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Brain dysfunction in tubular and tubulointerstitial kidney diseases.
Viggiano, Davide; Bruchfeld, Annette; Carriazo, Sol; de Donato, Antonio; Endlich, Nicole; Ferreira, Ana Carina; Figurek, Andreja; Fouque, Denis; Franssen, Casper F M; Giannakou, Konstantinos; Goumenos, Dimitrios; Hoorn, Ewout J; Nitsch, Dorothea; Ortiz, Alberto; Pesic, Vesna; Rastenyté, Daiva; Soler, Maria José; Rroji, Merita; Trepiccione, Francesco; Unwin, Robert J; Wagner, Carsten A; Wieçek, Andrzej; Zacchia, Miriam; Zoccali, Carmine; Capasso, Giovambattista.
Afiliação
  • Viggiano D; Department of Translational Medical Sciences, University of Campania 'L. Vanvitelli', Naples, Italy.
  • Bruchfeld A; Biogem, Institute of Molecular Biology and Genetics, Ariano Irpino, Italy.
  • Carriazo S; Department of Health, Medicine and Caring Sciences, Linköping University, Linköping, Sweden.
  • de Donato A; Department of Renal Medicine, Karolinska University Hospital and CLINTEC Karolinska Institutet, Stockholm, Sweden.
  • Endlich N; Department of Nephrology and Hypertension, IIS-Fundacion Jimenez Diaz-UAM, Madrid, Spain.
  • Ferreira AC; Department of Renal Medicine, Karolinska University Hospital and CLINTEC Karolinska Institutet, Stockholm, Sweden.
  • Figurek A; Department of Nephrology and Hypertension, IIS-Fundacion Jimenez Diaz-UAM, Madrid, Spain.
  • Fouque D; Department of Anatomy and Cell Biology, University Medicine Greifswald, Greifswald, Germany.
  • Franssen CFM; Nephrology Department, Centro Hospitalar e Universitário de Lisboa Central, Lisbon, Portugal.
  • Giannakou K; Universidade Nova de Lisboa, Faculdade de Ciências Médicas, Lisbon, Portugal.
  • Goumenos D; Institute of Anatomy, University of Zurich, Zurich, Switzerland.
  • Hoorn EJ; Department of Nephrology, Hospices Civils de Lyon, Centre Hospitalier Lyon-Sud, Pierre-Benite, University of Lyon, France.
  • Nitsch D; Department of Nephrology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • Ortiz A; Department of Health Sciences, School of Sciences, European University Cyprus, Nicosia, Cyprus.
  • Pesic V; Department of Nephrology and Renal Transplantation, Patras University Hospital, Patras, Greece.
  • Rastenyté D; Department of Internal Medicine, Division of Nephrology and Transplantation, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, The Netherlands.
  • Soler MJ; Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, UK.
  • Rroji M; Department of Nephrology and Hypertension, IIS-Fundacion Jimenez Diaz-UAM, Madrid, Spain.
  • Trepiccione F; Faculty of Pharmacy, Department of Physiology, University of Belgrade, Belgrade, Serbia.
  • Unwin RJ; Medical Academy, Department of Neurology, Lithuanian University of Health Sciences, Kaunas, Lithuania.
  • Wagner CA; Nephrology Department, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain.
  • Wieçek A; Department of Nephrology, University Hospital Center "Mother Tereza", Tirana, Albania.
  • Zacchia M; Biogem, Institute of Molecular Biology and Genetics, Ariano Irpino, Italy.
  • Zoccali C; Department of Translational Medical Sciences, University of Campania "L. Vanvitelli", Naples, Italy.
  • Capasso G; Department of Renal Medicine, Division of Medicine, University College London, London, UK.
Nephrol Dial Transplant ; 37(Suppl 2): ii46-ii55, 2021 12 28.
Article em En | MEDLINE | ID: mdl-34792176
ABSTRACT
Kidney function has two important elements glomerular filtration and tubular function (secretion and reabsorption). A persistent decrease in glomerular filtration rate (GFR), with or without proteinuria, is diagnostic of chronic kidney disease (CKD). While glomerular injury or disease is a major cause of CKD and usually associated with proteinuria, predominant tubular injury, with or without tubulointerstitial disease, is typically non-proteinuric. CKD has been linked with cognitive impairment, but it is unclear how much this depends on a decreased GFR, altered tubular function or the presence of proteinuria. Since CKD is often accompanied by tubular and interstitial dysfunction, we explore here for the first time the potential role of the tubular and tubulointerstitial compartments in cognitive dysfunction. To help address this issue we selected a group of primary tubular diseases with preserved GFR in which to review the evidence for any association with brain dysfunction. Cognition, mood, neurosensory and motor disturbances are not well characterized in tubular diseases, possibly because they are subclinical and less prominent than other clinical manifestations. The available literature suggests that brain dysfunction in tubular and tubulointerstitial diseases is usually mild and is more often seen in disorders of water handling. Brain dysfunction may occur when severe electrolyte and water disorders in young children persist over a long period of time before the diagnosis is made. We have chosen Bartter and Gitelman syndromes and nephrogenic diabetes insipidus as examples to highlight this topic. We discuss current published findings, some unanswered questions and propose topics for future research.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Insuficiência Renal Crônica / Nefropatias / Nefrite Intersticial Tipo de estudo: Diagnostic_studies / Etiology_studies Limite: Child / Child, preschool / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Insuficiência Renal Crônica / Nefropatias / Nefrite Intersticial Tipo de estudo: Diagnostic_studies / Etiology_studies Limite: Child / Child, preschool / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article