
Vasan, Ramachandran S.
Spector, Tim D.
Teslovich, Tanya M.
Tuomilehto, Jaakko
van Dijk, Ko Willems
Viikari, Jorma S.
Zhu, Na
Langenberg, Claudia
Ingelsson, Erik
Semple, Robert K.
Sinaiko, Alan R.
Palmer, Colin N.A.
Walker, Mark
Lam, Karen S.L.
Paulweber, Bernhard
Mohlke, Karen L.
van Duijn, Cornelia
Raitakari, Olli T.
Bidulescu, Aurelian
Wareham, Nick J.
Laakso, Markku
Waterworth, Dawn M.
Lawlor, Debbie A.
Meigs, James B.
Richards, J. Brent
Frayling, Timothy M.
author_facet Yaghootkar, Hanieh
Lamina, Claudia
Scott, Robert A.
Dastani, Zari
Hivert, Marie-France
Warren, Liling L.
Stancáková, Alena
Buxbaum, Sarah G.
Lyytikäinen, Leo-Pekka
Henneman, Peter
Wu, Ying
Cheung, Chloe Y.Y.
Pankow, James S.
Jackson, Anne U.
Gustafsson, Stefan
Zhao, Jing Hua
Ballantyne, Christie M.
Xie, Weijia
Bergman, Richard N.
Boehnke, Michael
el Bouazzaoui, Fatiha
Collins, Francis S.
Dunn, Sandra H.
Dupuis, Josee
Forouhi, Nita G.
Gillson, Christopher
Hattersley, Andrew T.
Hong, Jaeyoung
Kähönen, Mika
Kuusisto, Johanna
Kedenko, Lyudmyla
Kronenberg, Florian
Doria, Alessandro
Assimes, Themistocles L.
Ferrannini, Ele
Hansen, Torben
Hao, Ke
Häring, Hans
Knowles, Joshua W.
Lindgren, Cecilia M.
Nolan, John J.
Paananen, Jussi
Pedersen, Oluf
Quertermous, Thomas
Smith, Ulf
Lehtimäki, Terho
Liu, Ching-Ti
Loos, Ruth J.F.
McCarthy, Mark I.
Morris, Andrew D.
Vasan, Ramachandran S.
Spector, Tim D.
Teslovich, Tanya M.
Tuomilehto, Jaakko
van Dijk, Ko Willems
Viikari, Jorma S.
Zhu, Na
Langenberg, Claudia
Ingelsson, Erik
Semple, Robert K.
Sinaiko, Alan R.
Palmer, Colin N.A.
Walker, Mark
Lam, Karen S.L.
Paulweber, Bernhard
Mohlke, Karen L.
van Duijn, Cornelia
Raitakari, Olli T.
Bidulescu, Aurelian
Wareham, Nick J.
Laakso, Markku
Waterworth, Dawn M.
Lawlor, Debbie A.
Meigs, James B.
Richards, J. Brent
Frayling, Timothy M.
author_sort Yaghootkar, Hanieh
collection PubMed
description Adiponectin is strongly inversely associated with insulin resistance and type 2 diabetes, but its causal role remains controversial. We used a Mendelian randomization approach to test the hypothesis that adiponectin causally influences insulin resistance and type 2 diabetes. We used genetic variants at the ADIPOQ gene as instruments to calculate a regression slope between adiponectin levels and metabolic traits (up to 31,000 individuals) and a combination of instrumental variables and summary statistics–based genetic risk scores to test the associations with gold-standard measures of insulin sensitivity (2,969 individuals) and type 2 diabetes (15,960 case subjects and 64,731 control subjects). In conventional regression analyses, a 1-SD decrease in adiponectin levels was correlated with a 0.31-SD (95% CI 0.26–0.35) increase in fasting insulin, a 0.34-SD (0.30–0.38) decrease in insulin sensitivity, and a type 2 diabetes odds ratio (OR) of 1.75 (1.47–2.13). The instrumental variable analysis revealed no evidence of a causal association between genetically lower circulating adiponectin and higher fasting insulin (0.02 SD; 95% CI −0.07 to 0.11; N = 29,771), nominal evidence of a causal relationship with lower insulin sensitivity (−0.20 SD; 95% CI −0.38 to −0.02; N = 1,860), and no evidence of a relationship with type 2 diabetes (OR 0.94; 95% CI 0.75–1.19; N = 2,777 case subjects and 13,011 control subjects). Using the ADIPOQ summary statistics genetic risk scores, we found no evidence of an association between adiponectin-lowering alleles and insulin sensitivity (effect per weighted adiponectin-lowering allele: −0.03 SD; 95% CI −0.07 to 0.01; N = 2,969) or type 2 diabetes (OR per weighted adiponectin-lowering allele: 0.99; 95% CI 0.95–1.04; 15,960 case subjects vs. 64,731 control subjects). These results do not provide any consistent evidence that interventions aimed at increasing adiponectin levels will improve insulin sensitivity or risk of type 2 diabetes.
