34 datasets found
  1. Incidence of Down syndrome in the United States as of 2024, by age

    • statista.com
    Updated Oct 11, 2024
    Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    Statista (2024). Incidence of Down syndrome in the United States as of 2024, by age [Dataset]. https://www.statista.com/statistics/1497382/down-syndrome-incidence-by-age-us/
    Explore at:
    Dataset updated
    Oct 11, 2024
    Dataset authored and provided by
    Statistahttp://statista.com/
    Area covered
    United States
    Description

    Older women are at an increased risk of having a child with Down syndrome. For example, among women aged 20 years, the chances of conceiving a child with Down syndrome is about one in 2,000. In comparison, among women aged 49 years, the chances of conceiving a child with Down syndrome is about one in 10. This statistic shows the incidence of Down syndrome in the United States as of 2024, by maternal age.

  2. Global Down syndrome prevalence rate in 1990 and 2019, by region

    • statista.com
    Updated Oct 15, 2024
    + more versions
    Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    Statista (2024). Global Down syndrome prevalence rate in 1990 and 2019, by region [Dataset]. https://www.statista.com/statistics/1498089/global-down-syndrome-prevalence-rate-by-region/
    Explore at:
    Dataset updated
    Oct 15, 2024
    Dataset authored and provided by
    Statistahttp://statista.com/
    Area covered
    Worldwide
    Description

    In 2019, the global age-standardized prevalence rate of Down syndrome was around 21.51 per 100,000 population. At that time, the prevalence rate of Down syndrome was highest in Southern Latin America and Western Europe, with around 65 cases per 100,000 population. This statistic shows the age-standardized prevalence rate of Down syndrome worldwide in 1990 and 2019, by region.

  3. d

    Incidence of Down syndrome: percent (%) cases diagnosed prenatally by...

    • digital.nhs.uk
    Updated Jul 29, 2015
    + more versions
    Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    Incidence of Down syndrome: percent (%) cases diagnosed prenatally by maternal age, 3-year average, P [Dataset]. https://digital.nhs.uk/data-and-information/publications/statistical/compendium-public-health/current/chromosomal-abormalities-congential-malformations
    Explore at:
    Dataset updated
    Jul 29, 2015
    License

    https://digital.nhs.uk/about-nhs-digital/terms-and-conditionshttps://digital.nhs.uk/about-nhs-digital/terms-and-conditions

    Description

    Legacy unique identifier: P00443

  4. f

    Table5_Global, Regional, and National Burden and Trends of Down Syndrome...

    • figshare.com
    • frontiersin.figshare.com
    xlsx
    Updated Jun 16, 2023
    + more versions
    Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    Liyuan Chen; Lifei Wang; Yi Wang; Haishan Hu; Yuan Zhan; Zhilin Zeng; Lidan Liu (2023). Table5_Global, Regional, and National Burden and Trends of Down Syndrome From 1990 to 2019.XLSX [Dataset]. http://doi.org/10.3389/fgene.2022.908482.s006
    Explore at:
    xlsxAvailable download formats
    Dataset updated
    Jun 16, 2023
    Dataset provided by
    Frontiers
    Authors
    Liyuan Chen; Lifei Wang; Yi Wang; Haishan Hu; Yuan Zhan; Zhilin Zeng; Lidan Liu
    License

    Attribution 4.0 (CC BY 4.0)https://creativecommons.org/licenses/by/4.0/
    License information was derived automatically

