老年非酒精性脂肪性肝病患者100例的认知功能观察和临床特点

被引:10
作者
许旌
杨立
师璇
王丹
杨帆
机构
[1] 南京大学医学院附属鼓楼医院老年科
关键词
认知; 非酒精性脂肪性肝病; 可溶性转铁蛋白受体; 质子磁共振波谱;
D O I
暂无
中图分类号
R575.5 [肝代谢障碍];
学科分类号
1002 ; 100201 ;
摘要
目的观察老年非酒精性脂肪性肝病(NAFLD)患者认知功能、临床指标和海马组织结构的变化。方法纳入2014年12月至2016年6月在南京大学医学院附属鼓楼医院老年科住院的169例老年体检患者, 分成NAFLD组与非NAFLD组。收集两组患者的病史资料, 采用蒙特利尔认知评估量表(MoCA)进行认知功能障碍评估, 检测血清可溶性转铁蛋白受体(sTfR)水平, 进行肝脾比值测量和海马质子磁共振波谱(1H-MRS)检查。统计学方法采用t检验和线性回归分析。结果 169例老年患者中, NAFLD 100例, 非NAFLD 69例。NAFLD组患者的BMI和腰臀比分别为(25.9±3.4) kg/m2和1.03±0.13, 分别高于非NAFLD组的(24.2±3.7) kg/m2和0.95±0.06, 差异均有统计学意义(t=-2.714、-3.605, P均<0.01)。NAFLD组患者的MoCA评分为(20.1±5.8)分, 低于非NAFLD组的(22.1±4.4)分, 差异有统计学意义(t=2.154, P=0.033)。NAFLD组血清sTfR水平和肝脾CT比值分别为(8.78±4.31) mg/L和0.97±0.12, 分别低于非NAFLD组的(12.66±3.93) mg/L和1.19±0.15, 差异均有统计学意义(t=3.765、6.142, P均<0.01)。肝脾CT比值(β=7.597, 95%CI 2.938~12.935)、sTfR(β=0.552, 95%CI 0.304~0.787)与老年患者认知功能呈正相关(P均<0.01)。NAFLD组右侧海马高度为(0.410±0.074) mm, 低于非NAFLD组的(0.453±0.086) mm, 差异有统计学意义(t=2.078, P=0.042)。结论老年NAFLD患者认知功能减退, 这与铁负荷及肝脏脂肪密切相关。
引用
收藏
页码:35 / 39
页数:5
相关论文
共 18 条
[1]  
Systemic inflammation without gliosis mediates cognitive deficits through impaired BDNF expression in bile duct ligation model of hepatic encephalopathy.[J].Saurabh Dhanda;Smriti Gupta;Avishek Halder;Aditya Sunkaria;Rajat Sandhir.Brain Behavior and Immunity.2018,
[2]  
Cognitive assessment of patients with nonalcoholic fatty liver disease.[J].Asuman Celikbilek;Mehmet Celikbilek;Gurbet Bozkurt.European Journal of Gastroenterology & Hepatology.2018,
[3]  
Global epidemiology of non‐alcoholic fatty liver disease/non‐alcoholic steatohepatitis: What we need in the future.[J].Ana Ruth Araújo;Natalia Rosso;Giorgio Bedogni;Claudio Tiribelli;Stefano Bellentani.Liver International.2018,
[4]  
Association of Nonalcoholic Fatty Liver Disease With Lower Brain Volume in Healthy Middle-Aged Adults in the Framingham Study.[J].Galit Weinstein;Shira Zelber-Sagi;Sarah R. Preis;Alexa S. Beiser;Charles DeCarli;Elizabeth K. Speliotes;Claudia L. Satizabal;Ramachandran S. Vasan;Sudha Seshadri.JAMA Neurology.2017, 1
[5]  
Association of brain amyloidosis with pro-inflammatory gut bacterial taxa and peripheral inflammation markers in cognitively impaired elderly.[J].Annamaria Cattaneo;Nadia Cattane;Samantha Galluzzi;Stefania Provasi;Nicola Lopizzo;Cristina Festari;Clarissa Ferrari;Ugo Paolo Guerra;Barbara Paghera;Cristina Muscio;Angelo Bianchetti;Giorgio Dalla Volta;Marinella Turla;Maria Sofia Cotelli;Michele Gennuso;Alessandro Prelle;Orazio Zanetti;Giulia Lussignoli;Dario Mirabile;Daniele Bellandi;Simona Gentile;
[6]  
Nonalcoholic fatty liver disease is associated with cognitive function in adults.[J].Sang Won Seo;Rebecca F. Gottesman;Jeanne M. Clark;Ruben Hernaez;Yoosoo Chang;Changsoo Kim;Kyoung Hwa Ha;Eliseo Guallar;Mariana Lazo.Neurology.2016,
[7]   Alzheimer disease: Epidemiology, diagnostic criteria, risk factors and biomarkers [J].
Reitz, Christiane ;
Mayeux, Richard .
BIOCHEMICAL PHARMACOLOGY, 2014, 88 (04) :640-651
[8]   Genetic and biochemical markers in patients with Alzheimer's disease support a concerted systemic iron homeostasis dysregulation [J].
Crespo, Angela C. ;
Silva, Bruno ;
Marques, Liliana ;
Marcelino, Erica ;
Maruta, Carolina ;
Costa, Sonia ;
Timoteo, Angela ;
Vilares, Arminda ;
Couto, Frederico Simoes ;
Faustino, Paula ;
Correia, Ana Paula ;
Verdelho, Ana ;
Porto, Graca ;
Guerreiro, Manuela ;
Herrero, Ana ;
Costa, Cristina ;
de Mendonca, Alexandre ;
Costa, Luciana ;
Martins, Madalena .
NEUROBIOLOGY OF AGING, 2014, 35 (04) :777-785
[9]   Epidemiology of a fast emerging disease in the Asia-Pacific region: non-alcoholic fatty liver disease [J].
Wah-Kheong, Chan ;
Khean-Lee, Goh .
HEPATOLOGY INTERNATIONAL, 2013, 7 (01) :65-71
[10]   Gender and Iron Genes May Modify Associations Between Brain Iron and Memory in Healthy Aging [J].
Bartzokis, George ;
Lu, Po H. ;
Tingus, Kathleen ;
Peters, Douglas G. ;
Amar, Chetan P. ;
Tishler, Todd A. ;
Finn, J. Paul ;
Villablanca, Pablo ;
Altshuler, Lori L. ;
Mintz, Jim ;
Neely, Elizabeth ;
Connor, James R. .
NEUROPSYCHOPHARMACOLOGY, 2011, 36 (07) :1375-1384