Helena Enders-Seidlitz, Klemens Raile, Maolian Gong, Angela Galler, Peter Kuehnen, Susanna Wiegand
{"title":"儿童和青少年肥胖症患者的胰岛素分泌缺陷:临床和分子遗传特征","authors":"Helena Enders-Seidlitz, Klemens Raile, Maolian Gong, Angela Galler, Peter Kuehnen, Susanna Wiegand","doi":"10.1155/2024/5558634","DOIUrl":null,"url":null,"abstract":"<i>Introduction</i>. Childhood obesity is increasing worldwide and presents as a global health issue due to multiple metabolic comorbidities. About 1% of adolescents with obesity develop type 2 diabetes (T2D); however, little is known about the genetic and pathophysiological background at young age. The objective of this study was to assess the prevalence of impaired glucose regulation (IGR) in a large cohort of children and adolescents with obesity and to characterize insulin sensitivity and insulin secretion. We also wanted to investigate adolescents with insulin secretion disorder more closely and analyze possible candidate genes of diabetes in a subcohort. <i>Methods</i>. We included children and adolescents with obesity who completed an oral glucose tolerance test (OGTT, <span><svg height=\"12.7112pt\" style=\"vertical-align:-3.403299pt\" version=\"1.1\" viewbox=\"-0.0498162 -9.3079 49.422 12.7112\" width=\"49.422pt\" xmlns=\"http://www.w3.org/2000/svg\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"><g transform=\"matrix(.013,0,0,-0.013,0,0)\"></path></g><g transform=\"matrix(.013,0,0,-0.013,6.175,0)\"></path></g><g transform=\"matrix(.013,0,0,-0.013,9.308,0)\"></path></g><g transform=\"matrix(.013,0,0,-0.013,16.211,0)\"></path></g><g transform=\"matrix(.013,0,0,-0.013,21.71,0)\"></path></g><g transform=\"matrix(.013,0,0,-0.013,28.34,0)\"></path></g><g transform=\"matrix(.013,0,0,-0.013,33.215,0)\"></path></g><g transform=\"matrix(.013,0,0,-0.013,41.791,0)\"></path></g></svg><span></span><span><svg height=\"12.7112pt\" style=\"vertical-align:-3.403299pt\" version=\"1.1\" viewbox=\"52.277183799999996 -9.3079 36.313 12.7112\" width=\"36.313pt\" xmlns=\"http://www.w3.org/2000/svg\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"><g transform=\"matrix(.013,0,0,-0.013,52.327,0)\"></path></g><g transform=\"matrix(.013,0,0,-0.013,55.811,0)\"></path></g><g transform=\"matrix(.013,0,0,-0.013,62.818,0)\"><use xlink:href=\"#g190-116\"></use></g><g transform=\"matrix(.013,0,0,-0.013,67.524,0)\"><use xlink:href=\"#g190-118\"></use></g><g transform=\"matrix(.013,0,0,-0.013,74.492,0)\"><use xlink:href=\"#g190-109\"></use></g><g transform=\"matrix(.013,0,0,-0.013,77.781,0)\"><use xlink:href=\"#g190-106\"></use></g><g transform=\"matrix(.013,0,0,-0.013,81.265,0)\"><use xlink:href=\"#g190-111\"></use></g></svg>)</span></span> in the outpatient clinic. We calculated Matsuda index, the area under the curve (AUC (Ins/Glu)), and an oral disposition index (ISSI-2) to estimate insulin resistance and beta-cell function. We identified patients with IGR and low insulin secretion (maximum insulin during <span><svg height=\"9.39034pt\" style=\"vertical-align:-0.6370001pt\" version=\"1.1\" viewbox=\"-0.0498162 -8.75334 47.029 9.39034\" width=\"47.029pt\" xmlns=\"http://www.w3.org/2000/svg\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"><g transform=\"matrix(.013,0,0,-0.013,0,0)\"></path></g><g transform=\"matrix(.013,0,0,-0.013,9.946,0)\"></path></g><g transform=\"matrix(.013,0,0,-0.013,19.241,0)\"></path></g><g transform=\"matrix(.013,0,0,-0.013,27.614,0)\"><use xlink:href=\"#g190-85\"></use></g><g transform=\"matrix(.013,0,0,-0.013,39.398,0)\"></path></g></svg><span></span><svg height=\"9.39034pt\" style=\"vertical-align:-0.6370001pt\" version=\"1.1\" viewbox=\"50.6111838 -8.75334 18.919 9.39034\" width=\"18.919pt\" xmlns=\"http://www.w3.org/2000/svg\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"><g transform=\"matrix(.013,0,0,-0.013,50.661,0)\"></path></g><g transform=\"matrix(.013,0,0,-0.013,56.901,0)\"></path></g><g transform=\"matrix(.013,0,0,-0.013,63.141,0)\"><use xlink:href=\"#g113-49\"></use></g></svg></span> mU/l) and tested a subgroup using next generation sequencing to identify possible mutations in 103 candidate genes. <i>Results</i>. The total group consisted of 903 children and adolescents with obesity. 4.5% showed impaired fasting glucose, 9.4% impaired glucose tolerance, and 1.2% T2D. Matsuda index and Total AUC (Ins/Glu) showed a hyperbolic relationship. Out of 39 patients with low insulin secretion, we performed genetic testing on 12 patients. We found five monogenetic defects (ABCC8 (<span><svg height=\"8.55521pt\" style=\"vertical-align:-0.2063904pt\" version=\"1.1\" viewbox=\"-0.0498162 -8.34882 17.789 8.55521\" width=\"17.789pt\" xmlns=\"http://www.w3.org/2000/svg\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"><g transform=\"matrix(.013,0,0,-0.013,0,0)\"></path></g><g transform=\"matrix(.013,0,0,-0.013,10.158,0)\"></path></g></svg><span></span><span><svg height=\"8.55521pt\" style=\"vertical-align:-0.2063904pt\" version=\"1.1\" viewbox=\"21.3711838 -8.34882 6.416 8.55521\" width=\"6.416pt\" xmlns=\"http://www.w3.org/2000/svg\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"><g transform=\"matrix(.013,0,0,-0.013,21.421,0)\"></path></g></svg>),</span></span> GCK (<span><svg height=\"8.55521pt\" style=\"vertical-align:-0.2063904pt\" version=\"1.1\" viewbox=\"-0.0498162 -8.34882 17.789 8.55521\" width=\"17.789pt\" xmlns=\"http://www.w3.org/2000/svg\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"><g transform=\"matrix(.013,0,0,-0.013,0,0)\"><use xlink:href=\"#g113-111\"></use></g><g transform=\"matrix(.013,0,0,-0.013,10.158,0)\"><use xlink:href=\"#g117-34\"></use></g></svg><span></span><span><svg height=\"8.55521pt\" style=\"vertical-align:-0.2063904pt\" version=\"1.1\" viewbox=\"21.3711838 -8.34882 6.416 8.55521\" width=\"6.416pt\" xmlns=\"http://www.w3.org/2000/svg\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"><g transform=\"matrix(.013,0,0,-0.013,21.421,0)\"></path></g></svg>),</span></span> and GLI2/PTF1A (<span><svg height=\"8.55521pt\" style=\"vertical-align:-0.2063904pt\" version=\"1.1\" viewbox=\"-0.0498162 -8.34882 17.789 8.55521\" width=\"17.789pt\" xmlns=\"http://www.w3.org/2000/svg\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"><g transform=\"matrix(.013,0,0,-0.013,0,0)\"><use xlink:href=\"#g113-111\"></use></g><g transform=\"matrix(.013,0,0,-0.013,10.158,0)\"><use xlink:href=\"#g117-34\"></use></g></svg><span></span><span><svg height=\"8.55521pt\" style=\"vertical-align:-0.2063904pt\" version=\"1.1\" viewbox=\"21.3711838 -8.34882 6.416 8.55521\" width=\"6.416pt\" xmlns=\"http://www.w3.org/2000/svg\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"><g transform=\"matrix(.013,0,0,-0.013,21.421,0)\"><use xlink:href=\"#g113-50\"></use></g></svg>))</span></span>. <i>Conclusion</i>. Using surrogate parameters of beta-cell function and insulin resistance can help identify patients with insulin secretion disorder. A prevalence of 40% mutations of known diabetes genes in the subgroup with low insulin secretion suggests that at least 1.7% of patients with adolescent obesity have monogenic diabetes. A successful molecular genetic diagnosis can help to improve individual therapy.","PeriodicalId":15576,"journal":{"name":"Journal