    Description

    Introduction: Down syndrome (DS) is the leading cause of genetically defined intellectual disability and congenital birth defects worldwide. A large population of people diagnosed with DS globally is posing an enormous socioeconomic burden. However, the global burden and trends of DS have not been reported.Methods: Based on the data from the Global Burden of Disease database in 2019, we analyzed the incidence, prevalence, disability-adjusted life years (DALYs), and death of DS from 1990 to 2019 according to sex, age, regions, and social-demographic index (SDI). Then, age-standardized rates (ASRs) and estimated annual percentage change (EAPC) of these aforementioned indexes were calculated to evaluate the temporal trend of DS. Finally, the association of SDI with DS epidemiological parameters was assessed.Results: In the past 30 years, the incident cases, age-standardized incident rate (ASIR), and age-standardized prevalent rate (ASPR) of DS first decreased slightly and subsequently increased globally. The number of prevalent cases increased steadily, while the number and age-standardized rate (ASRs) of DALYs and deaths decreased gradually from 1990 to 2019. In the meantime, disease burdens were different across various SDI regions. The prevalent cases and ASPR for both sexes were increasing in all SDI regions except for the high-middle SDI region. At the national level, Brunei Darussalam, Ireland, and Haiti were the top three countries with the highest ASIR in 2019. Georgia was in the top three with the highest increase in ASRs of four parameters, while Serbia was consistently ranked in the top three with fastest declining. Furthermore, we found that ASIR and ASPR were positively correlated with SDI, yet the age-standardized DALYs and age-standardized death rate (ASDR) were negatively correlated with SDI.Conclusion: In the past 30 years, the burden and trends of DS were heterogeneous across different regions and countries with different sociodemographic characteristics. Great improvements had been achieved in reducing DALYs and deaths globally. However, the increased number and ASRs of incident and prevalent cases in some regions, especially in low SDI regions, were contributing to numerous challenges to public health. The findings may provide valuable information to the development or implementation of more effective measures.

  5. Rate of chromosome (gene) malformation birth defects in the U.S. 2016-2020,...

    • statista.com
    Updated Oct 14, 2024
    + more versions
    Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    Statista (2024). Rate of chromosome (gene) malformation birth defects in the U.S. 2016-2020, by age [Dataset]. https://www.statista.com/statistics/1497838/chromosome-gene-malformation-birth-defects-rate-by-age/
    Explore at:
    Dataset updated
    Oct 14, 2024
    Dataset authored and provided by
    Statistahttp://statista.com/
    Area covered
    United States
    Description

    In the period 2016-2020, babies born to women aged 40 years and older in the United States had the highest rates of Down syndrome, with around 121 babies born with this defect per 10,000 live births. Down syndrome is a genetic condition that can affect how the brain and body develop and is the most common chromosomal condition in the United States. This statistic shows the rate of select chromosome (gene) malformation birth defects in the United States from 2016 to 2020, by age.

  6. Global Down syndrome prevalence rate in 1990 and 2019, by gender

    • statista.com
    Updated Oct 15, 2024
    + more versions
    Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    Statista (2024). Global Down syndrome prevalence rate in 1990 and 2019, by gender [Dataset]. https://www.statista.com/statistics/1498090/global-down-syndrome-prevalence-rate-by-gender/
    Explore at:
    Dataset updated
    Oct 15, 2024
    Dataset authored and provided by
    Statistahttp://statista.com/
    Area covered
    Worldwide
    Description

    In 2019, the global age-standardized prevalence rate of Down syndrome was around 21.51 per 100,000 population. The prevalence rate of Down syndrome is slightly higher among males than females. This statistic shows the age-standardized prevalence rate of Down syndrome worldwide in 1990 and 2019, by gender.

  7. f

    Additional file 4: of Disentangling the roles of maternal and paternal age...

    • springernature.figshare.com
    txt
    Updated Feb 12, 2024
    Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    James Thompson (2024). Additional file 4: of Disentangling the roles of maternal and paternal age on birth prevalence of Down syndrome and other chromosomal disorders using a Bayesian modeling approach [Dataset]. http://doi.org/10.6084/m9.figshare.8032271.v2
    Explore at:
    txtAvailable download formats
    Dataset updated
    Feb 12, 2024
    Dataset provided by
    figshare
    Authors
    James Thompson
    License

    Attribution 4.0 (CC BY 4.0)https://creativecommons.org/licenses/by/4.0/
    License information was derived automatically

    Description

    5 year age categories. Fully conditional modeling of maternal and paternal ages as 5 year age categories. OpenBUGS code and data that can be used to repeat the analyses for the 5 year age categories. The data are arranged so that the DIC is comparable to the other fully conditional models (TXT 37 kb)

  8. d

    Incidence of Down syndrome: crude rate per 10,000 live births, at birth,...

