市场调查报告书
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胚胎着床前基因检测市场:按技术、产品、程序类型、应用、最终用户 - 2024-2030 年全球预测Preimplantation Genetic Testing Market by Technology, Offering, Procedure Type, Application, End User - Global Forecast 2024-2030 |
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预计2023年胚胎着床前基因检测市场规模为7.284亿美元,2024年将达8.2906亿美元,2030年将达18.8628亿美元,复合年增长率为14.56%。
胚胎着床前基因检测(PGT)是指在胚胎着床前检测影响胚胎的染色体异常的技术。 PGT是一项重要服务,能够在体外受精(IVF)方法中及早发现胚胎着床前胚胎的遗传异常,显着降低将遗传性疾病传给后代的风险并提高成功率。 PGT 的主要应用领域包括识别单发疾病、染色体异常、粒线体疾病以及潜在兄弟姐妹的人类白血球抗原 (HLA) 匹配。由于生活方式的改变以及夫妻选择生育的延迟导致不孕率不断上升,因此需要开发PGT技术。政府促进体外受精治疗的措施正在创造许多扩张机会。然而,与 IVF 治疗和 PGT 程序相关的高成本可能是潜在最终用户的主要阻碍力。围绕 PGT 的伦理问题和 IVF 治疗的有限保险范围阻碍了 PGT 服务的采用。领先的生物技术公司正在迅速加强应对道德和监管挑战,创造考虑道德和伦理因素的技术。次世代定序(NGS)和非侵入性胚胎着床前测试等新方法是新兴技术,为该技术的发展提供了巨大潜力。
主要市场统计 | |
---|---|
基准年[2023] | 7.284 亿美元 |
预测年份 [2024] | 82906万美元 |
预测年份 [2030] | 18.8628亿美元 |
复合年增长率(%) | 14.56% |
检测染色体异常和单基因疾病的下一代定序技术取得进展
比较基因组杂合反应(CGH) 已被用来比较两个样本的 DNA 来检测染色体失衡。检测胚胎着床前胚胎的染色体异常,有助于选择健康胚胎进行体外受精。萤光原位杂合反应(FISH) 是一种使用萤光探针来视觉化和绘製细胞内染色体上特定 DNA 序列的技术。可以检测染色体异常,包括非整倍体和易位。次世代定序(NGS) 能够快速且准确地对大量 DNA序列测定,因此成为胚胎着床前基因检测的强大工具。聚合酵素链锁反应(PCR) 是一种广泛使用的分子生物学技术,可扩增特定的 DNA 序列以进行分析和检测单基因疾病。单核苷酸多态性(SNP)评估基因组中单核苷酸水平的变异,用于识别遗传疾病的携带者并评估多因素疾病(包括癌症)的风险。
提供:利用多样化的产品来优化製程条件并获得准确的结果
该设备在 PGT 过程中发挥重要作用,因为它可以对胚胎进行准确、高效的基因筛检。关键设备包括次世代定序仪(NGS)、定量 PCR (qPCR) 系统和萤光原位杂合反应(FISH) 分析仪。 NGS具有高通量定序能力和广泛的检测范围,适合检测单基因和染色体异常。 PGT使用的试剂和耗材由基因检测所需的各种套件、探针、缓衝液、酵素、溶液等组成。探针对于检测特定染色体异常至关重要,缓衝液为最佳扩增条件提供了适当的条件。软体和服务是 PGT 不可或缺的一部分,因为它们可确保基因检测结果的可靠资料管理、分析、解释和报告。偏好围绕着使用者友善的介面、准确的变异检测演算法、用于变异註释的综合资料库、安全的资料储存选项等。
胚胎着床前遗传学诊断(PGD)程序变得普及,降低了遗传疾病的风险。
胚胎着床前遗传学诊断(PGD)是一种专门的程序,可以在植入或怀孕前诊断出胚胎中的基因突变和染色体异常。 PGD 的主要目的是降低某些遗传疾病的风险,如囊肿纤维化、亨廷顿舞蹈症和肌肉萎缩症。胚胎着床前遗传学筛检(PGS),也称为非整倍体染色体胚胎着床前遗传学检测(PGT-A),是在胚胎着床前胚胎中染色体非整倍性或不平衡的情况。透过识别具有正确染色体数量的胚胎,PGS旨在降低流产、死产、唐氏症和其他染色体异常的风险,并增加成功怀孕的机会。