of Diabetes Research","volume":"27 1","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2024-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Insulin Secretion Defect in Children and Adolescents with Obesity: Clinical and Molecular Genetic Characterization\",\"authors\":\"Helena Enders-Seidlitz, Klemens Raile, Maolian Gong, Angela Galler, Peter Kuehnen, Susanna Wiegand\",\"doi\":\"10.1155/2024/5558634\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<i>Introduction</i>. Childhood obesity is increasing worldwide and presents as a global health issue due to multiple metabolic comorbidities. About 1% of adolescents with obesity develop type 2 diabetes (T2D); however, little is known about the genetic and pathophysiological background at young age. The objective of this study was to assess the prevalence of impaired glucose regulation (IGR) in a large cohort of children and adolescents with obesity and to characterize insulin sensitivity and insulin secretion. We also wanted to investigate adolescents with insulin secretion disorder more closely and analyze possible candidate genes of diabetes in a subcohort. <i>Methods</i>. We included children and adolescents with obesity who completed an oral glucose tolerance test (OGTT, <span><svg height=\\\"12.7112pt\\\" style=\\\"vertical-align:-3.403299pt\\\" version=\\\"1.1\\\" viewbox=\\\"-0.0498162 -9.3079 49.422 12.7112\\\" width=\\\"49.422pt\\\" xmlns=\\\"http://www.w3.org/2000/svg\\\" xmlns:xlink=\\\"http://www.w3.org/1999/xlink\\\"><g transform=\\\"matrix(.013,0,0,-0.013,0,0)\\\"></path></g><g transform=\\\"matrix(.013,0,0,-0.013,6.175,0)\\\"></path></g><g transform=\\\"matrix(.013,0,0,-0.013,9.308,0)\\\"></path></g><g transform=\\\"matrix(.013,0,0,-0.013,16.211,0)\\\"></path></g><g transform=\\\"matrix(.013,0,0,-0.013,21.71,0)\\\"></path></g><g transform=\\\"matrix(.013,0,0,-0.013,28.34,0)\\\"></path></g><g transform=\\\"matrix(.013,0,0,-0.013,33.215,0)\\\"></path></g><g transform=\\\"matrix(.013,0,0,-0.013,41.791,0)\\\"></path></g></svg><span></span><span><svg height=\\\"12.7112pt\\\" style=\\\"vertical-align:-3.403299pt\\\" version=\\\"1.1\\\" viewbox=\\\"52.277183799999996 -9.3079 36.313 12.7112\\\" width=\\\"36.313pt\\\" xmlns=\\\"http://www.w3.org/2000/svg\\\" xmlns:xlink=\\\"http://www.w3.org/1999/xlink\\\"><g transform=\\\"matrix(.013,0,0,-0.013,52.327,0)\\\"></path></g><g transform=\\\"matrix(.013,0,0,-0.013,55.811,0)\\\"></path></g><g transform=\\\"matrix(.013,0,0,-0.013,62.818,0)\\\"><use xlink:href=\\\"#g190-116\\\"></use></g><g transform=\\\"matrix(.013,0,0,-0.013,67.524,0)\\\"><use xlink:href=\\\"#g190-118\\\"></use></g><g transform=\\\"matrix(.013,0,0,-0.013,74.492,0)\\\"><use xlink:href=\\\"#g190-109\\\"></use></g><g transform=\\\"matrix(.013,0,0,-0.013,77.781,0)\\\"><use xlink:href=\\\"#g190-106\\\"></use></g><g transform=\\\"matrix(.013,0,0,-0.013,81.265,0)\\\"><use xlink:href=\\\"#g190-111\\\"></use></g></svg>)</span></span> in the outpatient clinic. We calculated Matsuda index, the area under the curve (AUC (Ins/Glu)), and an oral disposition index (ISSI-2) to estimate insulin resistance and beta-cell function. We identified patients with IGR and low insulin secretion (maximum insulin during <span><svg height=\\\"9.39034pt\\\" style=\\\"vertical-align:-0.6370001pt\\\" version=\\\"1.1\\\" viewbox=\\\"-0.0498162 -8.75334 47.029 9.39034\\\" width=\\\"47.029pt\\\" xmlns=\\\"http://www.w3.org/2000/svg\\\" xmlns:xlink=\\\"http://www.w3.org/1999/xlink\\\"><g transform=\\\"matrix(.013,0,0,-0.013,0,0)\\\"></path></g><g