![]() |
市场调查报告书
商品编码
1813355
IVF遗传风险评分市场预测(至2032年):按测试类型、技术、应用、最终用户和地区进行的全球分析IVF Genetic Risk Scoring Market Forecasts to 2032 - Global Analysis By Test Type (Single-Gene Risk Scoring, Polygenic Risk Scoring, Carrier Screening Panels and Whole Genome Sequencing), Technology, Application, End User and By Geography |
根据 Stratistics MRC 的数据,全球 IVF 遗传风险评分市场预计在 2025 年达到 3.632 亿美元,到 2032 年将达到 8.813 亿美元,预测期内的复合年增长率为 13.5%。
体外受精(IVF)遗传风险评分(GRS)是一项尖端生殖技术,用于评估体外受精(IVF)胚胎的遗传健康状况。透过分析特定的遗传标记、单核苷酸多态性(SNP)和多基因风险因素,GRS可以预测胚胎未来患有特定遗传疾病或病症的可能性。此评分系统使临床医生和准父母能够做出明智的胚胎选择决策,从而提高健康怀孕的几率并降低遗传疾病的风险。 IVF GRS整合了先进的基因组学、生物资讯学和生殖医学技术,以更高的精准度和预测性提供个人化的不孕症治疗。
生殖技术的进步
基因组学、生物资讯学和胚胎筛检领域的快速创新推动了IVF遗传风险评分(GRS)的普及。多基因风险因子和单核苷酸多态性(SNP)检测技术的提升,使临床医生能够更有信心地进行个人化胚胎选择。人工智慧主导的分析技术与新一代定序(NGS)平台的整合进一步提高了预测准确性,使GRS成为现代不孕症治疗的基石。这些进步透过改善临床疗效和降低遗传性疾病的发病率,推动了市场扩张。
高成本且可近性有限
高成本和有限的可及性严重阻碍了IVF基因风险评分市场的成长。这些障碍将大量人群排除在早期基因组筛检之外,并阻碍了公平的医疗创新。新兴地区缺乏保险覆盖和基础设施,进一步加剧了差距,抑制了需求,并减缓了临床整合。因此,市场扩张仍受到限制,其变革潜力在服务不足的地区仍未充分发挥。
遗传性疾病发生率不断上升
囊肿纤维化、泰-萨克斯病和BRCA相关癌症等遗传性疾病的发生率不断上升,加剧了对预测性胚胎筛检的需求。 IVF遗传风险评分提供了一个主动的解决方案,能够及早识别遗传易感性,从而改善生殖决策。随着临床医生和准父母意识的不断增强,GRS有望成为生育治疗通讯协定的标准组成部分。这种日益增长的临床需求代表着巨大的成长机会,尤其是在遗传疾病高发生率地区。
胚胎受损的风险
基因检测过程中胚胎损伤的风险严重削弱了人们对体外受精(IVF)遗传风险评分的信心,阻碍了临床医生和准父母的采用。对侵入性切片检查技术及其对可存活胚胎的潜在危害的担忧引发了伦理和安全方面的担忧,阻碍了监管部门的核准和投资者的兴趣。这种不确定性阻碍了市场成长,限制了临床整合,并加剧了公众的怀疑,尤其是在生育政策保守、基因组学素养较低的地区。
COVID-19的影响
新冠疫情扰乱了体外受精(IVF)基因风险评分市场,扰乱了生育治疗,推迟了胚胎移植,并增加了患者的心理压力。诊所在关闭期间暂停运营,导致周期延迟和需求减少。然而,这场危机加速了人们对数位化咨商和基因组筛检的认知,刺激了长期成长。随着服务恢復,人们对个人化胚胎选择和基因分析的兴趣日益浓厚,推动了市场復苏和创新。
预测期内,性状筛检部分预计将成为最大的部分
预测期内,性状筛检细分市场预计将占据最大市场份额,这得益于其在评估多基因风险和遗传疾病方面广泛的临床效用。透过分析特定基因标记,可以早期发现与慢性疾病、认知障碍和身体异常相关的性状。它是一种非侵入性技术,适用于现有的体外受精 (IVF) 工作流程,因此具有高度的扩充性。随着个人化医疗的兴起,性状筛检正成为胚胎选择的重要组成部分,并推动其占据主导的市场份额。
预计在预测期内,不孕症治疗诊所部门的复合年增长率最高。
由于对综合生殖健康服务的需求不断增长,预计生育诊所细分市场将在预测期内呈现最高成长率。这些诊所提供端到端的IVF解决方案,包括遗传咨询、胚胎筛检和个人化治疗方案。采用先进的GRS平台将改善患者预后并提高临床效率。随着人们对遗传风险评分的认识不断提高,生育诊所正逐渐成为一个重要的销售管道,尤其是在患者数量众多且实验室设备先进的都市区。
在预测期内,由于生育治疗基础设施的不断扩大、人们对遗传疾病的认识不断提高以及政府的支持政策,预计亚太地区将占据最大的市场份额。由于人口结构的变化和中阶经济实力的不断增强,中国、印度和日本等国家正在越来越多地采用体外受精 (IVF)。区域性对基因组学和数位健康的投资正在进一步加速IVF GRS的整合。领先的生育诊所和研究机构的存在使亚太地区成为全球IVF GRS领域的主导力量。
预计北美将在预测期内呈现最高的复合年增长率。这得益于其强大的医疗基础设施、较高的患者认知度以及对基因检测强有力的监管支持。该地区率先采用精准医疗和先进的体外受精 (IVF)通讯协定,为 GRS 的扩张提供了肥沃的土壤。生物技术公司与生育中心之间的策略联盟正在推动创新和可及性。优惠的报销政策和对个人化生殖医学日益增长的需求预计将使北美在市场成长方面保持领先地位。
