Shapiro Allison L B, Coughlan Christina, Bettcher Brianne M, Pauley Meghan E, Kim Jeongchul, Bjornstad Petter, Rajic Benjamin, Truong Jennifer, Bell Christopher, Choi Ye Ji, Walker Keenan A, Potter Huntington, Liese Angela D, Dabelea Dana, Whitlow Christopher T
Lifecourse Epidemiology of Adiposity and Diabetes Center, University of Colorado at Anschutz (CU-Anschutz), Aurora, CO 80045, USA.
Section of Endocrinology, Department of Pediatrics, School of Medicine (SOM), CU-Anschutz, Aurora, CO 80045, USA.
Endocrines. 2024 Jun;5(2):197-213. doi: 10.3390/endocrines5020014. Epub 2024 May 6.
Adult-onset diabetes increases one's risk of neurodegenerative disease including Alzheimer's disease (AD); however, the risk associated with youth-onset diabetes (Y-DM) remains underexplored. We quantified plasma biomarkers of neurodegeneration and AD in participants with Y-DM from the SEARCH cohort at adolescence and young adulthood (Type 1, n = 25; Type 2, n = 25; 59% female; adolescence, age = 15 y/o [2.6]; adulthood, age = 27.4 y/o [2.2]), comparing them with controls (adolescence, n = 25, age = 14.8 y/o [2.7]; adulthood, n = 21, age = 24.9 y/o [2.8]). Plasma biomarkers, including glial fibrillary acidic protein (GFAP), neurofilament light chain protein (NfL), phosphorylated tau-181 (pTau181), and amyloid beta (Aβ40, Aβ42), were measured via Simoa. A subset of participants (n = 7; age = 27.5 y/o [5.7]) and six controls (age = 25.1 y/o [4.5]) underwent PET scans to quantify brain amyloid and tau densities in AD sensitive brain regions. Y-DM adolescents exhibited lower plasma levels of Aβ40, Aβ42, and GFAP, and higher pTau181 compared to controls ( < 0.05), a pattern persisting into adulthood ( < 0.001). All biomarkers showed significant increases from adolescence to adulthood in Y-DM ( < 0.01), though no significant differences in brain amyloid or tau were noted between Y-DM and controls in adulthood. Preliminary evidence suggests that preclinical AD neuropathology is present in young people with Y-DM, indicating a potential increased risk of neurodegenerative diseases.
成人发病型糖尿病会增加患神经退行性疾病(包括阿尔茨海默病(AD))的风险;然而,与青少年发病型糖尿病(Y-DM)相关的风险仍未得到充分研究。我们对SEARCH队列中处于青春期和青年期的Y-DM参与者(1型,n = 25;2型,n = 25;59%为女性;青春期,年龄 = 15岁[2.6];成年期,年龄 = 27.4岁[2.2])的神经退行性变和AD的血浆生物标志物进行了量化,并将其与对照组(青春期,n = 25,年龄 = 14.8岁[2.7];成年期,n = 21,年龄 = 24.9岁[2.8])进行比较。通过Simoa测量血浆生物标志物,包括胶质纤维酸性蛋白(GFAP)、神经丝轻链蛋白(NfL)、磷酸化tau-181(pTau181)和淀粉样β蛋白(Aβ40、Aβ42)。一部分参与者(n = 7;年龄 = 27.5岁[5.7])和六名对照组(年龄 = 25.1岁[4.5])接受了PET扫描,以量化AD敏感脑区的脑淀粉样蛋白和tau密度。与对照组相比,Y-DM青少年的Aβ40、Aβ42和GFAP血浆水平较低,pTau181较高(<0.05),这种模式持续到成年期(<0.001)。所有生物标志物在Y-DM中从青春期到成年期均显著增加(<0.01),尽管成年期Y-DM和对照组之间在脑淀粉样蛋白或tau方面没有显著差异。初步证据表明,患有Y-DM的年轻人存在临床前AD神经病理学,这表明神经退行性疾病的潜在风险增加。