    • digital.nhs.uk
    Updated Jul 29, 2015
    + more versions
    Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    (2015). Incidence of Down syndrome: crude rate per 10,000 live births, at birth, 3-year average, P [Dataset]. https://digital.nhs.uk/data-and-information/publications/statistical/compendium-public-health/current/chromosomal-abormalities-congential-malformations
    Explore at:
    Dataset updated
    Jul 29, 2015
    License

    https://digital.nhs.uk/about-nhs-digital/terms-and-conditionshttps://digital.nhs.uk/about-nhs-digital/terms-and-conditions

    Description

    Legacy unique identifier: P00441

  9. c

    Social Implications of One-Stop First Trimester Prenatal Screening,...

    • datacatalogue.cessda.eu
    • beta.ukdataservice.ac.uk
    Updated Nov 28, 2024
    + more versions
    Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    Hundt, G., University of Warwick, School of Health and Social Studies (2024). Social Implications of One-Stop First Trimester Prenatal Screening, 2002-2003 [Dataset]. http://doi.org/10.5255/UKDA-SN-5180-1
    Explore at:
    Dataset updated
    Nov 28, 2024
    Dataset provided by
    Institute of Health
    Authors
    Hundt, G., University of Warwick, School of Health and Social Studies
    Area covered
    England
    Variables measured
    Individuals, Subnational
    Measurement technique
    Postal survey
    Description

    Abstract copyright UK Data Service and data collection copyright owner.


    In 2003, the offer of screening for foetal abnormality and particularly Down’s syndrome became a routine part of antenatal care in the UK for the first time. The 2003 NICE antenatal care guidelines state that 'all pregnant women should be offered screening for Down’s syndrome with a policy that provides a minimum detection rate of 75% with a false-positive rate no greater than 3% by 2007', indicating a move to first trimester screening technologies which achieve this greater level of accuracy.

    Thus the findings of this study of the only NHS site in England offering combined first trimester screening in a one-stop clinic setting are of particular relevance at this time and has provided the opportunity to look at the implications of an IHT (Innovative Health Technology) prior to wide-scale implementation in the UK. The study findings raise questions about the implications for non-directiveness and informed decision-making of the resulting routinisation of screening, and the shift from an ‘opt-in’ to an ‘opt-out’ service.

    The implications of the introduction of a routine offer of screening for Down’s syndrome in the first trimester of pregnancy raises new issues for women and their partners, for the organisation and management of screening and for society. The development of prenatal screening technologies is a contested and politically charged arena with ethical and public policy considerations.

    In the light of the above concerns, the study aimed to explore:
  10. the impact of new screening technologies on the social management of pregnancy, service delivery and professional roles

  11. participants’ broader responses to the new reproductive technologies, and views about routinisation of screening

  12. perceptions of self, the foetus, and the management of reproductive risk


  13. The qualitative aspect of this study has not been deposited along with the quantitative data, as the staff interviewed could be identified as the NHS unit was the only place in the country which conducted this type of work at the time of the study.
    Main Topics:

    This study contains data from childbearing women over the age of 18 who completed a prenatal and postnatal questionnaire, with additional questions about amniocentesis for those who were offered the test.

    The data cover: details of pregnancy; information, decisions and facts about screening; having the screening test; scans; feelings and worries pre- and postnatal; views pre- and postnatal; previous pregnancies; demographic information; information about the baby and the birth.

