Beydoun May A, Nalls Michael A, Canas J Atilio, Evans Michele K, Zonderman Alan B
Laboratory of Epidemiology and Population Sciences, National Institute on Aging, NIH Biomedical Research Center,IRP 251, Bayview Boulevard, Suite 100, Room 04B118,Baltimore,MD21224,USA.
Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health,Bethesda,MD,USA.
Br J Nutr. 2014 Sep 28;112(6):992-1003. doi: 10.1017/S0007114514001706.
Gene polymorphisms provide a means to obtain unconfounded associations between carotenoids and various health outcomes. In the present study, we tested whether gene polymorphisms and gene scores linked to low serum carotenoid status are related to metabolic disturbance and depressive symptoms in African-American adults residing in Baltimore city, MD, using cross-sectional data from the Healthy Aging in Neighborhoods of Diversity across the Life Span study (age range 30-64 years, n 873-994). We examined twenty-four SNP of various gene loci that were previously shown to be associated with low serum carotenoid status (SNPlcar). Gene risk scores were created: five low specific-carotenoid risk scores (LSCRS: α-carotene, β-carotene, lutein+zeaxanthin, β-cryptoxanthin and lycopene) and one low total-carotenoid risk score (LTCRS: total carotenoids). SNPlcar, LSCRS and LTCRS were entered as predictors for a number of health outcomes. These included obesity, National Cholesterol Education Program Adult Treatment Panel III metabolic syndrome and its components, elevated homeostatic model assessment of insulin resistance, C-reactive protein, hyperuricaemia and elevated depressive symptoms (EDS, Center for Epidemiologic Studies-Depression score ≥ 16). Among the key findings, SNPlcar were not associated with the main outcomes after correction for multiple testing. However, an inverse association was found between the LTCRS and HDL-cholesterol (HDL-C) dyslipidaemia. Specifically, the α-carotene and β-cryptoxanthin LSCRS were associated with a lower odds of HDL-C dyslipidaemia. However, the β-cryptoxanthin LSCRS was linked to a higher odds of EDS, with a linear dose-response relationship. In summary, gene risk scores linked to low serum carotenoids had mixed effects on HDL-C dyslipidaemia and EDS. Further studies using larger African-American population samples are needed.
基因多态性为获取类胡萝卜素与各种健康结局之间无混杂因素的关联提供了一种手段。在本研究中,我们利用来自“全生命周期多元社区健康老龄化”研究(年龄范围30 - 64岁,n = 873 - 994)的横断面数据,测试了与低血清类胡萝卜素状态相关的基因多态性和基因评分是否与居住在马里兰州巴尔的摩市的非裔美国成年人的代谢紊乱和抑郁症状有关。我们检测了先前显示与低血清类胡萝卜素状态相关的24个不同基因位点的单核苷酸多态性(SNPlcar)。创建了基因风险评分:五个低特异性类胡萝卜素风险评分(LSCRS:α - 胡萝卜素、β - 胡萝卜素、叶黄素 + 玉米黄质、β - 隐黄质和番茄红素)和一个低总类胡萝卜素风险评分(LTCRS:总类胡萝卜素)。将SNPlcar、LSCRS和LTCRS作为多种健康结局的预测指标。这些结局包括肥胖、美国国家胆固醇教育计划成人治疗小组第三次报告定义的代谢综合征及其组分、胰岛素抵抗稳态模型评估升高、C反应蛋白、高尿酸血症以及抑郁症状加重(流行病学研究中心抑郁评分≥16)。在主要研究结果中,经多重检验校正后,SNPlcar与主要结局无关。然而,发现LTCRS与高密度脂蛋白胆固醇(HDL - C)血脂异常呈负相关。具体而言,α - 胡萝卜素和β - 隐黄质LSCRS与HDL - C血脂异常的较低几率相关。然而,β - 隐黄质LSCRS与抑郁症状加重的较高几率相关,且呈线性剂量反应关系。总之,与低血清类胡萝卜素相关的基因风险评分对HDL - C血脂异常和抑郁症状加重有混合效应。需要使用更大规模的非裔美国人群样本进行进一步研究。