The efficacy of Zingiber officinale on dyslipidaemia, blood pressure, and inflammation as cardiovascular risk factors: A systematic review

Clin Nutr ESPEN. 2022 Oct:51:72-82. doi: 10.1016/j.clnesp.2022.08.031. Epub 2022 Sep 3.

Abstract

Background & aims: Hypertension, dyslipidaemia, and chronic inflammation contribute to the development of cardiovascular disease (CVD). Zingiber officinale has been suggested to reduce these CVD risk factors; however, the clinical evidence remains unclear. This systematic review aims to analyse the effect of Z. officinale as a sole intervention on these risk factors.

Methods: In this PRISMA-based systematic review, we included randomised clinical trials from PubMed, Scopus and Cochrane Database of Systematic Reviews (July 2020) analysing triglycerides, low- and high-density lipoprotein (LDL, HDL), total cholesterol, C-reactive protein (CRP), tumor necrosis factor-alpha (TNF-α), interleukin 1, 6, 10, systolic and/or diastolic blood pressure as outcomes. Quality of studies was evaluated by JADAD and the Cochrane risk-of-bias tools.

Results: A total of 24 studies were included, mostly (79.2%) showing low risk of bias. These were based on obesity and cardio-metabolic derangements (33.3%), type 2 diabetes mellitus (37.5%), and miscellaneous conditions (29.2%). While total cholesterol and triglycerides levels mostly improved after Z. officinale, results were inconsistent for other blood lipids markers. Inflammatory markers (CRP, TNF-α) were more consistently reduced by Z. officinale, while only 3 studies reported a non-significant reduction of blood pressure.

Conclusions: Although there remains a paucity of studies, Z. officinale may be beneficial for improving dyslipidaemia and inflammation.

Keywords: Blood pressure; Cardiovascular disease; Dyslipidaemia; Inflammation; Systematic review; Zingiber officinale.

Publication types

  • Review
  • Systematic Review

MeSH terms

  • Blood Pressure
  • C-Reactive Protein
  • Cardiovascular Diseases* / prevention & control
  • Cholesterol
  • Diabetes Mellitus, Type 2*
  • Dyslipidemias* / drug therapy
  • Humans
  • Inflammation / drug therapy
  • Interleukin-1
  • Lipids
  • Lipoproteins, HDL
  • Triglycerides
  • Tumor Necrosis Factor-alpha
  • Zingiber officinale*

Substances

  • Interleukin-1
  • Lipids
  • Lipoproteins, HDL
  • Triglycerides
  • Tumor Necrosis Factor-alpha
  • C-Reactive Protein
  • Cholesterol