RT Conference Proceedings
T1 The andalusian “multiplex families with bipolar disorder “: a revaluation of the cohort study (1997-2013).
A1 Guzmán, José
A1 Mayoral Cleries, Fermín
A1 Moreno-Kustner, Berta
A1 Rivas, Fabio
A1 Romero, Pablo
A1 Gay, Eudoxia
A1 González, María José
A1 Gil, Susana
A1 Cabaleiro, Francisco
A1 Rio, Francisco
A1 Pérez, Fermín
A1 Haro, Jesús
A1 Nöthen, Markus
A1 Streit, Fabian
A1 Strohmaier, Jana
A1 Rietschel, Marcella
K1 Psicosis maniacodepresiva
AB Objectives. Bipolar disorder (BD) is highly heritable, and gene identification will elucidate biological factors and gene-environment interactions. Multiplex families represent a promising resource for identifying rare variants and polygenic effects. However, such families are difficult to recruit.In 1997, >100 multiplex Andalusian BD pedigrees - the largest of which contains >20 affected members- were recruited within an Andalusian-German collaboration study.  Since then, the Andalusian psychiatric network and biobank facilities have been expanded in order to facilitate psychiatric research. Therefore in 2013, the Andalusian-German collaborators initiated a follow-up study of this cohort in order to identify new genetic and environmental factors for BD aetiology and clinical course. Methods.In 1997, BD patients at Andalusian psychiatric hospitals who reported a family history of BD were asked to inform their families about the study. All consenting family members (N= 937; BPI/II=265; Recurrent Mayor Depression=149) were assessed using a structured psychiatric interview for life-time best estimate psychiatric diagnosis (SADS) and the family history method, and blood was obtained for DNA genetic analysis.Follow-up involves reassessment of diagnosis, neuropsychological testing (CANTAB), and the collection of biomaterials (RNA, Plasma, IPS, hair cortisol, etc.). Written informed consent is obtained for all study procedures and analyses. Results. For the first three families, follow-up assessments and biomaterial-processing have been completed. Follow-up of the remaining families is ongoing.  Conclusion.This cohort represents a unique resource for the investigation of BD aetiology and clinical course, and will be available to international researchers from other sciences.
YR 2014
FD 2014-12-01
LK http://hdl.handle.net/10630/8506
UL http://hdl.handle.net/10630/8506
LA eng
NO Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech.
DS RIUMA. Repositorio Institucional de la Universidad de Málaga
RD 20 ene 2026