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@ARTICLE{Montejo:274096,
author = {Montejo, Laura and Sole, Brisa and Fico, Giovanna and
Kalman, Janos L. and Budde, Monika and Heilbronner, Urs and
Oliva, Vincenzo and De Prisco, Michele and Martin-Parra,
Sara and Ruiz, Andrea and Martinez-Aran, Anabel and Adorjan,
Kristina and Falkai, Peter and Heilbronner, Maria and
Kohshour, Mojtaba Oraki and Reich-Erkelenz, Daniela and
Schaupp, Sabrina K. and Schulte, Eva C. and Senner, Fanny
and Vogl, Thomas and Anghelescu, Ion-George and Arolt,
Volker and Baune, Bernhard T. and Dannlowski, Udo and
Dietrich, Detlef E. and Fallgatter, Andreas J. and Figge,
Christian and Juckel, Georg and Konrad, Carsten and Reimer,
Jens and Reininghaus, Eva Z. and Schmauß, Max and Wiltfang,
Jens and Zimmermann, Jörg and Vieta, Eduard and Papiol,
Sergi and Schulze, Thomas G. and Torrent, Carla},
title = {{C}ontrasting genetic burden for bipolar disorder: {E}arly
onset versus late onset in an older adult bipolar disorder
sample},
journal = {European neuropsychopharmacology},
volume = {92},
issn = {0924-977X},
address = {Amsterdam},
publisher = {Elsevier},
reportid = {DZNE-2025-00052},
pages = {29 - 37},
year = {2025},
abstract = {Older Adults with Bipolar Disorder (OABD) represent a
heterogeneous group, including those with early and late
onset of the disorder. Recent evidence shows both groups
have distinct clinical, cognitive, and medical features,
tied to different neurobiological profiles. This study
explored the link between polygenic risk scores (PRS) for
bipolar disorder (PRS-BD), schizophrenia (PRS-SCZ), and
major depressive disorder (PRS-MDD) with age of onset in
OABD. PRS-SCZ, PRS-BD, and PRS-MDD among early vs late onset
were calculated. PRS was used to infer posterior SNP effect
sizes using a fully Bayesian approach. Demographic,
clinical, and cognitive variables were also analyzed.
Logistic regression analysis was used to estimate the amount
of variation of each group explained by standardized
PRS-SCZ, PRS-MDD, and PRS-BD. A total of 207 OABD subjects
were included (144 EOBD; 63 LOBD). EOBD showed higher PRS-BD
compared to LOBD (p = 0.005), while no association was found
between age of onset and PRS-SCZ or PRS-MDD. Compared to
LOBD, EOBD individuals also showed a higher likelihood for
suicide attempts (p = 0.01), higher presence of psychotic
symptoms (p = 0.003), higher prevalence of BD-I (p = 0.002),
higher rates of familiarity for any psychiatric disorder (p
= 0.004), and lower processing speed measured with
Trail-Making Test part A (p = 0.03). OABD subjects with an
early onset showed a greater genetic burden for BD compared
to subjects with a late onset. These findings contribute to
the notion that EOBD and LOBD may represent different forms
of OABD, particularly regarding the genetic predisposition
to BD.},
cin = {AG Wiltfang},
ddc = {610},
cid = {I:(DE-2719)1410006},
pnm = {353 - Clinical and Health Care Research (POF4-353)},
pid = {G:(DE-HGF)POF4-353},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:39718074},
doi = {10.1016/j.euroneuro.2024.12.001},
url = {https://pub.dzne.de/record/274096},
}