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Asian Journal of Urology, 2024, 11(2): 169-179    doi: 10.1016/j.ajur.2023.03.004
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Monogenic features of urolithiasis: A comprehensive review
Kyo Chul Kooa,Abdulghafour Halawanib,Victor K.F. Wongc,Dirk Langec,Ben H. Chewc*()
aDepartment of Urology, Yonsei University College of Medicine, Seoul, Republic of Korea
bDepartment of Urology, King Abdulaziz University, Jeddah, Saudi Arabia
cDepartment of Urological Sciences, University of British Columbia, Stone Centre at Vancouver General Hospital, Vancouver, British Columbia, Canada
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Abstract: 

Objective: Urolithiasis formation has been attributed to environmental and dietary factors. However, evidence is accumulating that genetic background can contribute to urolithiasis formation. Advancements in the identification of monogenic causes using high-throughput sequencing technologies have shown that urolithiasis has a strong heritable component.

Methods: This review describes monogenic factors implicated in a genetic predisposition to urolithiasis. Peer-reviewed journals were evaluated by a PubMed search until July 2023 to summarize disorders associated with monogenic traits, and discuss clinical implications of identification of patients genetically susceptible to urolithiasis formation.

Results: Given that more than 80% of urolithiases cases are associated with calcium accumulation, studies have focused mainly on monogenetic contributors to hypercalciuric urolithiases, leading to the identification of receptors, channels, and transporters involved in the regulation of calcium renal tubular reabsorption. Nevertheless, available candidate genes and linkage methods have a low resolution for evaluation of the effects of genetic components versus those of environmental, dietary, and hormonal factors, and genotypes remain undetermined in the majority of urolithiasis formers.

Conclusion: The pathophysiology underlying urolithiasis formation is complex and multifactorial, but evidence strongly suggests the existence of numerous monogenic causes of urolithiasis in humans.

Key words:  Gene    Genetic expression    Inheritance pattern    Urolithiasis
收稿日期:  2022-07-05           接受日期:  2023-03-28      出版日期:  2024-04-20      发布日期:  2024-04-28      整期出版日期:  2024-04-20
引用本文:    
. [J]. Asian Journal of Urology, 2024, 11(2): 169-179.
Kyo Chul Koo, Abdulghafour Halawani, Victor K.F. Wong, Dirk Lange, Ben H. Chew. Monogenic features of urolithiasis: A comprehensive review. Asian Journal of Urology, 2024, 11(2): 169-179.
链接本文:  
http://www.ajurology.com/CN/10.1016/j.ajur.2023.03.004  或          http://www.ajurology.com/CN/Y2024/V11/I2/169
Disorder Gene Inheritance Phenotype
Autosomal dominant idiopathic hypercalciuria ? ADCY10 and VDR AD ? Normocalcemia and normal PTH
Autosomal dominant hypocalcemia with hypercalciuria ? CASR and GNA11 AD ? Hypocalcemia, hyperphosphatemia, hypomagnesemia, and low to normal range PTH
Bartter syndrome
Type I ? NKCC2 (SLC12A1) AR ? Antenatal or postnatal nephrocalcinosis, hypokalemia, and metabolic alkalosis
Type II ? ROMK (KCNJ1) AR ? Antenatal/postnatal nephrocalcinosis, hyperkalemia in infancy, postnatal hypokalemia, late-onset nephrocalcinosis, and CKD
Type III ? CLCNKB AR ? Hypokalemic metabolic alkalosis, nephrocalcinosis, and late-onset symptoms
Type IVa ? BSND AR ? Sensorineural hearing loss and early-onset CKD
Type IVb ? CLCNKB and CLCNKA AR ? Renal salt wasting and sensorineural hearing loss
Type V ? MAGED2 XLR ? Salt wasting, polyuria, hypokalemia, nephrocalcinosis, and antenatal onset
Dent disease
Type 1 ? CLCN5 XLR ? LMW proteinuria, nephrocalcinosis, and CKD with progression to ESRD
Type 2 ? OCRL XLR ? LMW proteinuria and nephrocalcinosis (less frequent than type 1)
Hereditary hypophosphatemic rickets with hypercalciuria ? SLC34A1, SLC34A3, and SLC9A3R1 AR ? Low serum phosphate, hypophosphatemia, normocalcemia, and elevated 1,25(OH)2 vitamin D
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis ? CLDN16 and CLDN19 AR ? Hypomagnesemia, nephrocalcinosis, and progression to ESRD in adolescence
Distal renal tubular acidosis ? ATP6V1B1, ATP6V0A4, and SLC4A1 AD ? Hypokalemia, metabolic acidosis, nephrocalcinosis, growth delay, early-onset sensorineural deafness, and metabolic bone disease
Primary hyperoxaluria ? AGXT, GRHPR, and HOGA1 AR ? CKD with progression to ESRD and risk of systemic oxalosis
Infantile hypercalcemia ? CYP24A1 and SLC34A1 AR ? Hypercalcemia
Cystinuria ? SLC3A1 and SLC7A9 AR or AD ? Cystine stones and nephrocalcinosis
Hereditary hyperuricosuria ? HPRT1 XLR ? Hyperuricemia, neurologic deficits (psychomotor delay, intellectual disability), and renal failure
Hereditary xanthinuria ? XDH, MOCOS, MOCS1, MOCS2, and GPHN AR ? Myopathy, psychomotor deficit, growth delay, seizure, and hypotonia
Adenine phosphoribosyltransferase deficiency ? APRT AR ? Crystalluria and progressive CKD
  
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