Department of Neurosurgery, Kuopio University Hospital, P.O.Box 100, 70029, Kuopio, KYS, Finland.
Institute of Clinical Medicine-Neurosurgery, University of Eastern Finland, Kuopio, Finland.
Fluids Barriers CNS. 2020 Sep 15;17(1):57. doi: 10.1186/s12987-020-00217-0.
The pathophysiological basis of idiopathic normal pressure hydrocephalus (iNPH) is still unclear. Previous studies have shown a familial aggregation and a potential heritability when it comes to iNPH. Our aim was to conduct a novel case-controlled comparison between familial iNPH (fNPH) patients and their elderly relatives, involving multiple different families.
Questionnaires and phone interviews were used for collecting the data and categorising the iNPH patients into the familial (fNPH) and the sporadic groups. Identical questionnaires were sent to the relatives of the potential fNPH patients. Venous blood samples were collected for genetic studies. The disease histories of the probable fNPH patients (n = 60) were compared with their ≥ 60-year-old relatives with no iNPH (n = 49). A modified Charlson Comorbidity Index (CCI) was used to measure the overall disease burden. Fisher's exact test (two-tailed), the Mann-Whitney U test (two-tailed) and a multivariate binary logistic regression analysis were used to perform the statistical analyses.
Diabetes (32% vs. 14%, p = 0.043), arterial hypertension (65.0% vs. 43%, p = 0.033), cardiac insufficiency (16% vs. 2%, p = 0.020) and depressive symptoms (32% vs. 8%, p = 0.004) were overrepresented among the probable fNPH patients compared to their non-iNPH relatives. In the age-adjusted multivariate logistic regression analysis, diabetes remained independently associated with fNPH (OR = 3.8, 95% CI 1.1-12.9, p = 0.030).
Diabetes is associated with fNPH and a possible risk factor for fNPH. Diabetes could contribute to the pathogenesis of iNPH/fNPH, which motivates to further prospective and gene-environmental studies to decipher the disease modelling of iNPH/fNPH.
特发性正常压力脑积水(iNPH)的病理生理学基础仍不清楚。先前的研究表明,iNPH 存在家族聚集性和潜在遗传性。我们的目的是对家族性 iNPH(fNPH)患者及其老年亲属进行一项新的病例对照比较,涉及多个不同的家族。
使用问卷调查和电话访谈收集数据,并将 iNPH 患者分为家族性(fNPH)和散发性组。将相同的问卷发送给潜在 fNPH 患者的亲属。采集静脉血样进行遗传研究。将 60 名疑似 fNPH 患者的病史与无 iNPH 的≥60 岁亲属(n=49)进行比较。使用改良 Charlson 合并症指数(CCI)来衡量整体疾病负担。采用 Fisher 确切检验(双侧)、Mann-Whitney U 检验(双侧)和多元二项逻辑回归分析进行统计分析。
疑似 fNPH 患者比非 iNPH 亲属更常见糖尿病(32%比 14%,p=0.043)、动脉高血压(65.0%比 43%,p=0.033)、心功能不全(16%比 2%,p=0.020)和抑郁症状(32%比 8%,p=0.004)。在年龄调整后的多元逻辑回归分析中,糖尿病与 fNPH 仍独立相关(OR=3.8,95%CI 1.1-12.9,p=0.030)。
糖尿病与 fNPH 相关,是 fNPH 的一个可能危险因素。糖尿病可能导致 iNPH/fNPH 的发病机制,这促使我们进一步进行前瞻性和基因-环境研究,以阐明 iNPH/fNPH 的疾病模型。