Relationship between Adiponectin Gene Polymorphisms and Late-Onset Alzheimer's Disease

被引:20
作者
Yu, Zhuling [1 ]
Li, Wei [1 ,2 ]
Hou, Deren [1 ]
Zhou, Lin [3 ]
Deng, Yanyao [1 ]
Tian, Mi [1 ]
Feng, Xialu [1 ]
机构
[1] Cent S Univ, Dept Neurol, Xiangya Hosp 3, Changsha, Hunan, Peoples R China
[2] First Hosp Changsha, Dept Nerve Med Ctr, Changsha, Peoples R China
[3] Cent S Univ, Dept Geriatr Neurol, Xiangya Hosp, Changsha, Hunan, Peoples R China
来源
PLOS ONE | 2015年 / 10卷 / 04期
关键词
MILD COGNITIVE IMPAIRMENT; TYPE-2; DIABETES-MELLITUS; LINKAGE DISEQUILIBRIUM; INSULIN-RESISTANCE; METABOLIC SYNDROME; SERUM ADIPONECTIN; ASSOCIATION; VARIANTS; OBESITY; TRAITS;
D O I
10.1371/journal.pone.0125186
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In recent years, researchers have found that adiponectin (ANP) plays an important role in the pathogenesis of Alzheimer's disease (AD), and low serum concentrations of ANP are associated with AD. Higher plasma ANP level have a protective effect against the development of cognitive decline, suggesting that ANP may affect AD onset. Meanwhile, accumulating evidence supports the crucial role of ANP in the pathogenesis of AD. To study the relationship between ANP gene polymorphisms (rs266729, -11377C>G and rs1501299, G276T) and late-onset AD (LOAD), we carried out a case-control study that included 201 LOAD patients and 257 healthy control subjects. Statistically significant differences were detected in the genotype and allelotype frequency distributions of rs266729 and rs1501299 between the LOAD group and the control group, with a noticeable increase in the G and T allelotype frequency distributions in the LOAD group (P < 0.05). Logistic regression analysis using recessive model and additive model revealed that the rs266729 GG and rs1501299 TT genotypes are associated with a greater risk of LOAD. Haplotype analysis identified four haplotypes: CG, CT, GG, and GT. The frequencies of the CT and GG haplotypes were not significantly different (P > 0.05) between the LOAD group and control group, whereas the CG and GT haplotypes were significantly different (P < 0.05), suggesting a negative correlation between the CG haplotype and LOAD onset (OR = 0.74, 95% CI = 0.57-0.96, P = 0.022), and a positive correlation between the GT haplotype and LOAD onset (OR = 2.29, 95% CI = 1.42-3.68, P = 0.005). Therefore, we speculated that the rs266729 and rs1501299 of ANP gene polymorphisms and the GT and CG haplotypes were associated with LOAD.
引用
收藏
页数:11
相关论文
共 50 条
  • [21] The Relationship Between the Continuum of Elevated Adiposity, Hyperinsulinemia, and Type 2 Diabetes and Late-onset Alzheimer's Disease: An Epidemiological Perspective
    Luchsinger, Jose A.
    DIABETES, INSULIN AND ALZHEIMER'S DISEASE, 2010, : 89 - 107
  • [22] Meta-analysis of the association between CR1 polymorphisms and risk of late-onset Alzheimer's disease
    Luo, Jingrong
    Li, Shan
    Qin, Xue
    Song, Liuying
    Peng, Qiliu
    Chen, Siyuan
    Xie, Yantong
    Xie, Li
    Li, Taijie
    He, Yu
    Deng, Yan
    Wang, Jian
    Zeng, Zhiyu
    NEUROSCIENCE LETTERS, 2014, 578 : 165 - 170
  • [23] Roles of the Tau Gene Short Tandem Repeats in Late-Onset Alzheimer's Disease
    Dong, Shuai
    Chu, Lan
    Liu, Fang
    Xu, Zhu
    Li, Shirong
    Zhang, Yifan
    Wang, Hao
    Cai, Lijun
    Dai, Mingming
    INTERNATIONAL JOURNAL OF NEUROSCIENCE, 2012, 122 (05) : 271 - 276
  • [24] Amyloid Precursor Protein Gene (APP) Variation in Late-Onset Alzheimer's Disease
    Miar, Ana
    Alvarez, Victoria
    Corao, Ana I.
    Diaz, Marta
    Alonso, Belen
    Martinez, Carmen
    Calatayud, Maria T.
    Menendez, Manuel
    Moris, German
    Coto, Eliecer
    JOURNAL OF MOLECULAR NEUROSCIENCE, 2011, 45 (01) : 5 - 9
  • [25] ESTROGEN RECEPTOR ALPHA GENE POLYMORPHISMS IN PATIENTS WITH LATE ONSET ALZHEIMER'S DISEASE
    Sohrabifar, Nasim
    Gharesouran, Jalal
    Talebi, Mahnaz
    Ghojazadeh, Morteza
    Mohaddes Ardebili, Seiied Mojtaba
    GENETIKA-BELGRADE, 2014, 46 (02): : 437 - 444
  • [26] Type 2 Diabetes and Late-Onset Alzheimer's Disease
    Cheng, D.
    Noble, J.
    Tang, M. X.
    Schupf, N.
    Mayeux, R.
    Luchsinger, J. A.
    DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 2011, 31 (06) : 424 - 430
  • [27] Assessment of the genetic variance of late-onset Alzheimer's disease
    Ridge, Perry G.
    Hoyt, Kaitlyn B.
    Boehme, Kevin
    Mukherjee, Shubhabrata
    Crane, Paul K.
    Haines, Jonathan L.
    Mayeux, Richard
    Farrer, Lindsay A.
    Pericak-Vance, Margaret A.
    Schellenberg, Gerard D.
    Kauwe, John S. K.
    NEUROBIOLOGY OF AGING, 2016, 41
  • [28] ABCA7 and EphA1 Genes Polymorphisms in Late-Onset Alzheimer's Disease
    Talebi, Mahnaz
    Delpak, Azar
    Khalaj-kondori, Mohamad
    Sadigh-Eteghad, Saeed
    Talebi, Malihe
    Mehdizadeh, Elham
    Majdi, Alireza
    JOURNAL OF MOLECULAR NEUROSCIENCE, 2020, 70 (02) : 167 - 173
  • [29] Genetic discoveries and advances in late-onset Alzheimer's disease
    Rezazadeh, Maryam
    Hosseinzadeh, Hassan
    Moradi, Mohsen
    Esfahani, Behnaz Salek
    Talebian, Shahrzad
    Parvin, Shaho
    Gharesouran, Jalal
    JOURNAL OF CELLULAR PHYSIOLOGY, 2019, 234 (10) : 16873 - 16884
  • [30] Alpha-2 macroglobulin gene in early- and late-onset Alzheimer disease
    Korovaitseva, GI
    Premkumar, S
    Grigorenko, A
    Molyaka, Y
    Galimbet, V
    Selezneva, N
    Gavrilova, SI
    Farrer, LA
    Rogaev, EI
    NEUROSCIENCE LETTERS, 1999, 271 (02) : 129 - 131