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Bipolar I and bipolar II subtypes in older age: Results from the Global Aging and Geriatric Experiments in Bipolar Disorder (GAGE-BD) project
被引:10
|作者:
Beunders, Alexandra J. M.
[1
,2
,3
]
Klaus, Federica
[4
,5
]
Kok, Almar A. L.
[1
,2
,3
]
Schouws, Sigfried N. T. M.
[1
,2
,3
]
Kupka, Ralph W.
[1
,2
,3
]
Blumberg, Hilary P.
[6
]
Briggs, Farren
[7
]
Eyler, Lisa T.
[4
,5
]
Forester, Brent P.
[8
,9
]
Forlenza, Orestes, V
[10
]
Gildengers, Ariel
[11
]
Jimenez, Esther
[12
]
Mulsant, Benoit H.
[13
]
Patrick, Regan E.
[8
,9
]
Rej, Soham
[14
,15
]
Sajatovic, Martha
[16
]
Sarna, Kaylee
[16
]
Sutherland, Ashley
[4
,5
]
Yala, Joy
[16
]
Vieta, Eduard
[12
]
Villa, Luca M.
[6
,17
]
Korten, Nicole C. M.
[1
,2
,3
]
Dols, Annemieke
[1
,2
,3
,18
,19
]
机构:
[1] GGZ InGeest Specialized Mental Hlth Care, Old Age Psychiat, Oldenaller 1, NL-1081 HJ Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Psychiat, Amsterdam UMC Locat, Amsterdam, Netherlands
[3] Amsterdam Publ Hlth Res Inst, Mental Hlth, Amsterdam, Netherlands
[4] Univ Calif San Diego, Dept Psychiat, San Diego, CA 92103 USA
[5] VA San Diego Healthcare Syst, Desert Pacific Mental Illness Res Educ & Clin Ctr, San Diego, CA USA
[6] Yale Sch Med, Dept Psychiat, New Haven, CT USA
[7] Case Western Reserve Univ, Dept Populat & Quantitat Hlth Sci, Sch Med, Cleveland, OH USA
[8] McLean Hosp, Div Geriatr Psychiat, Belmont, MA USA
[9] Harvard Med Sch, Boston, MA USA
[10] Univ Sao Paulo HCFMUSP, Dept & Inst Psychiat, Lab Neurosci LIM27, Hosp Clin,Fac Med, Sao Paulo, Brazil
[11] Univ Pittsburgh, Dept Psychiat, Sch Med, Pittsburgh, PA USA
[12] Univ Barcelona, Hosp Clin, Bipolar & Depress Disorders Unit, CIBERSAM,IDIBAPS, Barcelona, Spain
[13] Univ Toronto, Ctr Addict & Mental Hlth, Dept Psychiat, Toronto, ON, Canada
[14] Jewish Gen Hosp, GeriPARTy Res Grp, Lady Davis Inst, Montreal, PQ, Canada
[15] McGill Univ, Montreal, PQ, Canada
[16] Case Western Reserve Univ, Univ Hosp Case Med Ctr, Sch Med, Cleveland, OH USA
[17] Univ Oxford, Dept Psychiat, Oxford, England
[18] Amsterdam Neurosci, Neurodegenerat, Amsterdam, Netherlands
[19] Univ Med Ctr Utrecht, UMC Utrecht Brain Ctr, Dept Psychiat, Utrecht, Netherlands
基金:
巴西圣保罗研究基金会;
英国医学研究理事会;
关键词:
bipolar disorder;
cognition;
comorbidities;
diagnostic subtypes;
elderly;
functioning;
geriatrics;
impairment;
older-age bipolar disorder (OABD);
psychiatry;
MEDICAL ILLNESS;
RATING-SCALE;
PREVALENCE;
COHORT;
COMORBIDITIES;
VALIDITY;
FEATURES;
D O I:
10.1111/bdi.13271
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Objectives: The distinction between bipolar I disorder (BD-I) and bipolar II disorder (BD-II) has been a topic of long-lasting debate. This study examined differences between BD-I and BD-II in a large, global sample of OABD, focusing on general functioning, cognition and somatic burden as these domains are often affected in OABD. Methods: Cross-sectional analyses were conducted with data from the Global Aging and Geriatric Experiments in Bipolar Disorder (GAGE-BD) database. The sample included 963 participants aged >= 50 years (714 BD-I, 249 BD-II). Sociodemographic and clinical factors were compared between BD subtypes including adjustment for study cohort. Multivariable analyses were conducted with generalized linear mixed models (GLMMs) and estimated associations between BD subtype and (1) general functioning (GAF), (2) cognitive performance (g-score) and (3) somatic burden, with study cohort as random intercept. Results: After adjustment for study cohort, BD-II patients more often had a late onset >= 50 years (p = 0.008) and more current severe depression (p = 0.041). BD-I patients were more likely to have a history of psychiatric hospitalization (p < 0.001) and current use of anti-psychotics (p = 0.003). Multivariable analyses showed that BD subtype was not related to GAF, cognitive g-score or somatic burden. Conclusion: BD-I and BD-II patients did not differ in terms of general functioning, cognitive impairment or somatic burden. Some clinical differences were observed between the groups, which could be the consequence of diagnostic definitions. The distinction between BD-I and BD-II is not the best way to subtype OABD patients. Future research should investigate other disease specifiers in this population.
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页码:43 / 55
页数:13
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