Quality of life in patients with autosomal dominant tubulointerstitial kidney disease

Clin Nephrol. 2019 Dec;92(6):302-311. doi: 10.5414/CN109842.


Aims: The reaction to diagnosis and quality of life (QOL) in autosomal dominant tubulointerstitial kidney disease (ADTKD) due to <i>UMOD</i> and <i>MUC</i> mutations from the time of diagnosis until treatment for end-stage kidney disease (ESKD) has not been characterized. It is unclear how asymptomatic patients react to a positive genetic test result.

Materials and methods: A cross-sectional survey concerning QOL and genetic testing was delivered to 622 individuals who had undergone genetic testing from families with known ADTKD.

Results: 286 of 622 individuals completed the survey, including 61 (21%) genetically unaffected, 36 (12%) with stage 1, 2 chronic kidney disease (CKD), 51 (18%) stage 3, 41 (14%) stage 4 pre-dialysis, 50 (17%) receiving dialysis, and 47 (16%) s/p kidney transplantation. Of 55 respondents who thought they had normal kidney function at the time of testing and were found to have ADTKD, 51 (93%) were happy testing was performed, 3 (5%) neutral, and 1 (2%) neutral/unhappy. 42 of 183 (23%) affected individuals stated that ADTKD "has a substantial effect and I think about it daily," 47 (26%) think about ADTKD weekly, 48 (26%) monthly, and 48 (26%) less than monthly. The mean PROMIS anxiety score was similar between unaffected and affected individuals and the general population. Depression was present in 41% of affected vs. 23% of unaffected individuals (p = 0.01).

Conclusion: Genetic testing of presymptomatic patients for ADTKD is reasonable when requested. This study provides reassurance regarding the impact on QOL of the increased use of genetic testing to diagnose kidney disease. ADTKD has a significant impact on QOL, with depression, not anxiety, being more prevalent in affected individuals.

MeSH terms

  • Adult
  • Aged
  • Cross-Sectional Studies
  • Female
  • Genetic Testing
  • Humans
  • Kidney Diseases / genetics*
  • Kidney Diseases / psychology*
  • Male
  • Middle Aged
  • Mucin-1 / genetics*
  • Mutation*
  • Quality of Life*
  • Uromodulin / genetics*
  • Young Adult


  • Mucin-1
  • Uromodulin