  • Global Down syndrome death rate in 1990 and 2019, by region

    • statista.com
    Updated Oct 15, 2024
    Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    Statista (2024). Global Down syndrome death rate in 1990 and 2019, by region [Dataset]. https://www.statista.com/statistics/1498107/global-down-syndrome-death-rate-by-region/
    Explore at:
    Dataset updated
    Oct 15, 2024
    Dataset authored and provided by
    Statistahttp://statista.com/
    Area covered
    Worldwide
    Description

    In 2019, the global age-standardized death rate for Down syndrome was around 0.3 per 100,000 population. At that time, the death rate for Down syndrome was highest in Tropical Latin America, with around 0.7 deaths per 100,000 population. The most common cause of death for adults and children with Down syndrome is respiratory infection. This statistic shows the age-standardized death rate for Down syndrome worldwide in 1990 and 2019, by region.

  • f

    Additional file 2: of Disentangling the roles of maternal and paternal age...

    • springernature.figshare.com
    txt
    Updated Feb 12, 2024
    + more versions
    Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    James Thompson (2024). Additional file 2: of Disentangling the roles of maternal and paternal age on birth prevalence of Down syndrome and other chromosomal disorders using a Bayesian modeling approach [Dataset]. http://doi.org/10.6084/m9.figshare.8032253.v2
    Explore at:
    txtAvailable download formats
    Dataset updated
    Feb 12, 2024
    Dataset provided by
    figshare
    Authors
    James Thompson
    License

    Attribution 4.0 (CC BY 4.0)https://creativecommons.org/licenses/by/4.0/
    License information was derived automatically

    Description

    Model 2. Paternal Age Random-walk (CAR). OpenBUGS code and data that can be used to repeat the analyses for Model 2. (TXT 2 kb)

  • d

    Incidence of Down syndrome: crude rate per 10,000 total (live and still)...

    • digital.nhs.uk
    Updated Jul 29, 2015
    Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    (2015). Incidence of Down syndrome: crude rate per 10,000 total (live and still) births, at birth, annual, P [Dataset]. https://digital.nhs.uk/data-and-information/publications/statistical/compendium-public-health/current/chromosomal-abormalities-congential-malformations
    Explore at:
    Dataset updated
    Jul 29, 2015
    License

    https://digital.nhs.uk/about-nhs-digital/terms-and-conditionshttps://digital.nhs.uk/about-nhs-digital/terms-and-conditions

    Description

    Legacy unique identifier: P00440

  • Global Down syndrome death rate in 1990 and 2019, by gender

    • statista.com
    Updated Oct 15, 2024
    Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    Statista (2024). Global Down syndrome death rate in 1990 and 2019, by gender [Dataset]. https://www.statista.com/statistics/1498105/global-down-syndrome-death-rate-by-gender/
    Explore at:
    Dataset updated
    Oct 15, 2024
    Dataset authored and provided by
    Statistahttp://statista.com/
    Area covered
    Worldwide
    Description

    In 2019, the global age-standardized death rate for Down syndrome was around 0.3 per 100,000 population. The most common cause of death for adults and children with Down syndrome is respiratory infection. This statistic shows the age-standardized death rate for Down syndrome worldwide in 1990 and 2019, by gender.

  • r

    Data from: Socioeconomic, ethnocultural, substance- and cannabinoid- related...

    • researchdata.edu.au
    Updated Aug 15, 2023
    + more versions
    Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    UWA Medical School; Albert Stuart Reece; Albert Reece (2023). Socioeconomic, ethnocultural, substance- and cannabinoid- related epidemiology of Down syndrome USA 1986-2016 dataset: An ecological geotemporospatial and causal inference investigation [Dataset]. http://doi.org/10.17632/TN46TDHC4C.2
    Explore at:
    Dataset updated
    Aug 15, 2023
    Dataset provided by
    Edith Cowan University
    Authors
    UWA Medical School; Albert Stuart Reece; Albert Reece
    License

    Attribution 4.0 (CC BY 4.0)https://creativecommons.org/licenses/by/4.0/
    License information was derived automatically

    Area covered
    United States
    Description

    Background. Downs syndrome (DS) is the commonest of the congenital genetic defects. Its incidence has been rising in recent years for unknown reasons. Objective. Investigate the relationship of DS to substance- and cannabinoid- exposure; and causality.

