One of the huge market factors driving the Non-Invasive Prenatal Testing (NIPT) market is the rising pattern of postponed pregnancies. As women decide to begin families sometime down the road, the chance of chromosomal abnormalities rises, prompting a more popularity for non-invasive prenatal testing to survey fetal wellbeing.
The prevalence of chromosomal disorders, like Down syndrome, has been on the ascent. NIPT offers a solid and precise technique for early recognition, cultivating its reception among would-be parents. This expanded awareness about the significance of early determination adds to the development of the NIPT market.
Continual progresses in genetic screening technologies have altogether worked on the precision and dependability of NIPT. The improvement of next-generation sequencing (NGS) and other inventive strategies upgrades the capacity to identify chromosomal abnormalities with high accuracy, supporting certainty among medical care experts and patients.
The non-invasive nature of prenatal testing is a critical component driving its market growth. Unlike other customary invasive methods like amniocentesis, NIPT presents insignificant risk to both the mother and the embryo. This security perspective urges more hopeful parents to choose NIPT, subsequently adding to the development of the market.
Expanding medical care use around the world, combined with the developing spotlight on maternal and child wellbeing, is encouraging the reception of advanced prenatal testing methods. Legislatures and confidential associations are putting resources into medical services foundation, making NIPT more open to a more extensive population and driving market growth.
The utilization of NIPT in various growth pregnancies, like twins or triplets, is acquiring noticeable quality. The capacity of NIPT to give exact outcomes to every embryo exclusively is a vital calculation driving its reception instances of various pregnancies, adding to the general market extension.
The worldwide shift towards customized medication is impacting the NIPT market elements. Fitting medical services arrangements considering individual genetic profiles is turning out to be progressively significant, and NIPT lines up with this pattern by offering exact and customized data about fetal wellbeing, accordingly adding to its market development.
Non-Invasive Prenatal Testing Market Size was valued at USD 6.36 Billion in 2023. The Global Non-Invasive Prenatal Testing industry is projected to grow from USD 7.21 Billion in 2024 to USD 19.74 Billion by 2032, exhibiting a compound annual growth rate (CAGR) of 13.89% during the forecast period (2024 - 2032).
Strand Life Sciences has announced the launch of its prenatal screening and diagnostics portfolio in April 2024. The portfolio includes two groundbreaking developments: MaatriSeq (Non-Invasive Prenatal Screening) and CNSeq (sequencing-based identification of aneuploidies and copy number variations). CNSeq represents a substantial advancement in prenatal diagnostics by incorporating the most recent Next Generation Sequencing technology into a critical prenatal test.
CNSeq provides unparalleled precision in the identification of Copy Number Variations (CNVs) by utilizing proprietary software, surpassing conventional molecular and cytogenetic methods. On the other hand, MaatriSeq is the first Non-Invasive Prenatal Screening (NIPS) solution to be validated on the most recent high-throughput Illumina NovaSeq X Plus sequencing platform. This innovation provides a cost-effective and highly precise solution that is accessible to a broader community in India. The company's dedication to the advancement of genetic diagnostics and the alleviation of the burden of rare diseases in India is emphasized by these innovations.
Yourgene Health, a prominent international molecular diagnostics group, has implemented the first non-invasive prenatal testing (NIPT) protocol in Morocco, which is based on the IONA® test, at the Centre de Biologie Riad (Laboriad), in November 2023. Laboriad can expand its service offerings and offer pregnant women fast, dependable results that reduce the necessity for invasive tests and the resulting tension and anxiety for expectant parents by providing this service locally.
The test can also be employed to ascertain the sex of the fetus. It is a comprehensive CE-IVD product designed for laboratories that desire to provide their own in-house NIPT service. The test results are available within three days after the analysis is conducted on a maternal blood sample using next-generation sequencing technology. It has been validated on a methodology that is highly scalable and flexible, making it suitable for sample throughputs ranging from low to high volume. This enables clinical laboratories to adapt and expand in response to their increasing demands.
Worldwide demand for NIPT is rising due to several factors, including a rise in doctors' preferences for sophisticated genetic screening for high-risk pregnancies, an eagerness to put off having children, and a boom in pregnancy-related problems in the last or second trimester. The devastating effect of COVID-19 has been unexpected and catastrophic worldwide, and NIPT has not seen any change regarding demand across all regions due to the pandemic. When the pandemic is finished, this market's demand and growth will resume to pre-pandemic levels, which will explain the increase in CAGR. A child's chance of developing genetic defects increases when genes and chromosomes mutate. According to reports, trisomy 21 is one of the most prevalent chromosomal disorders, affecting about 5,000 newborns annually in the United States.
The demand for an efficient screening tool for prenatal tests has increased due to the rising prevalence of chromosomal defects. Amniocentesis and chorionic villus sampling are invasive prenatal testing methods that might result in complications like miscarriage. As a result, there is a significant need for more effective, non-invasive, and safe tests and a fall in using these procedures. NIPT can be used to detect common trisomies in the fetus, such as Down syndrome, fetal rhesus D status, Turner syndrome, and sex chromosomal problems, as well as to determine the fetal sex. This is done using cell-free fetal DNA (cffDNA), which circulates in the mother's blood. Significant technological developments are being made in the sector to enhance testing capabilities. Many well-known companies and fresh start-ups seek financing for NIPT technique development and clinical testing. Government and business organizations are searching for research facilities and start-ups to provide cutting-edge testing methods to identify important genetic abnormalities through NIPT. Many nations have adopted rules that make non-invasive prenatal diagnostics the norm for prenatal screening rather than invasive examinations.
NIPT is the testing procedure done during the pregnancy period to monitor the fetal growth and related diagnosis. Annually it is predicted that around 21 million girls aged 15 to 19 years give birth in developing regions around the globe.
Thus, it is among the reasons why NIPT is needed for safe delivery of the baby.
The birth rate is expected to increase during the forecast period.
Rising cases of premature pregnancy in developing and underdeveloped countries.
The Non-Invasive Prenatal Testing (NIPT) Market based on product type is broadly segmented into devices, consumables, and others.
The non-Invasive prenatal testing (NIPT) market based on technique is segmented into biochemical screening tests and ultrasound detection.
Non-Invasive Prenatal Testing (NIPT) Market Key Players
November 2023
Natera, Inc. announces that it has received FDA approval for its Panorama NIPT test to detect Down syndrome, trisomy 18, and trisomy 13 in pregnancies as early as 9 weeks of gestation. This is the earliest gestational age at which any NIPT test has been approved by the FDA.
Sequenom Laboratories announces that it has launched its new MaterniT21 PLUS test, an NIPT test that can detect Down syndrome, trisomy 18, and trisomy 13, as well as several other genetic disorders, in pregnancies as early as 10 weeks of gestation. The MaterniT21 PLUS test is the first NIPT test to be able to detect a wider range of genetic disorders.
Ariosa Diagnostics, Inc. announces that it has partnered with Illumina, Inc. to develop a new NIPT test that can be used to detect a wider range of genetic disorders, including single gene disorders. The partnership will combine Ariosa's expertise in NIPT with Illumina's expertise in sequencing technology to develop a new test that is more accurate and comprehensive than current NIPT tests.
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