Brief communication

Am J Hypertens (2004) 17, 1056–1058; doi: 10.1016/j.amjhyper.2004.06.018

A randomized, double-blind, placebo-controlled trial of casein protein hydrolysate (C12 peptide) in human essential hypertension*

Raymond R. Townsend1, Christopher B. McFadden1, Virginia Ford1 and Jenny A. Cadée2

  1. 1Department of Medicine, Renal Electrolyte and Hypertension Division, University of Pennsylvania, Philadelphia, Pennsylvania
  2. 2DMV International, Veghel, The Netherlands

Correspondence: Dr. Raymond R. Townsend, University of Pennsylvania, 210 White Building, 3400 Spruce Street, Philadelphia, PA 19104 E-mail: townsend@mail.med.upenn.edu

*Supported in part by an unrestricted grant from DMV International, The Netherlands.

Received 14 January 2004; Revised 26 May 2004; Accepted 13 June 2004.

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Abstract

Background: Many patients seek complementary medicine treatments like neutraceuticals for common conditions such as hypertension.

Methods: We conducted a placebo-controlled prospective randomized crossover study in 10 hypertensive subjects to determine whether a single dose of a hydrolysate of bovine milk protein (designated C12 peptide; low and high dose), either alone or combined with alginic acid (low and high dose), reduced daytime blood pressure (BP), as determined by ambulatory BP monitoring.

Results: Within the five treatment regimens a significant reduction of 9.2 plusminus 3.2 mm Hg in systolic BP at h 6 compared with h 2 occurred on the higher dose of alginic acid (1754 mg) combined with C12 (P = .02). The C12 peptide with the higher dose of alginic acid also showed a significant reduction of 6.0 plusminus 2.0 mm Hg in diastolic BP at h 6 compared with h 2 (P = .015).

Conclusions: These preliminary data are encouraging and deserve testing in a larger and longer treatment trial.

Keywords:

Hypertension, caseins, complementary therapies

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