Malnutrition enteropathy in Zambian and Zimbabwean children with severe acute malnutrition: A multi-arm randomized phase II trial.
Kanta ChandweMutsa Bwakura-DangarembiziBeatrice AmadiGertrude TawodzeraDeophine NgosaAnesu DzikitiNivea ChuluRobert MakuyanaKanekwa ZyamboKuda MutasaChola MulengaEllen BesaJonathan P SturgeonShepherd MudzingwaBwalya SimunyolaLydia KazhilaMasuzyo ZyamboHazel SonkweBatsirai MutasaMiyoba ChipunzaVirginia SaurambaLisa F LanghaugVictor MudendaSimon H MurchSusan HillRaymond John PlayfordKelley VanBuskirkAndrew J PrendergastM Paul KellyPublished in: Nature communications (2024)
Malnutrition underlies almost half of all child deaths globally. Severe Acute Malnutrition (SAM) carries unacceptable mortality, particularly if accompanied by infection or medical complications, including enteropathy. We evaluated four interventions for malnutrition enteropathy in a multi-centre phase II multi-arm trial in Zambia and Zimbabwe and completed in 2021. The purpose of this trial was to identify therapies which could be taken forward into phase III trials. Children of either sex were eligible for inclusion if aged 6-59 months and hospitalised with SAM (using WHO definitions: WLZ <-3, and/or MUAC <11.5 cm, and/or bilateral pedal oedema), with written, informed consent from the primary caregiver. We randomised 125 children hospitalised with complicated SAM to 14 days treatment with (i) bovine colostrum (n = 25), (ii) N-acetyl glucosamine (n = 24), (iii) subcutaneous teduglutide (n = 26), (iv) budesonide (n = 25) or (v) standard care only (n = 25). The primary endpoint was a composite of faecal biomarkers (myeloperoxidase, neopterin, α 1 -antitrypsin). Laboratory assessments, but not treatments, were blinded. Per-protocol analysis used ANCOVA, adjusted for baseline biomarker value, sex, oedema, HIV status, diarrhoea, weight-for-length Z-score, and study site, with pre-specified significance of P < 0.10. Of 143 children screened, 125 were randomised. Teduglutide reduced the primary endpoint of biomarkers of mucosal damage (effect size -0.89 (90% CI: -1.69,-0.10) P = 0.07), while colostrum (-0.58 (-1.4, 0.23) P = 0.24), N-acetyl glucosamine (-0.20 (-1.01, 0.60) P = 0.67), and budesonide (-0.50 (-1.33, 0.33) P = 0.32) had no significant effect. All interventions proved safe. This work suggests that treatment of enteropathy may be beneficial in children with complicated malnutrition. The trial was registered at ClinicalTrials.gov with the identifier NCT03716115.
Keyphrases
- phase iii
- phase ii
- open label
- clinical trial
- placebo controlled
- double blind
- study protocol
- young adults
- randomized controlled trial
- physical activity
- healthcare
- type diabetes
- risk factors
- palliative care
- pain management
- preterm infants
- replacement therapy
- case report
- human milk
- human immunodeficiency virus
- chronic pain
- hepatitis c virus
- quality improvement
- coronary artery disease