Neurocognitive endophenotypes for bipolar disorder.

Full Abstract

OBJECTIVES: Neurocognitive deficits have been proposed as vulnerability markers or endophenotypes for the development of bipolar I disorder (BD I). However, few research studies have examined whether neurocognitive deficits also exist in first-degree relatives of individuals with BD I. METHODS: This prospective study examined neurocognitive function in individuals with BD I, their first-degree relatives and a normal control group using a comprehensive battery of neurocognitive tests. RESULTS: Results indicated that individuals with bipolar disorder and their unaffected relatives demonstrated neuropsychological deficits in comparison to the normal control group in the domains of visuospatial/constructional abilities, executive function, visual learning and memory, and motor speed. In general, the unaffected relatives demonstrated an intermediate level of performance in comparison to the normal control and bipolar group. After adjustment for mood symptoms, significant differences were present for the visuospatial/constructional, executive function, and motor domains. Individuals with bipolar disorder also demonstrated a differential right versus left hemisphere deficit with respect to neurocognitive tasks. CONCLUSIONS: Results suggest that deficits on specific neuropsychological tests, most notably Digit Symbol, Block Design and Judgment of Line Orientation, may be indicative of cognitive endophenotypes for bipolar disorder. Replication studies are needed to further identify these deficits as endophenotypes for BD I.

Author information

Author/s: Frantom, Linda V (LV); Allen, Daniel N (DN); Cross, Chad L (CL);

Affiliation: Department of Psychology, School of Public Health, University of Nevada, Las Vegas, NV 89154-5030, USA.

Journal and publication information

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal: Bipolar disorders (Bipolar Disord), published in Denmark. (Language: eng)

Reference: 2008-May; vol 10 (issue 3) : pp 387-99

Dates: Created 2008/04/11; Completed 2008/08/07;

PMID: 18402627, status: MEDLINE (last retrieval date: 2/18/2009, IMS Date: )

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