Evidence map›Paper›PMID 35137195›Full record

ArticleNephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association2022

Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study.

Maartje F A Verploegen, Rosa Vargas-Poussou, Stephen B Walsh, Harika Alpay, Atefeh Amouzegar, Gema Ariceta, Bahriye Atmis, Justine Bacchetta, Peter Bárány, Stéphanie Baron and 50 more

Open access · hybridAbstract read
In one paragraph

Article in Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Failure to thrive in children with tubulopathies.Pediatric nephrology (Berlin, Germany) · 2026
    Review
  2. Article
  3. Article
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  5. Article
  6. [The European Rare Kidney Disease Reference Network].Innere Medizin (Heidelberg, Germany) · 2024
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Bartter Syndrome Type 1 Due to NovelJCEM case reports · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

60 authors at 20 institutions in 18 countries.

Maartje F A VerploegenDepartment of Nephrology, Radboud University Medical Center, Nijmegen, The Netherlands.
Rosa Vargas-PoussouDepartment of Genetics, Centre de Références MARHEA, Hôpital Européen Georges Pompidou Assistance Publique Hôpitaux de Paris, Paris, France.ORCID 0000-0002-4169-0680
Stephen B WalshDepartment of Renal Medicine, University College London, London, UK.
Harika AlpayDivision of Paediatric Nephrology, Faculty of Medicine, Marmara University, Istanbul, Turkey.
Atefeh AmouzegarDivision of Nephrology, Department of Medicine, Firoozgar Clinical Research Development Center, Iran University of Medical Sciences, Tehran, Iran.ORCID 0000-0003-3090-1662
Gema AricetaPaediatric Nephrology Department, University Hospital Vall d'Hebron, Barcelona, Spain.
Bahriye AtmisDepartment of Paediatric Nephrology, Cukurova University Faculty of Medicine, Adana, Turkey.
Justine BacchettaDepartment of Paediatric Nephrology, Rheumatology and Dermatology, Reference Centre for Rare Renal Diseases, Reference Centre for Rare Diseases of Calcium and Phosphate Metabolism. University Children's Hospital, Lyon, France.ORCID 0000-0002-0578-2529
Peter BárányDivision of Renal Medicine, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Stéphanie BaronDepartment of Physiology, Hôpital Européen Georges Pompidou Assistance Publique Hôpitaux de Paris, Paris, France.
Umut Selda BayrakciDepartment of Paediatric Nephrology, Ankara City Hospital, Üniversiteler Mahallesi Bilkent Caddesi, Çankaya/Ankara, Turkey.
Hendrica BelgeCenter for Human Genetics, Institute of Pathology and Genetics, Gosselies, Belgium.
Martine BesouwDepartment of Paediatric Nephrology, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
Anne BlanchardClinical Research Centre 1418, Centre de Références MARHEA, Hôpital Européen Georges Pompidou Assistance Publique Hôpitaux de Paris, Paris, France.ORCID 0000-0002-0815-0586
Arend BökenkampDepartment of Paediatric Nephrology, Emma Children's Hospital, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Olivia BoyerDepartment of Paediatric Nephrology, Necker Hospital, APHP, MARHEA, Imagine Institute, Paris University, Paris, France.
Kathrin BurgmaierFaculty of Medicine, University Hospital of Cologne, Children's and Adolescents' Hospital, Paediatric Nephrology, University of Cologne, Cologne, Germany.ORCID 0000-0001-9787-1096
Lorenzo A CalòDepartment of Medicine (DIMED), Nephrology, Dialysis, Transplantation, University of Padova, Padova, Italy.
Stéphane DecramerDepartment of Paediatric Nephrology. Centre de Références SORARE, Toulouse University Hospital, Toulouse, France.
Olivier DevuystDivision of Nephrology, UCLouvain Medical School, Brussels, Belgium; Institute of Physiology, Mechanism of Inherited Kidney Disorders Group, University of Zurich, Zurich, Switzerland.ORCID 0000-0003-3744-4767
Maria van DyckDepartment of Paediatric Nephrology, University Hospital Leuven, Leuven, Belgium.
Pietro Manuel FerraroU.O.S. Terapia Conservativa della Malattia Renale Cronica, U.O.C. Nefrologia, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.ORCID 0000-0002-1379-022X
Marc FilaPediatric Nephrology, CHU Arnaud de Villeneuve, Montpellier University Hospital, Montpellier, France.
Telma FranciscoDepartment of Paediatric Nephrology, Centro Hospitalar Universitário de Lisboa Central, Lisbon, Portugal.
Gian Marco GhiggeriDivision of Nephrology, Dialysis and Transplantation, Istituto Giannina Gaslini, IRCCS, Genoa, Italy.ORCID 0000-0003-3659-9062
Leire GondraPediatric Nephrology Department, Cruces University Hospital, Barakaldo, Spain; Biocruces Bizkaia Health Research Institute, Barakaldo, Spain; Paediatric Department, University of the Basque Country UPV/EHU, Leioa, Spain.
Stefano GuarinoDepartment of Woman, Child and of General and Specialized Surgery, Università degli Studi della Campania 'Luigi Vanvitelli', Naples, Italy.
Nakysa HoomanAli-Asghar Clinical Research Development Centre, Iran University of Medical Sciences, Tehran, Iran.