广泛使用胚胎着床前基因检测来治疗应用性非整倍体疾病
非整倍体是一种由于细胞内染色体数量异常而导致唐氏症、爱德华兹氏症候群和帕陶氏症等遗传性疾病的疾病。胚胎着床前非整倍体基因检测(PGT-A)可在胚胎着床前辨识出染色体异常的胚胎,进而增加成功怀孕的机会。透过胚胎着床前基因检测进行性别鑑定,让夫妇选择孩子的性别,以平衡家庭并避免与性别相关的疾病。人类白血球抗原 (HLA) 分型可在干细胞和器官移植过程中匹配供体和受体的组织类型。胚胎着床前HLA型检测可以识别组织学相容的胚胎,并促进患有血液疾病或免疫系统缺陷的兄弟姐妹的成功植入。染色体结构异常涉及染色体结构的变化,包括缺失、重复和重排。此外,X连锁疾病是由X染色体上的基因突变引起的,对男性的影响比女性更严重。
最终用户:医疗研究机构越来越多地采用 PGT,以实现准确诊断和有效治疗
胚胎着床前基因检测广泛应用于各种医疗机构,并在临床研究中取得了成功。合约研究和製造组织 (CRMO) 是在产品开发、製造和商业化中发挥关键作用的关键组织。这些组织更喜欢外包服务,以确保品管、遵守监管标准和成本效率,同时专注于核心能力。同样,冷冻库是在极低的温度下储存精子、卵子和胚胎等生物样本以供将来使用的机构。胚胎着床前基因检测对于冷冻银行至关重要,可确保在体外受精和显微授精等移植程序之前储存样本的遗传活力。医院、诊断实验室和服务供应商正在利用胚胎着床前基因检测技术透过准确的诊断和有效的治疗为患者护理做出贡献。研究机构和学术机构透过尖端研究、技术开发和跨学科合作,在推动胚胎着床前基因检测的创新和进步方面发挥关键作用。这些机构专注于开发下一代定序(NGS)等新技术,以提高胚胎着床前基因检测方法的准确性。
区域洞察
在美洲,由于生活方式的改变和基因检测意识的增强导致不孕率上升,因此对胚胎着床前基因检测(PGT)的需求很高。改善的医疗基础设施和优惠的报销政策使美洲寻求不孕症治疗的夫妇更容易获得 PGT 服务。该地区企业拥有强大的研发能力,政府支持支持该领域的创新。亚洲是 PGT 的主要市场,因为 PGT 服务改善了 IVF 等先进生育技术的提供,扩大了医疗旅游业,并吸引了寻求具有成本效益的治疗选择的外国患者。由于政府对医疗保健研究的资助增加以及 IVF 在欧洲国家普及等因素,欧洲对全球 PGT 市场做出了巨大贡献。此外,围绕基因检测的严格法律规范确保了在进行 PGT 服务时的品管和道德考虑。该地区的主要企业正在为胚胎着床前基因检测实践的技术进步做出重大贡献。
FPNV定位矩阵
FPNV定位矩阵对于评估胚胎着床前基因检测市场至关重要。我们检视与业务策略和产品满意度相关的关键指标,以对供应商进行全面评估。这种深入的分析使用户能够根据自己的要求做出明智的决策。根据评估,供应商被分为四个成功程度不同的像限:前沿(F)、探路者(P)、利基(N)和重要(V)。
市场占有率分析
市场占有率分析是一种综合工具,可以对胚胎着床前基因测试市场供应商的现状进行深入而深入的研究。全面比较和分析供应商在整体收益、基本客群和其他关键指标方面的贡献,以便更好地了解公司的绩效及其在争夺市场占有率时面临的挑战。此外,该分析还提供了对该行业竞争特征的宝贵见解,包括在研究基准年观察到的累积、分散主导地位和合併特征等因素。详细程度的提高使供应商能够做出更明智的决策并制定有效的策略,从而在市场上获得竞争优势。
1. 市场渗透率:提供有关主要企业所服务的市场的全面资讯。
2. 市场开拓:我们深入研究利润丰厚的新兴市场,并分析其在成熟细分市场的渗透率。
3. 市场多元化:提供有关新产品发布、开拓地区、最新发展和投资的详细资讯。
4. 竞争评估和情报:对主要企业的市场占有率、策略、产品、认证、监管状况、专利状况和製造能力进行全面评估。
5. 产品开发与创新:提供对未来技术、研发活动和突破性产品开发的见解。
1.胚胎着床前基因检测市场规模及预测为何?
