Journal of cataract and refractive surgery · 2025
Genetic variants in genes regulating lens capsule structure and stability in dead bag syndrome: part 1.
СтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Vasavada Abhay R, Rajkumar Sankaranarayanan, Vasavada Shail A, Vasavada Vaishali, Dholu Suchi, Meena Vijaylaxmi
Аннотация
PURPOSE: To investigate potential genetic variants associated with spontaneous posterior capsule rupture (sPCR) in patients diagnosed with dead bag syndrome (DBS).
SETTING: Iladevi Cataract and IOL Research Centre and Raghudeep Eye Hospital, Ahmedabad, Gujarat, India.
DESIGN: Laboratory study.
METHODS: Blood samples were collected from 30 patients with DBS and 37 controls. Whole-exome sequencing was performed. Genetic variants in genes encoding extracellular matrix components of the lens capsule were screened. The association of selected variants with DBS was analyzed using the Optimal Unified Sequence Kernel Association Test in R and Logistic Regression. Genes showing significant associations were further analyzed using in silico predictions through the Ensembl Variant Effect Predictor to assess their potential impact on protein function.
RESULTS: Three genes- FBN2 ( P = .027, odds ratio [OR] = 4.9, 95% CI = 0.56-42.72), LAMB1 ( P = .005, OR = 11.0, 95% CI = 1.56-77.31), and LAMB2 ( P = .091, OR = 8.2, 95% CI = 1.03-65.57)-were found to be positively associated with DBS. A total of 15 distinct, functionally deleterious genetic variants, including 6 in FBN2 , 3 in LAMB1 , and 6 in LAMB2 genes, were identified across 17 (56.7%) patients with DBS. Of the 17 patients, 5 (29.4%) carried a common genetic variant (p.Ile1547Thr; rs35915664, minor allele frequency = 0.016) in the LAMB1 gene, which was absent in controls.
CONCLUSIONS: The genetic variants found in FBN2 , LAMB1 , and LAMB2 genes may compromise the strength and stability of the lens capsule over time, predisposing individuals to DBS and sPCR later in life. The study shows for the first time, to the authors' knowledge, that the DBS has a genetic predisposition.
SETTING: Iladevi Cataract and IOL Research Centre and Raghudeep Eye Hospital, Ahmedabad, Gujarat, India.
DESIGN: Laboratory study.
METHODS: Blood samples were collected from 30 patients with DBS and 37 controls. Whole-exome sequencing was performed. Genetic variants in genes encoding extracellular matrix components of the lens capsule were screened. The association of selected variants with DBS was analyzed using the Optimal Unified Sequence Kernel Association Test in R and Logistic Regression. Genes showing significant associations were further analyzed using in silico predictions through the Ensembl Variant Effect Predictor to assess their potential impact on protein function.
RESULTS: Three genes- FBN2 ( P = .027, odds ratio [OR] = 4.9, 95% CI = 0.56-42.72), LAMB1 ( P = .005, OR = 11.0, 95% CI = 1.56-77.31), and LAMB2 ( P = .091, OR = 8.2, 95% CI = 1.03-65.57)-were found to be positively associated with DBS. A total of 15 distinct, functionally deleterious genetic variants, including 6 in FBN2 , 3 in LAMB1 , and 6 in LAMB2 genes, were identified across 17 (56.7%) patients with DBS. Of the 17 patients, 5 (29.4%) carried a common genetic variant (p.Ile1547Thr; rs35915664, minor allele frequency = 0.016) in the LAMB1 gene, which was absent in controls.
CONCLUSIONS: The genetic variants found in FBN2 , LAMB1 , and LAMB2 genes may compromise the strength and stability of the lens capsule over time, predisposing individuals to DBS and sPCR later in life. The study shows for the first time, to the authors' knowledge, that the DBS has a genetic predisposition.