Longitudinal analysis of cognitive performances in recent-onset and late-life Bipolar Disorder: A systematic review and meta-analysis

被引:36
作者
Szmulewicz, Alejandro [1 ,2 ,3 ]
Valerio, Marina P. [2 ,4 ]
Martino, Diego J. [4 ,5 ]
机构
[1] Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
[2] Favaloro Univ, Neurosci Inst, Bipolar Disorder Program, Buenos Aires, DF, Argentina
[3] Univ Buenos Aires, Dept Pharmacol, Buenos Aires, DF, Argentina
[4] Natl Council Sci & Tech Res CONICET, Buenos Aires, DF, Argentina
[5] Favaloro Univ, INECO Fdn, Inst Cognit & Translat Neurosci INCyT, Buenos Aires, DF, Argentina
关键词
bipolar disorder; cognition; cognitive impairments; longitudinal studies; meta-analysis; 5-YEAR FOLLOW-UP; OLDER-ADULTS; EUTHYMIC PATIENTS; NEUROCOGNITIVE SUBTYPES; INTERNATIONAL SOCIETY; HEALTHY CONTROLS; STAGING MODEL; BRAIN CHANGES; NEUROPROGRESSION; SCHIZOPHRENIA;
D O I
10.1111/bdi.12841
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives Neurocognitive deficits have been widely reported in euthymic Bipolar Disorder (BD) patients and contribute to functional disability. However, the longitudinal trajectory of these deficits remains a subject of debate. Although most research to this date shows that neurocognitive deficits tend to be stable among middle-age BD patients, it remains plausible that deterioration occurs at either early or late stages of this condition. Methods We conducted a comprehensive meta-analysis of studies that reported longitudinal neurocognitive performance among individuals with BD either within the year of their diagnosis or among late-life BD patients. Pooled effects of standardized mean differences (SMDs) for changes in neuropsychological scores over follow-up were estimated using random effects model. We also examined effect moderators, such as length of follow-up, mood state, or pharmacological load. Results Eight studies met inclusion criteria for recent-onset and four studies for late-life BD analysis. No evidence for a deterioration in neurocognitive functioning was observed among recent-onset BD patients (8 studies, 284 patients, SMD: 0.12, 95% CI -0.06 to 0.30, mean follow-up: 17 months) nor for late-life BD patients (4 studies, 153 patients, SMD: -0.35, 95% CI -0.84 to 0.15, mean follow-up: 33 months). None of the moderators were shown to be significant. Conclusions These results, when appraised together with the findings in middle-life BD patients and individuals at genetic risk for BD, suggest that neurodevelopmental factors might play a significant role in cognitive deficits in BD and do not support the notion of progressive cognitive decline in most patients with BD.
引用
收藏
页码:28 / 37
页数:10
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