transform=\\\"matrix(.013,0,0,-0.013,9.946,0)\\\"></path></g><g transform=\\\"matrix(.013,0,0,-0.013,19.241,0)\\\"></path></g><g transform=\\\"matrix(.013,0,0,-0.013,27.614,0)\\\"><use xlink:href=\\\"#g190-85\\\"></use></g><g transform=\\\"matrix(.013,0,0,-0.013,39.398,0)\\\"></path></g></svg><span></span><svg height=\\\"9.39034pt\\\" style=\\\"vertical-align:-0.6370001pt\\\" version=\\\"1.1\\\" viewbox=\\\"50.6111838 -8.75334 18.919 9.39034\\\" width=\\\"18.919pt\\\" xmlns=\\\"http://www.w3.org/2000/svg\\\" xmlns:xlink=\\\"http://www.w3.org/1999/xlink\\\"><g transform=\\\"matrix(.013,0,0,-0.013,50.661,0)\\\"></path></g><g transform=\\\"matrix(.013,0,0,-0.013,56.901,0)\\\"></path></g><g transform=\\\"matrix(.013,0,0,-0.013,63.141,0)\\\"><use xlink:href=\\\"#g113-49\\\"></use></g></svg></span> mU/l) and tested a subgroup using next generation sequencing to identify possible mutations in 103 candidate genes. <i>Results</i>. The total group consisted of 903 children and adolescents with obesity. 4.5% showed impaired fasting glucose, 9.4% impaired glucose tolerance, and 1.2% T2D. Matsuda index and Total AUC (Ins/Glu) showed a hyperbolic relationship. Out of 39 patients with low insulin secretion, we performed genetic testing on 12 patients. We found five monogenetic defects (ABCC8 (<span><svg height=\\\"8.55521pt\\\" style=\\\"vertical-align:-0.2063904pt\\\" version=\\\"1.1\\\" viewbox=\\\"-0.0498162 -8.34882 17.789 8.55521\\\" width=\\\"17.789pt\\\" xmlns=\\\"http://www.w3.org/2000/svg\\\" xmlns:xlink=\\\"http://www.w3.org/1999/xlink\\\"><g transform=\\\"matrix(.013,0,0,-0.013,0,0)\\\"></path></g><g transform=\\\"matrix(.013,0,0,-0.013,10.158,0)\\\"></path></g></svg><span></span><span><svg height=\\\"8.55521pt\\\" style=\\\"vertical-align:-0.2063904pt\\\" version=\\\"1.1\\\" viewbox=\\\"21.3711838 -8.34882 6.416 8.55521\\\" width=\\\"6.416pt\\\" xmlns=\\\"http://www.w3.org/2000/svg\\\" xmlns:xlink=\\\"http://www.w3.org/1999/xlink\\\"><g transform=\\\"matrix(.013,0,0,-0.013,21.421,0)\\\"></path></g></svg>),</span></span> GCK (<span><svg height=\\\"8.55521pt\\\" style=\\\"vertical-align:-0.2063904pt\\\" version=\\\"1.1\\\" viewbox=\\\"-0.0498162 -8.34882 17.789 8.55521\\\" width=\\\"17.789pt\\\" xmlns=\\\"http://www.w3.org/2000/svg\\\" xmlns:xlink=\\\"http://www.w3.org/1999/xlink\\\"><g transform=\\\"matrix(.013,0,0,-0.013,0,0)\\\"><use xlink:href=\\\"#g113-111\\\"></use></g><g transform=\\\"matrix(.013,0,0,-0.013,10.158,0)\\\"><use xlink:href=\\\"#g117-34\\\"></use></g></svg><span></span><span><svg height=\\\"8.55521pt\\\" style=\\\"vertical-align:-0.2063904pt\\\" version=\\\"1.1\\\" viewbox=\\\"21.3711838 -8.34882 6.416 8.55521\\\" width=\\\"6.416pt\\\" xmlns=\\\"http://www.w3.org/2000/svg\\\" xmlns:xlink=\\\"http://www.w3.org/1999/xlink\\\"><g transform=\\\"matrix(.013,0,0,-0.013,21.421,0)\\\"></path></g></svg>),</span></span> and GLI2/PTF1A (<span><svg height=\\\"8.55521pt\\\" style=\\\"vertical-align:-0.2063904pt\\\" version=\\\"1.1\\\" viewbox=\\\"-0.0498162 -8.34882 17.789 8.55521\\\" width=\\\"17.789pt\\\" xmlns=\\\"http://www.w3.org/2000/svg\\\" xmlns:xlink=\\\"http://www.w3.org/1999/xlink\\\"><g transform=\\\"matrix(.013,0,0,-0.013,0,0)\\\"><use xlink:href=\\\"#g113-111\\\"></use></g><g transform=\\\"matrix(.013,0,0,-0.013,10.158,0)\\\"><use xlink:href=\\\"#g117-34\\\"></use></g></svg><span></span><span><svg height=\\\"8.55521pt\\\" style=\\\"vertical-align:-0.2063904pt\\\" version=\\\"1.1\\\" viewbox=\\\"21.3711838 -8.34882 6.416 8.55521\\\" width=\\\"6.416pt\\\" xmlns=\\\"http://www.w3.org/2000/svg\\\" xmlns:xlink=\\\"http://www.w3.org/1999/xlink\\\"><g transform=\\\"matrix(.013,0,0,-0.013,21.421,0)\\\"><use xlink:href=\\\"#g113-50\\\"></use></g></svg>))</span></span>. <i>Conclusion</i>. Using surrogate parameters of beta-cell function and insulin resistance can help identify patients with insulin secretion disorder. A prevalence of 40% mutations of known diabetes genes in the subgroup with low insulin secretion suggests that at least 1.7% of patients with adolescent obesity have monogenic diabetes. A successful molecular genetic diagnosis can help to improve individual therapy.