ASN's Mission

To create a world without kidney diseases, the ASN Alliance for Kidney Health elevates care by educating and informing, driving breakthroughs and innovation, and advocating for policies that create transformative changes in kidney medicine throughout the world.

learn more

Contact ASN

1401 H St, NW, Ste 900, Washington, DC 20005

email@asn-online.org

202-640-4660

The Latest on X

Kidney Week

Abstract: FR-PO0869

Attribute-Based Medicine for IgAN: A Nationwide Japanese Cohort Reveals Prognostic Interactions

Session Information

Category: Glomerular Diseases

  • 1402 Glomerular Diseases: Clinical, Outcomes, and Therapeutics

Authors

  • Kataoka, Hiroshi, Tokyo Joshi Ika Daigaku, Shinjuku, Tokyo, Japan
  • Manabe, Shun, Tokyo Joshi Ika Daigaku, Shinjuku, Tokyo, Japan
  • Moriyama, Takahito, Tokyo Ika Daigaku, Shinjuku, Tokyo, Japan
  • Ushio, Yusuke, Tokyo Joshi Ika Daigaku, Shinjuku, Tokyo, Japan
  • Nitta, Kosaku, Tokyo Joshi Ika Daigaku, Shinjuku, Tokyo, Japan
  • Hoshino, Junichi, Tokyo Joshi Ika Daigaku, Shinjuku, Tokyo, Japan
  • Hirano, Keita, Tokyo Jikeikai Ika Daigaku, Minato, Tokyo, Japan
  • Matsuzaki, Keiichi, Kitasato Daigaku Igakubu, Sagamihara, Kanagawa Prefecture, Japan
  • Yasuda, Takashi, Nagoya Daigaku Daigakuin Igakukei Kenkyuka Igakubu, Nagoya, Aichi Prefecture, Japan
  • Yasuda, Yoshinari, Kichijoji Asahi Byoin, Musashino, Tokyo, Japan
  • Kawamura, Tetsuya, Tokyo Jikeikai Ika Daigaku, Minato, Tokyo, Japan
  • Maruyama, Shoichi, Nagoya Daigaku, Nagoya, Aichi Prefecture, Japan
  • Yokoo, Takashi, Tokyo Jikeikai Ika Daigaku, Minato, Tokyo, Japan
  • Suzuki, Yusuke, Juntendo Daigaku, Bunkyo, Tokyo, Japan
Background

IgA nephropathy (IgAN) is a heterogeneous glomerular disease with variable progression patterns. Attribute-based medicine emphasizes tailoring treatment to individual characteristics. We hypothesized that this approach could clarify residual risks and inform personalized management.

Methods

This secondary analysis included 996 adults from the Japanese Nationwide Retrospective Cohort Study in IgAN. The primary outcome was kidney replacement therapy or a ≥1.5-fold increase in serum creatinine. Six attributes were assessed: age, sex, BMI, CKD stage, urinary protein excretion (U-Prot), and urine occult blood (U-OB). Cox regression and Kaplan–Meier analyses evaluated main effects and interactions with eight clinical variables (e.g., eGFR, corticosteroid use, hyperuricaemia).

Results

Over a median 7.0 years, 111 patients (11.1%) reached the primary outcome. Multivariable analysis identified low eGFR (HR=0.87 per 10 mL/min/1.73 m2), high U-Prot (log HR=4.54), and hyperuricaemia (HR=1.64) as risk factors; corticosteroids (HR=0.60) and tonsillectomy (HR=0.44) were protective. Key interactions included:
1. Hyperuricaemia with BMI <22 kg/m2 (HR=3.44, P=0.003),
2. Hypertension with female sex (HR=4.36, P=0.018),
3. The prognostic impact of age and eGFR differed between CKD stage 3 and stages 1–2, indicating a reversal in risk association,
4. Stronger association of U-Prot with outcomes in those with U-OB ≤2+,
5. Corticosteroids improved outcomes in patients with U-Prot ≥1 g/day, while tonsillectomy was most effective in those with U-OB ≥3+.

Conclusion

Attribute-based analysis uncovered critical risk modifiers and supports individualized treatment strategies in IgAN. This approach enables precision nephrology and may improve kidney outcomes by aligning therapy with patient attributes.

Digital Object Identifier (DOI)