Serum and urinary galactose-deficient IgA1 as a tool for diagnosis of IgA nephropathy in pediatric patients with hematuria

被引:0
|
作者
Abdelrahman, Nour A. [1 ]
EL Hakim, Ihab Z. [2 ]
Mohamed, Neama L. [3 ]
EL Farsy, Mohamed S. [2 ]
机构
[1] Ain Shams Univ, Fac Med, Publ Hlth Hosp, Paediat Dept, Cairo, Egypt
[2] Ain Shams Univ, Clin Pathol Dept, Cairo, Egypt
[3] Ain Shams Univ, Fac Med, Cairo, Egypt
关键词
IgA nephropathy; Serum galactose-deficient IgA1; Urinary galactose IgA1; IMMUNOGLOBULIN-A NEPHROPATHY; CHILDREN; LEVEL;
D O I
10.21608/ejpa.2024.277144.1064
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: IgA nephropathy (IgAN) is an immunopathologic diagnosis based on a renal biopsy. Diagnosis of IgAN may not be made in the milder cases or may be delayed until clinical manifestations are severe. We sought to assess the validity of serum and urinary galactose-deficient IgA1(GdIgA1) as a possible non-invasive diagnostic biomarker of IgAN. Methods: A cross-sectional study was conducted at Pediatric Nephrology Clinic, Children's Hospitals, Ain Shams University on 40 patients with recurrent gross glomerular hematuria diagnosed with renal biopsy and divided into two equal groups, group 1 patients with IgAN and group 2 with non-IgA glomerular diseases. Serum and urinary Gd-IgA1 levels were measured by ELISA using an anti-Gd-IgA1 monoclonal antibody (KM55). Laboratory investigations included complete blood count (CBC), erythrocyte sedimentation rate (ESR), complement 3 level in serum (C3), antinuclear antibody (ANA), anti-double strand DNA, urine protein/creatinine (UP/Cr) ratio, serum, and urinary total IgA levels (ELISA). . Results: The study included 20 patients with IgAN, of which 13 were males and 7 were females, in addition to 20 patients with non-IgAN, of which 12 were males and 8 were females. In the IgAN group median age was 6.5 (5-9) years old. In the nonIgAN group, median age was 9 (4.5-13) years old. Serum Gd-IgA1 levels were significantly elevated in children with IgAN compared with children with non-IgA glomerular diseases (p-value 0.001). The serum Gd-IgA1 cutoff point to differentiate between IgAN and non-IgA glomerular diseases was 240 ng/ml with 75 % sensitivity and 80 % specificity and AUC 80.2%. There was no statistically significant difference between IgAN and non-IgA glomerular diseases regarding urinary Gd-IgA1 (p-value 0.08), Ptn/Creat ratio (p-value 0.055), serum and urine total IgA (p-value 0.144 and 0.288). Conclusion: Serum Gd-IgA1 level is higher in IgAN patients compared to non-IgA glomerular diseases, serum Gd-IgA1 may be used as a non-invasive diagnostic biomarker for IgAN patients. .
引用
收藏
页码:73 / 80
页数:8
相关论文
共 50 条
  • [21] IgA nephropathy: characterization of IgG antibodies specific for galactose-deficient IgA1
    Suzuki, Hitoshi
    Moldoveanu, Zina
    Hall, Stacy
    Brown, Rhubell
    Julian, Bruce A.
    Wyatt, Robert J.
    Tomana, Milan
    Tomino, Yasuhiko
    Novak, Jan
    Mestecky, Jiri
    IGA NEPHROPATHY TODAY, 2007, 157 : 129 - 133
  • [22] Autoantibodies Targeting Galactose-Deficient IgA1 Associate with Progression of IgA Nephropathy
    Berthoux, Francois
    Suzuki, Hitoshi
    Thibaudin, Lise
    Yanagawa, Hiroyuki
    Maillard, Nicolas
    Mariat, Christophe
    Tomino, Yasuhiko
    Julian, Bruce A.
