Chourpiliadis Charilaos, Lovik Anikó, Seitz Christina, Hu Yihan, Wu Jing, Ljungman Petter, Press Rayomand, Samuelsson Kristin, Ingre Caroline, Fang Fang
Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Institute of Psychology, Leiden University, Leiden, the Netherlands.
Lancet Reg Health Eur. 2024 Dec 10;49:101173. doi: 10.1016/j.lanepe.2024.101173. eCollection 2025 Feb.
The evidence on the link between cardiometabolic diseases (CMDs) and motor neuron diseases (MNDs) remains inconsistent. We aimed to determine whether there is an association of CMDs, namely, any cardiovascular disease, cardiac arrhythmia, heart failure, thromboembolic disease, hypertension, cerebrovascular disease, ischemic heart disease, diabetes mellitus type 2, and hypercholesterolemia with the risk and progression of MNDs.
We included 1463 MND patients (amyotrophic lateral sclerosis (ALS), primary lateral sclerosis (PLS), progressive spinal muscular atrophy (PSMA), and unspecified MND) diagnosed from January 1, 2015, to July 1, 2023, in Sweden according to the Swedish Motor Neuron Disease Quality Registry (i.e., cases), up to 5 MND-free population controls per case (N = 7311) who were individually matched to the cases on age and sex, and the full siblings (N = 2002) and spouses (N = 1220) of MND patients (i.e., relative controls). Conditional logistic regression models were used to estimate the risk of MND diagnosis in relation to previous CMDs, through comparing MND patients to population controls or relative controls. MND patients were followed from diagnosis to assess the role of pre-diagnostic CMDs on disease progression. A joint longitudinal-survival model was used to estimate risk of mortality (or use of invasive ventilation) in relation to CMDs after taking into account the longitudinal changes of ALS functional rating scale-revised (ALSFRS-R) in the time-to-event analysis. Hierarchical clustering with the Ward's linkage and a dissimilarity matrix created by Gower's method was used to identify clusters of MND patients with distinct phenotypes.
Among the CMDs studied, a history of diabetes mellitus type 2 (OR 0.75; 95% CI 0.62, 0.93) or hypercholesterolemia (OR 0.82; 95% CI 0.71, 0.94) more than one year before diagnosis was associated with a lower risk for MNDs. The associations persisted for more than five years before MND diagnosis. MND patients with a history of any cardiovascular disease (HR 1.43; 95% CI 1.13, 1.81), arrhythmia (HR 1.42; 95% CI 1.04, 1.93), heart failure (HR 1.79; 95% CI 1.02, 3.14), hypertension (HR 1.41; 95% CI 1.12, 1.77), or hypercholesterolemia (HR 1.28; 95% CI 1.01, 1.62) had an increased mortality risk, compared to others, after taking into consideration the longitudinal changes in ALSFRS-R. Cluster analysis identified two clusters of MND patients, where one cluster demonstrated higher age, worse functional status, and higher prevalence of CMDs at the time of diagnosis as well as a higher mortality and faster functional decline during follow-up, compared to the ones included in the other cluster.
Diabetes mellitus type 2 and hypercholesterolemia were associated with a lower future risk of MND. On the other hand, most of the CMDs were indicative of a poor disease progression after an MND diagnosis.
European Research Council, US Center for Disease Control and Prevention, Swedish Research Council.
关于心脏代谢疾病(CMDs)与运动神经元疾病(MNDs)之间联系的证据仍不一致。我们旨在确定CMDs,即任何心血管疾病、心律失常、心力衰竭、血栓栓塞性疾病、高血压、脑血管疾病、缺血性心脏病、2型糖尿病和高胆固醇血症,是否与MNDs的风险和进展相关。
我们纳入了2015年1月1日至2023年7月1日在瑞典根据瑞典运动神经元疾病质量登记处诊断的1463例MND患者(肌萎缩侧索硬化症(ALS)、原发性侧索硬化症(PLS)、进行性脊髓性肌萎缩症(PSMA)和未明确的MND)(即病例),每个病例最多5名无MND的人群对照(N = 7311),这些对照在年龄和性别上与病例个体匹配,以及MND患者的全同胞(N = 2002)和配偶(N = 1220)(即亲属对照)。通过将MND患者与人群对照或亲属对照进行比较,使用条件逻辑回归模型来估计与先前CMDs相关的MND诊断风险。对MND患者从诊断开始进行随访,以评估诊断前CMDs对疾病进展的作用。在事件发生时间分析中,考虑到修订的ALS功能评定量表(ALSFRS-R)的纵向变化,使用联合纵向生存模型来估计与CMDs相关的死亡风险(或使用有创通气的风险)。使用Ward链接法进行层次聚类,并通过Gower方法创建的差异矩阵来识别具有不同表型的MND患者集群。
在所研究的CMDs中,诊断前一年以上的2型糖尿病病史(OR 0.75;95% CI 0.62,0.93)或高胆固醇血症病史(OR 0.82;95% CI 0.71,0.94)与MNDs风险较低相关。这些关联在MND诊断前持续超过五年。在考虑ALSFRS-R的纵向变化后,有任何心血管疾病病史(HR 1.43;95% CI 1.13,1.81)、心律失常病史(HR 1.42;95% CI 1.04,1.93)、心力衰竭病史(HR 1.79;95% CI 1.02,3.14)、高血压病史(HR 1.41;95% CI 1.12,1.77)或高胆固醇血症病史(HR 1.28;95% CI 1.01,1.62)的MND患者与其他患者相比,死亡风险增加。聚类分析确定了两组MND患者,其中一组与另一组相比,在诊断时年龄更大、功能状态更差、CMDs患病率更高,并且在随访期间死亡率更高、功能下降更快。
2型糖尿病和高胆固醇血症与未来较低的MND风险相关。另一方面,大多数CMDs表明MND诊断后疾病进展不良。
欧洲研究理事会、美国疾病控制与预防中心、瑞典研究理事会。