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J Neurovirol. 2010 Oct;16(5):399-404. doi: 10.3109/13550284.2010.504248.
2
Differential expression of immunophilins FKBP51 and FKBP52 in the frontal cortex of HIV-infected patients with major depressive disorder.免疫亲和蛋白FKBP51和FKBP52在患有重度抑郁症的HIV感染患者额叶皮质中的差异表达。
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Accumulation of cytoplasmic glucocorticoid receptor is related to elevation of FKBP5 in lymphocytes of depressed patients.抑郁患者淋巴细胞中细胞质糖皮质激素受体的积累与FKBP5的升高有关。
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The role of FKBP5 in mood disorders: action of FKBP5 on steroid hormone receptors leads to questions about its evolutionary importance.FKBP5 在心境障碍中的作用:FKBP5 对甾体激素受体的作用引发了对其进化重要性的质疑。
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FKBP5 polymorphisms and antidepressant response in geriatric depression.FKBP5 多态性与老年抑郁症的抗抑郁反应。
Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):554-560. doi: 10.1002/ajmg.b.31019.
2
The role of FKBP5, a co-chaperone of the glucocorticoid receptor in the pathogenesis and therapy of affective and anxiety disorders.FKBP5 作为糖皮质激素受体的共伴侣在情感和焦虑障碍的发病机制和治疗中的作用。
Psychoneuroendocrinology. 2009 Dec;34 Suppl 1:S186-95. doi: 10.1016/j.psyneuen.2009.05.021.
3
Modulation of glucocorticoid receptor nuclear translocation in neurons by immunophilins FKBP51 and FKBP52: implications for major depressive disorder.亲免素FKBP51和FKBP52对神经元中糖皮质激素受体核转位的调节:对重度抑郁症的影响。
Brain Res. 2009 Aug 25;1286:1-12. doi: 10.1016/j.brainres.2009.06.036. Epub 2009 Jun 21.
4
Differential expression of immunophilins FKBP51 and FKBP52 in the frontal cortex of HIV-infected patients with major depressive disorder.免疫亲和蛋白FKBP51和FKBP52在患有重度抑郁症的HIV感染患者额叶皮质中的差异表达。
J Neuroimmune Pharmacol. 2009 Jun;4(2):218-26. doi: 10.1007/s11481-009-9146-6. Epub 2009 Feb 6.
5
Genetic variants in FKBP5 affecting response to antidepressant drug treatment.FKBP5基因变异影响对抗抑郁药物治疗的反应。
Pharmacogenomics. 2008 Jul;9(7):841-6. doi: 10.2217/14622416.9.7.841.
6
Association of FKBP5 polymorphisms and childhood abuse with risk of posttraumatic stress disorder symptoms in adults.FKBP5基因多态性与童年期虐待经历和成年人创伤后应激障碍症状风险的关联。
JAMA. 2008 Mar 19;299(11):1291-305. doi: 10.1001/jama.299.11.1291.
7
The FKBP5-gene in depression and treatment response--an association study in the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) Cohort.抑郁症及治疗反应中的FKBP5基因——缓解抑郁症的序贯治疗方案(STAR*D)队列中的一项关联研究。
Biol Psychiatry. 2008 Jun 15;63(12):1103-10. doi: 10.1016/j.biopsych.2007.10.026. Epub 2008 Jan 11.
8
The corticotropin-releasing factor (CRF) family of peptides as local modulators of adrenal function.作为肾上腺功能局部调节因子的促肾上腺皮质激素释放因子(CRF)肽家族。
Cell Mol Life Sci. 2007 Jul;64(13):1638-55. doi: 10.1007/s00018-007-6555-7.
9
Diminished somatostatin gene expression in individuals with HIV and major depressive disorder.感染人类免疫缺陷病毒且患有重度抑郁症的个体中生长抑素基因表达降低。
Neurology. 2006 Nov 28;67(10):1867-9. doi: 10.1212/01.wnl.0000244436.04036.a2.
10
HPA axis activity and neuropathogenesis in HIV-1 clade C infection.HIV-1 C亚型感染中的下丘脑-垂体-肾上腺(HPA)轴活性与神经发病机制
Front Biosci. 2007 Jan 1;12:1271-7. doi: 10.2741/2145.

人类免疫缺陷病毒感染者中重度抑郁症状与 FKBP5 而非 FKBP4 表达的相关性。

Correlation of major depressive disorder symptoms with FKBP5 but not FKBP4 expression in human immunodeficiency virus-infected individuals.

机构信息

Department of Psychiatry, University of California San Diego, La Jolla, California 92093-0603, USA.

出版信息

J Neurovirol. 2010 Oct;16(5):399-404. doi: 10.3109/13550284.2010.504248.

DOI:10.3109/13550284.2010.504248
PMID:20726698
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3274491/
Abstract

Major depressive disorder (MDD) is a significant cause of morbidity in people living with the human immunodeficiency virus (HIV). FKBP5 is a candidate gene with single-nucleotide polymorphisms (SNPs) rs1360780 and rs3800373 associated with MDD. This gene product and its relative, FKBP4, physically associate with the glucocorticoid receptor whose function is implicated in MDD pathophysiology. Because these genes are expressed in blood and brain and elevated in HIV infection, we explored the relationship between gene expression, genotype, and MDD symptoms. Longitudinally followed subjects (N = 57) as part of the CNS HIV AntiRetroviral Effects Research study, with diagnosed MDD and who donated blood for genotyping and gene expression analysis, were assessed. Subjects donated blood on adjacent visits with and without meeting criteria for MDD episode. Changes in clinical parameters were compared changes in gene expression. Change in FKBP5 expression correlated with change in Beck Depression Inventory (BDI) for MDD → euthymic comparison in GG genotype of rs3800373 (P = .013) and TT carriers of rs1360780 (P = .02). In euthymic → MDD comparison, GG homozygous, FKBP5 expression correlated with more severe change in BDI. Change in FKBP4 expression did not correlate with changes in clinical or depression measurements. Higher FKBP5 expression correlated with greater symptom change for GG carriers of rs3800373.

摘要

重度抑郁症(MDD)是导致人类免疫缺陷病毒(HIV)感染者发病和致残的主要原因。FKBP5 是一个候选基因,其单核苷酸多态性(SNP)rs1360780 和 rs3800373 与 MDD 相关。该基因产物及其相关基因 FKBP4 与糖皮质激素受体物理结合,而后者的功能与 MDD 病理生理学有关。由于这些基因在血液和大脑中表达,并在 HIV 感染中升高,我们探讨了基因表达、基因型与 MDD 症状之间的关系。作为 CNS HIV AntiRetroviral Effects Research 研究的一部分,我们对纵向随访的受试者(N=57)进行了研究,这些受试者患有 MDD 并捐献了血液进行基因分型和基因表达分析。在符合或不符合 MDD 发作标准的相邻就诊期间,受试者均捐献了血液。比较了临床参数的变化与基因表达的变化。FKBP5 表达的变化与 MDD 向缓解状态的贝克抑郁量表(BDI)变化呈正相关,在 rs3800373 的 GG 基因型(P=.013)和 rs1360780 的 TT 携带者中(P=.02)。在缓解向 MDD 状态的比较中,FKBP5 表达与 BDI 的变化呈正相关,在 GG 纯合子中更为严重。FKBP4 表达的变化与临床或抑郁测量值的变化无关。FKBP5 表达的增加与 rs3800373 的 GG 携带者的症状变化更为明显相关。