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BMJ. 2008 Jul 15;337:a258. doi: 10.1136/bmj.a258.

Relation of iron and red meat intake to blood pressure: cross sectional epidemiological study.

Author information

  • 1Department of Epidemiology and Public Health, Imperial College London, St Mary's Campus, London W2 1PG. I.Tzoulaki@imperial.ac.uk

Abstract

OBJECTIVE:

To investigate associations of dietary iron (total, haem, and non-haem), supplemental iron, and red meat with blood pressure.

DESIGN:

Cross sectional epidemiological study.

SETTING:

17 population samples from Japan, China, the United Kingdom, and the United States participating in the international collaborative study on macro-/micronutrients and blood pressure (INTERMAP).

PARTICIPANTS:

4680 adults aged 40-59.

MAIN OUTCOME MEASURE:

Average of eight blood pressure readings.

RESULTS:

In multiple linear regression analyses dietary total iron and non-haem iron were consistently inversely associated with blood pressure. With adjustment for potential non-dietary and dietary confounders, dietary total iron intake higher by 4.20 mg/4.2 MJ (2 SD) was associated with -1.39 mm Hg (P<0.01) lower systolic blood pressure. Dietary non-haem iron intake higher by 4.13 mg/4.2 MJ (2 SD) was associated with -1.45 mm Hg (P<0.001) lower systolic blood pressure. Differences were smaller for diastolic blood pressure. In most models haem iron intake from food was positively, non-significantly associated with blood pressure. Iron intake from combined diet and supplements yielded smaller associations than dietary iron alone. Red meat intake was directly associated with blood pressure; 102.6 g/24 h (2 SD) higher intake was associated with 1.25 mm Hg higher systolic blood pressure. Associations between red meat and blood pressure persisted after adjustment for multiple confounders.

CONCLUSION:

Non-haem iron has a possible role in the prevention and control of adverse blood pressure levels. An unfavourable effect of red meat on blood pressure was observed. These results need confirmation including in prospective studies, clinical trials, and from experimental evidence on possible mechanisms.

Comment in

PMID:
18632704
[PubMed - indexed for MEDLINE]
PMCID:
PMC2658466
Free PMC Article
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