Martinelli Ilaria, Gianferrari Giulia, Santarelli Rebecca, Zucchi Elisabetta, Simonini Cecilia, Fini Nicola, Ghezzi Andrea, Gessani Annalisa, Ferri Laura, Smolik Krzysztof, Ferraro Diana, Bedin Roberta, Gizzi Matteo, Sette Elisabetta, Vacchiano Veria, Bonan Luigi, Zinno Lucia, De Massis Patrizia, Canali Elena, Medici Doriana, Terlizzi Emilio, Morresi Simonetta, Santangelo Mario, Patuelli Alberto, Currò Dossi Marco, Longoni Marco, Pugliatti Maura, Filippini Tommaso, Ferro Salvatore, Mandrioli Jessica
Department of Neurosciences, Azienda Ospedaliero Universitaria di Modena, 41126 Modena, Italy.
Neuroscience Ph.D. Program, University of Modena and Reggio Emilia, 41125 Modena, Italy.
Life (Basel). 2025 Jun 10;15(6):936. doi: 10.3390/life15060936.
Type 2 diabetes mellitus (T2DM) as a comorbidity in amyotrophic lateral sclerosis (ALS) has sparked interest for its potential impact on disease expression and prognosis. In this retrospective cohort study, we investigated the prevalence and clinical correlates of T2DM in a large cohort of patients from the ALS registry of a Northern Italy region, Emilia Romagna, established in 2009. Out of 1756 ALS patients enrolled up to 2021, 145 were affected by T2DM (diALS). Patients with diALS were older than those without T2DM (ndALS) (71.56 vs. 65.76 years, < 0.001), had a higher body mass index (25.63 vs. 24.23, < 0.001), but experienced greater weight loss at diagnosis (6.87% vs. 5.44%, < 0.007). Respiratory onset (6.2% vs. 2.6%, = 0.013) and respiratory phenotype (4.2% vs. 1.4%, = 0.04) were more frequent among diALS. Coherently, diALS presented a lower forced vital capacity (74.9% vs. 87.9%, ≤ 0.001) and more frequently adopted Non-Invasive Ventilation (NIV) (50.35% vs. 37.61%, = 0.003), with significant influence on time to NIV (HR 1.71, 95% CI 1.07-2.74, = 0.024). Exploring genetic background, among all the genes examined emerged as underrepresented among diALS (7.64% in ndALS vs. 0% in diALS, = 0.039). In conclusion, we confirmed a more severe respiratory dysfunction in diALS, suggesting a specific frailty in respiratory muscles, together with some peculiar clinical features consistent with the previous literature data, such as a later onset. The lower prevalence of expansion in this population may hint towards a specific role of the gene in metabolism and inflammation, granting more space to non-genetic causes, warranting further studies for confirmation.
2型糖尿病(T2DM)作为肌萎缩侧索硬化症(ALS)的一种合并症,因其对疾病表现和预后的潜在影响而引发了关注。在这项回顾性队列研究中,我们调查了来自意大利北部艾米利亚-罗马涅地区2009年建立的ALS登记处的一大群患者中T2DM的患病率及其临床相关性。在截至2021年登记的1756例ALS患者中,145例患有T2DM(糖尿病性ALS)。糖尿病性ALS患者比无T2DM的患者(非糖尿病性ALS)年龄更大(71.56岁对65.76岁,<0.001),体重指数更高(25.63对24.23,<0.001),但在诊断时体重减轻更多(6.87%对5.44%,<0.007)。呼吸起病(6.2%对2.6%,=0.013)和呼吸表型(4.2%对1.4%,=0.04)在糖尿病性ALS中更常见。相应地,糖尿病性ALS患者的用力肺活量较低(74.9%对87.9%,≤0.001),更频繁地采用无创通气(NIV)(50.35%对37.61%,=0.003),这对开始使用NIV的时间有显著影响(风险比1.71,95%置信区间1.07 - 2.74,=0.024)。在探索遗传背景时发现,在所有检测的基因中,某基因在糖尿病性ALS中出现的频率较低(非糖尿病性ALS中为7.64%,糖尿病性ALS中为0%,=0.039)。总之,我们证实糖尿病性ALS患者存在更严重的呼吸功能障碍,提示呼吸肌存在特定的脆弱性,同时还有一些与先前文献数据一致的特殊临床特征,如发病较晚。该人群中某基因扩增的患病率较低可能暗示该基因在代谢和炎症中具有特定作用,这使得非遗传因素的作用更为突出,有待进一步研究证实。