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Cover of Effects of Soy on Health Outcomes

Effects of Soy on Health Outcomes

Evidence Reports/Technology Assessments, No. 126

Investigators: , MD, MPH, Project Leader, , MPH, Research Associate, , MPH, Research Associate, , MD, Investigator, , MD, Research Associate, , BA, Research Associate, , MD, Research Associate, , DDS, Research Fellow, , BA, Research Assistant, , MLitt, Project Manager, and , MD, Principal Investigator.

Rockville (MD): Agency for Healthcare Research and Quality (US); .
Report No.: 05-E024-2

Structured Abstract

Context:

Soy products, including both protein and isoflavones, have been touted for a number of clinical benefits related to a putative estrogen-like effect. However, potential risks of chronic soy consumption are also of concern.

Objectives:

Systematic review to describe the range of soy products and outcomes that have been studied, to summarize the effects of soy consumption to prevent a wide variety of medical conditions in healthy adults, and to summarize adverse events related to soy consumption.

Data Sources:

We searched MEDLINE®, EMBASE, and the Commonwealth Agricultural Bureau (CAB) databases. Additional studies were identified in bibliographies of selected reviews and by technical experts.

Study Selection:

English-language, prospective studies of soy products in adults, of at least 4 weeks' duration were included. We reviewed outcomes related to cardiovascular health, menopausal symptoms and reproductive health, endocrine function, tumor-related biomarkers, bone health, neurocognitive health, kidney function, and glucose metabolism. Eligibility criteria were adjusted for several outcomes.

Data Extraction:

Selected studies were extracted for study design, demographics, amount of soy product, soy protein, and isoflavones, control, outcomes. Based on these data, studies were graded for quality and applicability.

Data Synthesis:

We screened almost 4,800 abstracts and retrieved 599 full text articles, of which 178 were eligible for review. Soy supplements (including soy milk) were used in about three quarters of all the trials analyzed in this report, with soy foods used in the remainder of the trials. Most used soy protein with isoflavones, one-third used isoflavones alone, and a few used soy protein without isoflavones. Textured soy protein and soy flour were the most common soy foods investigated. Among studies with soy protein, the range of soy protein consumed daily was 14 to 154 g, with a median of 36 g per day (equivalent to over a pound of tofu daily). Among studies with soy isoflavones, the range of isoflavones consumed daily was 10 to 185 mg, with a median of 80 mg per day. These ranges were the same for all lipid profile studies. There is a large degree of heterogeneity among the studies in terms of soy products evaluated, soy protein and isoflavone doses, study durations, background diet, controls used, and study design. No study evaluated clinical cardiovascular events. Meta-analysis indicates that consumption of soy products appears to exert a small benefit on low density lipoprotein (LDL) - the summary net change was -5 (95% confidence interval [CI] -8 to -3) mg/dL - and on triglycerides - net change -8 (95% CI -11, -5) mg/dL. No significant effect was seen on high density lipoprotein (HDL) - net change +0.6 (95% CI -0.5, +1.8). Across studies, there is the possible suggestion that higher doses of soy protein are associated with greater LDL reduction among those with elevated baseline LDL, but not with HDL or triglycerides. Dose of isoflavones was not associated with effect for any lipid. Higher baseline LDL or triglycerides may also be associated with net effect for these 2 lipids; the effect of baseline HDL is unclear. In individual studies, the effect of dose and baseline was generally inconsistent. Meta-analysis of blood pressure (BP) found no effect of soy consumption. The net effect on systolic BP was -1 (95% CI -3, +1) mm Hg, and on diastolic BP -1, (-2, +0) mm Hg. No association was found between baseline BP, soy protein or isoflavone dose and effect on BP. No significant effect of soy products was found for several markers of inflammation, vascular function, or lipid oxidation. Although the effect of soy products on menopausal symptoms are inconsistent across studies, the evidence of a benefit was stronger from the randomized trials of soy isoflavone supplements, but not of other soy products among post-menopausal women. This effect was not seen in the few studies among peri-menopausal women or those treated for breast cancer. Soy products do not appear to affect menstrual cycle length or estradiol level in pre-menopausal women, thyroid stimulating hormone, bone markers, or glucose metabolism. Small numbers of studies or inconsistency among studies precluded drawing conclusions regarding the effect of soy protein on other endocrine markers and other evaluated outcomes. For all outcomes, no soy protein or isoflavone dose-effect response or soy product type difference in effect was apparent across studies. The few studies that directly compared soy doses (generally isoflavone doses) for the most part also found no difference in effect based on dose. In general, soy products were well-tolerated, although study withdrawal due to aversion was more common in soy treatment arms than control arms. The most common adverse events reported were gastrointestinal or menstrual complaints although they were few in number.

