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Purpose: This study aims to compare baseline characteristics and treatment outcomes of type 1 and type 2 myopic choroidal neovascularization (CNV) after one year of anti-vascular endothelial growth factors (VEGF) therapy and identify clinical factors associated with visual outcomes, recurrence rates, and injection numbers.
Methods: In this retrospective study, we reviewed 171 patients with active mCNV treated with anti-VEGF therapy and followed for at least one year. CNV types were classified using optical coherence tomography (OCT). Baseline characteristics, including best-corrected visual acuity (BCVA), myopic maculopathy grade, and OCT findings, were compared.
Results: Type 1 CNVs (19.3% of cases) exhibited worse baseline BCVA and more advanced macular degeneration than type 2 CNVs. Both types showed significant visual improvement equivalent to 2.2 lines post-therapy, with no difference in recurrence rates or injection numbers. Multivariate analysis revealed that baseline BCVA, severity of myopic macular degeneration, and presence of subretinal hyperreflective exudation were significant predictors of final BCVA, while CNV type was not an independent predictor.
Conclusion: Despite more severe macular degeneration in type 1 CNV, both types myopic CNVs benefit significantly from anti-VEGF therapy. These findings support extending treatment to type 1 CNVs and highlight the need for individualized management strategies.
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http://dx.doi.org/10.1097/IAE.0000000000004611 | DOI Listing |
Acta Med Philipp
July 2025
Department of Biochemistry and Molecular Biology, College of Medicine, University of the Philippines Manila, Manila, Philippines.
Background And Objectives: Cell lines serve as invaluable tools in studying lung cancer biology and developing new therapies to combat the disease. However, commercially available cell lines are typically of Caucasian origin and may be less representative of the local genetic background. To address this, our lab previously immortalized cells from pleural fluid of a Filipino non-small cell lung cancer (NSCLC) patient via CDK4 transduction.
View Article and Find Full Text PDFGenes (Basel)
July 2025
Department for Personalized Medicine, University Hospital Center Zagreb, 10000 Zagreb, Croatia.
Background: Neurodevelopmental disorders (NDDs), including autism spectrum disorder (ASD), are genetically complex and often linked to structural genomic variations such as copy number variants (CNVs). Current diagnostic strategies face challenges in interpreting the clinical significance of such variants.
Methods: We developed a customized, gene-oriented chromosomal microarray (CMA) targeting 6026 genes relevant to neurodevelopment, aiming to improve diagnostic yield and candidate gene prioritization.
BMC Plant Biol
August 2025
State Key Laboratory of Plant Diversity and Specialty Crops, Institute of Botany, Chinese Academy of Sciences, Beijing, 100093, China.
Background: The columbine genus (Aquilegia) contains many species with horticultural and pharmaceutical importance. However, a well-resolved phylogeny for this genus remains lacking owing to recent and rapid radiation. We obtained plastomes of 75 Aquilegia species and six species of other genera in Thalictroideae to reconstruct a robust phylogeny for Aquilegia.
View Article and Find Full Text PDFAntimicrob Agents Chemother
August 2025
University Clinical Research Center, University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.
With growing concern about parasite resistance to sulfadoxine-pyrimethamine (SP) in West Africa, the effectiveness of dihydroartemisinin-piperaquine (DHA + PQ) was assessed as an alternative drug regimen for Seasonal Malaria Chemoprevention (SMC). This study aims to determine the prevalence of molecular markers of resistance to SP + AQ and DHA + PQ in Koulikoro (Mali), where SMC has been implemented since 2014. -positive samples were analyzed by either next-generation sequencing, focusing on SNPs in genes known to be associated with resistance: and genes, and using qPCR for copy number variations (CNVs) of and .
View Article and Find Full Text PDFJ Genet Couns
August 2025
Rutgers University Genetic Counseling Master's Program, Piscataway, New Jersey, USA.
We report pregnancy termination rates following a variety of fetal diagnoses and determine which factors may influence this decision. We conducted a retrospective chart review of pregnancies diagnosed with a genetic abnormality at a single institution from January 2012 to April 2023. The type of diagnosis, termination status, and thirteen demographic factors were collected.
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