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    Home»Health»Scientists Identify 117 Genes That Cause Type 2 Diabetes
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    Scientists Identify 117 Genes That Cause Type 2 Diabetes

    By University of Massachusetts AmherstJune 10, 20221 Comment9 Mins Read
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    Genetics Cancer DNA Mutation Illustration
    New research from the University of Massachusetts Amherst helps identify genetic links to type 2 diabetes risk.

    A Large-Scale Study of Diverse Populations Increases Our Understanding of Type 2 Diabetes

    According to the Centers for Disease Control and Prevention (CDC),  37.3 million Americans have diabetes. 95% of these people have type 2 diabetes, the most common type of diabetes.

    Type 2 diabetes (also known as non-insulin-dependent diabetes or adult-onset diabetes) is caused by the body’s poor utilization of insulin.  This long-term chronic illness causes an excess of sugar to circulate in the bloodstream. High blood sugar levels may eventually cause cardiovascular, neurological, and immunological problems.

    Genetic Link to Type 2 Diabetes

    Type 2 diabetes has no cure, although losing weight, eating healthily, and exercising can help you manage the condition. The exact of type 2 diabetes is unknown, however, researchers have recently found a genetic link to obtaining the disease. 

    An international team of scientists, including a genetic epidemiologist from the University of Massachusetts Amherst (UMass Amherst), is conducting an ongoing study in diverse populations throughout the globe, which has revealed new important insight into how genes contribute to type 2 diabetes.

    The study was published on May 12th, in Nature Genetics. “Our findings matter because we’re moving toward using genetic scores to weigh up a person’s risk of diabetes,” says co-author Cassandra Spracklen, assistant professor of biostatistics and epidemiology at the UMass Amherst School of Public Health and Health Sciences.

    Cassandra Spracklen UMass Amherst
    Cassandra Spracklen is an assistant professor of biostatistics and epidemiology at the UMass Amherst School of Public Health and Health Sciences. Credit: UMass Amherst

    Andrew Morris, professor of statistical genetics at the University of Manchester, and University of Oxford professors Mark McCarthy and Anubha Mahajan co-led the DIAMANTE (DIabetes Meta-ANalysis of Trans-Ethnic association studies) Consortium’s meta-analysis of 122 different genome-wide association studies (GWAS).

    Rapid Rise of Type 2 Diabetes Worldwide

    “The global prevalence of type 2 diabetes, a life-changing disease, has quadrupled over the last 30 years, affecting approximately 392 million people in 2015,” Morris says.

    The research is a major step toward the ultimate goal of identifying novel genes and understanding the biology of the disease, which has the potential to help scientists develop new treatments.

    It is also an important milestone in the development of “genetic risk scores” to identify individuals who are more predisposed to develop type 2 diabetes, regardless of their population background.

    The meta-analysis compared the DNA of almost 181,000 people with type 2 diabetes against 1.16 million people who didn’t have the disease. Searching across the entire human genome for sets of genetic markers called single nucleotide polymorphisms, or SNPs, genome-wide association studies look for genetic differences between people with and without a disease.

    The technique allows scientists to zero in on parts of the genome involved in disease risk, which helps pinpoint the genes that cause the disease.

    Addressing Ancestry Bias in Genetic Studies

    However, the largest genome-wide association studies of type 2 diabetes historically have involved the DNA of people of European descent, which has limited progress in understanding the disease in other population groups.

    To address this bias, scientists from the DIAMANTE Consortium assembled the world’s most diverse collection of genetic information on the disease, with almost 50% of individuals from East Asian, African, South Asian, and Hispanic population groups.

    “Up to now, over 80% of genomic research of this type has been conducted in white European-ancestry populations, but we know that scores developed exclusively in individuals of one ancestry don’t work well in people of a different ancestry,” says Spracklen, who helped analyze and coordinate the data sharing from the East Asian ancestry populations.

    The new paper builds off Spracklen’s previous research identifying genetic associations with type 2 diabetes in East Asian-ancestry populations and identifying genetic associations with diabetes-related traits (fasting glucose, fasting insulin, HbA1c) in multi-ancestry populations.

    “Because our research has included people from many different parts of the world, we now have a much more complete picture of the ways in which patterns of genetic risk for type 2 diabetes vary across populations,” McCarthy says.

    Mahajan adds, “We have now identified 117 genes that are likely to cause Type 2 diabetes, 40 of which have not been reported before. That is why we feel this constitutes a major step forward in understanding the biology of this disease.”

    The international study was partly funded by the National Institutes of Health, Wellcome, and the Medical Research Council in the United Kingdom.

