Preimplantation Genetic Testing (PGT) Market Share, Market Size, Market Segment Analysis to 2024

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Global Preimplantation Genetic Testing (PGT) Market Size,
Share, Emerging Trends, Analysis, Overview and Forecasts to
2024
The global preimplantation genetic testing market was valued at USD 129.3 million in 2015 and is
expected to reach a value of USD 221.1 million by 2024. Growth in number of offspring born with
inherited conditions is a high impact rendering factor for growth of this market. Emergence of
preimplantation genetic diagnosis for detection of nearly all genetically inherited conditions enable
couples, who are carriers of such conditions, screen their embryos before transferring to uterus and this
is the primary driver of this industry.
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Increase in adoption of IVF as a result of pregnancy-related complications is anticipated to drive demand
for preimplantation genetic testing services. Women who are undergoing IVF are expected to undergo
PGT cycles for prevention of inheritance of chromosomal abnormalities by offspring, which as a
consequence is augmenting growth. Growth in demand for these tests can be ascribed to the increase in
rate of infertility due to environmental and lifestyle factors, which in turn, emphasizes the need for
development in this vertical.
Preimplantation genetic testing is available for different types of services, which include X-linked
diseases, Human Leukocyte Antigen (HLA) typing, chromosomal abnormalities, freeze embryo testing,
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aneuploidy screening, detection of serious late-onset diseases, and gender selection. Preimplantation
genetic testing for chromosomal abnormalities accounted for approximately 29% of the market share
due to advancements in its screening by the use of noninvasive prenatal testing, which employs cell-free
DNA for early detection of chromosomal abnormalities, such as Patau syndrome, Edwards syndrome,
and Down syndrome.
This technology has various applications. Amongst all the applications, embryo HLA typing for stem cell
therapy dominated with a share of over 30%. This largest share can be attributed to the benefits
associated with the use of PGD for identification of HLA compatible embryos for stem cell therapy.
Although usage of these tests for inherited chromosomal disease is observed to have less penetration in
the current scenario, it is expected to witness tremendous growth in the coming years due to increasing
adoption rate of this service for detection of inherited genomic anomalies, such as sickle cell anemia and
Huntington's disease.
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Europe accounted for the largest share with respect to revenue as a result of growing awareness about
the scope of these diagnostic services for delivering genetically fit offspring. Also, developed
infrastructure, rising investments by governmental bodies, and presence of key players in this region,
collectively encourages growth of this industry in this region.
Some of the key players that have commercialized PGT services include:
 F. Hoffmann-La Roche AG
 Genea Limited
 Quest Diagnostics, Illumina, Inc.
 Natera, Inc
 CooperSurgical, Inc
 LabCorp; California Pacific Medical Center
 Thermo Fisher Scientific, Inc
 Igenomix
 Reproductive Genetic Innovations, LLC
 CombiMatrix
 Good Start Genetics, Inc
 Bioarray S.L
 Reproductive Health Science Ltd.
These key participants are actively involved in the R&D initiatives for development of novel PGT services.
Partnership between entities and acquisition of small companies by major companies in order to
reinforce its status in the market as well as to expand its product catalog for this vertical is expected
boost revenue generation in preimplantation genetic diagnostics.
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For instance, In December 2015, Natera, entered into a partnership with MedGenome, provider of
genomic solutions for personalized healthcare in India. As per this partnership, MedGenome will be
allowed to use the Panorama noninvasive prenatal test in its research laboratory. As a result,
MedGenome becomes the first provider of this service in India.
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