A meta-analytic investigation of neurocognitive deficits in bipolar illness: profile and effects of clinical state.
A meta-analytic investigation of neurocognitive deficits in bipolar illness: profile and effects of clinical state.
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DOI:
10.1037/a0016277
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发表时间:
2009-09
期刊:
影响因子:
2.4
通讯作者:
Gerraty, Raphael T.
中科院分区:
文献类型:
--
作者:
Kurtz, Matthew M.;Gerraty, Raphael T.
A meta-analysis of neuropsychological studies of patients with bipolar disorder in euthymic, manic/mixed or depressed phases of illness was conducted. Measures of attention, working memory, verbal and non-verbal memory, visuospatial function, psychomotor speed, language, and executive-function were evaluated in 42 studies of 1197 patients in euthymia, 13 studies consisting of 314 patients in a manic/mixed phase of illness, and 5 studies of 96 patients in a depressed state. Cohen d-values were calculated for each study as the mean difference between patient and control group score on each neuropsychological measure, expressed in pooled standard deviation units. Results for patients in euthymic, depressed and manic/mixed phases were evaluated separately and then a subset of measures on which patients in all three phases were tested were compared. For euthymia, results revealed impairment across all neuropsychological domains, with d-values in the moderate-large range (d=.5–.8) for the vast majority of measures. There was evidence of large effect-size impairment on measures of verbal learning (d=.81), and delayed verbal and non-verbal memory (d=.80-.92), while effect-size impairment on measures of visuospatial function was small-to-moderate (d≤.55). Patients tested during a manic/mixed or depressed phase of illness showed exaggerated impairment on measures of verbal learning, while patients tested during a depressed phase showed greater decrement on measures of phonemic fluency. Consistent with previous meta-analyses (Arts et al, 2007; Bora et al., 2009; Robinson et al., 2007), these results suggest that bipolar illness during euthymia is characterized by generalized moderate level impairment across an array of neurocognitive domains, with particular marked impairment in verbal learning and memory. These results also show that a subset of these deficits moderately worsen during acute disease states.
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