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氯氮平治疗的精神分裂症患者外周血神经调节蛋白 1(NRG1)mRNA 亚型表达升高。

Elevated peripheral expression of neuregulin-1 (NRG1) mRNA isoforms in clozapine-treated schizophrenia patients.

机构信息

Melbourne Neuropsychiatry Center, Department of Psychiatry, The University of Melbourne & Melbourne Health, Parkville, VIC, Australia.

The Cooperative Research Center (CRC) for Mental Health, Carlton, VIC, Australia.

出版信息

Transl Psychiatry. 2017 Dec 11;7(12):1280. doi: 10.1038/s41398-017-0041-2.

Abstract

Differential expression of neuregulin-1 (NRG1) mRNA isoforms and proteins has been reported in schizophrenia, primarily in post-mortem brain tissue. In this study, we examined 12 NRG1 SNPs, eight NRG1 mRNA isoforms (type I, type I, type II, type III, type IV, EGFα, EGFβ, pan-NRG1) in whole blood, and NRG1-β1 protein in serum of clozapine-treated schizophrenia patients (N = 71) and healthy controls (N = 57). In addition, using cultured peripheral blood mononuclear cells (PBMC) from 15 healthy individuals, we examined the effect of clozapine on NRG1 mRNA isoform and protein expression. We found elevated levels of NRG1 mRNA, specifically the EGFα (P = 0.0175), EGFβ (P = 0.002) and type I (P = 0.023) containing transcripts, but lower NRG1-β1 serum protein levels (P = 0.019) in schizophrenia patients compared to healthy controls. However, adjusting for smoking status attenuated the difference in NRG1-β1 serum levels (P = 0.050). Examination of clinical factors showed NRG1 EGFα (P = 0.02) and EGFβ (P = 0.02) isoform expression was negatively correlated with age of onset. However, we found limited evidence that NRG1 mRNA isoform or protein expression was associated with current chlorpromazine equivalent dose or clozapine plasma levels, the latter corroborated by our PBMC clozapine exposure experiment. Our SNP analysis found no robust expression quantitative trait loci. Our results represent the first comprehensive investigation of NRG1 isoforms and protein expression in the blood of clozapine-treated schizophrenia patients and suggest levels of some NRG1 transcripts are upregulated in those with schizophrenia.

摘要

神经调节蛋白 1(NRG1)mRNA 异构体和蛋白的差异表达已在精神分裂症中报道,主要在死后脑组织中。在这项研究中,我们检查了 12 个 NRG1 单核苷酸多态性、全血中的 8 个 NRG1 mRNA 异构体(I 型、I 型、II 型、III 型、IV 型、EGFα、EGFβ、pan-NRG1)和氯氮平治疗的精神分裂症患者(N=71)和健康对照组(N=57)的血清 NRG1-β1 蛋白。此外,使用来自 15 名健康个体的培养外周血单核细胞(PBMC),我们检查了氯氮平对 NRG1 mRNA 异构体和蛋白表达的影响。我们发现精神分裂症患者的 NRG1 mRNA 水平升高,特别是包含 EGFα(P=0.0175)、EGFβ(P=0.002)和 I 型(P=0.023)的转录物,但 NRG1-β1 血清蛋白水平较低(P=0.019)与健康对照组相比。然而,调整吸烟状态减弱了 NRG1-β1 血清水平的差异(P=0.050)。对临床因素的检查表明,NRG1 EGFα(P=0.02)和 EGFβ(P=0.02)异构体表达与发病年龄呈负相关。然而,我们发现 NRG1 mRNA 异构体或蛋白表达与当前氯丙嗪等效剂量或氯氮平血浆水平相关的证据有限,后者得到了我们的 PBMC 氯氮平暴露实验的证实。我们的 SNP 分析未发现稳健的表达数量性状基因座。我们的结果代表了氯氮平治疗的精神分裂症患者血液中 NRG1 异构体和蛋白表达的首次全面研究,表明一些 NRG1 转录物的水平在精神分裂症患者中上调。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11aa/5802529/8de98e01c691/41398_2017_41_Fig1_HTML.jpg

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