Miletić Marija, Stević Zorica, Vujović Svetlana, Rakočević Jelena, Tomić Ana, Tančić Gajić Milina, Stojanović Miloš, Palibrk Aleksa, Žarković Miloš
Clinic for Endocrinology, Diabetes and Metabolic Diseases, University Clinical Center of Serbia, 11000 Belgrade, Serbia.
Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.
Diagnostics (Basel). 2024 Sep 19;14(18):2078. doi: 10.3390/diagnostics14182078.
Spinal muscular atrophy type 3 (juvenile SMA, Kugelberg-Welander disease) is a genetic disease caused by changes in the survival motor neuron 1 (SMN) gene. However, there is increasing evidence of metabolic abnormalities in SMA patients, such as altered fatty acid metabolism, impaired glucose tolerance, and defects in the functioning of muscle mitochondria. Given that data in the literature are scarce regarding this subject, the purpose of this study was to estimate the prevalence of glucose and lipid metabolism disorders in adult patients with SMA type 3.
We conducted a cross-sectional study of 23 adult patients with SMA type 3 who underwent a comprehensive evaluation, including a physical examination, biochemical analysis, and an oral glucose tolerance test during 2020-2023.
At least one lipid abnormality was observed in 60.8% of patients. All four lipid parameters were atypical in 4.3% of patients, three lipid parameters were abnormal in 21.7% of patients, and two lipid parameters were altered in 8.7% patients. A total of 91.3% of SMA3 patients met the HOMA-IR criteria for insulin resistance, with 30.43% having impaired glucose tolerance. None of the patients met the criteria for a diagnosis of overt DM2.
The prevalence of dyslipidemia and altered glucose metabolism in our study sets apart the adult population with SMA3 from the general population, confirming a significant interplay between muscle, liver, and adipose tissue. Ensuring metabolic care for aging patients with SMA 3 is crucial, as they are vulnerable to metabolic derangements and cardiovascular risks.
脊髓性肌萎缩症3型(青少年型脊髓性肌萎缩症,库格尔贝格 - 韦兰德病)是一种由生存运动神经元1(SMN)基因变化引起的遗传性疾病。然而,越来越多的证据表明脊髓性肌萎缩症患者存在代谢异常,如脂肪酸代谢改变、葡萄糖耐量受损以及肌肉线粒体功能缺陷。鉴于关于该主题的文献数据稀缺,本研究的目的是评估成年脊髓性肌萎缩症3型患者中葡萄糖和脂质代谢紊乱的患病率。
我们对23例成年脊髓性肌萎缩症3型患者进行了横断面研究,这些患者在2020年至2023年期间接受了全面评估,包括体格检查、生化分析和口服葡萄糖耐量试验。
60.8%的患者观察到至少一种脂质异常。4.3%的患者所有四项脂质参数均不典型,21.7%的患者三项脂质参数异常,8.7%的患者两项脂质参数改变。共有91.3%的脊髓性肌萎缩症3型患者符合胰岛素抵抗的HOMA-IR标准,30.43%的患者葡萄糖耐量受损。没有患者符合2型糖尿病的诊断标准。
我们研究中血脂异常和葡萄糖代谢改变的患病率使成年脊髓性肌萎缩症3型患者群体与普通人群区分开来,证实了肌肉、肝脏和脂肪组织之间存在显著的相互作用。确保对老年脊髓性肌萎缩症3型患者进行代谢护理至关重要,因为他们易患代谢紊乱和心血管风险。