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Peer-reviewedCC BY 4.0Depression and Anxiety

Is It Possible to Establish Thresholds for Depressive Symptom Severity Associated With Cognitive Impairments in Bipolar Disorders? Findings From the FACE‐BD Cohort

12 more authors
26 affiliations
  1. 1Fondation FondaMental Créteil France
  2. 2DisAP MOODS Team INSERM UMR1018 CESP Université de Versailles Saint-Quentin-En-Yvelines Université Paris-Saclay Le Chesnay France universite-paris-saclay.fr
  3. 3Centre Hospitalier de Versailles Service Universitaire de Psychiatrie d’Adultes et d’Addictologie Le Chesnay France
  4. 4CHU Montpellier France chru-strasbourg.fr
  5. 5IGF University of Montpellier CNRS INSERM Montpellier France inserm.fr
  6. 6Pôle de Psychiatrie Centre Hospitalier Princesse Grace Monaco Monaco chpg.mc
  7. 7Department of Emergency Psychiatry and Acute Care Lapeyronie Hospital CHU Montpellier Montpellier France chu-montpellier.fr
  8. 8INSERM U1028 CNRS UMR5292 Lyon Neuroscience Research Center Psychiatric Disorders: From Resistance to Response Team University Lyon 1 Villeurbanne Lyon France univ-lyon1.fr
  9. 9Université de Paris Inserm UMR1266 Sorbonne Paris Cité Faculté de Médecine Paris France sorbonne-paris-cite.fr
  10. 10AP-HP Groupe Hospitalo-Universitaire AP-HP Nord DMU ESPRIT Service de Psychiatrie et Addictologie Hôpital Louis Mourier Colombes France aphp.fr
  11. 11Optimisation Thérapeutique en Neuropharmacologie OPTEN U1144 INSERM Université Paris Cité Paris 75006 France u-paris.fr
  12. 12Département de Psychiatrie et de Médecine Addictologique Hôpitaux Lariboisière-Fernand Widal GHU APHP Nord Université Paris Cité Paris F-75010 France u-paris.fr
  13. 13UMR INSERM 1322 LINC Université Marie et Louis Pasteur Besançon France
  14. 14Service de Psychiatrie de l’adulte CIC-1431 INSERM CHU de Besançon Besançon F-25000 France
  15. 15Université Sorbonne Paris Nord Bobigny Cedex 93017 France univ-paris13.fr
  16. 16Département de Recherche Clinique Pôle Universitaire 03 G03 EPS Ville Evrard Neuilly sur Marne France
  17. 17Inserm U 955 Neuropsychiatrie Translationnelle DMU IMPACT (AP-HP) Département de Psychiatrie, Fondation FondaMental Université Paris Est Créteil (UPEC) Créteil 94000 France u-pec.fr
  18. 18Pôle de Psychiatrie Assistance Publique Hôpitaux de Marseille Marseille France ap-hm.fr
  19. 19NT-UMR7289 CNRS Aix-Marseille Université Marseille France
  20. 20Centre Hospitalier et Universitaire Département de Psychiatrie EA 7280 Université d’Auvergne Clermont-Ferrand France u-clermont1.fr
  21. 21Centre Hospitalier Charles Perrens Pôle de Psychiatrie Générale et Universitaire Bordeaux France
  22. 22LabPsy UR 4139 Université de Bordeaux Bordeaux F-33000 France u-bordeaux.fr
  23. 23Université Grenoble Alpes Inserm U1216 CHU Grenoble Alpes Grenoble Institut Neurosciences Grenoble France univ-grenoble-alpes.fr
  24. 24Centre Psychothérapique de Nancy Inserm U1254 Université de Lorraine Nancy France univ-lorraine.fr
  25. 25Service Hospitalo-Universitaire de Psychiatrie Générale et de Réhabilitation Psycho Sociale 29G01 et 29G02 CHRU de Brest Hôpital de Bohars Brest France
  26. 26Service de Psychiatrie du Secteur 78G18 Centre Hospitalier de Plaisir Plaisir France

