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Background: Early childhood developmental delay, functional disability, and undernutrition pose critical public health challenges in low-resource settings. However, the co-occurrence of these conditions remains poorly understood. This study examined co-occurrence patterns of these three major global health concerns and associated risk factors among children aged 36-59 months in 15 sub-Saharan Africa (SSA) countries using cross-sectional data.
Methods: We analyzed data from 15 SSA countries, namely Benin, Central African Republic, Chad, Comoros, Democratic Republic of the Congo, Gambia, Ghana, Guinea-Bissau, Lesotho, Madagascar, Malawi, Sao Tome and Principe, Sierra Leone, Togo, and Zimbabwe, available from 2017 to 2022 from the Multiple Indicator Cluster Survey (MICS) online repository. Latent class analysis (LCA) was performed to identify the co-occurrence patterns of early childhood developmental delay, functional disability, and undernutrition. Multinomial logistic regression (MLR) was used to examine the risk factors associated with the co-occurrence patterns identified by LCA.
Findings: Five distinct co-occurrence patterns were identified: Relatively Healthy (66.7%), Co-occurrence of Wasting and Underweight with Developmental Delay (CWU-DD) (5.2%), Co-occurrence of Underweight, Stunting, Developmental Delay, and Functional Disability (CUS-DD-FD) (1.0%), Co-occurrence of Underweight and Stunting with Developmental Delay (CUS-DD) (15.7%), and Co-occurrence of Developmental Delay and Stunting with Functional Disability (CDD-S-FD) (11.4%). MLR revealed that maternal functional disabilities were positively associated with CUS-DD-FD (odds ratio [OR] = 2.56, 95% CI: 1.60-4.12) and CDD-S-FD (OR = 1.46, 95% CI: 1.18-1.82). Non-aggressive discipline was associated with decreased risks of CWU-DD (OR = 0.72, 95% CI: 0.55-0.95), CUS-DD-FD (OR = 0.31, 95% CI: 0.20-0.49), CUS-DD (OR = 0.81, 95% CI: 0.70-0.94), and CDD-S-FD (OR = 0.77, 95% CI: 0.65-0.92), while physical-aggressive discipline was associated with an increased risk of CDD-S-FD (OR = 1.17, 95% CI: 1.01-1.36). Additionally, sex, diarrhea, maternal education, and some socio-environmental factors were also identified as significantly associated risk factors that had differentiated effect on membership of co-occurrence patterns.
Interpretation: The identified co-occurrence patterns and their associated risk factors emphasize the need to address early childhood developmental delay, functional disability, and undernutrition as interconnected concerns. These findings support integrated approaches to early childhood interventions that account for the interconnected nature of developmental, functional, and nutritional vulnerabilities in young children.
Funding: None.
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http://dx.doi.org/10.1016/j.eclinm.2025.103305 | DOI Listing |
Pediatr Res
September 2025
Division of Developmental and Behavioral Pediatrics, Department of Pediatrics, University of Michigan Medical School, Ann Arbor, MI, USA.
Background: Children with congenital cytomegalovirus (cCMV) have a wide spectrum of possible neurodevelopmental outcomes.
Objectives: To describe neurodevelopmental (ND) Phenotypes of children with cCMV based on medical, developmental, and behavioral outcomes in childhood, and examine whether birth characteristics were associated with ND Phenotype.
Methods: Caregivers of children with cCMV (N = 242, child aged 12 months to <11 years) completed survey instruments reporting on the child's birth characteristics, reasons for cCMV testing, and present medical, developmental, and behavioral status.
Physiol Plant
September 2025
Department of Plant Physiology, Institute of Biology, Martin-Luther-Universität Halle-Wittenberg, Halle (Saale), Germany.
Several genes in the mitochondria of angiosperms are interrupted by introns, and their posttranscriptional excision involves numerous nucleus-encoded auxiliary factors. Most of these factors are of eukaryotic origin, among them members of the pentatricopeptide-repeat (PPR) family of RNA-binding proteins. This family divides into the PLS and P classes, with PLS-class proteins typically participating in C-to-U mRNA editing and P-class members contributing to transcript stabilization and intron splicing.
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September 2025
Division of Developmental Pediatrics, Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Türkiye.
Background: Autism spectrum disorder (ASD) is more frequently diagnosed in boys than in girls, possibly due to gender-based differences in symptom presentation or referral patterns. This study investigates gender-related variations in symptom severity and clinical presentation among preschool children referred for suspected ASD.
Methods: This study included 125 children (boys: n=103; girls: n=22) aged 2-5 years suspected of having ASD.
Ann Med
December 2025
Department of Physical & Rehabilitation Medicine, Chonnam National University Medical School & Hospital, Gwangju, Republic of Korea.
Purpose: This study aimed to investigate the epidemiological data of children with disabilities obtained by the INfants and Children's Health Screening (INCHS) program in South Korea.
Methods: We conducted a retrospective case-control study by extracting data from the Korean National Health Insurance Service Database for children who were diagnosed with disabilities within 60 months of birth. Chi-square and Fisher's exact tests were performed to compare 35,072 children born after the introduction of the INCHS program (2008-2014) with a control group born before (2002-2007).
Hum Genet
September 2025
College of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, Chinese PLA Medical School, 28 Fuxing Road, Beijing, 100853, China.
Recessive variants in TWNK cause syndromes arising from mitochondrial DNA (mtDNA) depletion. Hearing loss is the most prevalent manifestation in individuals with these disorders. However, the clinical and pathophysiological features have not been fully elucidated.
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