Angiotensin‐converting enzyme inhibitors increase anti‐fibrotic biomarkers in African Americans with left ventricular hypertrophy

Abstract Angiotensin‐converting enzyme inhibitors (ACEi) are part of the indicated treatment in hypertensive African Americans. ACEi have blood pressure‐independent effects that may make them preferred for certain patients. We aimed to evaluate the impact of ACEi on anti‐fibrotic biomarkers in Afric...

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Main Authors: Cesar A.Romero, Shobi Mathew, Benjamin Wasinski, Brian Reed, Aaron Brody, Rachelle Dawood, Michael J. Twiner, Candace D. McNaughton, Rafael Fridman, John M. Flack, Oscar A. Carretero, Phillip D. Levy
Format: Article
Language:English
Published: Wiley 2021-05-01
Series:The Journal of Clinical Hypertension
Subjects:
Online Access:https://doi.org/10.1111/jch.14206
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author Cesar A.Romero
Shobi Mathew
Benjamin Wasinski
Brian Reed
Aaron Brody
Rachelle Dawood
Michael J. Twiner
Candace D. McNaughton
Rafael Fridman
John M. Flack
Oscar A. Carretero
Phillip D. Levy
author_facet Cesar A.Romero
Shobi Mathew
Benjamin Wasinski
Brian Reed
Aaron Brody
Rachelle Dawood
Michael J. Twiner
Candace D. McNaughton
Rafael Fridman
John M. Flack
Oscar A. Carretero
Phillip D. Levy
author_sort Cesar A.Romero
collection DOAJ
description Abstract Angiotensin‐converting enzyme inhibitors (ACEi) are part of the indicated treatment in hypertensive African Americans. ACEi have blood pressure‐independent effects that may make them preferred for certain patients. We aimed to evaluate the impact of ACEi on anti‐fibrotic biomarkers in African American hypertensive patients with left ventricular hypertrophy (LVH). We conducted a post hoc analysis of a randomized controlled trial in which hypertensive African American patients with LVH and vitamin D deficiency were randomized to receive intensive antihypertensive therapy plus vitamin D supplementation or placebo. We selected patients who had detectable lisinopril (lisinopril group) in plasma using liquid‐chromatography/mass spectrometry analysis and compared them to subjects who did not (comparison group) at the one‐year follow‐up. The pro‐fibrotic marker type 1 procollagen C‐terminal propeptide (PICP) and the anti‐fibrotic markers matrix metalloproteinase‐1 (MMP‐1), tissue inhibitor of metalloproteinases 1 (TIMP‐1), telopeptide of collagen type I (CITP), and N‐acetyl‐seryl‐aspartyl‐lysyl‐proline (Ac‐SDKP) peptide were measured. Sixty‐six patients were included, and the mean age was 46.2 ± 8 years. No difference was observed in the number and intensity of antihypertensive medications prescribed in each group. Patients with detectable lisinopril had lower blood pressure than those in the comparison group. The anti‐fibrotic markers Ac‐SDKP, MMP‐1, and MMP‐1/TIMP‐1 ratio were higher in patients with detectable ACEi (all p < .05). In a model adjusted for systolic blood pressure, MMP‐1/TIMP‐1 (p = .02) and Ac‐SDKP (p < .001) levels were associated with lisinopril. We conclude that ACEi increase anti‐fibrotic biomarkers in hypertensive African Americans with LVH, suggesting that they may offer added benefit over other agents in such patients.
