Apolipoprotein L1 Risk Variants Associate with Systemic Lupus Erythematosus-Associated Collapsing Glomerulopathy

被引:158
作者
Larsen, Christopher P. [1 ,2 ]
Beggs, Marjorie L. [1 ]
Saeed, Mohammad [1 ]
Walker, Patrick D. [1 ,2 ]
机构
[1] Nephropath, Little Rock, AR 72211 USA
[2] Univ Arkansas Med Sci, Dept Pathol, Little Rock, AR 72205 USA
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2013年 / 24卷 / 05期
关键词
FOCAL SEGMENTAL GLOMERULOSCLEROSIS; HIV; KIDNEY; APOL1; GLOMERULONEPHRITIS; CLASSIFICATION; NEPHROPATHY; NEPHRITIS; AFRICAN; DISEASE;
D O I
10.1681/ASN.2012121180
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Collapsing glomerulopathy is a devastating renal disease that primarily affects African Americans and associates with numerous etiologies, such as HIV and autoimmune disease. The presence of APOL1 risk alleles associates with HIV-associated collapsing glomerulopathy, but it is unknown whether these risk alleles also associate with systemic lupus erythematosus (SLE)-associated collapsing glomerulopathy. Here, re-examination of 546 renal biopsies from African-American patients with SLE identified 26 cases of collapsing glomerulopathy, which we genotyped for APOL1 risk alleles using DNA extracted from archived biopsy tissue. APOL1 strongly associated with SLE-associated collapsing glomerulopathy (P<0.001). In a recessive model, two APOL1 risk alleles conferred 5.4-fold (95% CI=2.4 to 12.1) higher odds of developing SLE-associated collapsing glomerulopathy (P<0.001). In conclusion, APOL1 genotyping of African-American patients with SLE might help identify patients at risk for collapsing glomerulopathy, an entity with a poor prognosis that is often resistant to treatment. J Am Soc Nephrol 24: 722-725, 2013. doi: 10.1681/ASN.2012121180
引用
收藏
页码:722 / 725
页数:4
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