2.在胚胎着床前基因检测市场的预测期间内,有哪些产品、细分市场、应用和领域需要考虑投资?
3.胚胎着床前基因检测市场的技术趋势和法规结构是什么?
4.胚胎着床前基因检测市场主要厂商的市场占有率如何?
5. 进入胚胎着床前基因检测市场的合适型态和策略性手段是什么?
[192 Pages Report] The Preimplantation Genetic Testing Market size was estimated at USD 728.40 million in 2023 and expected to reach USD 829.06 million in 2024, at a CAGR 14.56% to reach USD 1,886.28 million by 2030.
Preimplantation genetic testing (PGT) refers to technologies used to detect chromosomal abnormalities affecting the embryos before implantation. PGT is a crucial service that allows for early detection of genetic abnormalities in embryos before implantation during in-vitro fertilization (IVF) procedures, significantly reducing the risk of passing on inheritable diseases to offspring and improving IVF success rates. The primary application areas for PGT include identifying monogenic disorders, chromosomal abnormalities, mitochondrial diseases, and human leukocyte antigen (HLA) matching for potential siblings. The rising infertility rates due to lifestyle changes and delayed parenthood choices among couples have necessitated the development of PGT technologies. Government initiatives promoting IVF treatments create numerous expansion opportunities. However, high costs associated with IVF treatments and PGT procedures can be a major deterrent to potential end-users. Ethical concerns surrounding PGT and limited insurance coverage for IVF treatments hinder the adoption of PGT services. Major biotechnology companies are rapidly expanding efforts to combat ethical and regulatory challenges and creating technologies that take moral and ethical issues under consideration. New approaches such as next-generation sequencing (NGS) and non-invasive preimplantation testing are emerging technologies that offer significant potential for the growth of the technology.
KEY MARKET STATISTICS | |
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Base Year [2023] | USD 728.40 million |
Estimated Year [2024] | USD 829.06 million |
Forecast Year [2030] | USD 1,886.28 million |
CAGR (%) | 14.56% |
Technology: Advancements in next-generation sequencing to detect chromosomal abnormalities and single-gene disorders
Comparative genomic hybridization (CGH) is adopted for detecting chromosomal imbalances by comparing the DNA of two samples. It can detect chromosomal abnormalities in embryos before implantation and help select healthy embryos for IVF. Fluorescence in situ hybridization (FISH) is a technique that uses fluorescent probes to visualize and map specific DNA sequences on chromosomes within cells. It can detect numerical chromosomal abnormalities, including aneuploidy or translocations. Next-generation sequencing (NGS) is a robust tool for preimplantation genetic testing owing to its ability to sequence large amounts of DNA quickly and accurately. Polymerase chain reaction (PCR) is a widely used molecular biology technique that amplifies specific DNA sequences for analysis and can detect monogenic diseases. Single-nucleotide polymorphism (SNP) evaluates variations at the single-nucleotide level within the genome and is used to identify carriers of inherited diseases or assess the risk of multifactorial disorders, including cancer.
