Inflammatory DEpression Advances in Schizophrenia (IDEAS): A precision medicine approach of the national FACE-SZ cohort

被引:6
作者
Fond, G. [1 ,4 ,10 ]
Godin, O. [1 ,15 ,16 ]
Schurhoff, F. [1 ,2 ,3 ,4 ]
Berna, F. [1 ,2 ,6 ]
Aouizerate, B. [1 ,5 ,13 ]
Capdevielle, D. [1 ,5 ,7 ]
Chereau, I. [1 ,8 ]
D'Amato, T. [1 ,6 ,9 ]
Dubertret, C. [1 ,9 ,10 ]
Dubreucq, J. [1 ,8 ,11 ]
Faget, C. [1 ,4 ,10 ]
Leignier, S. [1 ]
Lancon, C. [1 ,4 ]
Mallet, J. [1 ,9 ,10 ]
Marulaz, L. [1 ,2 ,3 ]
Misdrahi, D. [1 ,2 ,5 ,7 ,14 ]
Passerieux, C. [1 ,2 ,11 ,12 ]
Rey, R. [1 ,2 ,9 ]
Schandrin, A. [1 ,2 ,5 ,7 ]
Urbach, M. [1 ,2 ,11 ,12 ]
Vidailhet, P. [2 ,6 ]
Leboyer, M. [1 ,2 ,3 ,4 ]
Boyer, L. [1 ,4 ]
Llorca, P. M. [1 ,3 ,8 ]
Andrianarisoa, M. [4 ]
Aouizerate, B. [1 ,5 ,13 ]
Berna, F. [1 ,2 ,6 ]
Blanc, O. [3 ]
Brunel, L. [4 ]
Bulzacka, E. [4 ]
Capdevielle, D. [1 ,5 ,7 ]
Coulon, N.
Chereau-Boudet, I [3 ]
Chesnoy-Servanin, G. [6 ]
Danion, J. M. [2 ]
D'Amato, T. [1 ,6 ,9 ]
Deloge, A. [7 ]
Delorme, C. [8 ]
Denizot, H.
Dorey, J. M. [6 ]
Dubertret, C. [1 ,9 ,10 ]
Dubreucq, J. [1 ,8 ,11 ]
Faget, C. [1 ,4 ,10 ]
Fluttaz, C. [8 ]
Fond, G. [1 ,4 ,10 ]
Fonteneau, S. [11 ]
Gabayet, F. [8 ]
Giraud-Baro, E.
Hardy-Bayle, M. C. [11 ]
Lacelle, D.
机构
[1] Fdn FondaMental, Creteil, France
[2] INSERM U955, Equipe Psychiat Translat, Creteil, France
[3] Univ Paris Est Creteil, DHU Pe PSY, Pole Psychiat Hop Univ H Mondor, Creteil, France
[4] Aix Marseille Univ, Fac Med, Sect Timone, EA 3279 CEReSS Ctr Etud & Rech Serv Sante & Quali, 27 Blvd Jean Moulin, F-13005 Marseille, France
[5] Univ Bordeaux, Ctr Hosp Charles Perrens, F-33076 Bordeaux, France
[6] Univ Strasbourg, Hop Univ Strasbourg, INSERM U1114, Federat Med Translat Strasbourg, Strasbourg, France
[7] Univ Montpellier I, Serv Univ Psychiat Adulte, Hop Colombiere, CHRU Montpellier,Inserm 1061, Montpellier, France
[8] Univ Auvergne, EA Fac Med 7280, CHU, CMP B, BP 69 63003, Clermont Ferrand 1, France
[9] Univ Claude Bernard Lyon 1, Equipe PSYR2, Ctr Hosp Le Vinatier, INSERM U1028,CNRS UMR5292,Ctr Rech Neurosci Lyon, Pole Est,95 Bd Pinel,BP 30039, F-69678 Bron, France
[10] Univ Paris Diderot, Sorbonne Paris Cite, Fac Med, AP HP,Dept Psychiat,Louis Mourier Hosp,Inserm U89, Paris, France
[11] CH Alpes Isere, Ctr Referent Rehabil Psychosociale, Grenoble, France
[12] Univ Versailles St Quentin En Yvelines, Ctr Hosp Versailles, Serv Psychiat & Addictol Adulte, EA 4047 HANDIReSP,UFR Sci Sante Simone Veil, Versailles, France
[13] Univ Bordeaux, NutriNeuro, INRA, U1286, F-33076 Bordeaux, France
[14] INCIA, CNRS UMR 5287, Talence, France
[15] UPMC Univ Paris 06, Sorbonne Univ, UMR S 1136, Inst Pierre Louis Epidemiol & Sante Publ, F-75013 Paris, France
[16] INSERM, UMR S 1136, Inst Pierre Louis Epidemiol & Sante Publ, F-75013 Paris, France
关键词
Depression; Inflammation; Schizophrenia; Adiposity; Toxoplasma; TOXOPLASMA-GONDII; SYMPTOMS; DISORDER; ASSOCIATION; INFECTION; VALIDITY; OBESITY; SCALE;
D O I
10.1016/j.jad.2018.11.004
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Major Depressive Disorder (MDD) is a therapeutic challenge in schizophrenia (SZ). Untangling different forms of MDD appears as the best current strategy to improve remission to treatment in the so-called precision medicine approach. Aims: The objectives of the present study were to determine (i) the prevalence of Inflammatory Depression (ID) in stabilized SZ outpatients (ii) if ID was associated with clinical or cognitive profiles that may help clinicians detecting ID (iii) if antidepressants were effective in ID and (iv) the biological correlates of ID that may orientate personalized treatments. Method: Participants were consecutively included and received a thorough 2 days-clinical assessment. Results: 785 subjects were recruited in the FACE-SZ cohort. 289 (36.8%) were diagnosed with MDD (remitted or unremitted), of them 57 with ID (19.7%). No clinical or cognitive features were associated with ID (all p>0.05). ID has been associated with increased abdominal perimeter (aOR=4.48, p=0.002) and latent Toxoplasma infection (aOR=2.19, p=0.04). While antidepressants were associated with decreased depressive symptoms level in ID, 44% of the subjects remained unremitted under antidepressant, with no association with CRP blood levels. Conclusions: ID may not differ from other forms of depression by its clinical symptoms but by its aetiologies. ID is associated with increased perivisceral fat and latent Toxoplasma infection that are both potentially related to gut/microbiota disturbances. Specific anti-inflammatory drugs and microbiota-targeted therapeutics appear as promising strategies in the treatment of inflammatory depression in schizophrenia.
引用
收藏
页码:468 / 474
页数:7
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