Background: Early childhood wheezing is associated with asthma risk at later ages, emphasizing the need for understanding wheezing patterns and their implications for asthma development.
Methods: Children in the F2-generation (n = 603) of the Isle of Wight Birth Cohort (IOWBC) were followed-up at 3, 6, 12, 24, 36, and 72 months. Prevalence of wheeze and wheeze type (general, infectious, and non-infectious) were recorded. Group-based trajectory models covering ages 3 to 36 months were used to identify early childhood wheezing trajectories for each type of wheeze. These trajectories were examined for their association with asthma status and lung function at 6 years and later.
Results: Distinct trajectories for general ("Persistent", "Transient", "Progressive", and "Infrequent/Never"), infectious ("Persistent", "Transient", and "Infrequent/Never"), and non-infectious ("Progressive", "Early Occurrence", and "Infrequent/Never") wheezing were identified. Compared to the "Infrequent/Never" trajectories, four trajectories were associated with an increased risk of asthma, namely "Progressive" non-infectious, "Early Occurrence" non-infectious, "Persistent" infectious, and "Persistent" general wheeze trajectories.
Conclusions: The identification of wheeze trajectories across different etiologies as significant risk factors for asthma may aid in understanding the complex, multifactorial nature of asthma onset. The findings suggest that early identification of specific wheeze patterns, not just occurrence of wheezing, can inform clinical interventions and potentially mitigate the risk of developing asthma.
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http://dx.doi.org/10.1186/s12931-025-03153-5 | DOI Listing |
Indian J Otolaryngol Head Neck Surg
January 2025
Department of Data Science and Engineering, BITS Pilani, Pilani, Rajasthan India.
Hearing is crucial for the development of language skills. Many infants and young children with undiagnosed hearing impairments, particularly those with mild to moderate severity and no apparent risk factors, miss out on much of the critical early phase of language and speech development. This cross-sectional, hospital-based observational study was conducted at GSVM Medical College and LLRH Hospital on children aged 6 months to 5 years over a 12-month period.
View Article and Find Full Text PDFFront Pharmacol
February 2025
Department of Pediatric Respiratory Medicine, Immunology and Critical Care Medicine, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität, Berlin, Germany.
Objective: Intestinal current measurement (ICM) provides a sensitive bioassay for assessment of cystic fibrosis transmembrane conductance regulator (CFTR) function in rectal biopsies and is used as a diagnostic tool for cystic fibrosis (CF). Furthermore, ICM was shown to be sensitive to detect pharmacological rescue of CFTR function by CFTR modulators in people with CF carrying responsive mutations. Results from clinical trials of CFTR modulators across age groups indicate that CFTR function in the sweat duct may be age-dependent with children reaching higher levels than adults.
View Article and Find Full Text PDFInt J Womens Dermatol
March 2025
Department of Dermatology, Icahn School of Medicine at Mt Sinai, New York, New York.
Background: Early childhood sun exposure contributes to lifetime risk of skin cancer. Many individuals from diverse ethnic backgrounds believe their skin tone confers immunity to sun damage; however, evidence of negative outcomes exists. Best practice in photoprotection for children of color is unclear.
View Article and Find Full Text PDFFront Psychiatry
February 2025
Seaver Autism Center for Research and Treatment, Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Background: FOXP1 syndrome is a genetic neurodevelopmental disorder associated with complex clinical presentations including global developmental delay, mild to profound intellectual disability, speech and language impairment, autism traits, attention-deficit/hyperactivity disorder (ADHD), and a range of behavioral challenges. To date, much of the literature focuses on childhood symptoms and little is known about the FOXP1 syndrome phenotype in adolescence or adulthood.
Methods: A series of caregiver interviews and standardized questionnaires assessed psychiatric and behavioral features of 20 adolescents and adults with FOXP1 syndrome.
Cureus
February 2025
General Practice, Imam Abdulrahman Bin Faisal University, Dammam, SAU.
This systematic review evaluates the effectiveness of preventive strategies in pediatric primary care, focusing on immunization, developmental screening, nutrition counseling, physical activity programs, accident prevention, mental health screening, oral health programs, and parental education, which are essential for enhancing child health outcomes and preventing long-term health issues. Following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, a comprehensive literature search was conducted across multiple databases, including PubMed, MEDLINE, EMBASE, Cochrane Library, and PsycINFO, covering publications from January 2000 to December 2023, with 20 studies included encompassing randomized controlled trials (RCTs), cohort studies, observational studies, and systematic reviews. The review demonstrated that immunization programs significantly reduced disease incidence, while developmental screenings allowed for early intervention in developmental delays.
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