4.2 Article

Systematic assessment of monogenic etiology in adult-onset kidney stone formers undergoing urological intervention-evidence for genetic pretest probability

出版社

WILEY
DOI: 10.1002/ajmg.c.31991

关键词

cystinuria; genetics; kidney stone disease; nephrocalcinosis; nephrolithiasis; urolithiasis

资金

  1. Deutsche Forschungsgemeinschaft (DFG) [HA 6908/2-1]
  2. Else-Kroner Fresenius Foundation (EKFS)
  3. Fritz Thyssen Foundation (FTS)
  4. DFG [HA 6908/3-1, HA 6908/4-1, HA 6908/7-1, HA 6908/8-1]
  5. EKFS

向作者/读者索取更多资源

Kidney stone disease is a common condition associated with both genetic and environmental factors. This study used targeted next generation sequencing to identify hereditary kidney stone disorders in adults, providing insights into the underlying mechanisms of the disease and potential personalized treatments. Additionally, the study found that hereditary kidney stone disease is associated with increased disease severity.
Kidney stone disease (KSD) is a prevalent condition associated with high morbidity, frequent recurrence, and progression to chronic kidney disease (CKD). The etiology is multifactorial, depending on environmental and genetic factors. Although monogenic KSD is frequent in children, unbiased prevalence data of heritable forms in adults is scarce. Within 2 years of recruitment, all patients hospitalized for urological kidney stone intervention at our center were consecutively enrolled for targeted next generation sequencing (tNGS). Additionally, clinical and metabolic assessments were performed for genotype-phenotype analyses. The cohort comprised 155 (66%) males and 81 (34%) females, with a mean age at first stone of 47 years (4-86). The diagnostic yield of tNGS was 6.8% (16/236), with cystinuria (SLC3A1, SLC7A9), distal renal tubular acidosis (SLC4A1), and renal phosphate wasting (SLC34A1, SLC9A3R1) as underlying hereditary disorders. While metabolic syndrome traits were associated with late-onset KSD, hereditary KSD was associated with increased disease severity in terms of early-onset, frequent recurrence, mildly impaired kidney function, and common bilateral affection. By employing systematic genetic analysis to a less biased cohort of common adult kidney stone formers, we demonstrate its diagnostic value for establishing the underlying disorder in a distinct proportion. Factors determining pretest probability include age at first stone (<40 years), frequent recurrence, mild CKD, and bilateral KSD.

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