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Women's Isoflavone Soy Health (WISH) Trial

Primary Purpose

Atherosclerosis

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
25 gm soy protein supplement
Placebo
Sponsored by
University of Southern California
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Atherosclerosis focused on measuring Atherosclerosis, Cardiovascular Diseases, Carotid artery intima-media thickness (CIMT), Cognition, Complementary and alternative medicine, Daidzein, Genistein, Glycitein, Intervention, Isoflavones, Menopause, Prevention, Postmenopausal, Randomized controlled study, Soy, Soy Protein, Subclinical Vascular Disease, Ultrasonography, Women

Eligibility Criteria

30 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria: Postmenopausal, defined as no vaginal bleeding for at least 1 year and serum estradiol level lower than 20 pg/ml Exclusion Criteria: Signs, symptoms or personal history of cardiovascular disease Diabetes mellitus or fasting serum glucose of 126 mg/dL or greater Fasting plasma triglyceride of 500 mg/dL or greater Serum creatinine greater than 2.0 mg/dL Uncontrolled hypertension Untreated thyroid disease Life expectancy less than 5 years Current use of hormone replacement therapy (HRT) Soy, nut, or related food allergies More than 5 alcohol drinks per day or substance abuse

Sites / Locations

  • Atherosclerosis Research Unit, University of Southern California

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Isoflavone Soy Protein (ISP) Supplementation

Placebo

Arm Description

25 gm soy protein supplementation administered twice daily in equivalent dosages (12.5 gm)

Milk protein matching placebo administered twice daily in equivalent dosages

Outcomes

Primary Outcome Measures

Progression of Subclinical Atherosclerosis
Rate of change in right distal common carotid artery (CCA) far wall intima-media thickness (um per year) in computer image processed B-mode ultrasonograms.

Secondary Outcome Measures

Change in Neurocognitive Function (Global Cognition)
The specified primary cognitive endpoint compared between treatment groups was change from baseline on a global cognitive composite score calculated as an average of standardized scores for 14 neuropsychological tests weighted by the inverse intertest correlation matrix. Neuropsychological test scores at baseline and follow-up assessments were standardized ([raw score-mean score]/standard deviation) using the baseline means and standard deviations from the entire WISH sample. Each of 3 cognitive composite scores was calculated at baseline and follow-up as the weighted average of the individual donor standardized test scores weighted by the inverse correlation among tests. Change from baseline (endpoint minus baseline cognitive outcome) was computed for each cognitive score (verbal memory, global cognition, executive function). Since the outcome is not a single test but a weighted average of multiple tests, the range is not standardized and there are no established clinical thresholds.

Full Information

First Posted
July 7, 2005
Last Updated
April 16, 2023
Sponsor
University of Southern California
Collaborators
National Center for Complementary and Integrative Health (NCCIH), Office of Dietary Supplements (ODS), Office of Research on Women's Health (ORWH), Solae, LLC
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1. Study Identification

Unique Protocol Identification Number
NCT00118846
Brief Title
Women's Isoflavone Soy Health (WISH) Trial
Official Title
Phytoestrogens and Progression of Atherosclerosis
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Completed
Study Start Date
April 12, 2004 (Actual)
Primary Completion Date
March 19, 2009 (Actual)
Study Completion Date
March 19, 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Southern California
Collaborators
National Center for Complementary and Integrative Health (NCCIH), Office of Dietary Supplements (ODS), Office of Research on Women's Health (ORWH), Solae, LLC

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine whether soy supplementation can reduce hardening of the arteries and cognitive decline in postmenopausal women.
Detailed Description
Heart disease is the leading cause of death among women in the United States. Atherosclerosis, a primary cause of heart disease, accounts for more than 485,000 heart attacks and 370,000 strokes each year in American women. Data indicate that a woman's risk of suffering from an atherosclerosis-related cardiovascular event significantly increases after menopause; this risk may be due to reduced estrogen production associated with menopause. Soy isoflavones are plant compounds that are structurally similar to human estrogen. Evidence suggests that soy supplements may provide the same protection against heart disease as estrogen in postmenopausal women. This study will determine the effects of soy supplementation on subclinical atherosclerosis progression and cognitive decline in postmenopausal women. In this double-blinded, placebo-controlled trial, a total of 350 postmenopausal women were randomly assigned to receive either soy protein supplementation or placebo twice daily for 2.7 years. The initial 2.5-year treatment period was increased to 3 years. The active product, given as two divided doses, was 25 g soy protein containing 85 mg aglycone weight naturally-occurring isoflavones (150 mg total isoflavone) of genistein 45 mg aglycone weight (80 mg total weight), daidzein 35 mg aglycone weight (60 mg total weight), and glycitein 5 mg aglycone weight (10 mg total weight). The primary trial end point was the rate of change in the right distal common carotid artery intima-media thickness (CIMT) by ultrasonography. Participants underwent ultrasonography at baseline and every six months along with laboratory determinations and clinical measurements. Cognitive assessments were completed at baseline and the final follow-up visit (2.5 years).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atherosclerosis
Keywords
Atherosclerosis, Cardiovascular Diseases, Carotid artery intima-media thickness (CIMT), Cognition, Complementary and alternative medicine, Daidzein, Genistein, Glycitein, Intervention, Isoflavones, Menopause, Prevention, Postmenopausal, Randomized controlled study, Soy, Soy Protein, Subclinical Vascular Disease, Ultrasonography, Women