    Methods. Observational ecological population-based epidemiological study 1986-2016. Analysis performed January 2020. Geotemporospatial and causal inference analysis.

    Participants: Patients were diagnosed with DS and reported to state based registries; collated nationally. Data source: annual reports of National Birth Defects Prevention Network of Centres for Disease Control.

    Exposures: Drug exposure was taken from the National Survey of Drug Use and Health (NSDUH) conducted annually by Substance Abuse and Mental Health Services Administration. Nationally representative sample 67,000 participants annually. Drug exposures: cigarette consumption, alcohol abuse, analgesic/opioid abuse, cocaine use and last month cannabis use. Ethnicity and median household income: US Census Bureau. Maternal age of childbearing: CDC births registries. Cannabinoid concentrations: Drug Enforcement Agency seizures.

    Results. NSDUH report 74.1% mean annual response rate. All other data was population-wide. DS rate (DSR) was noted to be rising over time, cannabis use, and cannabis-use quintile. In the optimal geospatial model lagged to four years terms including Δ9-tetrahydrocannabinol and cannabigerol were significant (from β-est.=4189.96 (95%C.I. 1924.74, 6455.17), P=2.9x10-4). Ethnicity, income, and maternal age covariates were not significant. DSR in states where cannabis was not illegal was higher than elsewhere (β-est.=2.160 (1.5, 2.82), R.R.=1.81 (1.51, 2.16), P=4.7x10-10). In inverse probability-weighted mixed models terms including cannabinoids were significant (from β-estimate=18.82 (16.82, 20.82), P

    Conclusions. Our data show that the association between DSR and substance- and cannabinoid- exposure is robust to multivariable geotemporospatial adjustment, implicate particularly cannabigerol and Δ9-tetrahydrocannabinol, and fulfil causal crietria. Cannabis legalization was associated with elevated DSR’s. These findings are consistent with those from Hawaii, Colorado, Canada and Australia and concordant with several cellular mechanisms. Given that the cannabis industry is presently in a rapid growth-commercialization phase the present findings linking cannabis use with megabase scale genotoxicity suggest unrecognized DS risk factors, are of public health importance and suggest that re-focussing the cannabis debate on multigenerational and intergenerational health concerns is prudent.

  • D

    Prenatal Screening Market Research Report 2032

    • dataintelo.com
    csv, pdf, pptx
    Updated Dec 4, 2024
    Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    Dataintelo (2024). Prenatal Screening Market Research Report 2032 [Dataset]. https://dataintelo.com/report/global-prenatal-screening-market
    Explore at:
    csv, pptx, pdfAvailable download formats
    Dataset updated
    Dec 4, 2024
    Dataset authored and provided by
    Dataintelo
    License

    https://dataintelo.com/privacy-and-policyhttps://dataintelo.com/privacy-and-policy

    Time period covered
    2024 - 2032
    Area covered
    Global
    Description

    Prenatal Screening Market Outlook



    In 2023, the global prenatal screening market size was valued at approximately USD 5 billion and is projected to reach around USD 10 billion by 2032, growing at a compound annual growth rate (CAGR) of around 8%. The market is primarily driven by increasing awareness and advancements in prenatal screening technologies, leading to early and accurate detection of fetal anomalies. Additionally, the rising prevalence of genetic disorders, coupled with the growing demand for non-invasive testing methods, is expected to fuel further growth. The global healthcare industry’s emphasis on preventive care and the increasing maternal age are significant contributors to this upward trend in the prenatal screening market.



