Cognitive subgroups in first episode bipolar I disorder: Relation to clinical and brain volumetric variables

心理学 认知 大脑大小 言语记忆 智商 睡眠剥夺对认知功能的影响 听力学 工作记忆 双相情感障碍 白质 内科学 精神科 医学 磁共振成像 放射科
作者
Trisha Chakrabarty,Ivan J. Torres,Weizhong Su,Richard Sawatzky,Kamyar Keramatian,Lakshmi N. Yatham
出处
期刊:Acta Psychiatrica Scandinavica [Wiley]
卷期号:143 (2): 151-161 被引量:32
标识
DOI:10.1111/acps.13245
摘要

Abstract Objective Distinct cognitive subgroups are seen in patients with long duration bipolar I disorder (BDI), possibly reflective of underlying pathophysiological differences. It is unknown whether such cognitive heterogeneity is present at illness onset. We applied latent class analysis (LCA) to cognitive test scores in first episode BDI patients. Exploratory analysis elucidated whether impaired subgroups were characterized by ‘early neurodevelopmental’ (low premorbid IQ and intracranial volume) versus ‘later neurodevelopmental’ (decline from premorbid to current IQ, changes in relative grey (GM)/white (WM) matter volumes) pathology. Methods Recently recovered first manic episode BDI patients ( n = 91) and healthy controls (HC, n = 63) comprised the study sample. LCA identified subgroups based on processing speed, verbal memory, non‐verbal memory, executive functioning, attention and working memory scores. Subgroups were compared amongst each other and HC on premorbid/current IQ, intracranial (ICV), total brain and regional volumes. Results Three cognitive subgroups emerged: (i) globally impaired (GI, n = 31), scoring 0.5‐1 SD below demographically corrected norms across domains, (ii) selectively impaired (SI, n = 47), with predominant processing speed deficits and (iii) high performing (HP, n = 13), with above‐average cognitive performance. GI patients showed a ‘later neurodevelopmental’ pattern, with normal ICV, significant decline from premorbid to current IQ, higher total GM and lower total WM (with respect to total brain volume) versus SI and HC ( p = 0.003). GI patients had higher left frontal pole GM versus HC ( p < 0.05, FWE corrected). Conclusions A globally impaired patient subgroup is identifiable in first episode BDI, possibly characterized by unique neurodevelopmental pathologic processes proximal to illness onset.
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