Offering: Utilization of diverse offerings to optimize process conditions and derive accurate results
Instruments play a critical role in the PGT process as they enable accurate and efficient genetic screening of embryos. Key instruments include next-generation sequencers (NGS), quantitative PCR (qPCR) systems, and fluorescence in situ hybridization (FISH) analyzers. NGS offers high-throughput sequencing capabilities and a broader detection range, making it suitable for detecting single-gene disorders and chromosomal abnormalities. Reagents and consumables used for PGT consist of various kits, probes, buffers, enzymes, and solutions necessary for genetic testing procedures. Probes are vital in detecting specific chromosomal aberrations, and buffers provide appropriate conditions for optimal amplification conditions. Software and services are essential components of PGT, as they ensure reliable data management, analysis, interpretation, and reporting for genetic testing results. Need-based preferences revolve around user-friendly interfaces, accurate algorithms for variant detection, comprehensive databases for variant annotation, and secure data storage options.
Procedure: Increasing deployment of preimplantation genetic diagnosis (PGD) procedures to reduce the risk of genetic disorders
Preimplantation genetic diagnosis (PGD) is a specialized procedure that allows the identification of genetic mutations or chromosomal abnormalities in embryos diagnosed before implantation and pregnancy. The primary goal of PGD is to reduce the risk of developing specific genetic disorders such as cystic fibrosis, Huntington's disease, and muscular dystrophy. Preimplantation genetic screening (PGS), referred to as preimplantation genetic testing for aneuploidies (PGT-A), detects chromosomal aneuploidies or imbalances in embryos before implantation. PGS aims to improve the chances of successful pregnancies by identifying embryos with the correct number of chromosomes, reducing the risk of miscarriage, stillbirth, or having a child affected by Down syndrome or other chromosomal abnormalities.
Application: Wide use of preimplantation genetic testing for aneuploidy disorder
Aneuploidy is a disorder in which an abnormal number of chromosomes in a cell leads to genetic disorders, including Down syndrome, Edwards syndrome, and Patau syndrome. Preimplantation of genetic testing for aneuploidy (PGT-A) identifies embryos with chromosomal abnormalities before implantation, increasing the chances of a successful pregnancy outcome. Gender identification through preimplantation genetic testing allows couples to choose the gender of their child for family balancing or to avoid sex-linked disorders. Human leukocyte antigen (HLA) typing matches tissue types between donor and recipient for stem cell or organ transplantation procedures. Preimplantation HLA typing identifies embryos with compatible tissue types, potentially facilitating successful transplants in siblings with blood disorders or immune system deficiencies. Structural chromosomal abnormalities involve alterations in chromosome structure, including deletions, duplications, and rearrangements. In addition, X-linked diseases are caused by mutations in genes on the X chromosome, affecting males more severely than females.
End User: Increasing adoption of PGT in healthcare research organizations for accurate diagnosis and effective treatments
Preimplantation genetics testing is widely used in various healthcare facilities, providing successful outcomes in clinical research. Contract research and manufacturing organizations (CRMOs) are primary organizations that play a crucial role in developing, manufacturing, and commercializing preimplantation genetic testing products. These organizations prefer outsourcing their services to ensure quality control, compliance with regulatory standards, and cost efficiency while focusing on their core competencies. Similarly, cryobanks are institutions that store biological samples such as sperm, eggs, and embryos at extremely low temperatures for future use. Preimplantation genetic testing is crucial for cryobanks to ensure the genetic viability of stored samples before implantation procedures like IVF or ICSI. Hospitals, diagnostic labs, and service providers contribute to patient care through accurate diagnosis and effective treatments using preimplantation genetic testing technologies. Research laboratories and academic institutes play a vital role in driving innovation and advancements in preimplantation genetic testing through cutting-edge research, technological developments, and interdisciplinary collaborations. These institutions focus on developing novel techniques like next-generation sequencing (NGS) to enhance the accuracy of preimplantation genetic testing methods.
