Effects of Oral Butyrate on Blood Pressure in Patients With Hypertension: A Randomized, Placebo-Controlled Trial

• Published in: Hypertension (Dallas, Tex. 1979) Vol. 81; no. 10; pp. 2124 - 2136
• Main Authors: Verhaar, Barbara J.H., Wijdeveld, Madelief, Wortelboer, Koen, Rampanelli, Elena, Levels, Johannes H.M., Collard, Didier, Cammenga, Marianne, Nageswaran, Vanasa, Haghikia, Arash, Landmesser, Ulf, Li, Xinmin S., DiDonato, Joseph A., Hazen, Stanley L., Garrelds, Ingrid M., Danser, A.H. Jan, van den Born, Bert-Jan H., Nieuwdorp, Max, Muller, Majon
• Format: Journal Article
• Language: English
• Published: Hagerstown, MD Lippincott Williams & Wilkins 01.10.2024
• Subjects: Administration, Oral; Aged; Antihypertensive Agents - administration & dosage; Antihypertensive Agents - pharmacology; Antihypertensive Agents - therapeutic use; Blood Pressure - drug effects; Butyrates - administration & dosage; Butyrates - pharmacology; Double-Blind Method; Female; Humans; Hypertension - drug therapy; Hypertension - physiopathology; Male; Middle Aged; Original; Treatment Outcome; blood pressure; butyric acid; humans; hypertension; feces; gastrointestinal microbiome
• ISSN: 0194-911X; 1524-4563; 1524-4563
• DOI: 10.1161/HYPERTENSIONAHA.123.22437

BACKGROUND: The microbiota-derived short chain fatty acid butyrate has been shown to lower blood pressure (BP) in rodent studies. Nonetheless, the net effect of butyrate on hypertension in humans remains uncovered. In this study, for the first time, we aimed to determine the effect of oral butyrate on BP in patients with hypertension. METHODS: We performed a double-blind randomized placebo-controlled trial including 23 patients with hypertension. Antihypertensive medication was discontinued for the duration of the study with a washout period of 4 weeks before starting the intervention. Participants received daily oral capsules containing either sodium butyrate or placebo with an equivalent dosage of sodium chloride for 4 weeks. The primary outcome was daytime 24-hour systolic BP. Differences between groups over time were assessed using linear mixed models (group-by-time interaction). RESULTS: Study participants (59.0±3.7 years; 56.5% female) had an average baseline office systolic BP of 143.5±14.6 mm Hg and diastolic BP of 93.0±8.3 mm Hg. Daytime 24-hour systolic and diastolic BP significantly increased over the intervention period in the butyrate compared with the placebo group, with an increase of +9.63 (95% CI, 2.02-17.20) mm Hg in daytime 24-hour systolic BP and +5.08 (95% CI, 1.34-8.78) mm Hg in diastolic BP over 4 weeks. Butyrate levels significantly increased in plasma, but not in feces, upon butyrate intake, underscoring its absorption. CONCLUSIONS: Four-week treatment with oral butyrate increased daytime systolic and diastolic BP in subjects with hypertension. Our findings implicate that butyrate does not have beneficial effects on human hypertension, which warrants caution in future butyrate intervention studies. REGISTRATION: URL: https://onderzoekmetmensen.nl/; Unique identifier: NL8924.