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Evidence-Based Supplement Research
Evidence-Based Supplement Research

Study Design

Type
Review
Population
pregnant women at risk of PTB
Methods
Eight clinical studies involving pregnant women at risk of PTB were included. LF was administered orally, vaginally, or through combined regimens, with variations in dosage and duration.
  • Rigorous Journal

Background

Preterm birth (PTB) remains a leading cause of neonatal morbidity and mortality worldwide. Inflammatory cytokines, particularly IL-6, are central to PTB pathogenesis. Lactoferrin (LF), an iron-binding glycoprotein with antimicrobial and immunomodulatory properties, has been proposed as a potential protective factor against PTB. This narrative review aimed to synthesize current evidence on LF supplementation and its effects on inflammation, cytokine modulation, biochemical markers, and obstetric outcomes related to PTB.

Methods

Eight clinical studies involving pregnant women at risk of PTB were included. LF was administered orally, vaginally, or through combined regimens, with variations in dosage and duration. Reported outcomes encompassed inflammatory markers, cervical and uterine parameters, oxidative stress biomarkers, and obstetric or neonatal endpoints.

Results

Across the studies, LF supplementation was consistently associated with reduced pro-inflammatory cytokines, improvements in cervical length and uterine activity, and favorable changes in oxidative stress markers. Clinically, supplementation was linked with prolonged gestation, fewer preterm births, and reduced neonatal intensive care admissions. Immunological analyses further suggested a positive modulation of cytokine profiles in amniotic fluid.

Conclusions

LF appears to exert multifaceted immunomodulatory effects that mitigate inflammation and support pregnancy maintenance. Although findings point to its potential role in PTB prevention, they should be interpreted with caution given the limited and heterogeneous evidence. Further large-scale, multicenter randomized trials are needed to confirm efficacy and to establish optimal dosage, route, and timing of administration.

Research Insights

  • improvements in cervical length and uterine activity

    Effect
    Beneficial
    Effect size
    Moderate
    Dose
    oral, vaginal, or combined regimens with variations in dosage and duration
  • favorable changes in oxidative stress markers

    Effect
    Beneficial
    Effect size
    Moderate
    Dose
    oral, vaginal, or combined regimens with variations in dosage and duration
  • Immunological analyses further suggested a positive modulation of cytokine profiles in amniotic fluid

    Effect
    Beneficial
    Effect size
    Moderate
    Dose
    oral, vaginal, or combined regimens with variations in dosage and duration
  • supplementation was linked with prolonged gestation

    Effect
    Beneficial
    Effect size
    Moderate
    Dose
    oral, vaginal, or combined regimens with variations in dosage and duration
  • reduced neonatal intensive care admissions

    Effect
    Beneficial
    Effect size
    Moderate
    Dose
    oral, vaginal, or combined regimens with variations in dosage and duration
  • fewer preterm births

    Effect
    Beneficial
    Effect size
    Moderate
    Dose
    oral, vaginal, or combined regimens with variations in dosage and duration
  • Across the studies, LF supplementation was consistently associated with reduced pro-inflammatory cytokines

    Effect
    Beneficial
    Effect size
    Moderate
    Dose
    oral, vaginal, or combined regimens with variations in dosage and duration
  • improvements in cervical length and uterine activity

    Effect
    Beneficial
    Effect size
    Moderate
    Dose
    oral, vaginal, or combined regimens with variations in dosage and duration
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