Shang Ying, Nasr Patrik, Ekstedt Mattias, Widman Linnea, Stål Per, Hultcrantz Rolf, Kechagias Stergios, Hagström Hannes
Department of Neurobiology, Care Sciences and Society (NVS), Karolinska Institutet, Stockholm, Sweden.
Department of Gastroenterology and Hepatology, Department of Health, Medicine and Caring Sciences, Linköping University, Linköping, Sweden.
JHEP Rep. 2020 Dec 1;3(2):100218. doi: 10.1016/j.jhepr.2020.100218. eCollection 2021 Apr.
BACKGROUND & AIMS: Non-alcoholic fatty liver disease (NAFLD) is common in the general population, but its association with dementia is unclear. We aimed to assess the risk of dementia related to NAFLD, and to determine whether histological parameters could improve the predictive capacity of a conventional risk model for dementia in patients with biopsy-proven NAFLD.
A retrospective matched cohort study of 656 NAFLD patients underwent liver biopsy at 2 hospitals between 1971 and 2009. Up to 10 individuals (controls) from the general population (n = 6,436) were matched for age, sex, and municipality to each patient. Dementia was ascertained from National registers until 2014. Using Cox regression, we estimated hazard ratios for dementia with 95% confidence intervals. In the biopsy cohort, the discriminative power of adding histological markers to a conventional risk model was assessed by Harrell's C-index and compared with a likelihood-ratio test.
During a mean follow-up of 19.7 ± 8.7 years, 3.3% of the NAFLD patients and 4.9% of the controls developed dementia ( = 0.07). Overall, NAFLD was not significantly associated with incident dementia. In the biopsy cohort, the model of conventional risk factors (age, sex, hypertension, and cardiovascular diseases) had a C-index of 0.912 to predict incident dementia. Adding individual histological parameters significantly increased the prediction of dementia, with the most pronounced improvement for fibrosis stage (C-index = 0.938, <0.05).
Although NAFLD was not associated with the risk of dementia, we found that adding histological markers to a conventional risk model for dementia enhanced the predictive capacity, indicating a shared metabolic origin.
Both non-alcoholic fatty liver disease (NAFLD) and dementia are increasing in prevalence because of a more sedentary lifestyle, increased prevalence of obesity and population ageing. However, the link between these 2 diseases is not well studied. We investigated the association between NAFLD and the risk of dementia and found no association. However, liver histology parameters, especially fibrosis, could significantly improve the prediction of dementia risk.
非酒精性脂肪性肝病(NAFLD)在普通人群中很常见,但其与痴呆症的关联尚不清楚。我们旨在评估与NAFLD相关的痴呆症风险,并确定组织学参数是否可以提高经活检证实患有NAFLD患者的传统痴呆症风险模型的预测能力。
对1971年至2009年间在两家医院接受肝活检的656例NAFLD患者进行回顾性匹配队列研究。从普通人群(n = 6436)中为每位患者匹配多达10名个体(对照),匹配因素包括年龄、性别和所在城市。通过国家登记处确定截至2014年的痴呆症情况。使用Cox回归,我们估计了痴呆症的风险比及95%置信区间。在活检队列中,通过Harrell's C指数评估将组织学标志物添加到传统风险模型中的判别能力,并通过似然比检验进行比较。
在平均19.7±8.7年的随访期间,3.3%的NAFLD患者和4.9%的对照者发生了痴呆症(P = 0.07)。总体而言,NAFLD与新发痴呆症无显著关联。在活检队列中,传统风险因素(年龄、性别、高血压和心血管疾病)模型预测新发痴呆症的C指数为0.912。添加个体组织学参数显著提高了痴呆症的预测能力,其中纤维化阶段的改善最为显著(C指数 = 0.938,P<0.05)。
虽然NAFLD与痴呆症风险无关,但我们发现将组织学标志物添加到传统痴呆症风险模型中可增强预测能力,表明存在共同的代谢起源。
由于生活方式更加久坐、肥胖患病率增加和人口老龄化,非酒精性脂肪性肝病(NAFLD)和痴呆症的患病率都在上升。然而,这两种疾病之间的联系尚未得到充分研究。我们调查了NAFLD与痴呆症风险之间的关联,未发现关联。然而,肝脏组织学参数,尤其是纤维化,可显著改善痴呆症风险的预测。