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从 HIV 感染患者中分离的 CD14+细胞中鉴定出的与疲劳相关的基因网络:第二部分:统计分析。

Fatigue-related gene networks identified in CD14+ cells isolated from HIV-infected patients: part II: statistical analysis.

机构信息

Biobehavioral Nursing & Health Systems Department, School of Nursing, University of Washington, Seattle, WA 98195, USA.

出版信息

Biol Res Nurs. 2013 Apr;15(2):152-9. doi: 10.1177/1099800411423307. Epub 2011 Nov 14.

Abstract

PURPOSE

In limited samples of valuable biological tissues, univariate ranking methods of microarray analyses often fail to show significant differences among expression profiles. In order to allow for hypothesis generation, novel statistical modeling systems can be greatly beneficial. The authors applied new statistical approaches to solve the issue of limited experimental data to generate new hypotheses in CD14(+) cells of patients with HIV-related fatigue (HRF) and healthy controls.

METHODOLOGY

We compared gene expression profiles of CD14(+) cells of nucleoside reverse transcriptase inhibitor (NRTI)-treated HIV patients with low versus high fatigue to healthy controls (n = 5 each). With novel Bayesian modeling procedures, the authors identified 32 genes predictive of low versus high fatigue and 33 genes predictive of healthy versus HIV infection. Sparse association and liquid association networks further elucidated the possible biological pathways in which these genes are involved. RELEVANCE FOR NURSING PRACTICE: Genetic networks developed in a comprehensive Bayesian framework from small sample sizes allow nursing researchers to design future research approaches to address such issues as HRF.

IMPLICATION FOR PRACTICE

The findings from this pilot study may take us one step closer to the development of useful biomarker targets for fatigue status. Specific and reliable tests are needed to diagnosis, monitor and treat fatigue and mitochondrial dysfunction.

摘要

目的

在有限的有价值生物组织样本中,微阵列分析的单变量排序方法往往无法显示表达谱之间的显著差异。为了允许生成假设,可以极大地受益于新型统计建模系统。作者应用新的统计方法来解决有限实验数据的问题,以在 HIV 相关疲劳(HRF)患者和健康对照的 CD14(+)细胞中生成新的假设。

方法

我们比较了接受核苷逆转录酶抑制剂(NRTI)治疗的 HIV 患者中低疲劳与高疲劳的 CD14(+)细胞的基因表达谱,与健康对照组(每组各 5 例)进行比较。通过新颖的贝叶斯建模程序,作者确定了 32 个可预测低疲劳与高疲劳的基因和 33 个可预测健康与 HIV 感染的基因。稀疏关联和液体关联网络进一步阐明了这些基因所涉及的可能生物学途径。

对护理实践的意义

从小样本量综合贝叶斯框架中开发的遗传网络使护理研究人员能够设计未来的研究方法来解决 HRF 等问题。

实践意义

这项初步研究的结果可能使我们更接近开发用于疲劳状态的有用生物标志物靶标的目标。需要特定和可靠的测试来诊断、监测和治疗疲劳和线粒体功能障碍。

相似文献

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Fatigue-related gene networks identified in CD14+ cells isolated from HIV-infected patients: part II: statistical analysis.
Biol Res Nurs. 2013 Apr;15(2):152-9. doi: 10.1177/1099800411423307. Epub 2011 Nov 14.
2
Fatigue-related gene networks identified in CD(14)+ cells isolated from HIV-infected patients: part I: research findings.
Biol Res Nurs. 2013 Apr;15(2):137-51. doi: 10.1177/1099800411421957. Epub 2013 Jan 16.

引用本文的文献

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本文引用的文献

1
HIV infection and antiretroviral therapy have divergent effects on mitochondria in adipose tissue.
J Infect Dis. 2012 Jun 15;205(12):1778-87. doi: 10.1093/infdis/jis101. Epub 2012 Apr 3.
2
The potent anti-HIV activity of CXCL12gamma correlates with efficient CXCR4 binding and internalization.
J Virol. 2010 Mar;84(5):2563-72. doi: 10.1128/JVI.00342-09. Epub 2009 Dec 16.
3
Variable selection and dependency networks for genomewide data.
Biostatistics. 2009 Oct;10(4):621-39. doi: 10.1093/biostatistics/kxp018. Epub 2009 Jun 11.
4
Characterization and regulation of bv8 in human blood cells.
Clin Cancer Res. 2009 Apr 15;15(8):2675-84. doi: 10.1158/1078-0432.CCR-08-1954. Epub 2009 Mar 31.
5
Cofilin activation in peripheral CD4 T cells of HIV-1 infected patients: a pilot study.
Retrovirology. 2008 Oct 17;5:95. doi: 10.1186/1742-4690-5-95.
6
Cellular reservoirs of HIV-1 and their role in viral persistence.
Curr HIV Res. 2008 Sep;6(5):388-400. doi: 10.2174/157016208785861195.
7
Phosphoprotein associated with glycosphingolipid-enriched microdomains/Csk-binding protein: a protein that matters.
Pathol Res Pract. 2008;204(11):785-92. doi: 10.1016/j.prp.2008.06.006. Epub 2008 Aug 29.
8
Cytokine properties of prokineticins.
FEBS J. 2008 Aug;275(16):4014-21. doi: 10.1111/j.1742-4658.2008.06559.x. Epub 2008 Jul 18.
9
Ins and outs of ADF/cofilin activity and regulation.
Eur J Cell Biol. 2008 Sep;87(8-9):649-67. doi: 10.1016/j.ejcb.2008.04.001. Epub 2008 May 21.
10
Loss of prokineticin receptor 2 signaling predisposes mice to torpor.
Am J Physiol Regul Integr Comp Physiol. 2008 Jun;294(6):R1968-79. doi: 10.1152/ajpregu.00778.2007. Epub 2008 Apr 16.

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