Low LDL cholesterol, PCSK9 and HMGCR genetic variation, and risk of Alzheimer's disease and Parkinson's disease: Mendelian randomisation study

被引:90
作者
Benn, Marianne [1 ,2 ,3 ]
Nordestgaard, Borge G. [2 ,3 ,4 ,5 ]
Frikke-Schmidt, Ruth [1 ,2 ,3 ,5 ]
Tybjrg-Hansen, Anne [1 ,2 ,3 ,5 ]
机构
[1] Copenhagen Univ Hosp, Dept Clin Biochem, Rigshosp, Blegdamsvej 3, DK-2100 Copenhagen, Denmark
[2] Copenhagen Univ Hosp, Herlev & Gentofte Hosp, Copenhagen Gen Populat Study, Copenhagen, Denmark
[3] Univ Copenhagen, Fac Hlth & Med Sci, Copenhagen, Denmark
[4] Copenhagen Univ Hosp, Herlev & Gentofte Hosp, Dept Clin Biochem, Copenhagen, Denmark
[5] Copenhagen Univ Hosp, Frederiksberg Hosp, Copenhagen City Heart Study, Copenhagen, Denmark
来源
BMJ-BRITISH MEDICAL JOURNAL | 2017年 / 357卷
关键词
BODY-MASS INDEX; STATIN THERAPY; REDUCING LIPIDS; METAANALYSIS; EFFICACY; SAFETY; INSTRUMENTS; DEMENTIA; MUTATIONS; PEOPLE;
D O I
10.1136/bmj.j1648
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE To test the hypothesis that low density lipoprotein (LDL) cholesterol due to genetic variation in the genes responsible for LDL cholesterol metabolism and biosynthesis(PCSK9 and 3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR), respectively) is associated with a high risk of Alzheimer's disease, vascular dementia, any dementia, and Parkinson's disease in the general population. DESIGN Mendelian randomisation study. SETTING Copenhagen General Population Study and Copenhagen City Heart Study. PARTICIPANTS 111 194 individuals from the Danish general population. MAIN OUTCOME MEASURES Risk of Alzheimer's disease, vascular dementia, all dementia, and Parkinson's disease. RESULTS In observational analyses, the multifactorially adjusted hazard ratio for Parkinson's disease in participants with an LDL cholesterol level <1.8 mmol/L versus >= 4.0 mmol/L was 1.70 (95% confidence interval 1.03 to 2.79), whereas the corresponding hazard ratios for Alzheimer's disease, vascular dementia, or any dementia did not differ from 1.0. PCSK9 and HMGCR variants combined were associated with a 9.3% lower LDL cholesterol level. In genetic, causal analyses adjusted for age, sex, and year of birth, the risk ratios for a lifelong 1 mmol/L lower LDL cholesterol level were 0.57 (0.27 to 1.17) for Alzheimer's disease, 0.81 (0.34 to 1.89) for vascular dementia, 0.66 (0.34 to 1.26) for any dementia, and 1.02 (0.26 to 4.00) for Parkinson's disease. Summary level data from the International Genomics of Alzheimer's Project using Egger Mendelian randomisation analysis gave a risk ratio for Alzheimer's disease of 0.24 (0.02 to 2.79) for 26 PCSK9 and HMGCR variants, and of 0.64 (0.52 to 0.79) for 380 variants of LDL cholesterol level lowering. CONCLUSION Low LDL cholesterol levels due to PCSK9 and HMGCR variants had no causal effect on high risk of Alzheimer's disease, vascular dementia, any dementia, or Parkinson's disease; however, low LDL cholesterol levels may have a causal effect in reducing the risk of Alzheimer's disease.
引用
收藏
页数:11
相关论文
共 50 条
  • [31] Exploring the association between air pollution and Parkinson's disease or Alzheimer's disease: a Mendelian randomization study
    Ning, Pingping
    Guo, Xingzhi
    Qu, Qiumin
    Li, Rui
    ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH, 2023, 30 (59) : 123925 - 123938
  • [32] Life Course Adiposity and Alzheimer's Disease: A Mendelian Randomization Study
    Li, Xian
    Tian, Yan
    Yang, Yu-Xiang
    Ma, Ya-Hui
    Shen, Xue-Ning
    Chen, Shi-Dong
    Dong, Qiang
    Tan, Lan
    Yu, Jin-Tai
    JOURNAL OF ALZHEIMERS DISEASE, 2021, 82 (02) : 503 - 512
  • [33] Genetic Polymorphisms in the HMGCR Gene and Associations with Cognitive Decline in Parkinson's Disease Patients
    Pierzchlinska, Anna
    Slawek, Jaroslaw
    Kwasniak-Butowska, Magdalena
    Malinowski, Damian
    Komaniecka, Nina
    Mak, Monika
    Czerkawska, Anna
    Kukowka, Arnold
    Bialecka, Monika
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2024, 25 (16)
  • [34] A Possible Role for HMG-CoA Reductase Inhibitors and Its Association with HMGCR Genetic Variation in Parkinson's Disease
    Pierzchlinska, Anna
    Drozdzik, Marek
    Bialecka, Monika
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (22)
  • [35] Use of genetic variation to separate the effects of early and later life adiposity on disease risk: mendelian randomisation study
    Richardson, Tom G.
    Sanderson, Eleanor
    Elsworth, Benjamin
    Tilling, Kate
    Smith, George Davey
    BMJ-BRITISH MEDICAL JOURNAL, 2020, 369
  • [36] Plasma urate and risk of Parkinson's disease: A mendelian randomization study
    Kobylecki, Camilla J.
    Nordestgaard, Borge G.
    Afzal, Shoaib
    ANNALS OF NEUROLOGY, 2018, 84 (02) : 178 - 190
  • [37] Childhood obesity and risk of Alzheimer’s disease: a Mendelian randomization study
    Wenxiang Qing
    Yujie Qian
    Archives of Public Health, 82
  • [38] Effects of PCSK9 genetic variants on plasma LDL cholesterol levels and risk of premature myocardial infarction in the Italian population
    Guella, Ilaria
    Asselta, Rosanna
    Ardissino, Diego
    Merlini, Pier Angelica
    Peyvandi, Flora
    Kathiresan, Sekar
    Mannucci, Pier Mannuccio
    Tubaro, Marco
    Duga, Stefano
    JOURNAL OF LIPID RESEARCH, 2010, 51 (11) : 3342 - 3349
  • [39] Effects of Alzheimer's genetic risk scores and CSF biomarkers in de novo Parkinson's Disease
    Lee, Young-Gun
    Jeong, Seong Ho
    Park, Mincheol
    Kang, Sung Woo
    Baik, Kyoungwon
    Jeon, Seun
    Lee, Phil Hyu
    Sohn, Young Ho
    Ye, Byoung Seok
    NPJ PARKINSONS DISEASE, 2022, 8 (01)
  • [40] Total Cholesterol and APOE-Related Risk for Alzheimer's Disease in the Alzheimer's Disease Neuroimaging Initiative
    Dunk, Michelle M.
    Driscoll, Ira
    JOURNAL OF ALZHEIMERS DISEASE, 2022, 85 (04) : 1519 - 1528