    Reference: “Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation” by Anubha Mahajan, Cassandra N. Spracklen, Weihua Zhang, Maggie C. Y. Ng, Lauren E. Petty, Hidetoshi Kitajima, Grace Z. Yu, Sina Rüeger, Leo Speidel, Young Jin Kim, Momoko Horikoshi, Josep M. Mercader, Daniel Taliun, Sanghoon Moon, Soo-Heon Kwak, Neil R. Robertson, Nigel W. Rayner, Marie Loh, Bong-Jo Kim, Joshua Chiou, Irene Miguel-Escalada, Pietro della Briotta Parolo, Kuang Lin, Fiona Bragg, Michael H. Preuss, Fumihiko Takeuchi, Jana Nano, Xiuqing Guo, Amel Lamri, Masahiro Nakatochi, Robert A. Scott, Jung-Jin Lee, Alicia Huerta-Chagoya, Mariaelisa Graff, Jin-Fang Chai, Esteban J. Parra, Jie Yao, Lawrence F. Bielak, Yasuharu Tabara, Yang Hai, Valgerdur Steinthorsdottir, James P. Cook, Mart Kals, Niels Grarup, Ellen M. Schmidt, Ian Pan, Tamar Sofer, Matthias Wuttke, Chloe Sarnowski, Christian Gieger, Darryl Nousome, Stella Trompet, Jirong Long, Meng Sun, Lin Tong, Wei-Min Chen, Meraj Ahmad, Raymond Noordam, Victor J. Y. Lim, Claudia H. T. Tam, Yoonjung Yoonie Joo, Chien-Hsiun Chen, Laura M. Raffield, Cécile Lecoeur, Bram Peter Prins, Aude Nicolas, Lisa R. Yanek, Guanjie Chen, Richard A. Jensen, Salman Tajuddin, Edmond K. Kabagambe, Ping An, Anny H. Xiang, Hyeok Sun Choi, Brian E. Cade, Jingyi Tan, Jack Flanagan, Fernando Abaitua, Linda S. Adair, Adebowale Adeyemo, Carlos A. Aguilar-Salinas, Masato Akiyama, Sonia S. Anand, Alain Bertoni, Zheng Bian, Jette Bork-Jensen, Ivan Brandslund, Jennifer A. Brody, Chad M. Brummett, Thomas A. Buchanan, Mickaël Canouil, Juliana C. N. Chan, Li-Ching Chang, Miao-Li Chee, Ji Chen, Shyh-Huei Chen, Yuan-Tsong Chen, Zhengming Chen, Lee-Ming Chuang, Mary Cushman, Swapan K. Das, H. Janaka de Silva, George Dedoussis, Latchezar Dimitrov, Ayo P. Doumatey, Shufa Du, Qing Duan, Kai-Uwe Eckardt, Leslie S. Emery, Daniel S. Evans, Michele K. Evans, Krista Fischer, James S. Floyd, Ian Ford, Myriam Fornage, Oscar H. Franco, Timothy M. Frayling, Barry I. Freedman, Christian Fuchsberger, Pauline Genter, Hertzel C. Gerstein, Vilmantas Giedraitis, Clicerio González-Villalpando, Maria Elena González-Villalpando, Mark O. Goodarzi, Penny Gordon-Larsen, David Gorkin, Myron Gross, Yu Guo, Sophie Hackinger, Sohee Han, Andrew T. Hattersley, Christian Herder, Annie-Green Howard, Willa Hsueh, Mengna Huang, Wei Huang, Yi-Jen Hung, Mi Yeong Hwang, Chii-Min Hwu, Sahoko Ichihara, Mohammad Arfan Ikram, Martin Ingelsson, Md Tariqul Islam, Masato Isono, Hye-Mi Jang, Farzana Jasmine, Guozhi Jiang, Jost B. Jonas, Marit E. Jørgensen, Torben Jørgensen, Yoichiro Kamatani, Fouad R. Kandeel, Anuradhani Kasturiratne, Tomohiro Katsuya, Varinderpal Kaur, Takahisa Kawaguchi, Jacob M. Keaton, Abel N. Kho, Chiea-Chuen Khor, Muhammad G. Kibriya, Duk-Hwan Kim, Katsuhiko Kohara, Jennifer Kriebel, Florian Kronenberg, Johanna Kuusisto, Kristi Läll, Leslie A. Lange, Myung-Shik Lee, Nanette R. Lee, Aaron Leong, Liming Li, Yun Li, Ruifang Li-Gao, Symen Ligthart, Cecilia M. Lindgren, Allan Linneberg, Ching-Ti Liu, Jianjun Liu, Adam E. Locke, Tin Louie, Jian’an Luan, Andrea O. Luk, Xi Luo, Jun Lv, Valeriya Lyssenko, Vasiliki Mamakou, K. Radha Mani, Thomas Meitinger, Andres Metspalu, Andrew D. Morris, Girish N. Nadkarni, Jerry L. Nadler, Michael