Adiposity and the risk of dementia: mediating effects from inflammation and lipid levels.

Adiposity and the risk of dementia: mediating effects from inflammation and lipid levels.
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肥胖和痴呆症的风险:炎症和脂质水平的介导作用。

DOI:
10.1007/s10654-022-00918-w
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发表时间:
2022-12
影响因子:
13.6
通讯作者:
Reynolds, Chandra A.
Reynolds, Chandra A.
中科院分区:
医学1区
文献类型:
--
作者:
Karlsson, Ida K.;Zhan, Yiqiang;Wang, Yunzhang;Li, Xia;Jylhava, Juulia;Hagg, Sara;Aslan, Anna K. Dahl;Gatz, Margaret;Pedersen, Nancy L.;Reynolds, Chandra A.

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虽然中年肥胖是痴呆症的一个危险因素,但晚年肥胖似乎与较低的风险有关。人们对这种联系的驱动力知之甚少,尤其是晚年的逆联系。利用全基因组关联研究的结果,我们确定炎症和脂质代谢是肥胖和痴呆的生物学途径。为了测试这些因素是否介导中年和/或晚年肥胖对痴呆的影响,我们使用了瑞典双胞胎登记处的队列数据,测量了中年(40-64岁,n = 5999)或晚年(65-90岁,n = 7257)的肥胖和潜在介质。在生存和中介分析中,对体重指数(BMI)、腰臀比(WHR)、C反应蛋白(CRP)、血脂水平和痴呆之间的关系进行了检验。在所有模型中,年龄被用作基础时间尺度,性别和教育被用作协变量。空腹状态作为协变量纳入血脂模型。中年WHR高一个标准差(SD)与痴呆风险高25%(95%CI 2-52%)相关,当调整BMI时略有衰减。没有证据表明通过CRP或脂质水平的调解。65岁以后,BMI高一个SD,而不是WHR,与痴呆风险降低8%(95%CI 1-14%)相关。这种关联部分是由较高的CRP介导的,当高密度脂蛋白水平较低时,这种关联被抑制。总之,中年肥胖对痴呆风险的负面影响是由与体脂分布相关的因素直接驱动的,没有证据表明通过炎症或脂质水平进行调解。晚年肥胖和痴呆风险之间存在负相关,特别是在身体的炎症反应和脂质稳态完好无损的情况下。在线版本包含补充材料,可通过10.1007/s10654-022-00918-w获得。
While midlife adiposity is a risk factor for dementia, adiposity in late-life appears to be associated with lower risk. What drives the associations is poorly understood, especially the inverse association in late-life. Using results from genome-wide association studies, we identified inflammation and lipid metabolism as biological pathways involved in both adiposity and dementia. To test if these factors mediate the effect of midlife and/or late-life adiposity on dementia, we then used cohort data from the Swedish Twin Registry, with measures of adiposity and potential mediators taken in midlife (age 40–64, n = 5999) or late-life (age 65–90, n = 7257). Associations between body-mass index (BMI), waist-hip ratio (WHR), C-reactive protein (CRP), lipid levels, and dementia were tested in survival and mediation analyses. Age was used as the underlying time scale, and sex and education included as covariates in all models. Fasting status was included as a covariate in models of lipids. One standard deviation (SD) higher WHR in midlife was associated with 25% (95% CI 2–52%) higher dementia risk, with slight attenuation when adjusting for BMI. No evidence of mediation through CRP or lipid levels was present. After age 65, one SD higher BMI, but not WHR, was associated with 8% (95% CI 1–14%) lower dementia risk. The association was partly mediated by higher CRP, and suppressed when high-density lipoprotein levels were low. In conclusion, the negative effects of midlife adiposity on dementia risk were driven directly by factors associated with body fat distribution, with no evidence of mediation through inflammation or lipid levels. There was an inverse association between late-life adiposity and dementia risk, especially where the body’s inflammatory response and lipid homeostasis is intact. The online version contains supplementary material available at 10.1007/s10654-022-00918-w.
DOI: 10.1038/s41586-018-0579-z
发表时间: 2018-10
期刊: Nature
影响因子: 64.8
作者:
Bycroft C;Freeman C;Petkova D;Band G;Elliott LT;Sharp K;Motyer A;Vukcevic D;Delaneau O;O'Connell J;Cortes A;Welsh S;Young A;Effingham M;McVean G;Leslie S;Allen N;Donnelly P;Marchini J
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DOI: 10.1093/hmg/ddy327
发表时间: 2019-01-01
影响因子: 3.5
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DOI: 10.1002/ana.25396
发表时间: 2019-02-01
影响因子: 11.2
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通讯作者: Witte, A. Veronica
DOI: 10.1080/13825580490511152
发表时间: 2004-06-01
影响因子: 1.9
作者:
Finkel, D;Pedersen, NL
通讯作者: Pedersen, NL
DOI: 10.1038/nature14177
发表时间: 2015-02-12
期刊: NATURE
影响因子: 64.8
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Locke, Adam E.;Kahali, Bratati;Berndt, Sonja I.;Justice, Anne E.;Pers, Tune H.;Day, Felix R.;Powell, Corey;Vedantam, Sailaja;Buchkovich, Martin L.;Yang, Jian;Croteau-Chonka, Damien C.;Esko, Tonu;Fall, Tove;Ferreira, Teresa;Gustafsson, Stefan;Kutalik, Zoltan;Luan, Jian'an;Maegi, Reedik;Randall, Joshua C.;Winkler, Thomas W.;Wood, Andrew R.;Workalemahu, Tsegaselassie;Faul, Jessica D.;Smith, Jennifer A.;Zhao, Jing Hua;Zhao, Wei;Chen, Jin;Fehrmann, Rudolf;Hedman, Asa K.;Karjalainen, Juha;Schmidt, Ellen M.;Absher, Devin;Amin, Najaf;Anderson, Denise;Beekman, Marian;Bolton, Jennifer L.;Bragg-Gresham, L.;Buyske, Steven;Demirkan, Ayse;Deng, Guohong;Ehret, Georg B.;Feenstra, Bjarke;Feitosa, Mary F.;Fischer, Krista;Goel, Anuj;Gong, Jian;Jackson, Anne U.;Kanoni, Stavroula;Kleber, Marcus E.;Kristiansson, Kati;Lim, Unhee;Lotay, Vaneet;Mangino, Massimo;Leach, Irene Mateo;Medina-Gomez, Carolina;Medland, Sarah E.;Nalls, Michael A.;Palmer, Cameron D.;Pasko, Dorota;Pechlivanis, Sonali;Peters, Marjolein J.;Prokopenko, Inga;Shungin, Dmitry;Stancakova, Alena;Strawbridge, Rona J.;Sung, Yun Ju;Tanaka, Toshiko;Teumer, Alexander;Trompet, Stella;van der Laan, Sander W.;van Settee, Jessica;Van Vliet-Ostaptchouk, Jana V.;Wang, Zhaoming;Yengo, Loic;Zhang, Weihua;Isaacs, Aaron;Albrecht, Eva;Arnlov, Johan;Arscott, Gillian M.;Attwood, Antony P.;Bandinelli, Stefania;Barrett, Amy;Bas, Isabelita N.;Bellis, Claire;Bennett, Amanda J.;Berne, Christian;Blagieva, Roza;Blueher, Matthias;Bohringer, Stefan;Bonnycastle, Lori L.;Boettcher, Yvonne;Boyd, Heather A.;Bruinenberg, Marcel;Caspersen, Ida H.;Chen, Yii-Der Ida;Clarke, Robert;Daw, E. 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通讯作者: Speliotes, Elizabeth K.