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
350 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Isoflavone Soy Protein (ISP) Supplementation
Arm Type
Active Comparator
Arm Description
25 gm soy protein supplementation administered twice daily in equivalent dosages (12.5 gm)
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Milk protein matching placebo administered twice daily in equivalent dosages
Intervention Type
Dietary Supplement
Intervention Name(s)
25 gm soy protein supplement
Intervention Description
25 gm soy protein supplementation administered in equally divided dosage twice daily (12.5 gm)
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Milk protein administered twice daily
Primary Outcome Measure Information:
Title
Progression of Subclinical Atherosclerosis
Description
Rate of change in right distal common carotid artery (CCA) far wall intima-media thickness (um per year) in computer image processed B-mode ultrasonograms.
Time Frame
Baseline x 2 and then every 6 months, up to 2.5 years
Secondary Outcome Measure Information:
Title
Change in Neurocognitive Function (Global Cognition)
Description
The specified primary cognitive endpoint compared between treatment groups was change from baseline on a global cognitive composite score calculated as an average of standardized scores for 14 neuropsychological tests weighted by the inverse intertest correlation matrix. Neuropsychological test scores at baseline and follow-up assessments were standardized ([raw score-mean score]/standard deviation) using the baseline means and standard deviations from the entire WISH sample. Each of 3 cognitive composite scores was calculated at baseline and follow-up as the weighted average of the individual donor standardized test scores weighted by the inverse correlation among tests. Change from baseline (endpoint minus baseline cognitive outcome) was computed for each cognitive score (verbal memory, global cognition, executive function). Since the outcome is not a single test but a weighted average of multiple tests, the range is not standardized and there are no established clinical thresholds.
Time Frame
Baseline and 2.5 years

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Postmenopausal, defined as no vaginal bleeding for at least 1 year and serum estradiol level lower than 20 pg/ml Exclusion Criteria: Signs, symptoms or personal history of cardiovascular disease Diabetes mellitus or fasting serum glucose of 126 mg/dL or greater Fasting plasma triglyceride of 500 mg/dL or greater Serum creatinine greater than 2.0 mg/dL Uncontrolled hypertension Untreated thyroid disease Life expectancy less than 5 years Current use of hormone replacement therapy (HRT) Soy, nut, or related food allergies More than 5 alcohol drinks per day or substance abuse
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Howard N. Hodis, M.D.
Organizational Affiliation
Atherosclerosis Research Unit, University of Southern California
Official's Role
Principal Investigator
Facility Information:
Facility Name
Atherosclerosis Research Unit, University of Southern California
City
Los Angeles
State/Province
California
ZIP/Postal Code
90033
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
21903957
Citation
Hodis HN, Mack WJ, Kono N, Azen SP, Shoupe D, Hwang-Levine J, Petitti D, Whitfield-Maxwell L, Yan M, Franke AA, Selzer RH; Women's Isoflavone Soy Health Research Group. Isoflavone soy protein supplementation and atherosclerosis progression in healthy postmenopausal women: a randomized controlled trial. Stroke. 2011 Nov;42(11):3168-75. doi: 10.1161/STROKEAHA.111.620831. Epub 2011 Sep 8.
Results Reference
result
PubMed Identifier
22665144
Citation
Henderson VW, St John JA, Hodis HN, Kono N, McCleary CA, Franke AA, Mack WJ; WISH Research Group. Long-term soy isoflavone supplementation and cognition in women: a randomized, controlled trial. Neurology. 2012 Jun 5;78(23):1841-8. doi: 10.1212/WNL.0b013e318258f822.
Results Reference
result
PubMed Identifier
35526057
Citation
Lin F, Pa J, Karim R, Hodis HN, Han SD, Henderson VW, St John JA, Mack WJ. Subclinical carotid artery atherosclerosis and cognitive function in older adults. Alzheimers Res Ther. 2022 May 7;14(1):63. doi: 10.1186/s13195-022-00997-7.
Results Reference
derived
PubMed Identifier
23422867
Citation
Quaas AM, Kono N, Mack WJ, Hodis HN, Felix JC, Paulson RJ, Shoupe D. Effect of isoflavone soy protein supplementation on endometrial thickness, hyperplasia, and endometrial cancer risk in postmenopausal women: a randomized controlled trial. Menopause. 2013 Aug;20(8):840-4. doi: 10.1097/GME.0b013e3182804353.
Results Reference
derived

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Women's Isoflavone Soy Health (WISH) Trial

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