A. Nalls, Uma Nayak, Suraj S. Nongmaithem, Ioanna Ntalla, Yukinori Okada, Lorena Orozco, Sanjay R. Patel, Mark A. Pereira, Annette Peters, Fraser J. Pirie, Bianca Porneala, Gauri Prasad, Sebastian Preissl, Laura J. Rasmussen-Torvik, Alexander P. Reiner, Michael Roden, Rebecca Rohde, Kathryn Roll, Charumathi Sabanayagam, Maike Sander, Kevin Sandow, Naveed Sattar, Sebastian Schönherr, Claudia Schurmann, Mohammad Shahriar, Jinxiu Shi, Dong Mun Shin, Daniel Shriner, Jennifer A. Smith, Wing Yee So, Alena Stančáková, Adrienne M. Stilp, Konstantin Strauch, Ken Suzuki, Atsushi Takahashi, Kent D. Taylor, Barbara Thorand, Gudmar Thorleifsson, Unnur Thorsteinsdottir, Brian Tomlinson, Jason M. Torres, Fuu-Jen Tsai, Jaakko Tuomilehto, Teresa Tusie-Luna, Miriam S. Udler, Adan Valladares-Salgado, Rob M. van Dam, Jan B. van Klinken, Rohit Varma, Marijana Vujkovic, Niels Wacher-Rodarte, Eleanor Wheeler, Eric A. Whitsel, Ananda R. Wickremasinghe, Ko Willems van Dijk, Daniel R. Witte, Chittaranjan S. Yajnik, Ken Yamamoto, Toshimasa Yamauchi, Loïc Yengo, Kyungheon Yoon, Canqing Yu, Jian-Min Yuan, Salim Yusuf, Liang Zhang, Wei Zheng, FinnGen, eMERGE Consortium, Leslie J. Raffel, Michiya Igase, Eli Ipp, Susan Redline, Yoon Shin Cho, Lars Lind, Michael A. Province, Craig L. Hanis, Patricia A. Peyser, Erik Ingelsson, Alan B. Zonderman, Bruce M. Psaty, Ya-Xing Wang, Charles N. Rotimi, Diane M. Becker, Fumihiko Matsuda, Yongmei Liu, Eleftheria Zeggini, Mitsuhiro Yokota, Stephen S. Rich, Charles Kooperberg, James S. Pankow, James C. Engert, Yii-Der Ida Chen, Philippe Froguel, James G. Wilson, Wayne H. H. Sheu, Sharon L. R. Kardia, Jer-Yuarn Wu, M. Geoffrey Hayes, Ronald C. W. Ma, Tien-Yin Wong, Leif Groop, Dennis O. Mook-Kanamori, Giriraj R. Chandak, Francis S. Collins, Dwaipayan Bharadwaj, Guillaume Paré, Michèle M. Sale, Habibul Ahsan, Ayesha A. Motala, Xiao-Ou Shu, Kyong-Soo Park, J. Wouter Jukema, Miguel Cruz, Roberta McKean-Cowdin, Harald Grallert, Ching-Yu Cheng, Erwin P. Bottinger, Abbas Dehghan, E-Shyong Tai, Josée Dupuis, Norihiro Kato, Markku Laakso, Anna Köttgen, Woon-Puay Koh, Colin N. A. Palmer, Simin Liu, Goncalo Abecasis, Jaspal S. Kooner, Ruth J. F. Loos, Kari E. North, Christopher A. Haiman, Jose C. Florez, Danish Saleheen, Torben Hansen, Oluf Pedersen, Reedik Mägi, Claudia Langenberg, Nicholas J. Wareham, Shiro Maeda, Takashi Kadowaki, Juyoung Lee, Iona Y. Millwood, Robin G. Walters, Kari Stefansson, Simon R. Myers, Jorge Ferrer, Kyle J. Gaulton, James B. Meigs, Karen L. Mohlke, Anna L. Gloyn, Donald W. Bowden, Jennifer E. Below, John C. Chambers, Xueling Sim, Michael Boehnke, Jerome I. Rotter, Mark I. McCarthy, and Andrew P. Morris, 12 May 2022, Nature Genetics.
    DOI: 10.1038/s41588-022-01058-3

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    Diabetes Genetics Genomics University of Manchester University of Massachusetts Amherst University of Oxford
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    1 Comment

    1. Earlier the Better on June 12, 2022 4:29 pm

      Remember that this Diabetes starts after decades of Age; Same Genes in them and Same too in the Older that undergo it. WHY? Any amount of Prayers is USELESS.

      Reply
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