Cardiovascular DiseasesNCT03468127
Meta-analysis of 46 FDA Identified Studies on Lipid Markers
An observational study of Cardiovascular Diseases, run by University of Toronto at 2 sites in Canada.
Trial summary
The FDA have revised the data on soy and concluded that a heart health claim is no longer justified based on more recent studies. They are allowing and established panel for public input. Read more about this study
- Who is it for?
- Any ageHealthy volunteers can take part
- Conditions the study is for
- Cardiovascular Diseases
- What is being tested?
- Soy foods
- How many people
- 1 participants
- Where
- 2 sitesCanada
- Study dates
- 7 Mar 2018to 31 May 2018
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: All individuals, regardless of health status
Who may be able to join
- Studies pre-identified by the FDA [Docket No. FDA-2017-N-0763]
Who cannot join
- Studies with no viable outcome data
Trial locations and contacts
2 sites in 1 country.
Canada2 sites
Clinical Nutrition & Risk Factor Modification Centre, St. Michael's Hospital Health Centre
Toronto, Ontario, M5C 2T2
University of Toronto
Toronto, Ontario, M5S 3E2
About this study
Official title: A Meta-analysis of 46 Studies Identified by the FDA on the Effect of Soy Protein on Lipid Markers (LDL-Cholesterol [LDL-C] and Total Cholesterol [TC]) as Surrogates of Cardiovascular Disease
The FDA have revised the data on soy and concluded that a heart health claim is no longer justified based on more recent studies. They are allowing and established panel for public input. The selected studies have not been meta-analyzed, therefore we will conduct a meta-analysis of the 46 FDA selected studies to assess the effect of soy protein on surrogate markers of cardiovascular disease (LDL-C and TC).
Read the detailed description
Background: The FDA in their re-evaluation of the scientific evidence for a relationship between soy protein and reduced risk of coronary heart disease (CHD), has revised the data included in the 1999 soy protein and CHD health claim, as well as studies published after this authorized health claim and concluded that a heart health claim is no longer justified based on more recent studies. The 46 identified studies have not been meta-analyzed.
Need for proposed research: To meta-analyse the 46 identified studies to provide the highest level of evidence to aid in the final decision of the soy protein and reduced risk of CHD health claim.
Objective: To provide evidence-based guidance for publich health policy, health claims, and nutrition guidelines relating to soy, we will conduct a meta-analysis of the 46 FDA identified studies of the effect of soy protein on surrogate markers of cardiovascular disease.
Design: The conduct of the meta-analysis will follow the Cochrane handbook for Systematic Reviews of interventions. The reporting will follow the Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guidelines.
Data sources and study selection: We will include the 46 studies pre-selected by the FDA in the Proposed Rule, Soy Protein and Coronary Heart Disease (Docket No. FDA-2017-N-0763).
Data extraction: Two independent investigators will extract study information (study design, sample size, subject characteristics, soy form, dose, comparator, follow-up, background diet, outcome data).
Outcomes: Effects of soy protein intake on LDL-C and TC.
Data synthesis: Mean differences will be pooled using the generic inverse variance method with random-effects model even in the absence of statistically significance between-study heterogeneity, as they yield more conservative summary effect estimates in the presence of residual heterogeneity. Paired analysis will be applied fro crossover trials. Heterogeneity will e assessed by the Cochran Q statistic and quantified by the I2 statistic. To explore sources of heterogeneity, we will conduct sensitivity analysis, in which each study is systematically removed. We will also explore sources of heterogeneity by a priori subgroup analyses by baseline LDL-C levels (<135 mg/dl vs >=135mg/dl), soy dose (<25 g/d vs >= 25 g/d), soy protein food (Isolated soy protein, soy food, soy milk, etc), comparator (animal protein, dairy protein, meat protein), follow-up (median), and categories given by the FDA (baseline cholesterol level [desirable or borderline, high, or normal, borderline, and high], how soy was provided in the studies [feeding or substitution, added to diet], by a mixture of type of soy, how it was provided and baseline cholesterol level [1)Desirable or borderline cholesterol level, added ISP; 2) Desirable or borderline cholesterol level, feeding or substitution studies with ISP; 3) Desirable or borderline cholesterol level, added soy foods; 4)Desirable or borderline cholesterol level, feeding or substitution studies with soy foods; 5) Normal, borderline, and high cholesterol levels, feeding or substitution studies with ISP; 6) High cholesterol level, added ISP; 7) High cholesterol level, feeding or substitution studies with ISP; 8) High cholesterol level, added soy foods; and 9) High cholesterol level, feeding soy foods]), and risk of bias. Meta-regression analysis will assess the significance. Publication bias will be assess by visual inspection of funnel plots and by the use of Egger and Begg's tests. If publication bias is suspected, then we will attempt to adjust for funnel plot asymmetry by imputing the missing study data using the Duval and Tweedie trim and fill method. Dose-reponse analyses will be conducted using the metareg and mkspline commands.
