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Circulation. 2001;104:286-291

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(Circulation. 2001;104:286.)
© 2001 American Heart Association, Inc.


Clinical Investigation and Reports

Usefulness of Serum Carboxy-Terminal Propeptide of Procollagen Type I in Assessment of the Cardioreparative Ability of Antihypertensive Treatment in Hypertensive Patients

Begoña López, BSc; Ramón Querejeta, MD, PhD; Nerea Varo, DrPH; Arantxa González, BSc; Mariano Larman, MD; José L. Martínez Ubago, MD; Javier Díez, MD,PhD

From the Division of Cardiovascular Pathophysiology (B.L., A.G., J.D.), School of Medicine, University of Navarra, Pamplona, Spain; Departments of Cardiology and Cardiovascular Surgery (J.D.) and Clinical Chemistry (N.V.), University Clinic, University of Navarra, Pamplona, Spain; Division of Cardiology (R.Q.), Ntra Sra de Aránzazu Hospital, San Sebastian, Spain; and Division of Hemodynamics (M.L., J.L.M.U.), Guipuzcoa Policlinics, San Sebastian, Spain.

Correspondence to Javier Díez, MD, PhD, División de Fisiopatología Cardiovascular, Facultad de Medicina, C/Irunlarrea s/n, 31080 Pamplona, Spain. E-mail jadimar{at}unav.es

Background— We investigated whether serum concentration of carboxy-terminal propeptide of procollagen type I (PIP), a marker of collagen type I synthesis, can be used to assess the ability of antihypertensive treatment to regress myocardial fibrosis in hypertensive patients.

Methods and Results— The study was performed in 37 patients with essential hypertension and hypertensive heart disease. After randomization, 21 patients were assigned to losartan and 16 patients to amlodipine treatment. At baseline and after 12 months, right septal endomyocardial biopsies were performed to quantify collagen volume fraction (CVF) on picrosirius red–stained sections with an automated image-analysis system. Serum PIP was measured by specific radioimmunoassay. Nineteen patients in the losartan group and 11 in the amlodipine group finished the study. Time-course changes in blood pressure during treatment were similar in the 2 groups of patients. In losartan-treated patients, CVF decreased from 5.65±2.03% to 3.96±1.46% (P<0.01) and PIP from 127±30 to 99±26 µg/L (P<0.01). Neither CVF or PIP changed significantly in amlodipine-treated patients. CVF was directly correlated with PIP (r=0.44, P<0.001) in all hypertensives before and after treatment.

Conclusions— These findings suggest that the ability of antihypertensive treatment to regress fibrosis in hypertensives with biopsy-proven myocardial fibrosis is independent of its antihypertensive efficacy. Our data also suggest that blockade of the angiotensin II type 1 receptor is associated with inhibition of collagen type I synthesis and regression of myocardial fibrosis in hypertensives. Thus, determination of serum PIP may be useful to assess the cardioreparative properties of antihypertensive treatment in hypertensives.


Key Words: collagen • hypertension • myocardium • peptides • remodeling




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