Effect of Statin Treatment on Urinary AQP2 (uAQP2/01)
الكلمات الدالة
نبذة مختصرة
وصف
Statins are the first-line recommended pharmacological therapy in patients with dyslipidemias and play a key role in both primary and secondary prevention of coronary heart disease. By decreasing plasma total and low-density lipoprotein cholesterol (LDL-C) concentrations, statins decrease the risks for atherosclerotic cardiovascular disease and associated morbidity and mortality. Statins occupy part of the active binding site of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) and inhibit its enzymatic activity in the liver, a key step leading to the reduction of cellular sterol pool. Statins also have beneficial effects on the vascular wall by stabilizing the atherosclerotic plaques, ameliorating impaired endothelial function, and reducing vascular inflammation.
Besides the well-known metabolic and cardiovascular effects, it has been recently shown that statins increase the plasma membrane expression of the renal water channels Aquaporin 2 (AQP2). Water reabsorption in the kidney connecting tubule and collecting duct is regulated by the antidiuretic hormone arginine vasopressin (AVP), which promotes plasma membrane expression of the water channe aquaporin 2 (AQP2), the rate-limiting step controlling reabsorption of water, thus urine concentration, in this segment of the nephron. The investigators reported a number of evidences showing that statins accumulate AQP2 at the apical membrane of collecting duct cells by a AVP-independent mechanism. The effect of statins on AQP2 is independent of classical cholesterol homeostasis but rather depends on depletion of mevalonate-derived intermediates of cholesterol synthetic pathways, i.e. isoprenoid intermediates, including farnesylpyrophosphate (FPP) and geranylgeranylpyrophosphate (GGPP).
Water balance disorders are often associated with defects of AQP2 trafficking. Nephrogenic Diabetes Insipidus (NDI) is characterized by the inability of the kidney to respond to AVP stimulation and is caused by either mutations in AQP2 or vasopressin type-2 receptor (AVPR2) genes. Mutations in the AVPR2 gene lead to X-linked NDI (X-NDI). This cause of 90% of all diagnosed congenital NDI cases.
Conventional treatment of X-NDI patients consists in low-sodium, low-protein diet and the administration on thiazide diuretics sometimes in combination with indomethacin or amiloride. Although these drugs cause some relief of X-NDI symptoms, they most often do not eliminate them. Due to the partial beneficial effect of conventional treatments, much effort has been spent in the past years to uncover new and alternative methods to induce antidiuresis in X-NDI patients.
In this regard, the investigators recently reported that statins, in particular fluvastatin, accumulate AQP2 at the apical membrane of collecting duct cells by a AVP-independent mechanism and increase water reabsorption in both wild type and X-NDI mice.
The effect of statins on AQP2 trafficking in humans, however, deserves further investigation, also considering the potential efficacy of statins in patients with X-NDI. This was the reason to embark on the present study in which the investigators monitored the time-dependent effects of statin therapy on the urine excretion of AQP2, diuresis and urine osmolality in a cohort of hypercholesterolemic subjects initiating simvastatin therapy for three months. Two other groups of patients serve as controls: patients already on statin treatment and patients choosing to undergo an initial program with a standard hypolipidemic "mediterranean" style diet.
تواريخ
آخر التحقق: | 07/31/2015 |
تم الإرسال لأول مرة: | 08/09/2015 |
تم إرسال التسجيل المقدر: | 08/10/2015 |
أول نشر: | 08/13/2015 |
تم إرسال آخر تحديث: | 08/10/2015 |
آخر تحديث تم نشره: | 08/13/2015 |
تاريخ بدء الدراسة الفعلي: | 09/30/2013 |
تاريخ الإنجاز الأساسي المقدر: | 04/30/2014 |
التاريخ المتوقع لانتهاء الدراسة: | 06/30/2015 |
حالة أو مرض
مرحلة
مجموعات الذراع
ذراع | التدخل / العلاج |
---|---|
Naïve-S Patients with hypercholesterolemia starting statin treatment for primary or secondary prevention of cardiovascular diseases. | |
ONC-S Patients with hypercholesterolemia who had been treated with statin for at least one year and continued their previous therapy during the study period | |
Naïve-MC Patients with mild hypercholesterolemia either refusing initial statin treatment or intolerant to standard statin treatment and starting with monacolin K | |
Naïve-Diet Patients refusing an initial pharmacologic treatments and choosing the hypolipidic diet |
معايير الأهلية
الأعمار المؤهلة للدراسة | 40 Years إلى 40 Years |
الأجناس المؤهلة للدراسة | All |
طريقة أخذ العينات | Probability Sample |
يقبل المتطوعين الأصحاء | نعم |
المعايير | Inclusion criteria: - patients on primary prevention requiring moderate reduction of LDL-cholesterol according to the ACC/AHA Guidelines - age 40 to 75 years - estimated 10-year ASCVD risk ≥7.5% Exclusion criteria: - concomitant type 1 or type 2 diabetes - blood hypertension - concomitant use of diuretics or other drugs interfering with simvastatin |
النتيجة
مقاييس النتائج الأولية
1. uAQP2 [0, 1, 4, 12 weeks]
مقاييس النتائج الثانوية
1. Cholesterolemia [0, 1, 4, 12 weeks]