Regional Insights
The Americas exhibit a high need for preimplantation genetic testing (PGT) owing to rising infertility rates caused by lifestyle changes and increasing awareness regarding genetic testing. Well-established healthcare infrastructure facilities and favorable reimbursement policies have made PGT services more accessible to couples seeking infertility treatments in the Americas. Companies in the region have strong R&D capabilities and government support that drive innovation in the field. Asia is emerging as a big and opportunistic market for PGT owing to improved provision of advanced fertility techniques such as IVF with PGT services and growing medical tourism, attracting international patients seeking cost-effective treatment options. Europe contributes significantly to the global PGT market due to factors such as increased government funding for healthcare research and widespread adoption of IVF procedures across various European countries. Moreover, stringent regulatory frameworks surrounding genetic testing ensure quality control and ethical considerations when implementing PGT services. Key players within this region contribute significantly to technological advancements in preimplantation genetic testing practices.
FPNV Positioning Matrix
The FPNV Positioning Matrix is pivotal in evaluating the Preimplantation Genetic Testing Market. It offers a comprehensive assessment of vendors, examining key metrics related to Business Strategy and Product Satisfaction. This in-depth analysis empowers users to make well-informed decisions aligned with their requirements. Based on the evaluation, the vendors are then categorized into four distinct quadrants representing varying levels of success: Forefront (F), Pathfinder (P), Niche (N), or Vital (V).
Market Share Analysis
The Market Share Analysis is a comprehensive tool that provides an insightful and in-depth examination of the current state of vendors in the Preimplantation Genetic Testing Market. By meticulously comparing and analyzing vendor contributions in terms of overall revenue, customer base, and other key metrics, we can offer companies a greater understanding of their performance and the challenges they face when competing for market share. Additionally, this analysis provides valuable insights into the competitive nature of the sector, including factors such as accumulation, fragmentation dominance, and amalgamation traits observed over the base year period studied. With this expanded level of detail, vendors can make more informed decisions and devise effective strategies to gain a competitive edge in the market.
Key Company Profiles
The report delves into recent significant developments in the Preimplantation Genetic Testing Market, highlighting leading vendors and their innovative profiles. These include Abbott Laboratories, Agilent Technologies, Inc., Bio-Rad Laboratories, Inc., Bio-Techne Corporation, Bioarray S.L., EUROPE IVF International s.r.o., F. Hoffmann-La Roche AG, Genea Limited, GENETiKS, Illumina, Inc., Invicta Genetics, Invitae Corporation, Juno Genetics, US Inc., Laboratory Corporation of America Holdings, MedGenome Labs Ltd., Merck KGaA, Natera, Inc., NextGen Genetics Holdings, LLC, Ovation Fertility, PacGenomics, PerkinElmer, Inc., Progyny, Inc., Qiagen N.V., Quest Diagnostics Incorporated, Reproductive Genetic Innovations, LLC, SEQUENCE46, LLC, Sysmex Corporation, Takara Bio Inc., The Cooper Companies Inc., Thermo Fisher Scientific Inc., Vitrolife Sweden AB, and Yikon Genomics (Shanghai) Co., Ltd..
Market Segmentation & Coverage
1. Market Penetration: It presents comprehensive information on the market provided by key players.
2. Market Development: It delves deep into lucrative emerging markets and analyzes the penetration across mature market segments.
3. Market Diversification: It provides detailed information on new product launches, untapped geographic regions, recent developments, and investments.
4. Competitive Assessment & Intelligence: It conducts an exhaustive assessment of market shares, strategies, products, certifications, regulatory approvals, patent landscape, and manufacturing capabilities of the leading players.
5. Product Development & Innovation: It offers intelligent insights on future technologies, R&D activities, and breakthrough product developments.
1. What is the market size and forecast of the Preimplantation Genetic Testing Market?
2. Which products, segments, applications, and areas should one consider investing in over the forecast period in the Preimplantation Genetic Testing Market?
3. What are the technology trends and regulatory frameworks in the Preimplantation Genetic Testing Market?
4. What is the market share of the leading vendors in the Preimplantation Genetic Testing Market?
5. Which modes and strategic moves are suitable for entering the Preimplantation Genetic Testing Market?