According to Stratistics MRC, the Global IVF Genetic Risk Scoring Market is accounted for $363.2 million in 2025 and is expected to reach $881.3 million by 2032 growing at a CAGR of 13.5% during the forecast period. IVF Genetic Risk Scoring (GRS) is a cutting-edge reproductive technology that evaluates the genetic health of embryos created through in vitro fertilization (IVF). By analyzing specific genetic markers, single-nucleotide polymorphisms (SNPs), and polygenic risk factors, GRS predicts the likelihood of an embryo developing certain inherited diseases or conditions later in life. This scoring system enables clinicians and prospective parents to make informed decisions about embryo selection, aiming to improve the chances of a healthy pregnancy and reduce the risk of genetic disorders. IVF GRS integrates advanced genomics, bioinformatics, and reproductive medicine to personalize fertility care with greater precision and foresight.
Advancements in Reproductive Technologies
Rapid innovations in genomics, bioinformatics, and embryo screening are propelling the adoption of IVF Genetic Risk Scoring (GRS). Enhanced precision in detecting polygenic risk factors and single-nucleotide polymorphisms (SNPs) enables clinicians to personalize embryo selection with greater confidence. Integration of AI-driven analytics and next-generation sequencing (NGS) platforms is further improving predictive accuracy, making GRS a cornerstone of modern fertility care. These advancements are driving market expansion by elevating clinical outcomes and reducing the incidence of inherited disorders.
High Cost and Limited Accessibility
High cost and limited accessibility significantly hinder the growth of the IVF genetic risk scoring market by restricting adoption to affluent urban centers. These barriers exclude vast populations from early-stage genomic screening, stalling equitable healthcare innovation. The lack of insurance coverage and infrastructure in emerging regions further exacerbates disparities, curbing demand and slowing clinical integration. As a result, market expansion remains constrained, with transformative potential unrealized across underserved geographies.
Rising Incidence of Genetic Disorders
The increasing prevalence of hereditary conditions such as cystic fibrosis, Tay-Sachs, and BRCA-related cancers is intensifying demand for predictive embryo screening. IVF Genetic Risk Scoring offers a proactive solution by enabling early identification of genetic predispositions, thereby improving reproductive decision-making. As awareness grows among clinicians and prospective parents, GRS is poised to become a standard component of fertility protocols. This rising clinical need presents a significant growth opportunity, especially in regions with high rates of inherited diseases.