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spelling pubmed-37814442014-10-01 Mendelian Randomization Studies Do Not Support a Causal Role for Reduced Circulating Adiponectin Levels in Insulin Resistance and Type 2 Diabetes Yaghootkar, Hanieh Lamina, Claudia Scott, Robert A. Dastani, Zari Hivert, Marie-France Warren, Liling L. Stancáková, Alena Buxbaum, Sarah G. Lyytikäinen, Leo-Pekka Henneman, Peter Wu, Ying Cheung, Chloe Y.Y. Pankow, James S. Jackson, Anne U. Gustafsson, Stefan Zhao, Jing Hua Ballantyne, Christie M. Xie, Weijia Bergman, Richard N. Boehnke, Michael el Bouazzaoui, Fatiha Collins, Francis S. Dunn, Sandra H. Dupuis, Josee Forouhi, Nita G. Gillson, Christopher Hattersley, Andrew T. Hong, Jaeyoung Kähönen, Mika Kuusisto, Johanna Kedenko, Lyudmyla Kronenberg, Florian Doria, Alessandro Assimes, Themistocles L. Ferrannini, Ele Hansen, Torben Hao, Ke Häring, Hans Knowles, Joshua W. Lindgren, Cecilia M. Nolan, John J. Paananen, Jussi Pedersen, Oluf Quertermous, Thomas Smith, Ulf Lehtimäki, Terho Liu, Ching-Ti Loos, Ruth J.F. McCarthy, Mark I. Morris, Andrew D. Vasan, Ramachandran S. Spector, Tim D. Teslovich, Tanya M. Tuomilehto, Jaakko van Dijk, Ko Willems Viikari, Jorma S. Zhu, Na Langenberg, Claudia Ingelsson, Erik Semple, Robert K. Sinaiko, Alan R. Palmer, Colin N.A. Walker, Mark Lam, Karen S.L. Paulweber, Bernhard Mohlke, Karen L. van Duijn, Cornelia Raitakari, Olli T. Bidulescu, Aurelian Wareham, Nick J. Laakso, Markku Waterworth, Dawn M. Lawlor, Debbie A. Meigs, James B. Richards, J. Brent Frayling, Timothy M. Diabetes Original Research Adiponectin is strongly inversely associated with insulin resistance and type 2 diabetes, but its causal role remains controversial. We used a Mendelian randomization approach to test the hypothesis that adiponectin causally influences insulin resistance and type 2 diabetes. We used genetic variants at the ADIPOQ gene as instruments to calculate a regression slope between adiponectin levels and metabolic traits (up to 31,000 individuals) and a combination of instrumental variables and summary statistics–based genetic risk scores to test the associations with gold-standard measures of insulin sensitivity (2,969 individuals) and type 2 diabetes (15,960 case subjects and 64,731 control subjects). In conventional regression analyses, a 1-SD decrease in adiponectin levels was correlated with a 0.31-SD (95% CI 0.26–0.35) increase in fasting insulin, a 0.34-SD (0.30–0.38) decrease in insulin sensitivity, and a type 2 diabetes odds ratio (OR) of 1.75 (1.47–2.13). The instrumental variable analysis revealed no evidence of a causal association between genetically lower circulating adiponectin and higher fasting insulin (0.02 SD; 95% CI −0.07 to 0.11; N = 29,771), nominal evidence of a causal relationship with lower insulin sensitivity (−0.20 SD; 95% CI −0.38 to −0.02; N = 1,860), and no evidence of a relationship with type 2 diabetes (OR 0.94; 95% CI 0.75–1.19; N = 2,777 case subjects and 13,011 control subjects). Using the ADIPOQ summary statistics genetic risk scores, we found no evidence of an association between adiponectin-lowering alleles and insulin sensitivity (effect per weighted adiponectin-lowering allele: −0.03 SD; 95% CI −0.07 to 0.01; N = 2,969) or type 2 diabetes (OR per weighted adiponectin-lowering allele: 0.99; 95% CI 0.95–1.04; 15,960 case subjects vs. 64,731 control subjects). These results do not provide any consistent evidence that interventions aimed at increasing adiponectin levels will improve insulin sensitivity or risk of type 2 diabetes. American Diabetes Association 2013-10 2013-09-17 /pmc/articles/PMC3781444/ /pubmed/23835345 http://dx.doi.org/10.2337/db13-0128 Text en © 2013 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Original Research
Yaghootkar, Hanieh
Lamina, Claudia
Scott, Robert A.
