Melania Scarcella, Simona Fecarotta, Marianna Alagia, Ferdinando Barretta, Fabiana Uomo, Valeria De Pasquale, Hari S Patel, Pietro Strisciuglio, Giancarlo Parenti, Giulia Frisso, Luigi Michele Pavone, Margherita Ruoppolo
{"title":"坎帕尼亚地区(意大利)用于检测溶酶体积存病的干血斑新生儿的数字微流控平台:第一年试点项目的结果。","authors":"Melania Scarcella, Simona Fecarotta, Marianna Alagia, Ferdinando Barretta, Fabiana Uomo, Valeria De Pasquale, Hari S Patel, Pietro Strisciuglio, Giancarlo Parenti, Giulia Frisso, Luigi Michele Pavone, Margherita Ruoppolo","doi":"10.1016/j.ymgme.2024.109008","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Newborn screening (NBS) is a simple, non-invasive test that allows for the early identification of genetic diseases within the first days of a newborn's life. The aim of NBS is to detect potentially fatal or disabling conditions in newborns as early as possible, before the onset of disease symptoms. Early diagnosis enables timely treatments and improves the quality of life for affected patients.</p><p><strong>Results: </strong>A pilot project for dried blood spot (DBS) NBS of lysosomal storage diseases (LSDs), including Mucopolysaccharidosis I (MPSI, IDUA α-L-iduronidase deficiency), Pompe disease (GAA α-glucosidase acid deficiency), Gaucher disease (GBA β-glucosidase deficiency) and Fabry disease (GLA α-galactosidase deficiency), was conducted using the digital microfluidic (DMF) technique. DBS were analyzed in a multiplexed assays for the enzymatic activities of four lysosomal enzymes (IDUA, GAA, GBA, GLA), and subjects identified as deficient in any of these enzymes were referred to the clinical reference center for diagnosis confirmation. From June 6th, 2022, to May 12th, 2023, a total of 7650 newborns were analyzed and 1 subject affected by Pompe disease was identified together with two additional subjects, suspected of Pompe and Fabry disease respectively, for whom continued follow-up is mandatory to determine the phenotype.</p><p><strong>Conclusions: </strong>The pilot project for DBS NBS of four LSDs in Campania Region validated the effectiveness of DMF method, established enzymatic activity cut-offs, and identified newborns referred to the clinical center for integrated diagnostics, including genetic analyses. The results suggest that this technique can effectively detect potentially affected newborns, who will require further diagnostic confirmation and clinical follow-up. This diagnostic flow chart provides the opportunity to initiate early treatments and improve LSD patients' life span.</p>","PeriodicalId":18937,"journal":{"name":"Molecular genetics and metabolism","volume":" ","pages":"109008"},"PeriodicalIF":3.7000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Digital microfluidic platform for dried blood spot newborn screening of lysosomal storage diseases in Campania region (Italy): Findings from the first year pilot project.\",\"authors\":\"Melania Scarcella, Simona Fecarotta, Marianna Alagia, Ferdinando Barretta, Fabiana Uomo, Valeria De Pasquale, Hari S Patel, Pietro Strisciuglio, Giancarlo Parenti, Giulia Frisso, Luigi Michele Pavone, Margherita Ruoppolo\",\"doi\":\"10.1016/j.ymgme.2024.109008\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Newborn screening (NBS) is a simple, non-invasive test that allows for the early identification of genetic diseases within the first days of a newborn's life. The aim of NBS is to detect potentially fatal or disabling conditions in newborns as early as possible, before the onset of disease symptoms. Early diagnosis enables timely treatments and improves the quality of life for affected patients.</p><p><strong>Results: </strong>A pilot project for dried blood spot (DBS) NBS of lysosomal storage diseases (LSDs), including Mucopolysaccharidosis I (MPSI, IDUA α-L-iduronidase deficiency), Pompe disease (GAA α-glucosidase acid deficiency), Gaucher disease (GBA β-glucosidase deficiency) and Fabry disease (GLA α-galactosidase deficiency), was conducted using the digital microfluidic (DMF) technique. DBS were analyzed in a multiplexed assays for the enzymatic activities of four lysosomal enzymes (IDUA, GAA, GBA, GLA), and subjects identified as deficient in any of these enzymes were referred to the clinical reference center for diagnosis confirmation. 