Abstract

ndividuals with bipolar disorders (BDs) with depressive symptoms exhibit poorer cognitive performance and are often excluded from procognitive interventions and cognitive research. Threshold values on depression severity scales, based on cutoffs defining depressive episodes, have traditionally been used to exclude patients suspected of having depression-associated cognitive impairment. Identifying a threshold value for depression-associated cognitive impairment on these scales could help guide patient selection and treatment. We assessed neuropsychological performance in outpatients with BD with varying levels of depressive symptom severity measured by the Montgomery-Åsberg Depression Rating Scale (MADRS). The sample was divided based on the total MADRS score or subscores in MADRS theoretical domains. We then compared average cognitive performance between groups while adjusting for relevant covariates to determine a MADRS score above which cognition is significantly impaired. We included 2532 individuals with BD. The composite cognitive score was significantly lower in individuals with a MADRS score ≥ 12 than in those with a score ≤ 1 but did not differ from that of individuals with scores between 2 and 11. Symptoms of detachment and sadness were more strongly associated with cognitive impairment than other symptoms. Individuals with type I BD with MADRS detachment subscores higher than 4 and individuals with type II BD with nonzero sadness subscores had significant cognitive impairment compared to individuals with lower subscores. Excluding individuals with BD whose cognition may be affected by depressive symptoms would require omitting those with MADRS detachment subscores higher than 4 or nonzero sadness subscores. Our findings question the existence of a total depression severity threshold for cognitive impairment, as specific depressive symptoms seem more strongly associated with cognitive impairment than total symptom severity.

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BibTeX
@article{vidal2026possible,
  title = {{Is It Possible to Establish Thresholds for Depressive Symptom Severity Associated With Cognitive Impairments in Bipolar Disorders? Findings From the FACE‐BD Cohort}},
  author = {Nathan Vidal and Eric Brunet-Gouet and Alexandre Billard and Solène Frileux and Raoul Belzeaux and Anamaria Bogdan and Philippe Courtet and Thierry D’Amato and Caroline Dubertret and Bruno Etain and Emmanuel Haffen and Dominique Januel and Marion Leboyer and Antoine Lefrere and Pierre-Michel Llorca and Emeline Marlinge and Katia M’Bailara and Emilie Olié and Mircea Polosan and Raymund Schwan and Michel Walter and The FACE-BD (FondaMental Academic Centers of Expertise for Bipolar Disorders) group and Christine Passerieux and Paul Roux},
  journal = {Depression and Anxiety},
  year = {2026},
  month = oct,
  doi = {10.1155/da/9918396},
  url = {https://hal.science/hal-05842587v1},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Is It Possible to Establish Thresholds for Depressive Symptom Severity Associated With Cognitive Impairments in Bipolar Disorders? Findings From the FACE‐BD Cohort
AU  - Nathan Vidal
AU  - Eric Brunet-Gouet
AU  - Alexandre Billard
AU  - Solène Frileux
AU  - Raoul Belzeaux
AU  - Anamaria Bogdan
AU  - Philippe Courtet
AU  - Thierry D’Amato
AU  - Caroline Dubertret
AU  - Bruno Etain
AU  - Emmanuel Haffen
AU  - Dominique Januel
AU  - Marion Leboyer
AU  - Antoine Lefrere
AU  - Pierre-Michel Llorca
AU  - Emeline Marlinge
AU  - Katia M’Bailara
AU  - Emilie Olié
AU  - Mircea Polosan
AU  - Raymund Schwan
AU  - Michel Walter
AU  - The FACE-BD (FondaMental Academic Centers of Expertise for Bipolar Disorders) group
AU  - Christine Passerieux
AU  - Paul Roux
PY  - 2026
DA  - 2026/10/26
JO  - Depression and Anxiety
DO  - 10.1155/da/9918396
UR  - https://hal.science/hal-05842587v1
AB  - ndividuals with bipolar disorders (BDs) with depressive symptoms exhibit poorer cognitive performance and are often excluded from procognitive interventions and cognitive research. Threshold values on depression severity scales, based on cutoffs defining depressive episodes, have traditionally been used to exclude patients suspected of having depression-associated cognitive impairment. Identifying a threshold value for depression-associated cognitive impairment on these scales could help guide patient selection and treatment. We assessed neuropsychological performance in outpatients with BD with varying levels of depressive symptom severity measured by the Montgomery-Åsberg Depression Rating Scale (MADRS). The sample was divided based on the total MADRS score or subscores in MADRS theoretical domains. We then compared average cognitive performance between groups while adjusting for relevant covariates to determine a MADRS score above which cognition is significantly impaired. We included 2532 individuals with BD. The composite cognitive score was significantly lower in individuals with a MADRS score ≥ 12 than in those with a score ≤ 1 but did not differ from that of individuals with scores between 2 and 11. Symptoms of detachment and sadness were more strongly associated with cognitive impairment than other symptoms. Individuals with type I BD with MADRS detachment subscores higher than 4 and individuals with type II BD with nonzero sadness subscores had significant cognitive impairment compared to individuals with lower subscores. Excluding individuals with BD whose cognition may be affected by depressive symptoms would require omitting those with MADRS detachment subscores higher than 4 or nonzero sadness subscores. Our findings question the existence of a total depression severity threshold for cognitive impairment, as specific depressive symptoms seem more strongly associated with cognitive impairment than total symptom severity.
SN  - 1091-4269
SN  - 1520-6394
ER  -