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市場調查報告書
商品編碼
1813355
IVF遺傳風險評分市場預測(至2032年):按測試類型、技術、應用、最終用戶和地區進行的全球分析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 |
根據 Stratistics MRC 的數據,全球 IVF 遺傳風險評分市場預計在 2025 年達到 3.632 億美元,到 2032 年將達到 8.813 億美元,預測期內的複合年成長率為 13.5%。
體外受精(IVF)遺傳風險評分(GRS)是一項尖端生殖技術,用於評估體外受精(IVF)胚胎的遺傳健康狀況。透過分析特定的遺傳標記、單核苷酸多態性(SNP)和多基因風險因素,GRS可以預測胚胎未來患有特定遺傳疾病或病症的可能性。此評分系統使臨床醫生和準父母能夠做出明智的胚胎選擇決策,從而提高健康懷孕的幾率並降低遺傳疾病的風險。 IVF GRS整合了先進的基因組學、生物資訊學和生殖醫學技術,以更高的精準度和預測性提供個人化的不孕症治療。
生殖技術的進步
基因組學、生物資訊學和胚胎篩檢領域的快速創新推動了IVF遺傳風險評分(GRS)的普及。多基因風險因子和單核苷酸多態性(SNP)檢測技術的提升,使臨床醫生能夠更有信心地進行個人化胚胎選擇。人工智慧主導的分析技術與新一代定序(NGS)平台的整合進一步提高了預測準確性,使GRS成為現代不孕症治療的基石。這些進步透過改善臨床療效和降低遺傳性疾病的發病率,推動了市場擴張。
高成本且可近性有限
高成本和有限的可及性嚴重阻礙了IVF基因風險評分市場的成長。這些障礙將大量人群排除在早期基因組篩檢之外,並阻礙了公平的醫療創新。新興地區缺乏保險覆蓋和基礎設施,進一步加劇了差距,抑制了需求,並減緩了臨床整合。因此,市場擴張仍受到限制,其變革潛力在服務不足的地區仍未充分發揮。
遺傳性疾病發生率不斷上升
囊腫纖維化、泰-薩克斯病和BRCA相關癌症等遺傳性疾病的發生率不斷上升,加劇了對預測性胚胎篩檢的需求。 IVF遺傳風險評分提供了一個主動的解決方案,能夠及早識別遺傳易感性,從而改善生殖決策。隨著臨床醫生和準父母意識的不斷增強,GRS有望成為生育治療通訊協定的標準組成部分。這種日益成長的臨床需求代表著巨大的成長機遇,尤其是在遺傳疾病高發生率地區。
胚胎受損的風險
基因檢測過程中胚胎損傷的風險嚴重削弱了人們對體外受精(IVF)遺傳風險評分的信心,阻礙了臨床醫生和準父母的採用。對侵入性切片檢查技術及其對可存活胚胎的潛在危害的擔憂引發了倫理和安全方面的擔憂,阻礙了監管部門的核准和投資者的興趣。這種不確定性阻礙了市場成長,限制了臨床整合,並加劇了公眾的懷疑,尤其是在生育政策保守、基因組學素養較低的地區。
COVID-19的影響
新冠疫情擾亂了體外受精(IVF)基因風險評分市場,擾亂了生育治療,推遲了胚胎移植,並增加了患者的心理壓力。診所在關閉期間暫停營運,導致周期延遲和需求減少。然而,這場危機加速了人們對數位化諮商和基因組篩檢的認知,刺激了長期成長。隨著服務恢復,人們對個人化胚胎選擇和基因分析的興趣日益濃厚,推動了市場復甦和創新。
預測期內,性狀篩檢部分預計將成為最大的部分
預測期內,性狀篩檢細分市場預計將佔據最大市場佔有率,這得益於其在評估多基因風險和遺傳疾病方面廣泛的臨床效用。透過分析特定基因標記,可以早期發現與慢性疾病、認知障礙和身體異常相關的性狀。它是一種非侵入性技術,適用於現有的體外受精 (IVF) 工作流程,因此具有高度的擴充性。隨著個人化醫療的興起,性狀篩檢正成為胚胎選擇的重要組成部分,並推動其佔據主導的市場佔有率。
預計在預測期內,不孕症治療診所部門的複合年成長率最高。
由於對綜合生殖健康服務的需求不斷成長,預計生育診所細分市場將在預測期內呈現最高成長率。這些診所提供端到端的IVF解決方案,包括遺傳諮詢、胚胎篩檢和個人化治療方案。採用先進的GRS平台將改善患者預後並提高臨床效率。隨著人們對遺傳風險評分的認知不斷提高,生育診所正逐漸成為一個重要的銷售管道,尤其是在患者數量眾多且實驗室設備先進的都市區。
在預測期內,由於生育治療基礎設施的不斷擴大、人們對遺傳疾病的認知不斷提高以及政府的支持政策,預計亞太地區將佔據最大的市場佔有率。由於人口結構的變化和中階經濟實力的不斷增強,中國、印度和日本等國家正在擴大採用體外受精 (IVF)。區域性對基因組學和數位健康的投資正在進一步加速IVF GRS的整合。領先的生育診所和研究機構的存在使亞太地區成為全球IVF GRS領域的主導力量。
預計北美將在預測期內呈現最高的複合年成長率。這得益於其強大的醫療基礎設施、較高的患者認知度以及對基因檢測強力的監管支持。該地區率先採用精準醫療和先進的體外受精 (IVF)通訊協定,為 GRS 的擴張提供了肥沃的土壤。生物技術公司與生育中心之間的策略聯盟正在推動創新和可及性。優惠的報銷政策和對個人化生殖醫學日益成長的需求預計將使北美在市場成長方面保持領先地位。
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.