    One of the foremost growth factors for the prenatal screening market is the technological advancements in non-invasive prenatal testing (NIPT). NIPT has transformed prenatal screening by offering a highly accurate and risk-free method of detecting chromosomal abnormalities in the fetus. It’s a preferable choice for expecting mothers, particularly those in high-risk categories, as it eliminates the need for invasive sampling techniques like amniocentesis, which carry potential risks for both the mother and the fetus. The continuous improvements in sequencing technologies, coupled with increased availability and affordability, have expanded the accessibility of NIPT, driving the market growth substantially.



    Moreover, the rising maternal age worldwide is another critical factor propelling the prenatal screening market. As more women choose to start families later in life, the risk of chromosomal abnormalities rises, thereby increasing the demand for prenatal screening. Older maternal age is associated with a higher likelihood of chromosomal aneuploidies such as Down syndrome, spurring the need for reliable and early detection methods. Healthcare providers advocate prenatal screenings as a standard practice for expectant mothers over the age of 35, which indirectly boosts the market. The simultaneous increase in global birth rates also adds to the demand for comprehensive prenatal screenings.



    The growing awareness and emphasis on early diagnosis and preventive healthcare measures further bolster the market. With the support of government initiatives and healthcare policies aimed at improving maternal and fetal health outcomes, more expectant mothers are opting for prenatal screenings. These screenings allow for the early detection and management of potential chromosomal and genetic disorders, providing critical information for making informed healthcare decisions. Education campaigns and counseling services regarding the benefits and availability of prenatal screening are enhancing public perception and acceptance, contributing significantly to market expansion.



    Regionally, North America holds the largest share of the prenatal screening market due to the high adoption rate of advanced screening technologies and supportive healthcare infrastructure. The presence of major market players and the availability of comprehensive insurance coverage for prenatal tests drive market growth in this region. Europe follows closely, with countries like Germany, France, and the UK showing strong adoption rates due to increasing awareness and government support. The Asia Pacific region is expected to witness the highest growth rate due to an increasing population base and improving healthcare infrastructure. China and India, with their large populations, offer significant potential for market expansion. The market in Latin America and the Middle East & Africa is also growing steadily, albeit at a slower pace, due to improvements in healthcare access and rising awareness.



    Test Type Analysis



    The test type segment of the prenatal screening market includes non-invasive prenatal testing (NIPT), maternal serum screening, ultrasound, and others. Non-invasive prenatal testing (NIPT) is the fastest-growing segment within this category. It is favored for its high accuracy and safety, as it involves analyzing cell-free fetal DNA circulating in the maternal blood. Its ability to detect common chromosomal abnormalities like trisomy 21, 18, and 13 with high sensitivity and specificity has made it a popular choice among healthcare providers and expectant parents. The ease of the testing process and reduced risk compared to invasive methods are key factors driving the growth of NIPT in the prenatal screening market.



    Maternal serum screening is another significant segment in the prenatal screening market. This involves a blood test to evaluate the levels of

  • D

    Non-Invasive Prenatal Testing Kit Market Research Report 2032

    • dataintelo.com
    csv, pdf, pptx
    Updated Sep 12, 2024
    + more versions
    Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    Dataintelo (2024). Non-Invasive Prenatal Testing Kit Market Research Report 2032 [Dataset]. https://dataintelo.com/report/global-non-invasive-prenatal-testing-kit-market
    Explore at:
    csv, pdf, pptxAvailable download formats
    Dataset updated
    Sep 12, 2024
    Dataset authored and provided by
    Dataintelo
    License

    https://dataintelo.com/privacy-and-policyhttps://dataintelo.com/privacy-and-policy

    Time period covered
    2024 - 2032
    Area covered
    Global
    Description

    Non-Invasive Prenatal Testing Kit Market Outlook



    The global market size for Non-Invasive Prenatal Testing (NIPT) kits was valued at approximately USD 3.4 billion in 2023 and is anticipated to reach nearly USD 9.8 billion by 2032, showcasing a robust CAGR of 12.5% during the forecast period. This impressive growth is driven by several factors including advancements in diagnostic technology, increasing awareness among expectant parents, and the escalating incidences of chromosomal abnormalities.