Ewout J HoornDepartment of Internal Medicine, Division of Nephrology and Transplantation, Erasmus Medical Centre, University Medical Centre Rotterdam, Rotterdam, The Netherlands.ORCID 0000-0002-8738-3571
Pascal HouillierCentre de Recherche des Cordeliers, INSERM, Sorbonne Université, Université de Paris, Paris, France.
Konstantinos KamperisDepartment of Paediatrics and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark.
Jameela A KariPediatric Nephrology Centre of Excellence and Paediatric Department, Faculty of Medicine, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.
Martin KonradDepartment of General Paediatrics, Paediatric Nephrology, University Hospital Münster, Munster, Germany.
Elena LevtchenkoDepartment of Paediatric Nephrology & Department of Development and Regeneration, University Hospital Leuven, KU Leuven, Leuven, Belgium.
Laura LucchettiDepartment of Paediatric Subspecialties, Division of Nephrology, Bambino Gesù Children's Hospital - IRCCS, Rome, Italy.
Francesca LuganiDivision of Nephrology, Dialysis and Transplantation, Istituto Giannina Gaslini, IRCCS, Genoa, Italy.
Pierluigi MarzuilloDepartment of Woman, Child and of General and Specialized Surgery, Università degli Studi della Campania 'Luigi Vanvitelli', Naples, Italy.ORCID 0000-0003-4682-0170
Barian MohidinDepartment of Renal Medicine, University College London, London, UK.
Thomas J NeuhausDepartment of Paediatrics, Children's Hospital of Lucerne, Cantonal Hospital of Lucerne, Lucerne, Switzerland.
Abdaldafae OsmanPaediatric Nephrology Unit, Great Ormond Street Hospital, London, UK.
Svetlana PapizhDepartment of Hereditary and Acquired Kidney Diseases, Research and Clinical Institute for Pediatrics, Pirogov Russian National Research Medical University, Moscow, Russia.
Manel PerellóNephrology Department, Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.
Maarten B RookmaakerDepartment of Nephrology and Hypertension, University Medical Centre Utrecht, Utrecht, The Netherlands.
Valerie Said ContiDepartment of Paediatrics, Mater Dei Hospital Malta, Msida, Malta.
Fernando SantosDepartment of Paediatrics, Asturias Central University Hospital, University of Oviedo, Oviedo, Spain.
Ghalia SawafDepartment of Paediatric Nephrology, Damascus Hospital, Damascus, Syria.
Erkin SerdarogluDepartment of Paediatric Nephrology, Dr Behçet Uz Children's Hospital, Izmir, Turkey.
Maria SzczepanskaDepartment of Paediatrics, Faculty of Medical Sciences in Zabrze, SUM in Katowice, Katowice, Poland.
Francesca TaroniPaediatric Nephrology, Dialysis and Transplant Unit, Fondazione IRCCS Ca' Granda-Ospedale Maggiore Policlinico, Milan, Italy.
Rezan TopalogluDepartment of Paediatric Nephrology, Hacettepe University School of Medicine, Ankara, Turkey.ORCID 0000-0002-6423-0927
Francesco TrepiccioneDepartment of Translational Medical Sciences, University of Campania "L. Vanvitelli", Naples, Italy.
Enrico VidalDivision of Paediatrics, Department of Medicine, University of Udine, Udine, Italy.
Elizabeth R WanDepartment of Renal Medicine, University College London, London, UK.
Lutz WeberFaculty of Medicine, University Hospital of Cologne, Children's and Adolescents' Hospital, Paediatric Nephrology, University of Cologne, Cologne, Germany.
Zeynep Yuruk YildirimDepartment of Paediatrics, Division of Paediatric Nephrology, Istanbul University Istanbul Faculty of Medicine, Istanbul, Turkey.
Selçuk YükselDepartment of Paediatric Nephrology, Pamukkale University School of Medicine, Denizli, Turkey.ORCID 0000-0001-9415-1640
Galia ZlatanovaUniversity Children's Hospital Medical University, Sofia, Bulgaria.
Detlef BockenhauerDepartment of Renal Medicine, University College London, London, UK.
Francesco EmmaDepartment of Paediatric Subspecialties, Division of Nephrology, Bambino Gesù Children's Hospital - IRCCS, Rome, Italy.ORCID 0000-0002-0383-3468
Tom NijenhuisDepartment of Nephrology, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID 0000-0002-4375-7236
Assistance Publique – Hôpitaux de Paris · FRUniversity College London · GBUniversity of Campania "Luigi Vanvitelli" · ITBambino Gesù Children's Hospital · ITGreat Ormond Street Hospital · GBInserm · FRIran University of Medical Sciences · IRIstituto Giannina Gaslini · ITKU Leuven · BERadboud University Nijmegen · NLUniversity of Cologne · DEAarhus University Hospital · DKÇankaya University · TRCukurova University · TRDamascus Hospital · SYDr. Behçet Uz Çocuk Hastalıkları Hastanesi · TREmma Kinderziekenhuis · NLErasmus University Rotterdam · NLFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITHacettepe University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSmall cohort studies have reported high parathyroid hormone (PTH) levels in patients with Bartter syndrome and lower serum phosphate levels have anecdotally been reported in patients with Gitelman syndrome. In this cross-sectional study, we assessed PTH and phosphate homeostasis in a large cohort of patients with salt-losing tubulopathies.

