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系统性红斑狼疮中高肿瘤坏死因子α水平的家族聚集性。

Familial aggregation of high tumor necrosis factor alpha levels in systemic lupus erythematosus.

作者信息

Mangale Dorothy, Kariuki Silvia N, Chrabot Beverly S, Kumabe Marissa, Kelly Jennifer A, Harley John B, James Judith A, Sivils Kathy L, Niewold Timothy B

机构信息

Section of Rheumatology and Gwen Knapp Center for Lupus and Immunology Research, University of Chicago, Chicago, IL 60637, USA.

出版信息

Clin Dev Immunol. 2013;2013:267430. doi: 10.1155/2013/267430. Epub 2013 Sep 25.

Abstract

Systemic lupus erythematosus (SLE) patients frequently have high circulating tumor necrosis factor alpha (TNF-α) levels. We explored circulating TNF-α levels in SLE families to determine whether high levels of TNF-α were clustered in a heritable pattern. We measured TNF-α in 242 SLE patients, 361 unaffected family members, 23 unaffected spouses of SLE patients, and 62 unrelated healthy controls. Familial correlations and relative recurrence risk rates for the high TNF-α trait were assessed. SLE-affected individuals had the highest TNF-α levels, and TNF-α was significantly higher in unaffected first degree relatives than healthy unrelated subjects (P = 0.0025). No Mendelian patterns were observed, but 28.4% of unaffected first degree relatives of SLE patients had high TNF-α levels, resulting in a first degree relative recurrence risk of 4.48 (P = 2.9 × 10⁻⁵). Interestingly, the median TNF-α value in spouses was similar to that of the first degree relatives. Concordance of the TNF-α trait (high versus low) in SLE patients and their spouses was strikingly high at 78.2%. These data support a role for TNF-α in SLE pathogenesis, and TNF-α levels may relate with heritable factors. The high degree of concordance in SLE patients and their spouses suggests that environmental factors may also play a role in the observed familial aggregation.

摘要

系统性红斑狼疮(SLE)患者常常循环肿瘤坏死因子α(TNF-α)水平较高。我们探究了SLE患者家系中的循环TNF-α水平,以确定高水平的TNF-α是否以遗传模式聚集。我们测量了242例SLE患者、361名未患病的家庭成员、23名SLE患者的未患病配偶以及62名无亲缘关系的健康对照者的TNF-α水平。评估了高TNF-α性状的家族相关性和相对复发风险率。受SLE影响的个体TNF-α水平最高,未患病的一级亲属的TNF-α水平显著高于无亲缘关系的健康受试者(P = 0.0025)。未观察到孟德尔遗传模式,但SLE患者中28.4%的未患病一级亲属TNF-α水平较高,导致一级亲属复发风险为4.48(P = 2.9×10⁻⁵)。有趣的是,配偶的TNF-α中位数与一级亲属相似。SLE患者及其配偶中TNF-α性状(高与低)的一致性高达78.2%,令人惊讶。这些数据支持TNF-α在SLE发病机制中的作用,且TNF-α水平可能与遗传因素有关。SLE患者及其配偶之间的高度一致性表明环境因素可能也在观察到的家族聚集现象中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/944e/3800640/4edc481213e5/CDI2013-267430.001.jpg

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本文引用的文献

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Interferon regulatory factor 5 in the pathogenesis of systemic lupus erythematosus.
Clin Dev Immunol. 2012;2012:780436. doi: 10.1155/2012/780436. Epub 2012 Nov 1.
4
Genetic ancestry, serum interferon-α activity, and autoantibodies in systemic lupus erythematosus.
J Rheumatol. 2012 Jun;39(6):1238-40. doi: 10.3899/jrheum.111467. Epub 2012 Apr 15.
5
Large-scale analysis of tumor necrosis factor α levels in systemic lupus erythematosus.
Arthritis Rheum. 2012 Sep;64(9):2947-52. doi: 10.1002/art.34483.
7
Type I interferon signature is high in lupus and neuromyelitis optica but low in multiple sclerosis.
J Neurol Sci. 2012 Feb 15;313(1-2):48-53. doi: 10.1016/j.jns.2011.09.032. Epub 2011 Oct 27.
8
Interferon alpha as a primary pathogenic factor in human lupus.
J Interferon Cytokine Res. 2011 Dec;31(12):887-92. doi: 10.1089/jir.2011.0071. Epub 2011 Sep 16.
9
Functional study of TNF-α promoter polymorphisms: literature review and meta-analysis.
Eur Cytokine Netw. 2011 Jun;22(2):88-102. doi: 10.1684/ecn.2011.0285.

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