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      Markers of potassium homeostasis in salt losing tubulopathies- associations with hyperaldosteronism and hypomagnesemia

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          Abstract

          Background

          Renal loss of potassium (K +) and magnesium (Mg 2+) in salt losing tubulopathies (SLT) leads to significantly reduced Quality of Life (QoL) and higher risks of cardiac arrhythmia. The normalization of K + is currently the most widely accepted treatment target, however in even excellently designed RCTs the increase of K + was only mild and rarely normalized. These findings question the role of K + as the ideal marker of potassium homeostasis in SLT. Aim of this hypothesis-generating study was to define surrogate endpoints for future treatment trials in SLT in terms of their usefulness to determine QoL and important clinical outcomes.

          Methods

          Within this prospective cross-sectional study including 11 patients with SLTs we assessed the biochemical, clinical and cardiological parameters and their relationship with QoL (RAND SF-36). The primary hypothesis was that QoL would be more dependent of higher aldosterone concentration, assessed by the transtubular-potassium-gradient (TTKG). Correlations were evaluated using Pearson’s correlation coefficient.

          Results

          Included patients were mainly female (82%, mean age 34 ± 12 years). Serum K + and Mg 2+ was 3.3 ± 0.6 mmol/l and 0.7 ± 0.1 mmol/l (mean ± SD). TTKG was 9.5/3.4–20.2 (median/range). While dimensions of mental health mostly correlated with serum Mg 2+ (r = 0.68, p = 0.04) and K + (r = 0.55, p = 0.08), better physical health was associated with lower aldosterone levels (r = -0.61, p = 0.06). TTKG was neither associated with aldosterone levels nor with QoL parameters. No relevant abnormalities were observed in neither 24 h-ECG nor echocardiography.

          Conclusions

          Hyperaldosteronism, K + and Mg 2+ were the most important parameters of QoL. TTKG was no suitable marker for hyperaldosteronism or QoL. Future confirmatory studies in SLT should assess QoL as well as aldosterone, K + and Mg 2+.

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          Most cited references22

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          The number of subjects per variable required in linear regression analyses.

          To determine the number of independent variables that can be included in a linear regression model.
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            Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference

            Gitelman syndrome (GS) is a rare, salt-losing tubulopathy characterized by hypokalemic metabolic alkalosis with hypomagnesemia and hypocalciuria. The disease is recessively inherited, caused by inactivating mutations in the SLC12A3 gene that encodes the thiazide-sensitive sodium-chloride cotransporter (NCC). GS is usually detected during adolescence or adulthood, either fortuitously or in association with mild or nonspecific symptoms or both. The disease is characterized by high phenotypic variability and a significant reduction in the quality of life, and it may be associated with severe manifestations. GS is usually managed by a liberal salt intake together with oral magnesium and potassium supplements. A general problem in rare diseases is the lack of high quality evidence to inform diagnosis, prognosis, and management. We report here on the current state of knowledge related to the diagnostic evaluation, follow-up, management, and treatment of GS; identify knowledge gaps; and propose a research agenda to substantiate a number of issues related to GS. This expert consensus statement aims to establish an initial framework to enable clinical auditing and thus improve quality control of care.
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              Mechanism of hypokalemia in magnesium deficiency.

              Magnesium deficiency is frequently associated with hypokalemia. Concomitant magnesium deficiency aggravates hypokalemia and renders it refractory to treatment by potassium. Herein is reviewed literature suggesting that magnesium deficiency exacerbates potassium wasting by increasing distal potassium secretion. A decrease in intracellular magnesium, caused by magnesium deficiency, releases the magnesium-mediated inhibition of ROMK channels and increases potassium secretion. Magnesium deficiency alone, however, does not necessarily cause hypokalemia. An increase in distal sodium delivery or elevated aldosterone levels may be required for exacerbating potassium wasting in magnesium deficiency.
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                Author and article information

                Contributors
                zeljko.kikic@meduniwien.ac.at
                Journal
                BMC Nephrol
                BMC Nephrol
                BMC Nephrology
                BioMed Central (London )
                1471-2369
                6 July 2020
                6 July 2020
                2020
                : 21
                : 256
                Affiliations
                [1 ]GRID grid.22937.3d, ISNI 0000 0000 9259 8492, Division of Nephrology and Dialysis, Department of Medicine III, , Medical University Vienna, ; Währinger Gürtel 18-20, A-1090 Vienna, Austria
                [2 ]GRID grid.22937.3d, ISNI 0000 0000 9259 8492, Institute of Biometrics, Center for Medical Statistics, Informatics, and Intelligent Systems, , Medical University of Vienna, ; Vienna, Austria
                [3 ]GRID grid.415431.6, ISNI 0000 0000 9124 9231, Department of Internal Medicine and Gastroenterology (IMuG), Hepatology, , Endocrinology, Rheumatology, Nephrology and Emergency Medicine (ZAE), Klinikum Klagenfurt am Wörthersee, ; Klagenfurt, Austria
                Author information
                http://orcid.org/0000-0002-0093-5389
                Article
                1905
                10.1186/s12882-020-01905-7
                7336449
                a3694c7f-c97d-437e-a866-7ebd2f4363f9
                © The Author(s) 2020

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 21 August 2019
                : 24 June 2020
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2020

                Nephrology
                gitelman syndrome,bartter syndrome,transtubular potassium gradient,ttkg,quality of life
                Nephrology
                gitelman syndrome, bartter syndrome, transtubular potassium gradient, ttkg, quality of life

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