A Randomized Trial to Evaluate the Effects of Folic Acid and Zinc Supplementation on Male Fertility and Livebirth: Design and Baseline Characteristics

Author:

Schisterman Enrique F1,Clemons Traci2,Peterson C Matthew3,Johnstone Erica3,Hammoud Ahmad O4,Lamb Denise3,Carrell Douglas T5,Perkins Neil J1,Sjaarda Lindsey A1,Van Voorhis Bradley J6,Ryan Ginny6,Summers Karen6,Campbell Bruce7,Robins Jared8,Chaney Kayla2,Mills James L1,Mendola Pauline1,Chen Zhen9,DeVilbiss Elizabeth A1,Mumford Sunni L1

Affiliation:

1. Epidemiology Branch, Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland

2. The Emmes Company LLC, Rockville, Maryland

3. Division of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, University of Utah, Salt Lake City, Utah

4. IVF Michigan Fertility Centers, Bloomfield Hills, Michigan

5. Departments of Surgery (Urology) and Human Genetics, University of Utah School of Medicine, Salt Lake City, Utah

6. Department of Obstetrics and Gynecology, University of Iowa Carver College of Medicine, Iowa City, Iowa

7. Center for Reproductive Medicine, Minneapolis, Minnesota

8. Division of Reproductive Endocrinology and Infertility, Northwestern University Feinberg School of Medicine, Chicago, Illinois

9. Biostatistics and Bioinformatics Branch, Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland

Abstract

Abstract The Folic Acid and Zinc Supplementation Trial (FAZST) was a multicenter, double-blind, block-randomized, placebo-controlled trial to determine whether folic acid and zinc supplementation in men improves semen quality and increases livebirth rate among couples seeking infertility treatment (2013–2017). Eligible men were aged 18 years or older with female partners aged 18–45 years, seeking infertility treatment. Men were randomized (1:1) to 5 mg folic acid and 30 mg elemental zinc daily or matching placebo for 6 months. Randomization was stratified by site and intended infertility treatment (in vitro fertilization (IVF), non-IVF/study site, and non-IVF/outside clinic). Follow-up of men continued for 6 months, and female partners were passively followed for a minimum of 9 months. Women who conceived were followed throughout pregnancy. Overall, 2,370 men were randomized during 2013–2017 (1,185 folic acid and zinc, 1,185 placebo); they had a mean age of 33 years and body mass index (weight (kg)/height (m)2) of 29.8. Most participants were white (82%), well educated (83% with some college), and employed (72%). Participant characteristics were balanced across intervention arms. Study visits were completed by 89%, 77%, and 75% of men at months 2, 4, and 6, respectively. Here we describe the study design, recruitment, data collection, lessons learned, and baseline participant characteristics.

Funder

Intramural Research Program of the Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland

NIH

Publisher

Oxford University Press (OUP)

Subject

Epidemiology

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