Conclusions:

A wide variety of soy products and formulations have been investigated for a large number of conditions. However, a large proportion of the studies suffer from poor reporting or study design, limiting conclusions. Soy products appear to exert a small benefit on LDL and triglycerides; these effects may be of small clinical effect in individuals, although possibly large enough to have a population-wide effect. The inconsistent association between soy protein dose and effect, and the lack of association between soy isoflavone dose and effect, limit possible determination of an appropriate amount of soy product needed for lipid reduction. Soy products may reduce menopausal symptoms in post-menopausal women. The current literature does not support other effects of soy products. However, other than menopausal- and menstrual-related symptoms, no clinical outcomes were evaluated. The evidence from human studies does not suggest any worrisome adverse events beyond mild gastrointestinal intolerance. Conclusions were often limited due to small numbers of studies or heterogeneity across studies.

Given the large amount of heterogeneity and inadequate reporting, particularly related to soy protein and isoflavone dose, many questions remain as to whether specific soy products in adequate doses may be of benefit in specific populations. Further, well-conducted studies are needed to clarify the effect of soy dose on lipid parameters and to determine whether soy components other than protein or isoflavones may be responsible for the lipid effects seen.

Contents

Prepared for: Agency for Healthcare Research and Quality, U.S. Department of Health and Human Services.1 Contract No. 290-02-0022. Prepared by: Tufts-New England Medical Center Evidence-based Practice Center, Boston, Massachusetts.

Suggested citation:

Balk E, Chung M, Chew P, Ip S, Raman G, Kupelnick B, Tatsioni A, Sun Y, Wolk B, DeVine D, Lau J. Effects of Soy on Health Outcomes. Evidence Report/Technology Assessment No. 126. (Prepared by Tufts-New England Medical Center Evidence-based Practice Center under Contract No. 290-02-0022.) AHRQ Publication No. 05-E024-2. Rockville, MD: Agency for Healthcare Research and Quality. August 2005.

This report is based on research conducted by the Tufts-New England Medical Center Evidence-based Practice Center (EPC), under contract to the Agency for Healthcare Research and Quality (AHRQ), Rockville, MD (Contract No. 290-02-0022). The findings and conclusions in this document are those of the authors, who are responsible for its contents; the findings and conclusions do not necessarily represent the views of AHRQ. Therefore, no statement in this report should be construed as an official position of AHRQ or of the U.S. Department of Health and Human Services.

The information in this report is intended to help health care decisionmakers, patients and clinicians, health system leaders, and policymakers make well-informed decisions and thereby improve the quality of health care services. This report is not intended to be a substitute for the application of clinical judgment. Anyone who makes decisions concerning the provision of clinical care should consider this report as they would any medical reference and in conjunction with all other pertinent information, i.e., in the context of available resources and circumstances presented by individual patients.

This report may be used, in whole or in part, as the basis for development of clinical practice guidelines and other quality enhancement tools, or as a basis for reimbursement and coverage policies. Neither AHRQ's nor the U.S. Department of Health and Human Services' endorsement of such derivative products may be stated or implied.

1

540 Gaither Road, Rockville, MD 20850. www​.ahrq.gov

Bookshelf ID: NBK37881

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