Knowledge translation plan: The results will be disseminated in two stages, first, by the Soy Nutrition Institute in a response to the Proposed Rule, Soy Protein and Coronary Heart Disease, and by a publication in a high impact factor journal.
Significance: The meta-analysis will aid in knowledge translation related to the role of soy protein intake and surrogate markers of cardiovascular disease (LDL-C and TC), strengthening the evidence-based for guidelines and health claims, and improving health outcomes by educating healthcare providers and patients.
- Conditions
- Cardiovascular Diseases
- Being tested
- Soy foods
- Keywords
- Soy protein, LDL-Cholesterol, Total Cholesterol, Cardiovascular disease
- Medical subject headings
- Cardiovascular Diseases
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Soy foodsOther
Isolated soy protein, soy protein, soybean products, soy milk
What is being measured
The primary outcome is the main question the study is designed to answer.
Surrogate lipid markers of CVD
LDL-Cholesterol (LDL-C) Total Cholesterol (TC)
Measured: Long term (>3weeks)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Mar 2018
- Study start7 Mar 2018
- Primary completion19 Apr 2018 (estimated)
- Study completion31 May 2018 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Cardiovascular DiseasesStudies of the same condition, open and under way.
- More trials run by University of TorontoThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Prospective
- Enrolment
- 1 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Toronto
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, David Jenkins, University of Toronto
- Investigators
- David J Jenkins, MD, PhD, DSc, Principal investigator, University of TorontoJohn L Sievenpiper, MD, PhD, FRCPC, Principal investigator, University of Toronto
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03468127
- Sponsor's protocol ID
- FDA Soy meta 2018
- Status last verified
- Mar 2018
- First submitted
- 9 Mar 2018
- Last updated
- 16 Mar 2018
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: All data will be published
Publications
Blanco Mejia S, Messina M, Li SS, Viguiliouk E, Chiavaroli L, Khan TA, Srichaikul K, Mirrahimi A, Sievenpiper JL, Kris-Etherton P, Jenkins DJA. A Meta-Analysis of 46 Studies Identified by the FDA Demonstrates that Soy Protein Decreases Circulating LDL and Total Cholesterol Concentrations in Adults. J Nutr. 2019 Jun 1;149(6):968-981. doi: 10.1093/jn/nxz020.
PubMed 31006811
Study at a glance
From the registry record, last updated by the sponsor on 16 Mar 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Meta-analysis of 46 Studies Identified by the FDA on the Effect of Soy Protein on Lipid Markers (LDL-Cholesterol [LDL-C] and Total Cholesterol [TC]) as Surrogates of Cardiovascular Disease
- ClinicalTrials.gov ID
- NCT03468127
- Acronym / sponsor ID
- FDA Soy meta 2018
- Conditions
- Cardiovascular Diseases
- Keywords
- Soy protein, LDL-Cholesterol, Total Cholesterol, Cardiovascular disease
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 1 participants (estimated)
- Lead sponsor
- University of TorontoUniversity, hospital or other
- Study start
- 7 Mar 2018 (actual)
- Primary completion
- 19 Apr 2018 (estimated)
- Study completion
- 31 May 2018 (estimated)
- First posted
- 16 Mar 2018 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The FDA have revised the data on soy and concluded that a heart health claim is no longer justified based on more recent studies. They are allowing and established panel for public input. The selected studies have not been meta-analyzed, therefore we will conduct a meta-analysis of the 46 FDA selected studies to assess the effect of soy protein on surrogate markers of cardiovascular disease (LDL-C and TC).
Detailed description
Background: The FDA in their re-evaluation of the scientific evidence for a relationship between soy protein and reduced risk of coronary heart disease (CHD), has revised the data included in the 1999 soy protein and CHD health claim, as well as studies published after this authorized health claim and concluded that a heart health claim is no longer justified based on more recent studies. The 46 identified studies have not been meta-analyzed.
Need for proposed research: To meta-analyse the 46 identified studies to provide the highest level of evidence to aid in the final decision of the soy protein and reduced risk of CHD health claim.
Objective: To provide evidence-based guidance for publich health policy, health claims, and nutrition guidelines relating to soy, we will conduct a meta-analysis of the 46 FDA identified studies of the effect of soy protein on surrogate markers of cardiovascular disease.