    One of the primary growth factors for the NIPT kit market is the rising prevalence of genetic disorders like Down syndrome, Edwards syndrome, and Patau syndrome among newborns. With an increasing number of older women opting for pregnancies, the risk of chromosomal abnormalities has surged, thereby driving the demand for non-invasive prenatal testing. Additionally, advancements in cell-free DNA technology have significantly improved the accuracy and reliability of these tests, further propelling market growth.



    Another pivotal growth factor is the growing awareness and acceptance of non-invasive prenatal testing among healthcare providers and expectant parents. The non-invasive nature of these tests ensures that they pose minimal risk to both the mother and the fetus, making them a preferred option over invasive methods like amniocentesis. Furthermore, increasing educational campaigns and endorsements from healthcare organizations are enhancing the adoption rates of NIPT kits globally.



    The market is also experiencing growth due to the continuous innovations and improvements in prenatal testing technologies. Companies are investing heavily in research and development to introduce advanced testing kits that offer quicker results, higher accuracy, and comprehensive genetic screening capabilities. This has led to the development of more sophisticated instruments and software that streamline the testing process and improve diagnostic outcomes.



    Regionally, North America dominates the NIPT kit market due to its advanced healthcare infrastructure, high awareness levels, and supportive government policies. However, the Asia Pacific region is expected to exhibit the highest growth rate during the forecast period, driven by increasing healthcare expenditure, rising awareness, and the growing number of late maternal age pregnancies. Europe also holds a significant share, owing to advancements in healthcare technologies and increased acceptance of prenatal screening methods.



    Product Type Analysis



    In the NIPT kit market, the product type segment is classified into consumables, instruments, and software. Consumables, which include reagents, test kits, and other supplies used in the testing process, form a substantial part of the market. Due to the recurrent need for these items with each test conducted, consumables are expected to maintain a significant market share. The constant demand from laboratories and hospitals contributes significantly to the revenue generated in this segment.



    Instruments used in NIPT, such as sequencers and analyzers, form another crucial segment. With continuous advancements in technology, newer and more efficient instruments are introduced, enhancing the accuracy and speed of prenatal tests. This segment, although requiring a higher initial investment, promises substantial growth due to the increasing adoption of advanced diagnostic tools in hospitals and diagnostic centers. The integration of AI and machine learning in these instruments further adds to their efficacy, making them indispensable in prenatal diagnostics.



    Software solutions form the backbone of NIPT, as they are essential for analyzing the vast amounts of genetic data generated during testing. Robust software solutions enable precise interpretation of test results, ensuring accurate detection of genetic anomalies. Companies are focusing on developing advanced software that can handle complex genetic data and provide user-friendly interfaces for healthcare professionals. This segment is expected to grow significantly as software innovations continue to improve data analysis and reporting capabilities in prenatal testing.



    Report Scope




    Attributes Details
    Report

  • c

    Non-invasive prenatal testing market size was $1,567.9 million in 2022!

    • cognitivemarketresearch.com
    pdf,excel,csv,ppt
    Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    Cognitive Market Research, Non-invasive prenatal testing market size was $1,567.9 million in 2022! [Dataset]. https://www.cognitivemarketresearch.com/non-invasive-prenatal-testing-market-report
    Explore at:
    pdf,excel,csv,pptAvailable download formats
    Dataset authored and provided by
    Cognitive Market Research
    License

    https://www.cognitivemarketresearch.com/privacy-policyhttps://www.cognitivemarketresearch.com/privacy-policy

    Time period covered
    2021 - 2033
    Area covered
    Global
    Description

    Global Non-invasive prenatal testing market size was $1,567.9 million in 2022. Non-invasive prenatal testing Industry's Compound Annual Growth Rate will be 18.9% from 2023 to 2030. Factors Affecting Non-Invasive Prenatal Testing market growth.

