Aberrant galactosylation of IgA1 is involved in the genetic susceptibility of Chinese patients with IgA nephropathy
Author(s) -
Xiaojie Lin,
Jie Ding,
Li Zhu,
S. Shi,
Liping Jiang,
Mingming Zhao,
H. Zhang
Publication year - 2009
Publication title -
nephrology dialysis transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.654
H-Index - 168
eISSN - 1460-2385
pISSN - 0931-0509
DOI - 10.1093/ndt/gfp294
Subject(s) - medicine , nephropathy , pathogenesis , gastroenterology , immunology , diabetes mellitus , endocrinology
Immunoglobulin A nephropathy (IgAN) is associated with genetic and environmental factors, and undergalactosylation of IgA1 in the serum is considered to be a contributor to pathogenesis of IgAN. The present study was conducted to detect the galactose- (Gal) deficient IgA1 level in Chinese IgAN patients and their family members.
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