Actively Recruiting
Probiotic Supplementation in Optimizing Iron and Hematological Status Among Pregnant Females
Led by University of Illinois at Chicago · Updated on 2026-05-01
250
Participants Needed
1
Research Sites
251 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Maternal iron deficiency (ID) and iron deficiency anemia (IDA) is associated with maternal and infant mortality, spontaneous preterm birth, maternal postpartum hemorrhage, and neurocognitive defects in the neonate. Therefore, preventing maternal IDA in at-risk women is critical. The standard approach to improving iron status in pregnancy (i.e., oral iron supplements) is suboptimal and gastrointestinal discomforts associated with this approach (i.e., constipation) impairs adherence. The incidence of ID (18%) and IDA (5%) in pregnant populations suggest alternative interventions are needed to optimize iron status in pregnancy. There is increasing evidence that consuming the probiotic Lactoplantibacillus plantarum 299v (LP299V®) can enhance dietary non-heme iron absorption by changes in the composition and metabolic patterns of gut microbiota that reduce intestinal pH, enhance mucin production and favor an anti-inflammatory milieu. This immunomodulatory effect may be important because inflammation stimulates hepatic production of hepcidin, a master regulator of systemic iron homeostasis, which inhibits iron flow into circulation from diet and body stores. Further, the effects of LP299V® may extend to the placenta. The investigators' team showed previously that maternal iron deficiency is associated with changes to placental iron metabolism with more iron sequestered in the placenta and less iron transferring to the fetus. Given its positive effects on maternal iron status, the investigators surmise that LP299V® supplementation will result in higher placenta protein expression of iron transporters, transferrin receptor-1 and ferrroportin-1, and lower placental iron accumulation/content. The primary goal of this study is to test the efficacy of this low-cost, safe, innovative approach to optimizing maternal iron status in individuals at risk for ID in pregnancy \[Hb 11.0 - 11.9 g/dL (first trimester) and Hb 10.5 - 11.5 g/dL (second trimester) based on new OB clinical complete blood count (CBC) results obtained from the EHR\] from 10-16 weeks gestational age (GA) until the time of labor. The investigators will also test the effects on neonatal (cord blood) iron status and (cord blood + newborn heel stick) Hb at birth and determine the effect of maternal LP299V® supplementation on the maternal gut microbiome, hepcidin-ferroportin axis and placenta iron and placenta transport of iron as its primary mechanisms of action. Finally, the investigators will explore the effect of maternal LP299V® supplementation on infant neurodevelopment at birth. This study is an essential first step toward evaluating if twice daily oral LP299V® is an efficacious, safe, inexpensive, and scalable clinical strategy for the prevention of maternal ID and its related complications in at-risk women.
CONDITIONS
Official Title
Probiotic Supplementation in Optimizing Iron and Hematological Status Among Pregnant Females
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Singleton naturally conceived pregnancy
- At risk of iron deficiency anemia with hemoglobin 11.0-11.9 g/dL (first trimester) or 10.5-11.5 g/dL (second trimester) based on recent blood tests
- Age between 18 and 45 years
- 10 to 16 weeks gestational age
- Fluent in English to provide consent and complete study procedures
- Able to provide consent
- Own a smartphone
You will not qualify if you...
- Diagnosed or suspected iron deficiency anemia or other nutritional anemia (e.g., B12 or folate deficiency)
- Recent blood transfusion
- Autoimmune disorders such as rheumatoid arthritis
- Inflammatory bowel disease
- Oral or intravenous antibiotic use in past 2 months
- Previous spontaneous preterm birth
- History of bariatric surgery
- Malabsorptive diseases
- Current hyperemesis
- Current eating disorder
- Hematologic disorders or carrier traits such as hemochromatosis or beta-thalassemia
- Current use of tobacco, alcohol, or illicit drugs (excluding marijuana)
AI-Screening
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Trial Site Locations
Total: 1 location
1
University of Illinois at Chicago
Chicago, Illinois, United States, 60612
Actively Recruiting
Research Team
M
Mary Dawn Koenig, PhD, RN, CNM
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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