Genotype-phenotype analysis in pediatric patients with distal renal tubular acidosis

Eujin Park, Myung Hyun Cho, Hye Sun Hyun, Jaeil Shin, Joo Hoon Lee, Young Seo Park, Hyun Jin Choi, Hee Gyung Kang, Hae Il Cheong

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Background/Aims: Primary distal renal tubular acidosis (dRTA) in children is a rare genetic disorder, and three causative mutated genes have been identified: SLC4A1, ATP6V1B1, and ATP6V0A4. We analyzed the prevalence and phenotypic differences of genetic mutations in children with dRTA. Methods: A total of 17 children with dRTA were enrolled in the study. All patients underwent genetic testing for all three candidate genes. Results: Pathogenic mutations, including six novel mutations, were detected in 15 (88.2%) patients: dominant SLC4A1 mutations in ten (58.8%) patients, recessive ATP6V0A4 mutations in three (17.6%) patients, and recessive ATP6V1B1 mutations in two (11.8%) patients. Compared to other patients, patients with SLC4A1 mutations showed an older age of onset (3.7 ± 2.6 years) and less severe metabolic acidosis at initial presentation. All patients developed nephrocalcinosis, and sensorineural hearing loss was observed in two patients with ATP6V1B1 mutations. Three (17.6%) patients had decreased renal function (chronic kidney disease stage 2), and five (29.4%) patients had persistent growth retardation at the last follow-up. Long-term prognosis showed no genotype-phenotype correlation. Conclusions: SLC4A1 is the most common defective gene in Korean children with dRTA. Patients with SLC4A1 mutations show later onset and milder disease severity. Long-term follow-up of hearing ability, renal function, and growth is necessary for patients with dRTA.

Original languageEnglish
Pages (from-to)513-521
Number of pages9
JournalKidney and Blood Pressure Research
Volume43
Issue number2
DOIs
Publication statusPublished - 2018 Jan 1

Fingerprint

Renal Tubular Acidosis
Genotype
Pediatrics
Phenotype
Mutation
Nephrocalcinosis
Genes
Kidney
Inborn Genetic Diseases
Aptitude
Sensorineural Hearing Loss
Genetic Testing
Genetic Association Studies
Growth
Acidosis
Chronic Renal Insufficiency
Age of Onset
Hearing

All Science Journal Classification (ASJC) codes

  • Nephrology
  • Cardiology and Cardiovascular Medicine

Cite this

Park, Eujin ; Cho, Myung Hyun ; Hyun, Hye Sun ; Shin, Jaeil ; Lee, Joo Hoon ; Park, Young Seo ; Choi, Hyun Jin ; Kang, Hee Gyung ; Cheong, Hae Il. / Genotype-phenotype analysis in pediatric patients with distal renal tubular acidosis. In: Kidney and Blood Pressure Research. 2018 ; Vol. 43, No. 2. pp. 513-521.
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title = "Genotype-phenotype analysis in pediatric patients with distal renal tubular acidosis",
abstract = "Background/Aims: Primary distal renal tubular acidosis (dRTA) in children is a rare genetic disorder, and three causative mutated genes have been identified: SLC4A1, ATP6V1B1, and ATP6V0A4. We analyzed the prevalence and phenotypic differences of genetic mutations in children with dRTA. Methods: A total of 17 children with dRTA were enrolled in the study. All patients underwent genetic testing for all three candidate genes. Results: Pathogenic mutations, including six novel mutations, were detected in 15 (88.2{\%}) patients: dominant SLC4A1 mutations in ten (58.8{\%}) patients, recessive ATP6V0A4 mutations in three (17.6{\%}) patients, and recessive ATP6V1B1 mutations in two (11.8{\%}) patients. Compared to other patients, patients with SLC4A1 mutations showed an older age of onset (3.7 ± 2.6 years) and less severe metabolic acidosis at initial presentation. All patients developed nephrocalcinosis, and sensorineural hearing loss was observed in two patients with ATP6V1B1 mutations. Three (17.6{\%}) patients had decreased renal function (chronic kidney disease stage 2), and five (29.4{\%}) patients had persistent growth retardation at the last follow-up. Long-term prognosis showed no genotype-phenotype correlation. Conclusions: SLC4A1 is the most common defective gene in Korean children with dRTA. Patients with SLC4A1 mutations show later onset and milder disease severity. Long-term follow-up of hearing ability, renal function, and growth is necessary for patients with dRTA.",
author = "Eujin Park and Cho, {Myung Hyun} and Hyun, {Hye Sun} and Jaeil Shin and Lee, {Joo Hoon} and Park, {Young Seo} and Choi, {Hyun Jin} and Kang, {Hee Gyung} and Cheong, {Hae Il}",
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Park, E, Cho, MH, Hyun, HS, Shin, J, Lee, JH, Park, YS, Choi, HJ, Kang, HG & Cheong, HI 2018, 'Genotype-phenotype analysis in pediatric patients with distal renal tubular acidosis', Kidney and Blood Pressure Research, vol. 43, no. 2, pp. 513-521. https://doi.org/10.1159/000488698

