Potassium Magnesium Citrate (KMgCit)
DrugKMgCit will be administer for 4 months with chlorthalidone.
Other names: KMgCit
NCT Number: NCT02665117
Chlorthalidone (CTD) may produce various metabolic disturbances, including hypokalemia, activation of Renin-Angiotensin- Aldosterone (RAA) system, oxidative stress, dyslipidemia, Fibroblast growth factor 23 (FGF23) synthesis, and magnesium depletion. These factors may interact with each other to contribute to the development of insulin resistances and metabolic syndrome. Smaller studies have suggested that Potassium magnesium Citrate (KMgCit) can ameliorate CTD- induced metabolic side effects independent of correction of hypokalemia. This study will tests if KMgCit ameliorates CTD induced metabolic effects independent of correction of hypokalemia.
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Notify Me21 year and older
All sexes
Interventional
Not applicable
UT Southwestern Medical Center, Dallas, Texas, United States
CTD- induced metabolic side effects were though to be dependent on hypokalemia, but subsequent studies suggested that CTD - induced side effects were independent from hypokalemia. On the other hand, magnesium depletion has been linked to increased Renin-Angiotensin- Aldosterone (RAA) system, the development of metabolic syndrome and insulin resistance with magnesium supplementation ameliorating these effects.
Participants will participate in a double-blinded, parallel design study. After baseline evaluation participants will take Chlorthalidone (CTD) alone for 2-3 weeks. They will then be randomized to two equal groups to take KMgCit powder or Potassium Chloride (KCl) powder along with CTD for 4 months.
We speculate that Mg depletion is responsible for hepatic fat deposition, which then produces insulin resistance. Co-administration of KMgCit powder would avert magnesium (Mg) depletion, block hepatic fat deposition by restoring normal Mg status and direct intestinal binding of fat, thereby ameliorating insulin resistance. To test this hypothesis, we shall quantitate muscle Mg status and hepatic fat content by magnetic resonance spectroscopy (MRS) before and after KMgCit. Change in fasting glucose, insulin resistance, serum potassium, FGF23, and aldosterone will be compared between KCL and KMgCit groups after 4 months.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
KMgCit will be administer for 4 months with chlorthalidone.
Other names: KMgCit
KCl will be administer for 4 months with chlorthalidone.
Other names: KCl
Chlorthalidone will be administered for 2-3 weeks. Then either KCL or KMgCit will be added to Chlorthalidone and the combination will be taken for 4 months.
Time frame: week 4 and week 16
Fasting plasma glucose was measured from venous blood sample at week 4 and week 16
Time frame: baseline to week 16
Will be measured using hepatic magnetic resonance imaging at baseline and at week 16
Time frame: baseline to week 16
Will be measured using magnetic resonance imaging at baseline and at week 16
Time frame: week 4 to week 16
Will be measured from venous blood sample from week 4 to week 16
University of Texas Southwestern Medical Center
Other
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