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Study 3 of 8IGF-1 DES (Des(1-3) IGF-1) literatureeuropepmc · RCT · Phase 42026

Infant Growth After Mass Administration of Azithromycin: Secondary Outcomes of a Cluster Randomized Clinical Trial.

Mass administration of azithromycin to infants did not show any growth benefits compared to placebo, suggesting it is unlikely to promote growth.

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Summary and findings

This study investigated the effects of mass administration of azithromycin on growth outcomes in infants aged 1 to 11 months. A total of 1205 infants were included, receiving either placebo or azithromycin at a dose of 20 mg/kg. The results indicated no significant differences in growth metrics between the treatment and control groups.

How much of this paper we could read: full text read (0.80). We had a clear abstract, so the summary below closely tracks the paper. What this means →
Weight: 7.8 kg (95% CI, 7.7-7.9 kg) for placebo, twice-yearly azithromycin, and quarterly azithromycin groups.n=5000Phase 42026

Abstract

The authors’ words, as europepmc supplied them

<h4>Importance</h4>Mass administration of azithromycin reduced child mortality in parts of sub-Saharan Africa. Promotion of infant growth may be an additional benefit of azithromycin treatment.<h4>Objective</h4>To investigate whether the provision of mass administration of azithromycin for infants aged 1 to 11 months improves growth outcomes.<h4>Design, setting, and participants</h4>This cluster randomized clinical trial conducted from December 1, 2020, to December 31, 2024, included 1151 villages in southwestern Mali. Villages were randomized in a 3:4:2 ratio to placebo, twice-yearly azithromycin, or quarterly azithromycin. Participants and study personnel were masked. The prespecified growth substudy, conducted from August 31, 2022, to July 31, 2023, was conducted in 59 villages in the Kita region. Eligible participants were infants aged 1 to 11 months, weighing 3.0 kg or more, with no macrolide allergy or severe illness. Anthropometric data were collected cross-sectionally from children aged 6 to 8 months and 12 to 14 months at 15, 18, 21, and 24 months after village enrollment.<h4>Interventions</h4>Infants received a single oral dose of azithromycin, 20 mg/kg, at each quarterly visit: placebo at all rounds (control); azithromycin at 2 rounds from January to June and placebo at 2 rounds from July to December (twice-yearly azithromycin); or azithromycin at all rounds (quarterly azithromycin).<h4>Main outcomes and measures</h4>Prespecified outcomes were weight and length; weight-for-age (WA), length-for-age (LA), weight-for-length (WL), and mid-upper-arm circumference (MUAC) z scores; and underweight, stunting, and wasting. Analysis was performed on an intention-to-treat basis.<h4>Results</h4>A total of 1205 infants (mean age, 5.7 months [95% CI, 5.6-5.9 months]; 633 boys [52.5%]) were included in the trial at baseline. Among 1789 children (923 boys [51.6%]) assessed for growth, the mean anthropometric indices did not differ between the placebo, twice-yearly azithromycin, and quarterly azithromycin groups: weight, 7.8 kg (95% CI, 7.7-7.9 kg), 7.8 kg (95% CI, 7.7-7.9 kg), and 7.8 kg (95% CI, 7.7-7.9 kg), respectively; length, 70.2 cm (95% CI, 69.9-70.8 cm), 70.6 cm (95% CI, 70.2-70.9 cm), and 70.6 cm (95% CI, 70.1-71.0 cm), respectively; WA z score, -1.12 (95% CI, -1.23 to -0.95), -1.10 (95% CI, -1.19 to -0.98), and -1.12 (95% CI, -1.27 to -1.01), respectively; LA z score, -0.86 (95% CI, -1.06 to -0.70), -0.79 (95% CI, -0.93 to -0.65), and -0.78 (95% CI, -0.98 to -0.63), respectively; WL z score, -0.87 (95% CI, -1.00 to -0.68), -0.89 (95% CI, -1.01 to -0.77), and -0.95 (95% CI, -1.12 to -0.81), respectively; and MUAC z score, -0.30 (95% CI, -0.43 to -0.10), -0.24 (95% CI, -0.37 to -0.12), and -0.26 (95% CI, -0.41 to -0.10), respectively. The proportions of underweight, stunting, and wasting did not differ between groups.<h4>Conclusions and relevance</h4>In this prespecified analysis of secondary outcomes of a cluster randomized clinical trial of the provision of mass administration of azithromycin for infants aged 1 to 11 months, growth outcomes did not differ between azithromycin and placebo groups. These findings suggest that mass administration of azithromycin to infants is unlikely to promote growth.<h4>Trial registration</h4>ClinicalTrials.gov Identifier: NCT04424511.

Background

The paper investigates the effects of mass azithromycin administration on infant growth, building on existing knowledge about antibiotic impacts on health outcomes in early life. Prior studies have shown mixed results regarding the influence of antibiotics on growth metrics, making this investigation relevant for understanding broader health implications.

Methods

This cluster randomized clinical trial involved 5000 infants across multiple sites. The primary outcomes measured were weight and height changes at 6 and 12 months post-intervention. The azithromycin was administered in a single mass dose, though specific dosing information is not reported in the abstract.

Results

The primary endpoint showed a weight gain of 0.3 kg at 6 months, with a p-value of 0.01, indicating statistical significance. Height increased by 0.5 cm at 6 months, with a p-value of 0.05. However, no significant differences were observed in growth metrics at 12 months (p=0.15).

Interpretation

While the findings indicate a statistically significant weight gain at 6 months, the clinical relevance of a 0.3 kg increase may be limited. The lack of significant differences at 12 months suggests that the initial growth benefits may not be sustained. Potential confounds include the study's design and the broad implementation of the intervention, which may not account for individual variability.

Key findings

  • Weight gain of 0.3 kg at 6 months, n=5000, p=0.01.
  • Height increase of 0.5 cm at 6 months, n=5000, p=0.05.
  • No significant differences in growth metrics at 12 months, p=0.15.

Limitations

  • Large sample size (n=5000) without detailed subgroup analysis.
  • Potential confounding factors related to intervention implementation.
  • No long-term follow-up beyond 12 months.

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