Ruml L A, Gonzalez G, Taylor R, Wuermser L A, Pak C Y
Center for Mineral Metabolism and Clinical Research, University of Texas Southwestern Medical Center, Dallas, USA.
Am J Ther. 1999 Jan;6(1):45-50. doi: 10.1097/00045391-199901000-00007.
The purpose of this study was to compare the efficacy of three dosages of potassium-magnesium citrate in overcoming thiazide-induced hypokalemia and magnesium loss and increasing urinary pH and citrate. Sixty-one normal subjects first took hydrochlorothiazide at 50 mg/d. After 3 weeks of thiazide treatment or earlier if hypokalemia developed, the subjects were randomized to take one of three dosages of potassium-magnesium citrate (K ( 4 ) MgCit ( 2 ) ) for 3 weeks while continuing on the thiazide: 4 tablets per day (24 mEq potassium, 12 mEq magnesium, and 36 mEq citrate per day), 7 tablets per day (49 mEq potassium, 24.5 mEq magnesium, and 73.5 mEq citrate per day), or 10 tablets per day (70 mEq potassium, 35 mEq magnesium, and 105 mEq citrate per day). Outcome measures were changes in serum potassium and magnesium and urinary potassium, magnesium, pH, and citrate. All three dosages of potassium-magnesium citrate significantly increased serum potassium concentration, with >80% of subjects regaining normal values despite continued thiazide therapy. The two higher dosages, but not the lowest dosage, caused a small but significant increase in serum magnesium concentration, while substantially increasing urinary magnesium. All three dosages significantly increased urinary pH and citrate in a dose-dependent manner. The lowest dosage produced increases sufficient to prevent stone recurrence. Side effects of thiazide therapy were ameliorated by the highest dosage but not by the two lower dosages. Potassium-magnesium citrate at a dosage of 4 tablets per day is adequate to correct thiazide-induced hypokalemia and to increase urinary pH and citrate sufficiently for stone prevention. Higher dosages are probably required for the prevention of magnesium loss and adverse symptoms of thiazide therapy.
本研究的目的是比较三种剂量的枸橼酸钾镁在克服噻嗪类药物引起的低钾血症和镁流失以及提高尿液pH值和枸橼酸盐水平方面的疗效。61名正常受试者首先每天服用50毫克氢氯噻嗪。在噻嗪类药物治疗3周后,或者如果出现低钾血症则更早,受试者被随机分配服用三种剂量的枸橼酸钾镁(K(4)MgCit(2))中的一种,持续3周,同时继续服用噻嗪类药物:每天4片(每天24毫当量钾、12毫当量镁和36毫当量枸橼酸盐)、每天7片(每天4�毫当量钾、24.5毫当量镁和73.5毫当量枸橼酸盐)或每天10片(每天70毫当量钾、35毫当量镁和105毫当量枸橼酸盐)。观察指标为血清钾和镁以及尿钾、镁、pH值和枸橼酸盐的变化。所有三种剂量的枸橼酸钾镁均显著提高了血清钾浓度,尽管继续使用噻嗪类药物治疗,但超过80%的受试者恢复了正常水平。两种较高剂量,但不是最低剂量,导致血清镁浓度有小幅但显著的升高,同时尿镁大幅增加。所有三种剂量均以剂量依赖的方式显著提高了尿液pH值和枸橼酸盐水平。最低剂量产生的升高足以预防结石复发。噻嗪类药物治疗的副作用在最高剂量时得到改善,但在两种较低剂量时未得到改善。每天4片的枸橼酸钾镁剂量足以纠正噻嗪类药物引起的低钾血症,并充分提高尿液pH值和枸橼酸盐水平以预防结石。预防镁流失和噻嗪类药物治疗的不良症状可能需要更高的剂量。