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Clinical correlates of late‐onset versus early‐onset bipolar disorder in a global sample of older adults

Paola Lavín, Gabriella Buck, Osvaldo P. Almeida, Chien‐Lin Su, Lisa T. Eyler, Annemiek Dols, Hilary P. Blumberg, Brent P. Forester, Orestes Vicente Forlenza, Ariel Gildengers, Benoit H. Mulsant, Shang‐Ying Tsai, Eduard Vieta, Sigfried Schouws, Farren Briggs, Ashley Sutherland, Kaylee Sarna, Joy Yala, Melis Orhan, Nicole Korten, Martha Sajatovic, Soham Rej, GAGE‐BD Investigators

2022International Journal of Geriatric Psychiatry19 citationsDOIOpen Access PDF

Abstract

OBJECTIVES: Late-onset bipolar disorder (LOBD) represents a significant subgroup of bipolar disorder (BD). However, knowledge for this group is mostly extrapolated from small studies in subjects with early/mixed age of illness onset. In this global sample of older adults with BD (OABD: ≥50 years old) we aim to characterize the sociodemographic and clinical presentation of LOBD (≥40 years at BD onset) compared to early-onset BD (EOBD: <40 years at BD onset). METHODS: The Global Aging and Geriatric Experiments in Bipolar Disorder consortium provided international data on 437 older age bipolar disorder participants. We compared LOBD versus EOBD on depression, mania, functionality, and physical comorbidities. Exploratory analyses were performed on participants with BD onset ≥50 years old. RESULTS: LOBD (n = 105) did not differ from EOBD (n = 332) on depression, mania, global functioning, nor employment status (p > 0.05). Late-onset bipolar disorder was associated with higher endocrine comorbidities (odds ratio = 1.48, [95%CI = 1.0,12.1], p = 0.03). This difference did not remain significant when subjects with BD onset ≥50 years old were analyzed. LIMITATIONS: This study is limited by the retrospective nature of the variable age of onset and the differences in evaluation methods across studies (partially overcame by harmonization processes). CONCLUSION: The present analysis is in favor of the hypothesis that LOBD might represent a similar clinical phenotype as classic EOBD with respect to core BD symptomatology, functionality, and comorbid physical conditions. Large-scale global collaboration to improve our understanding of BD across the lifespan is needed.

Topics & Concepts

Bipolar disorderManiaAge of onsetDepression (economics)PsychologyPsychiatryComorbidityBipolar I disorderMedicineMoodClinical psychologyInternal medicineDiseaseEconomicsMacroeconomicsBipolar Disorder and TreatmentSchizophrenia research and treatmentTryptophan and brain disorders
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