Introduction: The growth of preterm newborns can be affected during the fetal period, hospitalization, and post discharge.
Objective: to describe the anthropometric development of preterm newborns with or without intrauterine and postnatal growth restriction, and with or without recovery at 40 weeks from birth to 24 months of age.
Patients And Method: Retrospective, descriptive study with Z-scores (Fen ton and WHO) of weight, length, head circumference, and weight/length of preterm infants of less than 32 weeks of gestational age at birth up to 24 months of corrected age. 4 groups were defined ac cording to prenatal, postnatal, post-discharge growth as follows: Group AAA: newborns born AGA, with no postnatal growth restriction; Group APA: newborns born AGA, with postnatal growth res triction, weight < p10 at discharge, and weight > p10 at 40 weeks; Group APP: newborns born AGA, with postnatal growth restriction, weight < p10 at discharge and at 40w; and Group PPP: newborns born with intrauterine growth restriction and who maintained postnatal growth restriction (< p10 at birth, at discharge, and at 40w). We used descriptive statistics with ANOVA, Chi-squared, and linear mixed model analysis.
Results: 710 preterm newborns were included, birth weight 1272 grams (SD 360) and gestational age 29 weeks (SD 1.9). Group AAA had weight, length, and head circumference Z-scores close to the median until 2 years of age. AGA preterm newborns and with postnatal growth restriction can evolve in two ways: one group presents recovery at 40 weeks (Group APA) while the other group presents weight Z-score < -1 up to 6 months (Group APP). Group PPP (with intraute rine and postnatal growth restriction) presents slow weight and length Z-score recovery, weight Z- score -2.3 at discharge, and slow improvement to < -1 at 2 years of age. All groups had weight/height Z-scores above the median in the first 2 months of corrected age.
Conclusion: Preterm newborns with good fetal growth but restricted postnatal growth, may recover at 40 weeks, with subsequent normal development or recover at 6 months.
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http://dx.doi.org/10.32641/andespediatr.v93i1.3600 | DOI Listing |
BMC Plant Biol
January 2025
Maize and Millet Research Institute, Yousafwala, Sahiwal, Pakistan.
Heat stress poses a significant challenge for maize production, especially during the spring when high temperatures disrupt cellular processes, impeding plant growth and development. The B-cell lymphoma-2 (Bcl-2) associated athanogene (BAG) gene family is known to be relatively conserved across various species. It plays a crucial role as molecular chaperone cofactors that are responsible for programmed cell death and tumorigenesis.
View Article and Find Full Text PDFBMC Plant Biol
January 2025
Hebei Agricultural University, Baoding, China.
Background: Nitrogen (N) deposition has become a major driving factor affecting the balance of terrestrial ecosystems, changing the soil environment, element balance and species coexistence relationships, driving changes in biodiversity and ecosystem structure and function. Human-induced nitrogen input leads to a high NH/ NO ratio in soil. However, relatively few studies have investigated the effects of different nitrogen sources on forest plant-microbial symbionts.
View Article and Find Full Text PDFBMC Plant Biol
January 2025
Agricultural College, Faculty of Agricultural College, Inner Mongolia Agricultural University, Hohhot, 010019, China.
Background: Drought stress is a major environmental constraint affecting crop yields. Plants in agricultural and natural environments have developed various mechanisms to cope with drought stress. Identifying genes associated with drought stress tolerance in potato and elucidating their regulatory mechanisms is crucial for the breeding of new potato germplasms.
View Article and Find Full Text PDFCNS Neurosci Ther
January 2025
Jiujiang Clinical Precision Medicine Research Center, Jiujiang, Jiangxi, China.
Background: Adenosine deaminase action on RNA 1 (ADAR1) can convert the adenosine in double-stranded RNA (dsRNA) molecules into inosine in a process known as A-to-I RNA editing. ADAR1 regulates gene expression output by interacting with RNA and other proteins; plays important roles in development, including growth; and is linked to innate immunity, tumors, and central nervous system (CNS) diseases.
Results: In recent years, the role of ADAR1 in tumors has been widely discussed, but its role in CNS diseases has not been reviewed.
Acta Pharmacol Sin
January 2025
Jiangsu Key Laboratory of Neuropsychiatric Diseases and College of Pharmaceutical Sciences, The Fourth Affiliated Hospital of Soochow University, Jiangsu Province Engineering Research Center of Precision Diagnostics and Therapeutics Development, Jiangsu Key Laboratory of Preventive and Translational Medicine for Geriatric Diseases, Suzhou Key Laboratory of Drug Research for Prevention and Treatment of Hyperlipidemic Diseases, Soochow University, Suzhou, 215123, China.
Gastric cancer is a malignant gastrointestinal disease characterized by high morbidity and mortality rates worldwide. The occurrence and progression of gastric cancer are influenced by various factors, including the abnormal alternative splicing of key genes. Recently, RBM39 has emerged as a tumor biomarker that regulates alternative splicing in several types of cancer.
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