School of Medicine, University of Patras, Patras, Greece.
Department of Endocrinology and Diabetes Center, Hellenic Red Cross Hospital, Athens, Greece.
Endocrine. 2024 Sep;85(3):965-978. doi: 10.1007/s12020-024-03772-w. Epub 2024 Mar 12.
The incidence and prevalence of type 2 diabetes mellitus (T2DM) in young individuals (aged <40 years) have significantly increased in recent years, approximating two to threefold increase in the respective rates. Numerous risk factors including severe obesity, family history, ethnicity, maternal diabetes or gestational diabetes, and female sex contribute to a younger age of onset. In terms of pathogenesis, impaired insulin secretion is the key operating mechanism, alongside with ectopic adiposity-related insulin resistance. T2DM diagnosis in a young adult requires the exclusion of type 1 diabetes mellitus (T1DM), latent autoimmune diabetes of adults (LADA) and maturity-onset diabetes of the young (MODY). The establishment of such diagnosis is critical for prognosis, because early-onset T2DM is associated with rapid deterioration in pancreatic β-cell secretory function leading to earlier initiation of insulin therapy. Furthermore, mortality and lifetime risk of developing complications, especially microvascular, is increased in these patients compared to both later-onset T2DM and T1DM patients; also, the latter are often developed earlier in the course of disease. The management of early-onset T2DM follows the same guidelines as in later-onset T2DM; yet patients aged 18-39 years are underrepresented in the big clinical trials on which the development of guidelines is based. Finally, young people with T2DM face significant challenges associated with social determinants, which compromise their adherence to therapy and induce diabetes distress. Future research focusing on the pathogenesis of β-cell decline and complications, as well as on specific treatment shall lead to better understanding and management of early-onset T2DM.
近年来,年轻人(年龄<40 岁)2 型糖尿病(T2DM)的发病率和患病率显著增加,相应的发病率增加了两到三倍。许多危险因素,包括严重肥胖、家族史、种族、母亲糖尿病或妊娠糖尿病以及女性,导致发病年龄提前。就发病机制而言,胰岛素分泌受损是关键的作用机制,同时还伴有异位脂肪相关的胰岛素抵抗。年轻成人的 T2DM 诊断需要排除 1 型糖尿病(T1DM)、成人隐匿性自身免疫性糖尿病(LADA)和青少年起病的成年型糖尿病(MODY)。确立这样的诊断对于预后至关重要,因为早发 T2DM 与胰岛β细胞分泌功能的迅速恶化有关,导致更早开始胰岛素治疗。此外,与晚发 T2DM 和 T1DM 患者相比,这些患者的死亡率和发生并发症(特别是微血管并发症)的终身风险增加;而且,这些并发症在疾病过程中往往更早出现。早发 T2DM 的管理遵循与晚发 T2DM 相同的指南;然而,指南制定所依据的大型临床试验中,年龄在 18-39 岁的患者代表性不足。最后,患有 T2DM 的年轻人面临与社会决定因素相关的重大挑战,这会影响他们对治疗的依从性,并导致糖尿病困扰。未来专注于β细胞衰退和并发症发病机制以及特定治疗的研究将有助于更好地理解和管理早发 T2DM。