Genotype-phenotype analysis in pediatric patients with distal renal tubular acidosis. / Park, Eujin; Cho, Myung Hyun; Hyun, Hye Sun; Shin, Jaeil; Lee, Joo Hoon; Park, Young Seo; Choi, Hyun Jin; Kang, Hee Gyung; Cheong, Hae Il.

In: Kidney and Blood Pressure Research, Vol. 43, No. 2, 01.01.2018, p. 513-521.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Genotype-phenotype analysis in pediatric patients with distal renal tubular acidosis

AU - Park, Eujin

AU - Cho, Myung Hyun

AU - Hyun, Hye Sun

AU - Shin, Jaeil

AU - Lee, Joo Hoon

AU - Park, Young Seo

AU - Choi, Hyun Jin

AU - Kang, Hee Gyung

AU - Cheong, Hae Il

PY - 2018/1/1

Y1 - 2018/1/1

N2 - Background/Aims: Primary distal renal tubular acidosis (dRTA) in children is a rare genetic disorder, and three causative mutated genes have been identified: SLC4A1, ATP6V1B1, and ATP6V0A4. We analyzed the prevalence and phenotypic differences of genetic mutations in children with dRTA. Methods: A total of 17 children with dRTA were enrolled in the study. All patients underwent genetic testing for all three candidate genes. Results: Pathogenic mutations, including six novel mutations, were detected in 15 (88.2%) patients: dominant SLC4A1 mutations in ten (58.8%) patients, recessive ATP6V0A4 mutations in three (17.6%) patients, and recessive ATP6V1B1 mutations in two (11.8%) patients. Compared to other patients, patients with SLC4A1 mutations showed an older age of onset (3.7 ± 2.6 years) and less severe metabolic acidosis at initial presentation. All patients developed nephrocalcinosis, and sensorineural hearing loss was observed in two patients with ATP6V1B1 mutations. Three (17.6%) patients had decreased renal function (chronic kidney disease stage 2), and five (29.4%) patients had persistent growth retardation at the last follow-up. Long-term prognosis showed no genotype-phenotype correlation. Conclusions: SLC4A1 is the most common defective gene in Korean children with dRTA. Patients with SLC4A1 mutations show later onset and milder disease severity. Long-term follow-up of hearing ability, renal function, and growth is necessary for patients with dRTA.

AB - Background/Aims: Primary distal renal tubular acidosis (dRTA) in children is a rare genetic disorder, and three causative mutated genes have been identified: SLC4A1, ATP6V1B1, and ATP6V0A4. We analyzed the prevalence and phenotypic differences of genetic mutations in children with dRTA. Methods: A total of 17 children with dRTA were enrolled in the study. All patients underwent genetic testing for all three candidate genes. Results: Pathogenic mutations, including six novel mutations, were detected in 15 (88.2%) patients: dominant SLC4A1 mutations in ten (58.8%) patients, recessive ATP6V0A4 mutations in three (17.6%) patients, and recessive ATP6V1B1 mutations in two (11.8%) patients. Compared to other patients, patients with SLC4A1 mutations showed an older age of onset (3.7 ± 2.6 years) and less severe metabolic acidosis at initial presentation. All patients developed nephrocalcinosis, and sensorineural hearing loss was observed in two patients with ATP6V1B1 mutations. Three (17.6%) patients had decreased renal function (chronic kidney disease stage 2), and five (29.4%) patients had persistent growth retardation at the last follow-up. Long-term prognosis showed no genotype-phenotype correlation. Conclusions: SLC4A1 is the most common defective gene in Korean children with dRTA. Patients with SLC4A1 mutations show later onset and milder disease severity. Long-term follow-up of hearing ability, renal function, and growth is necessary for patients with dRTA.

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