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Effects of betaine supplementation on cardiovascular markers: A systematic review and Meta-analysis

Damoon Ashtary-Larky, Reza Bagheri, Matin Ghanavati, Omid Asbaghi, Grant M Tinsley, Delsa Mombaini, Wesam Kooti, Sara Kashkooli, Alexei Wong
Critical reviews in food science and nutrition 2022 62(23):6516-6533

Bibliography

PubMed
PMID 33764214
Funding
Funding was not specified in the indexed record or accessible funding metadata.
Competing interests
A competing-interest declaration was not available in the indexed record or accessible disclosure metadata.

Study snapshot

DesignSystematic review and meta-analysis of RCTs
ModelEvidence synthesis; mixed research models
SampleHuman betaine trials; sample differs by outcome
InterventionBetaine versus controls; dose subgroups
DurationSearch through February 2021
EndpointsHomocysteine; LDL and total cholesterol; Blood pressure

What the study showed, in plain terms

Published in 2022, this source examined safety assessments and evidence synthesis. Its evidence base was Human betaine trials; sample differs by outcome. It evaluated Betaine versus controls; dose subgroups across Search through February 2021.

Homocysteine fell by about 1.30 micromol/L, while pooled total and LDL cholesterol increased. Blood pressure and several other markers did not improve.

Small heterogeneous trials and exploratory dose subgroups; a suggested lower-dose advantage is not a definitive safety threshold.

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Continue with TMG and Homocysteine: How Much Can Betaine Lower It?

Key findings

  • Homocysteine fell by about 1.30 micromol/L, while pooled total and LDL cholesterol increased.
  • Blood pressure and several other markers did not improve.
  • The recorded outcome domains were Homocysteine; LDL and total cholesterol; Blood pressure.
  • This synthesis reuses the included study populations; it is not an additional randomized participant cohort.

What this study can and cannot tell us

  • Small heterogeneous trials and exploratory dose subgroups; a suggested lower-dose advantage is not a definitive safety threshold.
  • Pooled estimates depend on the included trials and may share participants with companion publications or other reviews. A statistically significant surrogate outcome does not establish disease prevention.
  • Source basis: Indexed abstract and bibliographic data. Missing method details, funding information or participant denominators are not inferred.

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