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Kidney Cysts in Hypophosphatemic Rickets With Hypercalciuria: A Case Series
RATIONALE & OBJECTIVE: Hereditary hypophosphatemic rickets with hypercalciuria (HHRH) is a rare monogenic disorder caused by SLC34A3 pathogenic variants. HHRH is characterized by kidney phosphate wasting, hypophosphatemia, hypercalciuria, an elevated 1,25-dihydroxyvitamin D level, nephrocalcinos...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8978140/ https://www.ncbi.nlm.nih.gov/pubmed/35386604 http://dx.doi.org/10.1016/j.xkme.2022.100419 |
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author | Hanna, Christian Potretzke, Theodora A. Chedid, Maroun Rangel, Laureano J. Arroyo, Jennifer Zubidat, Dalia Tebben, Peter J. Cogal, Andrea G. Torres, Vicente E. Harris, Peter C. Sas, David J. Lieske, John C. Milliner, Dawn S. Chebib, Fouad T. |
author_facet | Hanna, Christian Potretzke, Theodora A. Chedid, Maroun Rangel, Laureano J. Arroyo, Jennifer Zubidat, Dalia Tebben, Peter J. Cogal, Andrea G. Torres, Vicente E. Harris, Peter C. Sas, David J. Lieske, John C. Milliner, Dawn S. Chebib, Fouad T. |
author_sort | Hanna, Christian |
collection | PubMed |
description | RATIONALE & OBJECTIVE: Hereditary hypophosphatemic rickets with hypercalciuria (HHRH) is a rare monogenic disorder caused by SLC34A3 pathogenic variants. HHRH is characterized by kidney phosphate wasting, hypophosphatemia, hypercalciuria, an elevated 1,25-dihydroxyvitamin D level, nephrocalcinosis, and urinary stone disease. Previously, we reported a 100% prevalence of kidney cysts in the related CYP24A1 deficiency. Thus, in the current study, we characterized cysts’ presence in HHRH, another monogenic cause of hypercalciuria, nephrocalcinosis, and urinary stone disease. STUDY DESIGN: Case series. SETTING & PARTICIPANTS: Medical records from the Mayo Clinic and the Rare Kidney Stone Consortium monogenic stone disease database were queried for patients with a genetically confirmed HHRH diagnosis. The number, sizes, and locations of kidney cysts in each patient were recorded. RESULTS: Twelve patients with SLC34A3 pathogenic variants were identified (7 monoallelic, 5 biallelic). Of these, 5 (42%) were males, and the median (Q1, Q3) ages were 16 years (13, 35 years) at clinical presentation and 42 years (20, 57 years) at genetic confirmation. Kidney cysts were present in 9 of 12 (75%) patients, and the median (Q1, Q3) age at first cyst detection was 41 years (13, 50 years). The median number of cysts per patient was 2.0 (0.5, 3.5). Fifty percent of adult patients had a cyst number that exceeded the 97.5th percentile of an age- and sex-matched control population. All children had at least 2 or more total cysts. None had a family history of cystic kidney disease. LIMITATIONS: Retrospective study, possible selection bias, single-center experience. CONCLUSIONS: A strong association between HHRH and kidney cysts was observed. Similarities in the biochemical profiles of HHRH and CYP24A1 deficiency suggest elevated active vitamin D and hypercalciuria may be potential cystogenic factors. Further studies are needed to understand how genetic changes in SLC34A3 favor cyst formation. |
format | Online Article Text |
id | pubmed-8978140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-89781402022-04-05 Kidney Cysts in Hypophosphatemic Rickets With Hypercalciuria: A Case Series Hanna, Christian Potretzke, Theodora A. Chedid, Maroun Rangel, Laureano J. Arroyo, Jennifer Zubidat, Dalia Tebben, Peter J. Cogal, Andrea G. Torres, Vicente E. Harris, Peter C. Sas, David J. Lieske, John C. Milliner, Dawn S. Chebib, Fouad T. Kidney Med Original Research RATIONALE & OBJECTIVE: Hereditary hypophosphatemic rickets with hypercalciuria (HHRH) is a rare monogenic disorder caused by SLC34A3 pathogenic variants. HHRH is characterized by kidney phosphate wasting, hypophosphatemia, hypercalciuria, an elevated 1,25-dihydroxyvitamin D level, nephrocalcinosis, and urinary stone disease. Previously, we reported a 100% prevalence of kidney cysts in the related CYP24A1 deficiency. Thus, in the current study, we characterized cysts’ presence in HHRH, another monogenic cause of hypercalciuria, nephrocalcinosis, and urinary stone disease. STUDY DESIGN: Case series. SETTING & PARTICIPANTS: Medical records from the Mayo Clinic and the Rare Kidney Stone Consortium monogenic stone disease database were queried for patients with a genetically confirmed HHRH diagnosis. The number, sizes, and locations of kidney cysts in each patient were recorded. RESULTS: Twelve patients with SLC34A3 pathogenic variants were identified (7 monoallelic, 5 biallelic). Of these, 5 (42%) were males, and the median (Q1, Q3) ages were 16 years (13, 35 years) at clinical presentation and 42 years (20, 57 years) at genetic confirmation. Kidney cysts were present in 9 of 12 (75%) patients, and the median (Q1, Q3) age at first cyst detection was 41 years (13, 50 years). The median number of cysts per patient was 2.0 (0.5, 3.5). Fifty percent of adult patients had a cyst number that exceeded the 97.5th percentile of an age- and sex-matched control population. All children had at least 2 or more total cysts. None had a family history of cystic kidney disease. LIMITATIONS: Retrospective study, possible selection bias, single-center experience. CONCLUSIONS: A strong association between HHRH and kidney cysts was observed. Similarities in the biochemical profiles of HHRH and CYP24A1 deficiency suggest elevated active vitamin D and hypercalciuria may be potential cystogenic factors. Further studies are needed to understand how genetic changes in SLC34A3 favor cyst formation. Elsevier 2022-01-24 /pmc/articles/PMC8978140/ /pubmed/35386604 http://dx.doi.org/10.1016/j.xkme.2022.100419 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Research Hanna, Christian Potretzke, Theodora A. Chedid, Maroun Rangel, Laureano J. Arroyo, Jennifer Zubidat, Dalia Tebben, Peter J. Cogal, Andrea G. Torres, Vicente E. Harris, Peter C. Sas, David J. Lieske, John C. Milliner, Dawn S. Chebib, Fouad T. Kidney Cysts in Hypophosphatemic Rickets With Hypercalciuria: A Case Series |
title | Kidney Cysts in Hypophosphatemic Rickets With Hypercalciuria: A Case Series |
title_full | Kidney Cysts in Hypophosphatemic Rickets With Hypercalciuria: A Case Series |
title_fullStr | Kidney Cysts in Hypophosphatemic Rickets With Hypercalciuria: A Case Series |
title_full_unstemmed | Kidney Cysts in Hypophosphatemic Rickets With Hypercalciuria: A Case Series |
title_short | Kidney Cysts in Hypophosphatemic Rickets With Hypercalciuria: A Case Series |
title_sort | kidney cysts in hypophosphatemic rickets with hypercalciuria: a case series |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8978140/ https://www.ncbi.nlm.nih.gov/pubmed/35386604 http://dx.doi.org/10.1016/j.xkme.2022.100419 |
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