methodsClinical and laboratory data of 589 patients with Bartter and Gitelman syndrome were provided by members of the European Rare Kidney Diseases Reference Network (ERKNet) and the European Society for Paediatric Nephrology (ESPN).

resultsA total of 285 patients with Bartter syndrome and 304 patients with Gitelman syndrome were included for analysis. Patients with Bartter syndrome type I and II had the highest median PTH level (7.5 pmol/L) and 56% had hyperparathyroidism (PTH >7.0 pmol/L). Serum calcium was slightly lower in Bartter syndrome type I and II patients with hyperparathyroidism (2.42 versus 2.49 mmol/L; P = .038) compared to those with normal PTH levels and correlated inversely with PTH (rs -0.253; P = .009). Serum phosphate and urinary phosphate excretion did not correlate with PTH. Overall, 22% of patients had low serum phosphate levels (phosphate-standard deviation score < -2), with the highest prevalence in patients with Bartter syndrome type III (32%). Serum phosphate correlated with tubular maximum reabsorption of phosphate/glomerular filtration rate (TmP/GFR) (rs 0.699; P < .001), suggesting renal phosphate wasting.

conclusionsHyperparathyroidism is frequent in patients with Bartter syndrome type I and II. Low serum phosphate is observed in a significant number of patients with Bartter and Gitelman syndrome and appears associated with renal phosphate wasting.

Indexed as

Bartter SyndromeGitelman SyndromeHyperparathyroidismAdenomaCalciumChildCross-Sectional StudiesFibromaHomeostasisHumansJaw NeoplasmsParathyroid HormonePhosphatesCalciumParathyroid HormonePhosphatesBartter syndromeGitelman syndromeparathyroid hormonephosphatesalt losing tubulopathies

Identifiers

PMID35137195
PMCPMC9681919
OpenAlexW4210556139

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.