Dastani, Zari
Hivert, Marie-France
Warren, Liling L.
Stancáková, Alena
Buxbaum, Sarah G.
Lyytikäinen, Leo-Pekka
Henneman, Peter
Wu, Ying
Cheung, Chloe Y.Y.
Pankow, James S.
Jackson, Anne U.
Gustafsson, Stefan
Zhao, Jing Hua
Ballantyne, Christie M.
Xie, Weijia
Bergman, Richard N.
Boehnke, Michael
el Bouazzaoui, Fatiha
Collins, Francis S.
Dunn, Sandra H.
Dupuis, Josee
Forouhi, Nita G.
Gillson, Christopher
Hattersley, Andrew T.
Hong, Jaeyoung
Kähönen, Mika
Kuusisto, Johanna
Kedenko, Lyudmyla
Kronenberg, Florian
Doria, Alessandro
Assimes, Themistocles L.
Ferrannini, Ele
Hansen, Torben
Hao, Ke
Häring, Hans
Knowles, Joshua W.
Lindgren, Cecilia M.
Nolan, John J.
Paananen, Jussi
Pedersen, Oluf
Quertermous, Thomas
Smith, Ulf
Lehtimäki, Terho
Liu, Ching-Ti
Loos, Ruth J.F.
McCarthy, Mark I.
Morris, Andrew D.
Vasan, Ramachandran S.
Spector, Tim D.
Teslovich, Tanya M.
Tuomilehto, Jaakko
van Dijk, Ko Willems
Viikari, Jorma S.
Zhu, Na
Langenberg, Claudia
Ingelsson, Erik
Semple, Robert K.
Sinaiko, Alan R.
Palmer, Colin N.A.
Walker, Mark
Lam, Karen S.L.
Paulweber, Bernhard
Mohlke, Karen L.
van Duijn, Cornelia
Raitakari, Olli T.
Bidulescu, Aurelian
Wareham, Nick J.
Laakso, Markku
Waterworth, Dawn M.
Lawlor, Debbie A.
Meigs, James B.
Richards, J. Brent
Frayling, Timothy M.
Mendelian Randomization Studies Do Not Support a Causal Role for Reduced Circulating Adiponectin Levels in Insulin Resistance and Type 2 Diabetes
title Mendelian Randomization Studies Do Not Support a Causal Role for Reduced Circulating Adiponectin Levels in Insulin Resistance and Type 2 Diabetes
title_full Mendelian Randomization Studies Do Not Support a Causal Role for Reduced Circulating Adiponectin Levels in Insulin Resistance and Type 2 Diabetes
title_fullStr Mendelian Randomization Studies Do Not Support a Causal Role for Reduced Circulating Adiponectin Levels in Insulin Resistance and Type 2 Diabetes
title_full_unstemmed Mendelian Randomization Studies Do Not Support a Causal Role for Reduced Circulating Adiponectin Levels in Insulin Resistance and Type 2 Diabetes
title_short Mendelian Randomization Studies Do Not Support a Causal Role for Reduced Circulating Adiponectin Levels in Insulin Resistance and Type 2 Diabetes
title_sort mendelian randomization studies do not support a causal role for reduced circulating adiponectin levels in insulin resistance and type 2 diabetes
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781444/
https://www.ncbi.nlm.nih.gov/pubmed/23835345
http://dx.doi.org/10.2337/db13-0128
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