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This diagnostic flow chart provides the opportunity to initiate early treatments and improve LSD patients' life span.</p>\",\"PeriodicalId\":18937,\"journal\":{\"name\":\"Molecular genetics and metabolism\",\"volume\":\" \",\"pages\":\"109008\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular genetics and metabolism\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1016/j.ymgme.2024.109008\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/12/31 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"ENDOCRINOLOGY & METABOLISM\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular genetics and metabolism","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.ymgme.2024.109008","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/12/31 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0
摘要
背景:新生儿筛查(NBS)是一种简单、无创的检测方法,可在新生儿出生后几天内早期发现遗传疾病。国家统计局的目标是在新生儿出现疾病症状之前尽早发现可能致命或致残的病症。早期诊断能够及时治疗并改善受影响患者的生活质量。结果:采用数字微流控(DMF)技术对溶酶体贮积病(包括粘多糖病I型(MPSI, IDUA α- l -伊杜糖苷酶缺乏症)、Pompe病(GAA α-葡萄糖苷酶缺乏症)、戈谢病(GBA β-葡萄糖苷酶缺乏症)和Fabry病(GLA α-半乳糖糖苷酶缺乏症)的干血斑(DBS) NBS进行了中试研究。对DBS患者进行四种溶酶体酶(IDUA、GAA、GBA、GLA)活性的多重检测,发现其中任何一种酶缺乏的受试者将被转至临床参考中心进行诊断确认。从2022年6月6日至2023年5月12日,共分析7650例新生儿,发现1例Pompe病患者,另外2例疑似Pompe病和Fabry病患者,需继续随访以确定表型。结论:Campania地区4个lsd的DBS NBS试点项目验证了DMF方法的有效性,建立了酶活性截止点,并确定了新生儿转介到临床中心进行综合诊断,包括遗传分析。结果表明,该技术可以有效地发现潜在的受影响的新生儿,需要进一步的诊断确认和临床随访。该诊断流程图提供了早期治疗和改善LSD患者寿命的机会。
Digital microfluidic platform for dried blood spot newborn screening of lysosomal storage diseases in Campania region (Italy): Findings from the first year pilot project.
Background: Newborn screening (NBS) is a simple, non-invasive test that allows for the early identification of genetic diseases within the first days of a newborn's life. The aim of NBS is to detect potentially fatal or disabling conditions in newborns as early as possible, before the onset of disease symptoms. Early diagnosis enables timely treatments and improves the quality of life for affected patients.
Results: A pilot project for dried blood spot (DBS) NBS of lysosomal storage diseases (LSDs), including Mucopolysaccharidosis I (MPSI, IDUA α-L-iduronidase deficiency), Pompe disease (GAA α-glucosidase acid deficiency), Gaucher disease (GBA β-glucosidase deficiency) and Fabry disease (GLA α-galactosidase deficiency), was conducted using the digital microfluidic (DMF) technique. DBS were analyzed in a multiplexed assays for the enzymatic activities of four lysosomal enzymes (IDUA, GAA, GBA, GLA), and subjects identified as deficient in any of these enzymes were referred to the clinical reference center for diagnosis confirmation. From June 6th, 2022, to May 12th, 2023, a total of 7650 newborns were analyzed and 1 subject affected by Pompe disease was identified together with two additional subjects, suspected of Pompe and Fabry disease respectively, for whom continued follow-up is mandatory to determine the phenotype.
Conclusions: The pilot project for DBS NBS of four LSDs in Campania Region validated the effectiveness of DMF method, established enzymatic activity cut-offs, and identified newborns referred to the clinical center for integrated diagnostics, including genetic analyses. The results suggest that this technique can effectively detect potentially affected newborns, who will require further diagnostic confirmation and clinical follow-up. This diagnostic flow chart provides the opportunity to initiate early treatments and improve LSD patients' life span.
期刊介绍:
Molecular Genetics and Metabolism contributes to the understanding of the metabolic and molecular basis of disease. This peer reviewed journal publishes articles describing investigations that use the tools of biochemical genetics and molecular genetics for studies of normal and disease states in humans and animal models.