Pan Guanrui, Fu Qingan, Xu Yuan, Jiang Long
Department of Cardiovascular Medicine, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China.
Department of Medical Big Data Center, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China.
J Affect Disord. 2025 Apr 1;374:397-407. doi: 10.1016/j.jad.2025.01.038. Epub 2025 Jan 12.
Lipoprotein (a) [Lp(a)] is a biomarker of atherosclerotic cardiovascular disease, but its role in mental disorders is controversial. Our study aimed to explore the causality between Lp(a) levels and mental disorders by combining retrospective and Mendelian randomization (MR) studies.
All genome-wide association study datasets used in the MR study were obtained from UK Biobank, FinnGen, and the Psychiatric Genomics Consortium. The matched case-control study were based on electronic health records from the Second Affiliated Hospital of Nanchang University and NHANES III cohort.
In the MR analysis, Lp(a) had a positive causal effect on the longest period of depression [1.05 (1.02-1.08), P = 0.0001], the number of depressive episodes [1.03 (1.01-1.06), P = 0.009] and a weak negative effect on memory loss [0.84 (0.72-0.99), P = 0.039]. Meanwhile, bipolar and major depressive disorder status was causally associated with significantly lower Lp(a) levels [0.96 (0.93-0.98), P = 0.003]. Retrospective study revealed low Lp(a) levels were associated with a significantly higher risk of depression (n = 670) [1.273 (1.007, 1.609), P = 0.044], anxiety (n = 1284) [1.231 (1.041, 1.456), P = 0.015] and major depression (n = 538) [1.364 (1.012,1.841), P = 0.042].
This study found there is a causal relationship between the number and longest period of depressive episodes or memory loss and Lp(a), while bipolar disorder and major depressive disorder were associated with a significant causal effect on reduced Lp(a) levels. Future studies should focus on whether a sustained decrease in Lp(a) levels could cause the development of mental disorders, and which target value is suitable for clinical practice.
脂蛋白(a)[Lp(a)]是动脉粥样硬化性心血管疾病的生物标志物,但其在精神障碍中的作用存在争议。我们的研究旨在通过回顾性研究和孟德尔随机化(MR)研究相结合的方法,探讨Lp(a)水平与精神障碍之间的因果关系。
MR研究中使用的所有全基因组关联研究数据集均来自英国生物银行、芬兰基因库和精神疾病基因组学联盟。配对病例对照研究基于南昌大学第二附属医院的电子健康记录和美国国家健康与营养检查调查(NHANES)III队列。
在MR分析中,Lp(a)对最长抑郁期[1.05(1.02 - 1.08),P = 0.0001]、抑郁发作次数[1.03(1.01 - 1.06),P = 0.009]有正向因果效应,对记忆力减退有较弱的负向效应[0.84(0.72 - 0.99),P = 0.039]。同时,双相情感障碍和重度抑郁症状态与显著较低的Lp(a)水平存在因果关联[0.96(0.93 - 0.98),P = 0.003]。回顾性研究显示,低Lp(a)水平与抑郁症(n = 670)[1.273(1.007, 1.609),P = 0.044]、焦虑症(n = 1284)[1.231(1.041, 1.456),P = 0.015]和重度抑郁症(n = 538)[1.364(1.012, 1.841),P = 0.042]的风险显著升高相关。
本研究发现抑郁发作的次数和最长持续时间或记忆力减退与Lp(a)之间存在因果关系,而双相情感障碍和重度抑郁症与Lp(a)水平降低存在显著因果效应。未来的研究应关注Lp(a)水平的持续降低是否会导致精神障碍的发生,以及哪种目标值适用于临床实践。