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2023-2028 年按产品类型、筛检、疾病、最终用户和地区分類的产前和新生儿基因检测市场报告Prenatal and Newborn Genetic Testing Market Report by Product Type, Screening, Disease, End User, and Region 2023-2028 |
2022年,全球产前和新生儿基因检测市场规模达到53亿美元。展望未来, IMARC Group预计到2028年市场规模将达到112亿美元,2022-2028年复合年增长率(CAGR)为13.3%。对先进诊断和筛检设备的需求不断增长、世界各地新生儿先天畸形和遗传异常患病率不断上升以及医疗行业的蓬勃发展是推动市场的一些关键因素。
产前和新生儿基因检测包括血液检测、特定类型的超音波检测和产前游离 DNA 筛检,为未出生婴儿和新生儿的基因组成提供宝贵的见解。它可以识别某些出生缺陷,其中许多是未出生或新生儿的遗传性疾病。它为准父母、医疗保健专业人员和研究人员提供重要信息,使他们能够就婴儿的健康和福祉做出明智的决定。它有助于改善患者的治疗结果并指导医疗干预,同时能够准确识别怀孕和婴儿早期的遗传变异和异常。它还有助于检测各种先天性疾病,如唐氏症、囊性纤维化、镰状细胞疾病和苯酮尿症。由于它有助于分析父母血液中的各种蛋白质水平,以确定婴儿染色体数量异常的风险,因此全球对产前和新生儿基因检测的需求正在增加。
目前,全球大众对先进诊断和筛检设备的需求不断增长,是支持市场成长的关键因素之一。此外,全世界新生儿先天畸形和基因异常的盛行率增加。这与蓬勃发展的医疗产业一起推动了市场的成长。此外,与传统方法相比,非侵入性产前筛检方法具有多种优点,例如准确度高、精确度高、痛苦少、诊断快速等,对市场的需求不断增长,正在对市场产生积极影响。除此之外,人们对产前和新生儿基因检测的好处的认识不断提高,为行业投资者提供了利润丰厚的成长机会。此外,由于注重健康的个人数量不断增加,对产前和新生儿基因检测的需求不断增加,也促进了市场的成长。除此之外,各国政府机构都致力于改善医疗基础设施,为国民提供更好的医疗服务。为此,主要参与者正在开发基因眼科测试,以确定患者罹患圆锥角膜和其他角膜营养不良的风险。此外,用于检测遗传性疾病风险的母体血浆检测对无细胞 DNA 的需求不断增长,这提供了有利的市场前景。
The global prenatal and newborn genetic testing market size reached US$ 5.3 Billion in 2022. Looking forward, IMARC Group expects the market to reach US$ 11.2 Billion by 2028, exhibiting a growth rate (CAGR) of 13.3% during 2022-2028. The growing demand for advanced diagnostic and screening devices, rising prevalence of congenital malformations and genetic abnormalities in newborn babies around the world, and thriving medical industry represent some of the key factors driving the market.
Prenatal and newborn genetic testing comprises blood tests, a specific type of ultrasound, and prenatal cell-free DNA screening that offers invaluable insights into the genetic makeup of unborn babies and newborns. It can identify certain birth defects, many of which are genetic disorders in unborn or newborn babies. It provides critical information to expectant parents, healthcare professionals, and researchers, enabling them to make informed decisions about the health and well-being of infants. It assists in improving patient outcomes and guiding medical interventions while enabling accurate identification of genetic variations and abnormalities during pregnancy and early infancy. It also aids in detecting various congenital conditions, such as Down syndrome, cystic fibrosis, sickle cell disease, and phenylketonuria. As it helps analyze various protein levels in the blood of parents to determine the risk for abnormal chromosome numbers in babies, the demand for prenatal and newborn genetic testing is rising across the globe.