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spelling doaj.art-9e2ff4d99bdc4f658ac0a41ad2fa6f0f2023-10-30T13:30:30ZengWileyThe Journal of Clinical Hypertension1524-61751751-71762021-05-012351008101610.1111/jch.14206Angiotensin‐converting enzyme inhibitors increase anti‐fibrotic biomarkers in African Americans with left ventricular hypertrophyCesar A.Romero0Shobi Mathew1Benjamin Wasinski2Brian Reed3Aaron Brody4Rachelle Dawood5Michael J. Twiner6Candace D. McNaughton7Rafael Fridman8John M. Flack9Oscar A. Carretero10Phillip D. Levy11Hypertension and Vascular Research Division Internal Medicine Department Henry Ford Hospital Detroit MI USADepartment of Emergency Medicine and Integrative Biosciences Center Wayne State University Detroit MI USADepartment of Emergency Medicine and Integrative Biosciences Center Wayne State University Detroit MI USADepartment of Emergency Medicine and Integrative Biosciences Center Wayne State University Detroit MI USADepartment of Emergency Medicine and Integrative Biosciences Center Wayne State University Detroit MI USADepartment of Emergency Medicine and Integrative Biosciences Center Wayne State University Detroit MI USADepartment of Emergency Medicine and Integrative Biosciences Center Wayne State University Detroit MI USADepartment of Emergency Medicine Vanderbilt University Medical Center and Geriatric Research Education Clinical Center VA Medical Center Nashville TN USADepartment of Pathology and Oncology Wayne State University Detroit MI USASchool of Medicine Department of Internal Medicine Southern Illinois University Springfield IL USAHypertension and Vascular Research Division Internal Medicine Department Henry Ford Hospital Detroit MI USADepartment of Emergency Medicine and Integrative Biosciences Center Wayne State University Detroit MI USAAbstract Angiotensin‐converting enzyme inhibitors (ACEi) are part of the indicated treatment in hypertensive African Americans. ACEi have blood pressure‐independent effects that may make them preferred for certain patients. We aimed to evaluate the impact of ACEi on anti‐fibrotic biomarkers in African American hypertensive patients with left ventricular hypertrophy (LVH). We conducted a post hoc analysis of a randomized controlled trial in which hypertensive African American patients with LVH and vitamin D deficiency were randomized to receive intensive antihypertensive therapy plus vitamin D supplementation or placebo. We selected patients who had detectable lisinopril (lisinopril group) in plasma using liquid‐chromatography/mass spectrometry analysis and compared them to subjects who did not (comparison group) at the one‐year follow‐up. The pro‐fibrotic marker type 1 procollagen C‐terminal propeptide (PICP) and the anti‐fibrotic markers matrix metalloproteinase‐1 (MMP‐1), tissue inhibitor of metalloproteinases 1 (TIMP‐1), telopeptide of collagen type I (CITP), and N‐acetyl‐seryl‐aspartyl‐lysyl‐proline (Ac‐SDKP) peptide were measured. Sixty‐six patients were included, and the mean age was 46.2 ± 8 years. No difference was observed in the number and intensity of antihypertensive medications prescribed in each group. Patients with detectable lisinopril had lower blood pressure than those in the comparison group. The anti‐fibrotic markers Ac‐SDKP, MMP‐1, and MMP‐1/TIMP‐1 ratio were higher in patients with detectable ACEi (all p < .05). In a model adjusted for systolic blood pressure, MMP‐1/TIMP‐1 (p = .02) and Ac‐SDKP (p < .001) levels were associated with lisinopril. We conclude that ACEi increase anti‐fibrotic biomarkers in hypertensive African Americans with LVH, suggesting that they may offer added benefit over other agents in such patients.https://doi.org/10.1111/jch.14206ACE inhibitorsAc‐SDKPAfrican Americancollagenleft ventricular hypertrophyMMP‐1
spellingShingle Cesar A.Romero
Shobi Mathew
Benjamin Wasinski
Brian Reed
Aaron Brody
Rachelle Dawood
Michael J. Twiner
Candace D. McNaughton
Rafael Fridman
John M. Flack
Oscar A. Carretero
Phillip D. Levy
Angiotensin‐converting enzyme inhibitors increase anti‐fibrotic biomarkers in African Americans with left ventricular hypertrophy
The Journal of Clinical Hypertension
ACE inhibitors
Ac‐SDKP
African American
collagen
left ventricular hypertrophy
MMP‐1
title Angiotensin‐converting enzyme inhibitors increase anti‐fibrotic biomarkers in African Americans with left ventricular hypertrophy
title_full Angiotensin‐converting enzyme inhibitors increase anti‐fibrotic biomarkers in African Americans with left ventricular hypertrophy
title_fullStr Angiotensin‐converting enzyme inhibitors increase anti‐fibrotic biomarkers in African Americans with left ventricular hypertrophy
title_full_unstemmed Angiotensin‐converting enzyme inhibitors increase anti‐fibrotic biomarkers in African Americans with left ventricular hypertrophy
title_short Angiotensin‐converting enzyme inhibitors increase anti‐fibrotic biomarkers in African Americans with left ventricular hypertrophy
title_sort angiotensin converting enzyme inhibitors increase anti fibrotic biomarkers in african americans with left ventricular hypertrophy
topic ACE inhibitors
Ac‐SDKP
African American
collagen
left ventricular hypertrophy
MMP‐1
url https://doi.org/10.1111/jch.14206
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