Department of Anatomy and Anthropology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Department of Epidemiology and Preventive Medicine, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
PLoS One. 2019 Feb 22;14(2):e0212464. doi: 10.1371/journal.pone.0212464. eCollection 2019.
Bone mineral density (BMD) and lipid levels are two of the most extensively studied risk factors for common diseases of aging, such as cardiovascular disease (CVD) and osteoporosis (OP). These two risk factors are also correlated with each other, but little is known about the molecular mechanisms behind this correlation. Recent studies revealed that circulating levels of several metabolites involved in the biosynthesis of androsterone correlate significantly with BMD and have the capacity to affect cholesterol and lipids levels. A main aim of the present study was to investigate the hypothesis that androsterone-related metabolites could provide a link between CVD and OP, as a common cause of lipid levels and BMD. The present study employed data from the NIHR BRC TwinsUK BioResource, comprising 1909 and 1994 monozygotic and dizygotic twin pairs, respectively, to address the causal relationships among BMD and lipids, and their associated metabolites, using reciprocal causation twin modelling, as well as Mendelian randomization (MR) using large publicly-available GWAS datasets on lipids and BMD, in conjunction with TwinsUK metabolite data. While results involving the twin modelling and MR analyses with metabolites were unable to establish a causal link between metabolite levels and either lipids or BMD, MR analyses of BMD and lipids suggest that lipid levels have a causal impact on BMD, which is consistent with findings from clinical trials of lipid-lowering drugs, which have also increased BMD.
骨密度(BMD)和血脂水平是研究最广泛的两种与衰老相关疾病的风险因素,如心血管疾病(CVD)和骨质疏松症(OP)。这两个风险因素也相互关联,但对于这种关联的分子机制知之甚少。最近的研究表明,几种参与雄甾酮生物合成的循环代谢物的水平与 BMD 显著相关,并且具有影响胆固醇和脂质水平的能力。本研究的主要目的是检验这样一个假设,即与雄甾酮相关的代谢物可以提供 CVD 和 OP 之间的联系,因为它们是脂质水平和 BMD 的共同原因。本研究利用了来自 NIHR BRC TwinsUK 生物资源的数据,其中分别包括 1909 年和 1994 年的同卵双胞胎和异卵双胞胎,采用双向因果关系双胞胎模型,以及使用大型公共脂质和 BMD GWAS 数据集进行的孟德尔随机化(MR),结合 TwinsUK 代谢物数据,研究了 BMD 和脂质及其相关代谢物之间的因果关系。虽然涉及代谢物的双胞胎模型和 MR 分析的结果未能确定代谢物水平与脂质或 BMD 之间的因果关系,但对 BMD 和脂质的 MR 分析表明,脂质水平对 BMD 有因果影响,这与降脂药物临床试验的结果一致,降脂药物也增加了 BMD。