A cross-sectional study of cognitive performance in bipolar disorder across the lifespan: the cog-BD project

被引:14
作者
Jones, Brett D. M. [1 ]
Fernandes, Brisa S. [1 ]
Husain, M. Ishrat [1 ,2 ]
Ortiz, Abigail [1 ,2 ]
Rajji, Tarek K. [1 ,2 ,3 ]
Blumberger, Daniel M. [1 ,2 ]
Butters, Meryl A. [4 ]
Gildengers, Ariel G. [4 ]
Shablinski, Tatiana [2 ]
Voineskos, Aristotle [1 ,2 ]
Mulsant, Benoit H. [1 ,2 ,3 ,4 ]
机构
[1] Univ Toronto, Temerty Fac Med, Dept Psychiat, Toronto, ON, Canada
[2] Ctr Addict & Mental Hlth, Campbell Family Res Inst, Toronto, ON, Canada
[3] Univ Toronto, Temerty Fac Med, Toronto Dementia Res Alliance, Toronto, ON, Canada
[4] Univ Pittsburgh, Dept Psychiatry, Pittsburgh, PA 15213 USA
基金
加拿大创新基金会; 美国国家卫生研究院; 加拿大健康研究院;
关键词
Bipolar disorder; cognition; geriatric psychiatry; mood disorder; LONGITUDINAL COURSE; RATING-SCALE; OLDER-ADULTS; METAANALYSIS; RELIABILITY; IMPAIRMENT; DEFICITS; BATTERY;
D O I
10.1017/S0033291722003622
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
BackgroundNeuroprogressive models of the trajectory of cognitive dysfunction in patients with bipolar disorder (BD) have been proposed. However, few studies have explored the relationships among clinical characteristics of BD, cognitive dysfunction, and aging. MethodsWe conducted a cross-sectional analysis in euthymic participants with the MATRICS Cognitive Consensus Battery, the Trail Making Test B, the Stroop Test, and the Wechsler Test of Adult Reading. Age- and gender-equated control participants without a mental disorder ['Healthy Controls' - HC)] were assessed similarly. We compared cognitive performance both globally and in seven domains in four groups: younger BD (age <= 49 years; n = 70), older BD (age > 50 years; n = 48), younger HC (n = 153), and older HC (n = 44). We also compared the BD and HC groups using age as a continuous measure. We controlled for relevant covariates and applied a Bonferroni correction. ResultsOur results support both an early impairment ('early hit') model and an accelerated aging model: impairment in attention/vigilance, processing speed, and executive function/working memory were congruent with the accelerated aging hypothesis whereas impairment in verbal memory was congruent with an early impairment model. BD and HC participants exhibited similar age-related decline in reasoning/problem solving and visuospatial memory. There were no age- or diagnosis-related differences in social cognition. ConclusionOur findings support that different cognitive domains are affected differently by BD and aging. Longitudinal studies are needed to explore trajectories of cognitive performance in BD across the lifespan.
引用
收藏
页码:6316 / 6324
页数:9
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