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… Click to show full 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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