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Meta-Analysis
. 2017 Aug 24;8(8):CD005051.
doi: 10.1002/14651858.CD005051.pub3.

Whole grain cereals for the primary or secondary prevention of cardiovascular disease

Affiliations
Meta-Analysis

Whole grain cereals for the primary or secondary prevention of cardiovascular disease

Sarah Am Kelly et al. Cochrane Database Syst Rev. .

Abstract

Background: There is evidence from observational studies that whole grains can have a beneficial effect on risk for cardiovascular disease (CVD). Earlier versions of this review found mainly short-term intervention studies. There are now longer-term randomised controlled trials (RCTs) available. This is an update and expansion of the original review conducted in 2007.

Objectives: The aim of this systematic review was to assess the effect of whole grain foods or diets on total mortality, cardiovascular events, and cardiovascular risk factors (blood lipids, blood pressure) in healthy people or people who have established cardiovascular disease or related risk factors, using all eligible RCTs.

Search methods: We searched CENTRAL (Issue 8, 2016) in the Cochrane Library, MEDLINE (1946 to 31 August 2016), Embase (1980 to week 35 2016), and CINAHL Plus (1937 to 31 August 2016) on 31 August 2016. We also searched ClinicalTrials.gov on 5 July 2017 and the World Health Organization International Clinical Trials Registry Platform (WHO ICTRP) on 6 July 2017. We checked reference lists of relevant articles and applied no language restrictions.

Selection criteria: We selected RCTs assessing the effects of whole grain foods or diets containing whole grains compared to foods or diets with a similar composition, over a minimum of 12 weeks, on cardiovascular disease and related risk factors. Eligible for inclusion were healthy adults, those at increased risk of CVD, or those previously diagnosed with CVD.

Data collection and analysis: Two review authors independently selected studies. Data were extracted and quality-checked by one review author and checked by a second review author. A second review author checked the analyses. We assessed treatment effect using mean difference in a fixed-effect model and heterogeneity using the I2 statistic and the Chi2 test of heterogeneity. We assessed the overall quality of evidence using GRADE with GRADEpro software.

Main results: We included nine RCTs randomising a total of 1414 participants (age range 24 to 70; mean age 45 to 59, where reported) to whole grain versus lower whole grain or refined grain control groups. We found no studies that reported the effect of whole grain diets on total cardiovascular mortality or cardiovascular events (total myocardial infarction, unstable angina, coronary artery bypass graft surgery, percutaneous transluminal coronary angioplasty, total stroke). All included studies reported the effect of whole grain diets on risk factors for cardiovascular disease including blood lipids and blood pressure. All studies were in primary prevention populations and had an unclear or high risk of bias, and no studies had an intervention duration greater than 16 weeks.Overall, we found no difference between whole grain and control groups for total cholesterol (mean difference 0.07, 95% confidence interval -0.07 to 0.21; 6 studies (7 comparisons); 722 participants; low-quality evidence).Using GRADE, we assessed the overall quality of the available evidence on cholesterol as low. Four studies were funded by independent national and government funding bodies, while the remaining studies reported funding or partial funding by organisations with commercial interests in cereals.

Authors' conclusions: There is insufficient evidence from RCTs of an effect of whole grain diets on cardiovascular outcomes or on major CVD risk factors such as blood lipids and blood pressure. Trials were at unclear or high risk of bias with small sample sizes and relatively short-term interventions, and the overall quality of the evidence was low. There is a need for well-designed, adequately powered RCTs with longer durations assessing cardiovascular events as well as cardiovascular risk factors.

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Conflict of interest statement

SK: None known.

LH: None known.

EL: None known.

JC: None known.

HJ: None known.

LA: None known.

CC: None known.

RG: None known.

HL: None known.

GF: None of the relationships described are felt to be a conflict of interest regarding this publication. Consultancy for appetite regulation with Unilever; grant application to Nestle on modified cereal fibre and glycaemic control (awaiting outcome); patent on compounds and their effects on appetite control and insulin sensitivity (WO2014020344 A1).

KR: None known.

Figures

1
1
Study flow diagram for updated searches 2016.
2
2
Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.
3
3
Risk of bias summary: review authors' judgements about each risk of bias item for each included study.
1.1
1.1. Analysis
Comparison 1: Whole grain versus control, Outcome 1: Body weight change (kg)
1.2
1.2. Analysis
Comparison 1: Whole grain versus control, Outcome 2: BMI change
1.3
1.3. Analysis
Comparison 1: Whole grain versus control, Outcome 3: Total cholesterol change (mmol/L)
1.4
1.4. Analysis
Comparison 1: Whole grain versus control, Outcome 4: LDL cholesterol change (mmol/L)
1.5
1.5. Analysis
Comparison 1: Whole grain versus control, Outcome 5: HDL cholesterol change (mmol/L)
1.6
1.6. Analysis
Comparison 1: Whole grain versus control, Outcome 6: Triglycerides change (mmol/L)
1.7
1.7. Analysis
Comparison 1: Whole grain versus control, Outcome 7: Systolic blood pressure change (mmHg)
1.8
1.8. Analysis
Comparison 1: Whole grain versus control, Outcome 8: Diastolic blood pressure (mmHg)

