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本文引用的文献

1
Chronic fluoxetine treatment changes S100B expression during postnatal rat brain development.慢性氟西汀治疗会改变新生大鼠大脑发育过程中S100B的表达。
J Child Adolesc Psychopharmacol. 2013 Sep;23(7):481-9. doi: 10.1089/cap.2011.0065. Epub 2013 Sep 11.
2
S100B-immunopositive astrocytes and oligodendrocytes in the hippocampus are differentially afflicted in unipolar and bipolar depression: a postmortem study.在单相和双相抑郁症中,海马体中 S100B 免疫阳性星形胶质细胞和少突胶质细胞受到不同程度的影响:一项尸检研究。
J Psychiatr Res. 2013 Nov;47(11):1694-9. doi: 10.1016/j.jpsychires.2013.07.005. Epub 2013 Jul 26.
3
Serum S100B represents a new biomarker for mood disorders.血清 S100B 是一种新的情绪障碍生物标志物。
Curr Drug Targets. 2013 Oct;14(11):1237-48. doi: 10.2174/13894501113149990014.
4
5-HT and mechanisms of defence.5-羟色胺与防御机制
J Psychopharmacol. 1991 Jan;5(4):305-15. doi: 10.1177/026988119100500414.
5
Chronic mild stress induces fluoxetine-reversible decreases in hippocampal and cerebrospinal fluid levels of the neurotrophic factor S100B and its specific receptor.慢性轻度应激导致神经营养因子S100B及其特异性受体在海马体和脑脊液中的水平出现氟西汀可逆性降低。
Int J Mol Sci. 2010;11(12):5310-22. doi: 10.3390/ijms11125310. Epub 2010 Dec 21.
6
S100B protein in neurodegenerative disorders.S100B 蛋白与神经退行性疾病。
Clin Chem Lab Med. 2011 Mar;49(3):409-24. doi: 10.1515/CCLM.2011.083. Epub 2011 Feb 9.
7
The dual role of serotonin in defense and the mode of action of antidepressants on generalized anxiety and panic disorders.血清素在防御中的双重作用以及抗抑郁药对广泛性焦虑症和恐慌症的作用模式。
Cent Nerv Syst Agents Med Chem. 2010 Sep 1;10(3):207-17. doi: 10.2174/1871524911006030207.
8
Elevated serum levels of the glial marker protein S100B are not specific for schizophrenia or mood disorders.血清中神经胶质标志物蛋白S100B水平升高并非精神分裂症或心境障碍所特有。
Mol Psychiatry. 2009 Mar;14(3):235-7. doi: 10.1038/mp.2008.85.
9
Secretion of S100B, an astrocyte-derived neurotrophic protein, is stimulated by fluoxetine via a mechanism independent of serotonin.S100B是一种由星形胶质细胞产生的神经营养蛋白,其分泌受到氟西汀的刺激,该机制独立于血清素。
Prog Neuropsychopharmacol Biol Psychiatry. 2008 Aug 1;32(6):1580-3. doi: 10.1016/j.pnpbp.2008.06.001. Epub 2008 Jun 8.
10
Serum markers support disease-specific glial pathology in major depression.血清标志物支持重度抑郁症中特定疾病的胶质细胞病理学。
J Affect Disord. 2008 Dec;111(2-3):271-80. doi: 10.1016/j.jad.2008.03.005. Epub 2008 Apr 21.

惊恐障碍患者血清 S100B 蛋白水平:选择性 5-羟色胺再摄取抑制剂治疗的影响。

Serum S100B Protein Levels in Patients with Panic Disorder: Effect of Treatment with Selective Serotonine Reuptake Inhibitors.

机构信息

Zonguldak Ataturk Government Hospital, Psychiatry Department, Zonguldak, Turkey.

Yıldırım Beyazit Diskapi Training and Research Hospital, Psychiatry Department, Ankara, Turkey.

出版信息

Psychiatry Investig. 2015 Apr;12(2):260-2. doi: 10.4306/pi.2015.12.2.260. Epub 2014 Dec 12.

DOI:10.4306/pi.2015.12.2.260
PMID:25866528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4390598/
Abstract

OBJECTIVE

Altered serum S100B protein levels have been shown in several psychiatric disorders. Our aim was to investigate whether plasma S100B is different in patients with panic disorder (PD) when compared with controls. Our second aim was to investigate whether treatment with SSRIs have an effect on S100B levels in patients with PD.

METHODS

The sample included 32 patients diagnosed with PD (21 women, 11 men) per DSM-IV criteria and 21 healthy controls (11 women, 10 men). S100B levels were measured with BioVendor Human S100B ELISA (Enzyme Linked Immunosorbent Assay) kit.

RESULTS

14 patients were not on drug treatment (43.8%) while 18 patients were taking various SSRIs. Median S100B value was 151.7 pg/mL (minimum-maximum: 120.4-164.7 pg/mL) in the control group, 147.4 pg/mL (minimum-maximum: 138.8-154.1 pg/mL) in the drug free group and 153.0 pg/mL (minimum-maximum: 137.9-164.7 pg/mL) in the treatment group. Kruskal-Wallis analysis showed a significant diffrerence among the three groups (z=9.9, df=2, p=0.007). Follow up Mann-Whitney-U tests indicated that while the control and the patients with treatment were not significantly different (z=-0.05, p=0.96), there were significant differences between the control group and untreated patients (z=-2.6, p=0.009) and treated and untreated patients (z=-3.0, p=0.003).

CONCLUSION

Our results suggested that, serum S100B protein level might be decreased in untreated PD patients and that patients who were treated with SSRIs had similar S100B level to healthy controls.

摘要

目的

多项精神疾病的血清 S100B 蛋白水平已发生改变。我们的目的是探究与对照组相比,惊恐障碍(PD)患者的血浆 S100B 是否存在差异。我们的第二个目的是探究 SSRI 治疗是否对 PD 患者的 S100B 水平有影响。

方法

该样本纳入 32 名符合 DSM-IV 标准的 PD 患者(21 名女性,11 名男性)和 21 名健康对照者(11 名女性,10 名男性)。采用 BioVendor Human S100B ELISA(酶联免疫吸附测定)试剂盒测量 S100B 水平。

结果

14 名患者未接受药物治疗(43.8%),18 名患者服用各种 SSRI。对照组 S100B 值中位数为 151.7pg/mL(最小值-最大值:120.4-164.7pg/mL),未用药组为 147.4pg/mL(最小值-最大值:138.8-154.1pg/mL),治疗组为 153.0pg/mL(最小值-最大值:137.9-164.7pg/mL)。Kruskal-Wallis 分析显示三组间存在显著差异(z=9.9,df=2,p=0.007)。随后进行的 Mann-Whitney-U 检验显示,对照组与治疗组间无显著差异(z=-0.05,p=0.96),而对照组与未用药组间存在显著差异(z=-2.6,p=0.009),治疗组与未用药组间也存在显著差异(z=-3.0,p=0.003)。

结论

我们的研究结果表明,未经治疗的 PD 患者的血清 S100B 蛋白水平可能降低,而接受 SSRI 治疗的患者的 S100B 水平与健康对照组相似。