ROLE OF ALLELIC VARIANTS OF FK506-BINDING PROTEIN 51 (FKBP5) GENE IN THE DEVELOPMENT OF ANXIETY DISORDERS

被引:43
作者
Minelli, Alessandra [1 ]
Maffioletti, Elisabetta [1 ]
Cloninger, Claude Robert [2 ]
Magri, Chiara [1 ]
Sartori, Riccardo [3 ]
Bortolomasi, Marco [4 ]
Congiu, Chiara [1 ]
Bignotti, Stefano [5 ]
Segala, Matilde [4 ]
Giacopuzzi, Mario [4 ]
Gennarelli, Massimo [1 ,6 ]
机构
[1] Univ Brescia, Dept Mol & Translat Med, I-25123 Brescia, Italy
[2] Washington Univ, Sch Med, Dept Psychiat, St Louis, MO 63110 USA
[3] Univ Verona, Dept Philosophy Educ & Psychol, I-37100 Verona, Italy
[4] Psychiat Hosp Villa Santa Chiara, Verona, Italy
[5] IRCCS San Giovanni Dio Fatebenefratelli, Psychiat Unit, Brescia, Italy
[6] IRCCS San Giovanni Dio Fatebenefratelli, Genet Unit, Brescia, Italy
关键词
FKBP5; major depressive disorder; anxiety; harm avoidance; temperament & character inventory; GENOME-WIDE ASSOCIATION; GLUCOCORTICOID-RECEPTOR; DEPRESSIVE DISORDER; POLYMORPHISMS; STRESS; RISK; PERSONALITY; OUTPATIENTS; MODEL; MINI;
D O I
10.1002/da.22158
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
BackgroundAnxiety disorders exhibit remarkably high rates of comorbidity with major depressive disorder (MDD). Mood and anxiety disorders are considered stress-related diseases. Genetic variations in the co-chaperone FK506-binding protein 51, FKBP5, which modulates the function of glucocorticoid receptors, have been associated with an increased risk for the development of posttraumatic stress disorder, but data regarding its role in MDD are controversial. The aims of this study were to clarify the role of the FKBP5 gene in depression and anxiety disorders through a case-control study and an association study with personality traits using the Temperament and Character Inventory (TCI) in healthy subjects. MethodsSix hundred fifty-seven MDD patients, with or without an anxiety disorder in comorbidity, and 462 healthy volunteers were enrolled in the study. Two hundred fifty-six controls agreed to fill out the TCI. ResultsThe results showed that the T allele of rs1360780 was more frequent among the patients affected by MDD with a comorbidity of anxiety disorders, compared to those without (P < .001). Among the controls, we found that the T allele more often exhibited personality traits associated with an increased vulnerability to anxiety. ConclusionsThese results support the hypothesis that allelic variants of FKBP5 are a risk factor for anxiety disorders. The identification of genetic variants involved in anxiety may have implications for the optimization of therapeutic interventions. (C) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:1170 / 1176
页数:7
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