Antihypertensive Mechanisms of Minocycline in Resistant Hypertension

Официальное название

Antihypertensive Mechanisms of Minocycline in Resistant Hypertension: Role of the Gut Microbiota-brain-immune Axis

Обзор

The goal of this clinical trial is to learn about the mechanisms by which minocycline effect blood pressure in individuals with treatment-resistant hypertension. The main questions it aims to answer are: * To what extent does minocycline lower blood pressure? * Are such blood pressure effects mediated through changes in gut microbiota, gut leakiness, systemic inflammation, neuroinflammation, or some combination of these? Participants will be randomly assigned to treatment with minocycline or placebo, treated daily for 3 months, to evaluate these questions.

Подробное описание

One hundred twenty patients with treatment-resistant hypertension will be enrolled. A total of 34 patients (17 from each treatment arm), who are participants in the main study, will also be enrolled in a substudy that includes neuroimaging. The study will last 3 months, and will include 3 visit time points (screening, randomization visit, 3-month follow-up visit).

Participants will be randomly assigned, in a 1:1 allocation, to minocycline 100 mg twice per day, or matching placebo, each provided by the study, and investigators will be blinded to treatment assignment.

At the baseline and 3-month follow-up visit, subjects will undergo:

* A comprehensive medical history and examination, including assessment of antihypertensive treatment history * A series of behavioral activity questionnaires * Blood tests (plasma renin activity, aldosterone, catecholamines, serum creatinine, lipid panel, hemoglobin a1c, as well as various biomarkers of immune and inflammatory activity, and gut leakiness markers) * Urine/saliva tests for antihypertensive adherence * Gut microbiota profiling via whole metagenomic sequencing of stool samples * Blood pressure (BP) measurement, including unattended office BP and 24-hour ambulatory BP

Subjects enrolled in the neuroimaging substudy will also have PET/MR imaging performed at each visit. Neuroimaging activities will take place at Emory University in Atlanta, GA.

At the final visit (3-month follow-up), participants will also have blood tests to measure study drug concentration, as a measure of adherence to the assigned treatment.

Вмешательства

• Препарат Minocycline Hydrochloride
  Minocycline Hydrochloride 100 mg twice daily
• Препарат Placebo
  Placebo

Первичные конечные точки

• 24-h systolic blood pressure [Срок оценки: 3 months]
• Gut microbiome [Срок оценки: 3 months]
• Gut inflammation and leakiness [Срок оценки: 3 months]
• Neuroinflammation [Срок оценки: 3 months]

Вторичные конечные точки (6)

• Mucin-degrading gene abundance [Срок оценки: 3 months]
• IgA+ coated plasma cells [Срок оценки: 3 months]
• Gut leakiness markers [Срок оценки: 3 months]
• 24-h diastolic blood pressure [Срок оценки: 3 months]
• 24-h heart rate [Срок оценки: 3 months]
• Adverse Events [Срок оценки: 3 months]

Критерии участия

Критерии включения

• Age ≥18 years
• Uncontrolled TRH, defined as uncontrolled blood pressure (mean 24-hour ambulatory systolic BP ≥125 mm Hg or diastolic BP ≥80 mm Hg) while being adherent to a stable (no changes in ≥14 days prior) antihypertensive regimen of 3 or more drugs, including an adequately dosed diuretic or unable to tolerate a diuretic.
• The participant agrees to have all study procedures performed

Критерии исключения

• Known hypersensitivity or contraindication to minocycline or other tetracyclines
• Recent (≤3 months prior), ongoing, or expected use of oral antibiotics
• Estimated glomerular filtration rate (eGFR) of <45mL/min/1.73m2, using the MDRD equation
• Known secondary hypertension
• History of hypertensive crisis, defined as any in-patient hospitalizations for hypertensive crisis/emergency within the past year
• History of orthostatic hypotension, defined as two or more episode(s) of orthostatic hypotension (reduction of SBP of >20 mm Hg or DBP of >10 mm Hg within 3 minutes of standing) in the past year
• History of myocardial infarction, unstable angina, syncope, or cerebrovascular accident in prior 6 months
• Evidence of alcoholism or drug abuse
• Severe comorbid conditions (i.e., neoplasms or HIV positive or AIDS)
• Current pregnancy or anticipated pregnancy during the study.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Рандомизированное

Модель

Параллельные группы

Маскирование

Тройное слепое

Основная цель

Лечение

Центры проведения

США · 1 центр

• UF Clinical Research Center (UF CRC) - CTSI — Gainesville

Идентификаторы

NCT: NCT06246396 · IRB202301939 · 2R01HL132448-05A1

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

Открыть это исследование на ClinicalTrials.gov ↗