At present, the rising demand for advanced diagnostic and screening devices among the masses across the globe represents one of the key factors supporting the growth of the market. In addition, there is an increase in the prevalence of congenital malformations and genetic abnormalities in newborn babies worldwide. This, along with the thriving medical industry, is propelling the growth of the market. Moreover, the growing demand for non-invasive prenatal screening methods due to their various benefits, such as high accuracy and precision, less pain, and fast diagnosis, as compared to conventional methods, is positively influencing the market. Besides this, the rising awareness among individuals about the benefits of prenatal and newborn genetic testing is offering lucrative growth opportunities to industry investors. Additionally, the escalating demand for prenatal and newborn genetic testing due to the increasing number of health-conscious individuals is contributing to the growth of the market. Apart from this, governing agencies of various countries are focusing on improving healthcare infrastructure to provide enhanced healthcare services to citizens. In line with this, key players are developing genetic eye tests to identify the risk of keratoconus and other corneal dystrophies in patients. Furthermore, the growing demand for cell-free DNA in maternal plasma tests to detect the risk of genetic disorders is offering a favorable market outlook.
IMARC Group provides an analysis of the key trends in each segment of the global prenatal and newborn genetic testing market, along with forecasts at the global, regional, and country levels from 2023-2028. Our report has categorized the market based on product type, screening, disease, and end user.
Consumables
Instruments
The report has provided a detailed breakup and analysis of the prenatal and newborn genetic testing market based on the product type. This includes consumables and instruments. According to the report, consumables represented the largest segment.
Non-invasive Prenatal Testing
Chorionic Villus Sampling
Amniocentesis
Maternal Serum Screening
A detailed breakup and analysis of the prenatal and newborn genetic testing market based on the screening has also been provided in the report. This includes non-invasive prenatal testing, chorionic villus sampling, amniocentesis, and maternal serum screening. According to the report, non-invasive prenatal testing accounted for the largest market share.
Downs Syndrome
Phenylketonuria
Cystic Fibrosis
Sickle Cell Anemia
A detailed breakup and analysis of the prenatal and newborn genetic testing market based on the disease has also been provided in the report. This includes downs syndrome, phenylketonuria, cystic fibrosis, and sickle cell anemia. According to the report, downs syndrome accounted for the largest market share.
Hospital
Maternity and Specialty Clinics
Diagnostic Centers
A detailed breakup and analysis of the prenatal and newborn genetic testing market based on the end user has also been provided in the report. This includes hospital, maternity and specialty clinics, and diagnostic centers. According to the report, hospital accounted for the largest market share.
North America
United States
Canada
Asia Pacific
China
Japan
India
South Korea
Australia
Indonesia
Others
Europe
Germany
France
United Kingdom
Italy
Spain
Russia
Others
Latin America
Brazil
Mexico
Others
Middle East and Africa
The report has also provided a comprehensive analysis of all the major regional markets, which include North America (the United States and Canada); Asia Pacific (China, Japan, India, South Korea, Australia, Indonesia, and others); Europe (Germany, France, the United Kingdom, Italy, Spain, Russia, and others); Latin America (Brazil, Mexico, and others); and the Middle East and Africa. According to the report, North America was the largest market for prenatal and newborn genetic testing. Some of the factors driving the North America prenatal and newborn genetic testing market included the growing number of pregnant women undergoing genetic screening, rising awareness about various inborn genetic diseases, enhanced healthcare infrastructure, etc.
The report has also provided a comprehensive analysis of the competitive landscape in the global prenatal and newborn genetic testing market. Detailed profiles of all major companies have been provided. Some of the companies covered include Abbott Laboratories, BGI Group, Bio-Rad Laboratories Inc., F. Hoffmann-La Roche AG, Illumina Inc., Laboratory Corporation of America Holdings, Natera Inc., PerkinElmer Inc., Quest Diagnostics Incorporated, Ravgen Inc., etc. Kindly note that this only represents a partial list of companies, and the complete list has been provided in the report.
Kindly note that this only represents a partial list of companies, and the complete list has been provided in the report.