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系统性红斑狼疮患者的血清补体和免疫球蛋白谱:一家教学医院的观察性研究。

Serum complements and immunoglobulin profiles in systemic lupus erythematosus patients: An observational study at a teaching hospital.

作者信息

Rana Ranjan Singh, Naik Bitan, Yadav Mahima, Singh Usha, Singh Anup, Singh Shailja

机构信息

Department of Pathology, Institute of Medical Sciences (IMS), Banaras Hindu University (BHU), Varanasi, Uttar Pradesh, India.

Department of Medicine, Institute of Medical Sciences (IMS), Banaras Hindu University (BHU), Varanasi, Uttar Pradesh, India.

出版信息

J Family Med Prim Care. 2022 Feb;11(2):608-613. doi: 10.4103/jfmpc.jfmpc_960_21. Epub 2022 Feb 16.

Abstract

CONTEXT

Serum complement proteins and autoantibodies play an important role in the pathogenesis and diagnosis of systemic lupus erythematosus (SLE). Abnormalities in various immunoglobulin levels are described in patients of SLE.

AIMS

To study the spectrum of clinical manifestations and measure the serum levels of complement C3, complement C4, autoantibodies and immunoglobulin G (IgG) in patients of SLE and compare with healthy controls.

SETTINGS AND DESIGN

The present study is a prospective hospital-based observational study conducted between May 2014 and December 2018.

STATISTICAL ANALYSIS USED

Unpaired t-test was used to compare the mean values between the SLE patients and healthy controls.

MATERIAL AND METHODS

A total of 100 cases of SLE and 100 healthy controls were included in the study. The clinical data were retrieved. Serum antinuclear antibody, anti-ds DNA antibody, and anti-Smith antibody levels, and complements C3, C4 and IgG were measured.

RESULTS

Arthritis (89%) and anaemia (65%) were two common clinical presentations. The low complement C3 levels and C4 were detected in 64 and 62% of the SLE patients. Serum IgG was increased in 41% of the patients. A reduced level of IgG was detected in 6% of the patients.

CONCLUSION

Primary care physicians should be aware of the clinical and serological manifestations of SLE as early detection will reduce end-organ damage. Autoantibody testing and complement testing should be done in all suspected cases. This study showed a significantly reduced C3 and C4 and elevated IgG in many cases of SLE as compared to control. Hypogammaglobulinemia was also present in a minority of the cases.

摘要

背景

血清补体蛋白和自身抗体在系统性红斑狼疮(SLE)的发病机制和诊断中起重要作用。SLE患者存在各种免疫球蛋白水平异常。

目的

研究SLE患者的临床表现谱,检测其血清补体C3、补体C4、自身抗体和免疫球蛋白G(IgG)水平,并与健康对照进行比较。

设置与设计

本研究是一项于2014年5月至2018年12月在医院进行的前瞻性观察性研究。

所用统计分析方法

采用非配对t检验比较SLE患者和健康对照的均值。

材料与方法

本研究共纳入100例SLE患者和100名健康对照。收集临床资料。检测血清抗核抗体、抗双链DNA抗体、抗史密斯抗体水平以及补体C3、C4和IgG。

结果

关节炎(89%)和贫血(65%)是两种常见的临床表现。64%和62%的SLE患者检测到补体C3水平降低和C4降低。41%的患者血清IgG升高。6%的患者检测到IgG水平降低。

结论

基层医疗医生应了解SLE的临床和血清学表现,因为早期发现可减少终末器官损害。所有疑似病例均应进行自身抗体检测和补体检测。本研究表明,与对照组相比,许多SLE病例的C3和C4显著降低,IgG升高。少数病例还存在低丙种球蛋白血症。

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