Design: The conduct of the meta-analysis will follow the Cochrane handbook for Systematic Reviews of interventions. The reporting will follow the Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guidelines.
Data sources and study selection: We will include the 46 studies pre-selected by the FDA in the Proposed Rule, Soy Protein and Coronary Heart Disease (Docket No. FDA-2017-N-0763).
Data extraction: Two independent investigators will extract study information (study design, sample size, subject characteristics, soy form, dose, comparator, follow-up, background diet, outcome data).
Outcomes: Effects of soy protein intake on LDL-C and TC.
Data synthesis: Mean differences will be pooled using the generic inverse variance method with random-effects model even in the absence of statistically significance between-study heterogeneity, as they yield more conservative summary effect estimates in the presence of residual heterogeneity. Paired analysis will be applied fro crossover trials. Heterogeneity will e assessed by the Cochran Q statistic and quantified by the I2 statistic. To explore sources of heterogeneity, we will conduct sensitivity analysis, in which each study is systematically removed. We will also explore sources of heterogeneity by a priori subgroup analyses by baseline LDL-C levels (<135 mg/dl vs >=135mg/dl), soy dose (<25 g/d vs >= 25 g/d), soy protein food (Isolated soy protein, soy food, soy milk, etc), comparator (animal protein, dairy protein, meat protein), follow-up (median), and categories given by the FDA (baseline cholesterol level [desirable or borderline, high, or normal, borderline, and high], how soy was provided in the studies [feeding or substitution, added to diet], by a mixture of type of soy, how it was provided and baseline cholesterol level [1)Desirable or borderline cholesterol level, added ISP; 2) Desirable or borderline cholesterol level, feeding or substitution studies with ISP; 3) Desirable or borderline cholesterol level, added soy foods; 4)Desirable or borderline cholesterol level, feeding or substitution studies with soy foods; 5) Normal, borderline, and high cholesterol levels, feeding or substitution studies with ISP; 6) High cholesterol level, added ISP; 7) High cholesterol level, feeding or substitution studies with ISP; 8) High cholesterol level, added soy foods; and 9) High cholesterol level, feeding soy foods]), and risk of bias. Meta-regression analysis will assess the significance. Publication bias will be assess by visual inspection of funnel plots and by the use of Egger and Begg's tests. If publication bias is suspected, then we will attempt to adjust for funnel plot asymmetry by imputing the missing study data using the Duval and Tweedie trim and fill method. Dose-reponse analyses will be conducted using the metareg and mkspline commands.
Knowledge translation plan: The results will be disseminated in two stages, first, by the Soy Nutrition Institute in a response to the Proposed Rule, Soy Protein and Coronary Heart Disease, and by a publication in a high impact factor journal.
Significance: The meta-analysis will aid in knowledge translation related to the role of soy protein intake and surrogate markers of cardiovascular disease (LDL-C and TC), strengthening the evidence-based for guidelines and health claims, and improving health outcomes by educating healthcare providers and patients.
Study design
- Observational model
- Other
- Time perspective
- Prospective
Who may qualify
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- All individuals, regardless of health status
Key inclusion criteria (1 listed)
- Studies pre-identified by the FDA [Docket No. FDA-2017-N-0763]
Key exclusion criteria (1 listed)
- Studies with no viable outcome data
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Soy foodsIsolated soy protein, soy protein, soybean products, soy milk | Other | – |
Primary outcome
Surrogate lipid markers of CVD
Time frame: Long term (>3weeks)
LDL-Cholesterol (LDL-C) Total Cholesterol (TC)
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Mar 2018.
- Derived from this study: PubMed 31006811Blanco Mejia S, Messina M, Li SS, Viguiliouk E, Chiavaroli L, Khan TA, Srichaikul K, Mirrahimi A, Sievenpiper JL, Kris-Etherton P, Jenkins DJA. A Meta-Analysis of 46 Studies Identified by the FDA Demonstrates that Soy Protein Decreases Circulating LDL and Total Cholesterol Concentrations in Adults. J Nutr. 2019 Jun 1;149(6):968-981. doi: 10.1093/jn/nxz020.
- Individual participant dataSharing planned: No. All data will be published
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
David J Jenkins, MD, PhD, DSc principal investigator
University of Toronto
John L Sievenpiper, MD, PhD, FRCPC principal investigator
University of Toronto
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Cardiovascular Diseases, run by University of Toronto at 2 sites in Canada.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 16 Mar 2018. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Surrogate lipid markers of CVD (time frame: Long term (>3weeks)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03468127, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Mar 2018.