Tubulointerstitial nephritis and uveitis (TINU) syndrome: a review

Br J Ophthalmol. 2020 Jun;104(6):742-747. doi: 10.1136/bjophthalmol-2019-314926. Epub 2019 Nov 12.

Abstract

Inflammation of renal interstitium and uveal tissue establishes the two components of tubulointerstitial nephritis and uveitis (TINU) syndrome. Although believed to occur more frequently in young females, a broad spectrum of patients can be affected. Both renal and eye disease can be asymptomatic and may not manifest simultaneously, having independent progressions. Renal disease manifests as acute kidney injury and may cause permanent renal impairment. Eye inflammation can manifest in different anatomical forms, most commonly as bilateral anterior uveitis and may progress to a chronic course. TINU syndrome accounts for approximately 1%-2% of uveitis in tertiary referral centres. A literature review covering the clinical features, pathogenesis, diagnosis and treatment is presented.

Publication types

  • Review

MeSH terms

  • Biopsy
  • Humans
  • Kidney / diagnostic imaging*
  • Nephritis, Interstitial / diagnosis*
  • Risk Factors
  • Syndrome
  • Uvea / diagnostic imaging*
  • Uveitis / diagnosis*

Supplementary concepts

  • Tubulointerstitial nephritis and uveitis