Risk of Embryo Damage
The risk of embryo damage during genetic testing significantly undermines confidence in IVF genetic risk scoring, deterring adoption among clinicians and prospective parents. Concerns over invasive biopsy techniques and potential harm to viable embryos raise ethical and safety alarms, stalling regulatory approvals and investor interest. This uncertainty hampers market growth, limits clinical integration, and fuels public skepticism, especially in regions with conservative reproductive policies and limited genomic literacy.
Covid-19 Impact
The COVID-19 pandemic disrupted the IVF Genetic Risk Scoring market by halting fertility treatments, delaying embryo transfers, and increasing emotional stress for patients. Clinics paused operations during lockdowns, leading to postponed cycles and reduced demand. However, the crisis accelerated digital consultations and genomic screening awareness, fostering long-term growth. As services resumed, heightened interest in personalized embryo selection and genetic profiling positioned the market for resilient recovery and innovation.
The trait screening segment is expected to be the largest during the forecast period
The trait screening segment is expected to account for the largest market share during the forecast period, due to its broad clinical utility in assessing polygenic risks and inherited conditions. By analyzing specific genetic markers, this segment enables early detection of traits linked to chronic diseases, cognitive disorders, and physical anomalies. Its non-invasive nature and compatibility with existing IVF workflows make it highly scalable. As personalized medicine gains traction, trait screening is becoming integral to embryo selection, driving its leadership in market share.
The fertility clinics segment is expected to have the highest CAGR during the forecast period
Over the forecast period, the fertility clinics segment is predicted to witness the highest growth rate, due to rising demand for integrated reproductive services. These clinics offer end-to-end IVF solutions, including genetic counseling, embryo screening, and personalized treatment plans. Their adoption of advanced GRS platforms enhances patient outcomes and boosts clinical efficiency. As awareness of genetic risk scoring grows, fertility clinics are emerging as key distribution channels, particularly in urban centers with high patient volumes and advanced lab capabilities.
During the forecast period, the Asia Pacific region is expected to hold the largest market share due to its expanding fertility infrastructure, rising awareness of genetic disorders, and supportive government initiatives. Countries like China, India, and Japan are witnessing increased IVF adoption, driven by demographic shifts and growing middle-class affordability. Regional investments in genomics and digital health are further accelerating GRS integration. The presence of leading fertility clinics and research institutions positions Asia Pacific as a dominant force in the global IVF GRS landscape.
Over the forecast period, the North America region is anticipated to exhibit the highest CAGR, owing to robust healthcare infrastructure, high patient awareness, and strong regulatory support for genetic testing. The region's early adoption of precision medicine and advanced IVF protocols makes it fertile ground for GRS expansion. Strategic collaborations between biotech firms and fertility centers are enhancing innovation and accessibility. Favorable reimbursement policies and growing demand for personalized reproductive care are expected to sustain North America's leadership in market growth.
Key players in the market
Some of the key players profiled in the IVF Genetic Risk Scoring Market include Illumina, Inc., Agilent Technologies, Inc., Natera, Inc., CooperSurgical, Inc., Thermo Fisher Scientific, Inc., Vitrolife AB, Igenomix, Genea Limited, PerkinElmer, Inc., Quest Diagnostics Incorporated, Invicta Genetics, Juno Genetics, US Inc., Bioarray S.L., Reproductive Health Science Ltd. and Genesis Genetics Ltd.
In July 2025, Thermo Fisher Scientific has agreed to acquire Sanofi's sterile manufacturing site in Ridgefield, New Jersey. This expansion aims to bolster U.S. drug product manufacturing capabilities, enhancing capacity to meet the increasing demand from pharmaceutical and biotech customers.
In July 2020, PerkinElmer partnered with Sonora Quest Laboratories to expand COVID-19 testing in Arizona. This collaboration aimed to increase testing capacity in response to rising case numbers, supported by funding from the state of Arizona.