    The increasing prevalence of chromosomal abnormalities with increasing maternal age is anticipated to drive the demand in the global non-invasive prenatal testing market. In addition, rising incidences of down syndrome are driving the growth of the global market. Furthermore, an increase in the number of kids with chromosomal disorders and improved diagnostic imaging technology provide an opportunity for the target market. However, the high cost of these tests to its relatively low affordability may hamper the growth of the global market. What is Non-Invasive Prenatal Testing?

    Non-invasive prenatal testing is a DNA-based blood test that is used to assess the risk of genetic disorders in the developing fetus. This is done to see if a person suffers from down syndrome, Patau syndrome, Edwards syndrome, and others.

  • d

    Incidence of spina bifida: crude rate, at birth, annual, P

    • digital.nhs.uk
    Updated Jul 29, 2015
    + more versions
    Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    (2015). Incidence of spina bifida: crude rate, at birth, annual, P [Dataset]. https://digital.nhs.uk/data-and-information/publications/statistical/compendium-public-health/current/chromosomal-abormalities-congential-malformations
    Explore at:
    Dataset updated
    Jul 29, 2015
    License

    https://digital.nhs.uk/about-nhs-digital/terms-and-conditionshttps://digital.nhs.uk/about-nhs-digital/terms-and-conditions

    Description

    Legacy unique identifier: P00448

  • d

    Incidence of all central nervous system anomalies: crude rate, at birth,...

    • digital.nhs.uk
    Updated Jul 29, 2015
    + more versions
    Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    (2015). Incidence of all central nervous system anomalies: crude rate, at birth, annual, P [Dataset]. https://digital.nhs.uk/data-and-information/publications/statistical/compendium-public-health/current/chromosomal-abormalities-congential-malformations
    Explore at:
    Dataset updated
    Jul 29, 2015
    License

    https://digital.nhs.uk/about-nhs-digital/terms-and-conditionshttps://digital.nhs.uk/about-nhs-digital/terms-and-conditions

    Description

    Legacy unique identifier: P00434

  • d

    Incidence of cleft palate and/or cleft lip: crude rate, at birth, 3-year...

    • digital.nhs.uk
    Updated Jul 29, 2015
    + more versions
    Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    Incidence of cleft palate and/or cleft lip: crude rate, at birth, 3-year average, P [Dataset]. https://digital.nhs.uk/data-and-information/publications/statistical/compendium-public-health/current/chromosomal-abormalities-congential-malformations
    Explore at:
    Dataset updated
    Jul 29, 2015
    License

    https://digital.nhs.uk/about-nhs-digital/terms-and-conditionshttps://digital.nhs.uk/about-nhs-digital/terms-and-conditions

    Description

    Legacy unique identifier: P00439

  • Share
    FacebookFacebook
    TwitterTwitter
    Email
    Click to copy link
    Link copied
    Close
    Cite
    Statista (2024). Incidence of Down syndrome in the United States as of 2024, by age [Dataset]. https://www.statista.com/statistics/1497382/down-syndrome-incidence-by-age-us/
    Organization logo

    Incidence of Down syndrome in the United States as of 2024, by age

    Explore at:
    Dataset updated
    Oct 11, 2024
    Dataset authored and provided by
    Statistahttp://statista.com/
    Area covered
    United States
    Description

    Older women are at an increased risk of having a child with Down syndrome. For example, among women aged 20 years, the chances of conceiving a child with Down syndrome is about one in 2,000. In comparison, among women aged 49 years, the chances of conceiving a child with Down syndrome is about one in 10. This statistic shows the incidence of Down syndrome in the United States as of 2024, by maternal age.

    Search
    Clear search
    Close search
    Google apps
    Main menu