Observational studyIndian pediatrics2025
Incidence and Risk Factors for Metabolic Bone Disease of Prematurity in Indian Infants: A Prospective Observational Study.
Observational study in Indian pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
6 citing papers in PubMed.
- Bone Mineral Density and Its Association with Serum Biochemical Markers of Metabolic Bone Disease of Prematurity in Neonates of <34 weeks Gestation: Correspondence.Indian journal of pediatrics · 2026Article
- Bone Mineral Density and Its Association with Serum Biochemical Markers of Metabolic Bone Disease of Prematurity in Neonates of <34 weeks Gestation: Authors' Reply.Indian journal of pediatrics · 2026Article
- Bone Mineral Density and Its Association with Serum Biochemical Markers of Metabolic Bone Disease of Prematurity in Neonates of <34 weeks Gestation.Indian journal of pediatrics · 2026Article
- Article
- Article
- Interventions for metabolic bone disease of prematurity: A systematic review and meta-analysis.Metabolism open · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
purposeTo assess the incidence and risk factors for metabolic bone disease of prematurity (MBDP).
methodsInfants born at ≤ 33 weeks' gestation were screened for MBDP using serum calcium, phosphorus, and alkaline phosphatase levels. Screening began at 3-6 weeks and was repeated as indicated until three months of corrected age. Feed volume, nutrient supplementation, and morbidity data were compared between the infants with and without MBDP.
resultsAmong the 153 infants, 22 (14.4%) had moderate MBDP and 28 (18.3%) had severe MBDP. Lower birth weight was independently associated with severe MBDP (P-0.009).
conclusionsNearly 40% of the preterm infants in our cohort had moderate-to-severe MBDP.
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Identifiers
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.