Joseph Biju, Shanmugam Mahesh Palanivelu, Srinivasan Madhuravasal Krishnan, Kumaramanickavel Govindasamy
SN ONGC, Department of Genetics and Molecular Biology, Vision Research Foundation, Sankara Nethralaya, Chennai, India.
Mol Diagn. 2004;8(4):237-43. doi: 10.1007/BF03260068.
Genetic testing is increasingly being used to evaluate susceptibility to hereditary diseases because it is a cost effective screening method. Predictive testing for retinoblastoma can help to save the vision and avoid unnecessary (and invasive) eye examinations for probands and their close relatives. This study was undertaken to evaluate the cost effectiveness of the retinoblastoma genetic screening strategy established in our hospital.
Cytogenetic study of peripheral blood, mutational, and methylation analyses from the tumor DNA of 25 patients with retinoblastoma was undertaken. The cost for retinoblastoma (RB1) gene screening was calculated based on the cost of the chemicals and consumables used and the clinical examination charges at our hospital. A comparison was made between the cost of genetic screening and clinical testing for retinoblastoma. Retinoblastoma patients underwent clinical management and genetic testing at Sankara Nethralaya, Chennai, India.
By adopting a genetic screening strategy, a 3.5-fold cost saving was seen for a proband while a 6-fold saving was seen for a family with two sibs compared to the cost of clinical examination. The clinical examination fee and cost of genetic screening for a proband was dollarUS536 and dollarUS152, respectively, while for a nuclear family with two sibs the costs were dollarUS1071 and dollarUS175, respectively.
Savings for a family will be higher if indirect costs, such as savings in travel times to and from the hospital and labor savings, were taken into account. Cost will be a major factor in determining the implementation of genetic screening for RB1 gene in the clinical practice.
In our study in India, genetic screening for retinoblastoma was cheaper than conventional screening and was useful in the genetic counseling of the families.
基因检测作为一种经济高效的筛查方法,越来越多地用于评估遗传性疾病的易感性。视网膜母细胞瘤的预测性检测有助于挽救视力,并避免先证者及其近亲进行不必要的(且具有侵入性的)眼部检查。本研究旨在评估我院建立的视网膜母细胞瘤基因筛查策略的成本效益。
对25例视网膜母细胞瘤患者的外周血进行细胞遗传学研究,对肿瘤DNA进行突变和甲基化分析。视网膜母细胞瘤(RB1)基因筛查的成本是根据我院使用的化学品和耗材成本以及临床检查费用计算得出的。对视网膜母细胞瘤的基因筛查成本与临床检测成本进行了比较。视网膜母细胞瘤患者在印度金奈的桑卡拉奈特拉亚医院接受临床管理和基因检测。
与临床检查成本相比,采用基因筛查策略时,先证者的成本节省了3.5倍,而有两个兄弟姐妹的家庭成本节省了6倍。先证者的临床检查费用和基因筛查成本分别为536美元和152美元,而对于有两个兄弟姐妹的核心家庭,成本分别为1071美元和175美元。
如果考虑间接成本,如往返医院的时间节省和劳动力节省,家庭的节省将更高。成本将是决定临床实践中RB1基因进行基因筛查实施情况的主要因素。
在我们印度的研究中,视网膜母细胞瘤的基因筛查比传统筛查更便宜,并且对家庭的遗传咨询很有用。