    Novak, Jan
    JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2012, 23 (09): : 1579 - 1587
  • [23] Oxidative Stress and Galactose-Deficient IgA1 as Markers of Progression in IgA Nephropathy
    Camilla, Roberta
    Suzuki, Hitoshi
    Dapra, Valentina
    Loiacono, Elisa
    Peruzzi, Licia
    Amore, Alessandro
    Ghiggeri, Gian Marco
    Mazzucco, Gianna
    Scolari, Francesco
    Gharavi, Ali G.
    Appel, Gerald B.
    Troyanov, Stephan
    Novak, Jan
    Julian, Bruce A.
    Coppo, Rosanna
    CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2011, 6 (08): : 1903 - 1911
  • [24] The level of galactose-deficient IgA1 in the sera of patients with IgA nephropathy is associated with disease progression
    Zhao, Na
    Hou, Ping
    Lv, Jicheng
    Moldoveanu, Zina
    Li, Yifu
    Kiryluk, Krzysztof
    Gharavi, Ali G.
    Novak, Jan
    Zhang, Hong
    KIDNEY INTERNATIONAL, 2012, 82 (07) : 790 - 796
  • [25] A case of paraneoplastic IgA nephropathy with glomerular capillary IgA and galactose-deficient IgA1 deposition
    Isogai, Erika
    Iwazu, Yoshitaka
    Akimoto, Tetsu
    Kuro-o, Makoto
    Niki, Toshiro
    Nagata, Daisuke
    CEN CASE REPORTS, 2024, 13 (02) : 104 - 109
  • [26] Changes in Nephritogenic Serum Galactose-Deficient IgA1 in IgA Nephropathy following Tonsillectomy and Steroid Therapy
    Nakata, Junichiro
    Suzuki, Yusuke
    Suzuki, Hitoshi
    Sato, Daisuke
    Kano, Tatsuya
    Yanagawa, Hiroyuki
    Matsuzaki, Keiichi
    Horikoshi, Satoshi
    Novak, Jan
    Tomino, Yasuhiko
    PLOS ONE, 2014, 9 (02):
  • [27] Clinical Significance of Galactose-Deficient IgA1 by KM55 in Patients with IgA Nephropathy
    Zhang, Kai
    Li, Qiongqiong
    Zhang, Yaru
    Shang, Wenya
    Wei, Li
    Li, Hongfen
    Gao, Shan
    Yan, Tiekun
    Jia, Junya
    Liu, Youxia
    Lin, Shan
    KIDNEY & BLOOD PRESSURE RESEARCH, 2019, 44 (05): : 1196 - 1206
  • [28] Clinical Relevance of Serum Galactose Deficient IgA1 in Patients with IgA Nephropathy
    Kim, Jin Sug
    Hwang, Hyeon Seok
    Lee, Sang Ho
    Kim, Yang Gyun
    Moon, Ju-Young
    Kong, Ji Yoon
    Jeong, Kyung Hwan
    JOURNAL OF CLINICAL MEDICINE, 2020, 9 (11) : 1 - 11
  • [29] A case of paraneoplastic IgA nephropathy with glomerular capillary IgA and galactose-deficient IgA1 deposition
    Erika Isogai
    Yoshitaka Iwazu
    Tetsu Akimoto
    Makoto Kuro-o
    Toshiro Niki
    Daisuke Nagata
    CEN Case Reports, 2024, 13 : 104 - 109
  • [30] Characterization of a recombinant IgG autoantibody specific for galactose-deficient IgA1 in IgA nephropathy
    Knoppova, Barbora
    Hansen, Alyssa
    Moldoveanu, Zina
    Hall, Stacy D.
    Huang, Zhi-Qiang
    Novak, Lea
    Julian, Bruce A.
    Renfrow, Matthew B.
    Novak, Jan
    Green, Todd J.
    GLYCOBIOLOGY, 2020, 30 (12) : 1068 - 1068