The potential role of gray matter volume differences in the association between smoking and depression: A narrative review

被引:2
|
作者
van de Weijer, Margot P. [1 ,4 ]
Vermeulen, Jentien [1 ]
Schrantee, Anouk [2 ]
Munafo, Marcus R. [3 ]
Verweij, Karin J. H. [1 ]
Treur, Jorien L. [1 ]
机构
[1] Univ Amsterdam, Amsterdam Univ Med Ctr, Dept Psychiat, Amsterdam, Netherlands
[2] Amsterdam Univ Med Ctr, Univ Amsterdam, Dept Radiol & Nucl Med, Amsterdam, Netherlands
[3] Univ Bristol, Sch Psychol Sci, Bristol, England
[4] Dept Psychiat, Genet Epidemiol, Amsterdam UMC locat AMC, Meibergdreef 5, NL-1105 AZ Amsterdam, Netherlands
来源
基金
欧洲研究理事会;
关键词
Depression; Smoking; Neuroimaging; Brain volume; Causality; MAJOR DEPRESSION; MENDELIAN RANDOMIZATION; HIPPOCAMPAL VOLUME; CIGARETTE-SMOKING; NICOTINE EXPOSURE; RISK-FACTORS; BRAIN; METAANALYSIS; DISORDER; SYSTEM;
D O I
10.1016/j.neubiorev.2023.105497
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Tobacco use and major depression are both leading contributors to the global burden of disease and are also highly comorbid. Previous research indicates bi-directional causality between tobacco use and depression, but the mechanisms that underlie this causality are unclear, especially for the causality from tobacco use to depression. Here we narratively review the available evidence for a potential causal role of gray matter volume in the association. We summarize the findings of large existing neuroimaging meta-analyses, studies in UK Biobank, and the Enhancing NeuroImaging Genetics through MetaAnalysis (ENIGMA) consortium and assess the overlap in implicated brain areas. In addition, we review two types of methods that allow us more insight into the causal nature of associations between brain volume and depression/smoking: longitudinal studies and Mendelian Randomization studies. While the available evidence suggests overlap in the alterations in brain volumes implicated in tobacco use and depression, there is a lack of research examining the underlying pathophysiology. We conclude with recommendations on (genetically-informed) causal inference methods useful for studying these associations.
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收藏
页数:12
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