Update of

References

References to studies included in this review

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Johnston 1998 {published data only}
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Judd 1981 {published data only}
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Juntunen 2002 {published data only}
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Juntunen 2003 {published data only}
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Kabir 2002 {published data only}
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Karl 2016 {published data only}
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Karlstrom 1984 {published data only}
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Karmally 2005 {published data only}
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Katz 2001a {published data only}
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Katz 2001b {published data only}
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Kay 1981 {published data only}
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Keenan 2002 {published data only}
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Kesaniemi 1990 {published data only}
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Kim 2008 {published data only}
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Kirwan 2016 {published data only}
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Kleemola 1999 {published data only}
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Kris‐Etherton 2002 {published data only}
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Lakshmi 1996 {published data only}
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Leinonen 1999 {published data only}
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Leinonen 2000 {published data only}
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Liese 2003 {published data only}
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Lousley 1984 {published data only}
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MacKay 2012 {published data only}
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MacMahon 1998 {published data only}
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Maki 2003 {published data only}
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Maki 2007 {published data only}
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Manhire 1981 {published data only}
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Mathur 1968 {published data only}
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McGeoch 2013 {published data only}
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McIntosh 1991 {published data only}
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McIntosh 2003 {published data only}
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Melanson 2006 {published data only}
    1. Melanson KJ, Angelopoulos TJ, Nguyen VT, Martini M, Zukley L, Lowndes J. Consumption of whole-grain cereals during weight loss: effects on dietary quality, dietary fiber, magnesium, vitamin B-6, and obesity. Journal of the American Dietetic Association 2006;106(9):1380-8. - PubMed
Meydani 2016 {published data only}
    1. Meydani M, Thomas M, Barnett JB, Vanegas S, Chen O, Dolnikowski G, et al. Short term consumption of whole grain foods independent of weight loss does not affect surrogate markers of CVD. FASEB Journal 2016;30(1 Suppl):678.10.
Moazzami 2012 {published data only}
    1. Moazzami AA, Bondia-Pons I, Hanhineva K, Juntunen K, Antl N, Poutanen K, et al. Metabolomics reveals the metabolic shifts following an intervention with rye bread in postmenopausal women - a randomized control trial. Nutrition Journal 2012;11:88. - PMC - PubMed
Montonen 2003 {published data only}
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Nielsen 1988 {published data only}
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O'Kell 1988 {published data only}
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Pacy 1986 {published data only}
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Pereira 2002 {published data only}
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Pins 2002 {published data only}
    1. Keenan JM, Pins JJ, Geleva D, Frazel C, O'Connor PJ, Cherney LM. Whole-grain oat cereal consumption reduces antihypertensive medication need: a cost analysis. Preventive Medicine in Managed Care 2002;3(1):9-17.
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Poulter 1993 {published data only}
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Rave 2007 {published data only}
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Reynolds 1989 {published data only}
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Reynolds 2000 {published data only}
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Rigaud 1990 {published data only}
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Ross 2012 {published data only}
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Roth 1985 {published data only}
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Russ 1985 {published data only}
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Rytter 1996 {published data only}
    1. Rytter E, Erlanson-Albertsson C, Lindahl L, Lundquist I, Viberg U, Akesson B, et al. Changes in plasma insulin, enterostatin, and lipoprotein levels during an energy-restricted dietary regimen including a new oat-based liquid food. Annals of Nutrition and Metabolism 1996;40:212-20. - PubMed
Saltzman 2001a {published data only}
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Saltzman 2001b {published data only}
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Schlamowitz 1987 {published data only}
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Turnbull 1987 {published data only}
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Turpeinen 2000 {published data only}
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Vitaglione 2015 {published data only}
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Willms 1987 {published data only}
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Wolever 2003 {published data only}
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Wolever 2016 {published data only}
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Wolffenbuttel 1992 {published data only}
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References to studies awaiting assessment

Bi 2013 {published data only}
    1. Bi M, Niu Y, Li X, Li Y, Sun C. Effects of barley flake on metabolism of glucose and lipids in patients with impaired fasting glucose. Wei sheng yan jiu [Journal of Hygiene Research] 2013;42(5):719-23. - PubMed
Li 2016 {published data only}
    1. Li X, Cai X, Ma X, Jing L, Gu J, Bao L, et al. Short-and long-term effects of wholegrain oat intake on weight management and glucolipid metabolism in overweight type-2 diabetics: a randomized control trial. Nutrients 2016;8(9):549. - PMC - PubMed

References to ongoing studies

NCT02615444 {published data only}
    1. NCT02615444. The effects of beta-glucan enriched oatcake consumption on metabolic disease risk factors. clinicaltrials.gov/ct2/show/NCT02615444 (first received 5 November 2015).
Wedick 2015 {published data only}
    1. Wedick NM, Sudha V, Spiegelman D, Bai MR, Malik VS, Venkatachalam SS, et al. Study design and methods for a randomized crossover trial substituting brown rice for white rice on diabetes risk factors in India. International Journal of Food Sciences and Nutrition 2015;66(7):797-804. - PMC - PubMed

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References to other published versions of this review

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