How lipids may affect risk for suicidal behavior

被引:36
|
作者
Daray, Federico M. [1 ]
Mann, J. John [2 ,3 ,4 ]
Sublette, M. Elizabeth [2 ,3 ]
机构
[1] Univ Buenos Aires, Sch Med, Inst Pharmacol, Paraguay 2155,Piso 9,C1121ABG, Buenos Aires, DF, Argentina
[2] Columbia Univ, Dept Psychiat, 1051 Riverside Dr, New York, NY 10032 USA
[3] New York State Psychiat Inst & Hosp, Div Mol Imaging & Neuropathol, 1051 Riverside Dr,Unit 42, New York, NY 10032 USA
[4] Columbia Univ, Dept Radiol, 622 West 168th St, New York, NY 10032 USA
关键词
POLYUNSATURATED FATTY-ACIDS; PLASMA EICOSAPENTAENOIC ACID; MAJOR DEPRESSIVE DISORDER; BLOOD-CELL MEMBRANES; ALTERS SERUM N-3; NF-KAPPA-B; DOCOSAHEXAENOIC-ACID; SEROTONIN BINDING; STATIN TREATMENT; ADIPOSE-TISSUE;
D O I
10.1016/j.jpsychires.2018.06.007
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Suicide and nonfatal suicidal behaviors are major causes of mortality and morbidity worldwide. Variability in rates of suicide and suicidal behaviors within and between countries has been attributed to population and individual risk factors, including economic status and cultural differences, both of which can have suicide risk effects mediated through a variety of factors, of which perhaps the least understood is the role of diet. We therefore review the scientific literature concerning two major dietary lipid classes, cholesterol and polyunsaturated fatty acids (PUFAs), that have been associated with higher risk of suicide attempts and suicide. We consider potential mechanistic intermediates including serotonin transporters and receptors, toll-like receptors (TLRs), nuclear factor kappa-light-chain-enhancer of activated B cells (NF kappa B), and peroxisome proliferator activated receptors (PPARs). Based on this review, we describe a theoretical model linking cholesterol and PUFA status to suicide risk, taking into account the effects of cholesterol-lowering interventions on PUFA balance, membrane lipid microdomains (rafts) as a nexus of interaction between cholesterol and omega-3 PUFAs, and downstream effects on serotonergic neurotransmission and specific inflammatory pathways.
引用
收藏
页码:16 / 23
页数:8
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