\",\"PeriodicalId\":15576,\"journal\":{\"name\":\"Journal of Diabetes Research\",\"volume\":\"27 1\",\"pages\":\"\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2024-03-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Diabetes Research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1155/2024/5558634\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENDOCRINOLOGY & METABOLISM\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Diabetes Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1155/2024/5558634","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
Insulin Secretion Defect in Children and Adolescents with Obesity: Clinical and Molecular Genetic Characterization
Introduction. Childhood obesity is increasing worldwide and presents as a global health issue due to multiple metabolic comorbidities. About 1% of adolescents with obesity develop type 2 diabetes (T2D); however, little is known about the genetic and pathophysiological background at young age. The objective of this study was to assess the prevalence of impaired glucose regulation (IGR) in a large cohort of children and adolescents with obesity and to characterize insulin sensitivity and insulin secretion. We also wanted to investigate adolescents with insulin secretion disorder more closely and analyze possible candidate genes of diabetes in a subcohort. Methods. We included children and adolescents with obesity who completed an oral glucose tolerance test (OGTT, ) in the outpatient clinic. We calculated Matsuda index, the area under the curve (AUC (Ins/Glu)), and an oral disposition index (ISSI-2) to estimate insulin resistance and beta-cell function. We identified patients with IGR and low insulin secretion (maximum insulin during mU/l) and tested a subgroup using next generation sequencing to identify possible mutations in 103 candidate genes. Results. The total group consisted of 903 children and adolescents with obesity. 4.5% showed impaired fasting glucose, 9.4% impaired glucose tolerance, and 1.2% T2D. Matsuda index and Total AUC (Ins/Glu) showed a hyperbolic relationship. Out of 39 patients with low insulin secretion, we performed genetic testing on 12 patients. We found five monogenetic defects (ABCC8 (), GCK (), and GLI2/PTF1A ()). Conclusion. Using surrogate parameters of beta-cell function and insulin resistance can help identify patients with insulin secretion disorder. A prevalence of 40% mutations of known diabetes genes in the subgroup with low insulin secretion suggests that at least 1.7% of patients with adolescent obesity have monogenic diabetes. A successful molecular genetic diagnosis can help to improve individual therapy.
期刊介绍:
Journal of Diabetes Research is a peer-reviewed, Open Access journal that publishes research articles, review articles, and clinical studies related to type 1 and type 2 diabetes. The journal welcomes submissions focusing on the epidemiology, etiology, pathogenesis, management, and prevention of diabetes, as well as associated complications, such as diabetic retinopathy, neuropathy and nephropathy.