論文

国際誌
2022年11月18日

Racial heterogeneity of IgA1 hinge-region O-glycoforms in patients with IgA nephropathy.

iScience
  • Yukako Ohyama
  • Hisateru Yamaguchi
  • Soshiro Ogata
  • Samantha Chiurlia
  • Sharon N Cox
  • Nikoletta-Maria Kouri
  • Maria J Stangou
  • Kazuki Nakajima
  • Hiroki Hayashi
  • Daijo Inaguma
  • Midori Hasegawa
  • Yukio Yuzawa
  • Naotake Tsuboi
  • Matthew B Renfrow
  • Jan Novak
  • Aikaterini A Papagianni
  • Francesco P Schena
  • Kazuo Takahashi
  • 全て表示

25
11
開始ページ
105223
終了ページ
105223
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.isci.2022.105223

Galactose (Gal)-deficient IgA1 (Gd-IgA1) is involved in IgA nephropathy (IgAN) pathogenesis. To reflect racial differences in clinical characteristics, we assessed disease- and race-specific heterogeneity in the O-glycosylation of the IgA1 hinge region (HR). We determined serum Gd-IgA1 levels in Caucasians (healthy controls [HCs], n = 31; IgAN patients, n = 63) and Asians (HCs, n = 20; IgAN patients, n = 60) and analyzed profiles of serum IgA1 HR O-glycoforms. Elevated serum Gd-IgA1 levels and reduced number of Gal residues per HR were observed in Caucasians. Reduced number of N-acetylgalactosamine (GalNAc) residues per HR and elevated relative abundance of IgA1 with three HR O-glycans were common features in IgAN patients; these features were associated with elevated blood pressure and reduced renal function. We speculate that the mechanisms underlying the reduced GalNAc content in IgA1 HR may be relevant to IgAN pathogenesis.

リンク情報
DOI
https://doi.org/10.1016/j.isci.2022.105223
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/36277451
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9583103
ID情報
  • DOI : 10.1016/j.isci.2022.105223
  • PubMed ID : 36277451
  • PubMed Central 記事ID : PMC9583103

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