Your browser doesn't support javascript.
loading
Anticardiolipin Antibody Plays a More Important Role Than Anti-ß2-Glycoprotein I Antibody in Activating Complement in Patients with Lupus Nephritis.
Zhang, Qiankun; Ren, Zhuoqin; Li, Jie; Zou, Zhengping.
Afiliación
  • Zhang Q; Department of Nephrology, the Fifth Affiliated Hospital of Wenzhou University, Lishui, Zheiang, People's Republic of China.
  • Ren Z; Department of Nephrology, Lishui Central Hospital, Lishui, Zhejiang, People's Republic of China.
  • Li J; Department of Nephrology and Rheumatology, Qianjiang Central Hospital, Qianjiang, Hubei, People's Republic of China.
  • Zou Z; Department of Nephrology and Rheumatology, Qianjiang Hospital Affiliated to Renmin Hospital of Wuhan University, Qianjiang, Hubei, People's Republic of China.
Int J Gen Med ; 17: 517-523, 2024.
Article en En | MEDLINE | ID: mdl-38356686
ABSTRACT

Objective:

This research aimed to explore the correlation between antiphospholipid antibodies (aPLs) and complement activation in lupus nephritis (LN) patients.

Methods:

A retrospective analysis was carried out on patients diagnosed with LN based on renal biopsy from June 2019 to June 2022. The study assessed levels of IgM, IgA, and IgG subtypes of anticardiolipin antibodies (aCLs) and anti-ß2-glycoprotein I (anti-ß2-GPI) antibodies. Pathological and clinical data were collected concurrently with the renal biopsy.

Results:

The analysis included 76 LN patients, with 44.7% testing positive for aPLs. LN patients with positive aPLs exhibited increased hematuria, higher SLEDAI scores, reduced serum C3 and C4 levels, and more C1q deposits in the glomerulus compared to those with negative aPLs (P<0.05). Correlation analysis demonstrated the inverse relationships between IgG-aCL levels and serum C3 and C4 levels (r=-0.29, P=0.005; r=-0.24, P=0.016, respectively), as well as a positive correlation with C4 deposits in the glomerulus (r=0.20, P=0.041).

Conclusion:

This investigation suggests that aPLs, particularly IgG-aCLs, may be associated with the severity of LN and could contribute to the activation of classical complement pathways.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Int J Gen Med Año: 2024 Tipo del documento: Article Pais de publicación: Nueva Zelanda

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Int J Gen Med Año: 2024 Tipo del documento: Article Pais de publicación: Nueva Zelanda