{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,7]],"date-time":"2026-08-07T17:02:45Z","timestamp":1786122165701,"version":"build-2736575974"},"reference-count":123,"publisher":"Wiley","issue":"9","license":[{"start":{"date-parts":[[2026,6,17]],"date-time":"2026-06-17T00:00:00Z","timestamp":1781654400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2026,6,17]],"date-time":"2026-06-17T00:00:00Z","timestamp":1781654400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["dom-pubs.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Diabetes Obesity Metabolism"],"published-print":{"date-parts":[[2026,9]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>Gestational diabetes mellitus (GDM) represents far more than a transient glycaemic disorder: it is a sentinel metabolic event that unveils pre\u2010existing defects in \u03b2\u2010cell function and insulin action, with profound implications for both maternal and offspring cardiometabolic health across the lifespan. The physiological insulin resistance of pregnancy, driven by placental hormones and maternal immune modulation, intensifies progressively, resulting in a 60%\u201365% reduction in insulin sensitivity by the third trimester. This metabolic challenge necessitates a compensatory 200%\u2013250% increase in insulin secretion to maintain euglycaemia. When pancreatic \u03b2\u2010cells fail to meet this demand, maternal hyperglycaemia develops, triggering foetal hyperinsulinemia and establishing an intrauterine environment that promotes accelerated foetal growth, adipogenesis and adverse metabolic programming.<\/jats:p>\n                  <jats:p>The intergenerational consequences of GDM extend beyond the perinatal period. Landmark studies in Pima Indians demonstrate that intrauterine exposure to maternal diabetes confers an elevated risk of childhood obesity and early\u2010onset type 2 diabetes in offspring, independent of shared genetic susceptibility, thereby perpetuating a transgenerational cycle of metabolic disease, potentially mediated in part by epigenetic mechanisms.<\/jats:p>\n                  <jats:p>Diagnostic strategies for GDM vary internationally, with the one\u2010step 75\u2010g OGTT (IADPSG\/ADA criteria) and the two\u2010step Carpenter\u2013Coustan approach yielding comparable maternal and neonatal outcomes.<\/jats:p>\n                  <jats:p>In GDM, management typically starts with individualized medical nutrition therapy and physical activity, with insulin as the preferred pharmacological treatment when glycaemic targets are not achieved. Metformin and glyburide, despite their convenience and oral administration, remain controversial due to placental transfer and still limited long\u2010term safety data in offspring.<\/jats:p>\n                  <jats:p>Given its increasing prevalence and long\u2010term implications, GDM is both a clinical and public health concern. Early recognition and evidence\u2010based management provide an opportunity to interrupt the intergenerational transmission of metabolic risk and preserve long\u2010term cardiometabolic health.<\/jats:p>","DOI":"10.1111\/dom.70987","type":"journal-article","created":{"date-parts":[[2026,6,17]],"date-time":"2026-06-17T08:09:08Z","timestamp":1781683748000},"page":"7705-7718","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["How the First 9\u2009Months Shape the Rest of Your Life: The Impact of Gestational Diabetes on the Metabolic Future"],"prefix":"10.1111","volume":"28","author":[{"given":"Mustafa","family":"Kanat","sequence":"first","affiliation":[{"name":"DIMER Diabetes and Obesity Research Center, Department of Medicine Istanbul Atlas University  Istanbul Turkiye"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4556-1787","authenticated-orcid":false,"given":"Muhammad","family":"Abdul\u2010Ghani","sequence":"additional","affiliation":[{"name":"Division of Diabetes University of Texas Health Science Center at San Antonio  San Antonio Texas USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-3839-1724","authenticated-orcid":false,"given":"Ralph A.","family":"DeFronzo","sequence":"additional","affiliation":[{"name":"Division of Diabetes University of Texas Health Science Center at San Antonio  San Antonio Texas USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2026,6,17]]},"reference":[{"key":"e_1_2_14_2_1","doi-asserted-by":"publisher","DOI":"10.2337\/dc07-s225"},{"key":"e_1_2_14_3_1","doi-asserted-by":"publisher","DOI":"10.2337\/diabetes.51.7.2207"},{"key":"e_1_2_14_4_1","doi-asserted-by":"publisher","DOI":"10.1210\/clinem\/dgae709"},{"key":"e_1_2_14_5_1","doi-asserted-by":"publisher","DOI":"10.2337\/dbi24-0012"},{"key":"e_1_2_14_6_1","doi-asserted-by":"publisher","DOI":"10.2337\/diab.28.12.1039"},{"key":"e_1_2_14_7_1","doi-asserted-by":"publisher","DOI":"10.2337\/dc14-S081"},{"key":"e_1_2_14_8_1","doi-asserted-by":"publisher","DOI":"10.1080\/08830185.2020.1777292"},{"key":"e_1_2_14_9_1","doi-asserted-by":"publisher","DOI":"10.3389\/fendo.2025.1486848"},{"key":"e_1_2_14_10_1","first-page":"931","article-title":"Distribution of Glucose Transporter Isoforms in Tissues of Rat and Human","volume":"103","author":"Totawa N. 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