市場調查報告書
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1533074
歐洲基因檢測服務市場預測至 2030 年 - 區域分析 - 按服務類型、疾病和服務提供者Europe Genetic Testing Services Market Forecast to 2030 - Regional Analysis - by Service Type, Disease, and Service Provider |
2022年歐洲基因檢測服務市值9.3111億美元,預計2030年將達27.7842億美元;預計2022年至2030年複合年成長率為14.6%。
對個人化藥物的認知和接受度不斷提高推動歐洲基因檢測服務市場
個人化醫療是利用患者的遺傳和環境資料提供最佳醫療保健的領域。它基於每個患者都是獨特的並且需要個別化藥物治療的原則。由於它是一個快速發展的領域,目前已納入多個醫療保健系統。 2003年人類基因組計畫(HGP)的成功完成以及人類基因組定序成本的快速下降鼓勵了一種新的醫療方法的發展,即個人化醫療。隨著分子層級個人化資料儲存庫的不斷擴大,分子診斷公司在釋放價值方面處於特殊地位。大規模藥物發現是提高個人化藥物在疾病和病症診斷的可行性和有用性的關鍵。基因組學是醫學科學中發展最快的部門之一。它正在推動疾病研究方法以及疾病診斷和治療的範式轉移。基因檢測已廣泛應用於藥物基因組學,也稱為藥物基因檢測。它有助於加速藥物發現及其開發。法國也制定了一項名為「法國基因組醫學 2025」的個人化醫療國家計畫。 2016 年6 月,阿維桑國家生命與健康科學聯盟主席兼Inserm 首席執行官伊夫·利維(Yves Levy) 向總理曼努埃爾·瓦爾斯(Manuel Valls) 提交了該計劃。保健和製造公司試點基因組定序平台。該計劃得到了政府的支持,並於 2020 年啟動了 7.608 億美元(6.7 億歐元)的公共融資,用於基因組學和個性化醫療項目。預計未來十年內法國將成為基因組醫學領域的領先國家。 2023 年 1 月,人類基因組計畫將開啟個人化醫療保健時代。現在,新的研究表明,使用基因檢測進行精確處方最終已達到全球採用的臨界點。這項經過同行評審的研究由劍橋大學出版社出版,研究了大規模使用臨床遺傳學所需的關鍵因素的成熟度。這些進步為支持將基於基因組的臨床決策建立為新的護理標準鋪平了道路。基因知情處方提供了成功降低醫療保健系統總體成本和改善個別患者護理的現實機制之一。基因檢測透過了解疾病背後的科學、治療的影響以及針對特定個體特徵的療法的開發,鼓勵採用個人化醫療方法。它還可以幫助醫護人員利用基因檢測結果做出有關疾病診斷、治療和預防的明智決策,從而改善患者的治療結果。
歐洲基因檢測服務市場概況
歐洲基因檢測服務市場分為德國、英國、法國、義大利、西班牙和歐洲其他地區。基因檢測一直以驚人的速度成長。現在提供大量測試來篩檢多種遺傳疾病。許多罕見遺傳疾病都有治療方法,而且這個過程在攜帶者檢測、新生兒篩檢、預測性和症狀前檢測等場景中變得越來越重要。此外,歐洲國家也採取了一系列措施來提高人們對基因檢測益處的認知。最終目標是確保基因檢測的各個方面都是高品質的,從而提供準確可靠的結果,造福患者。
歐洲基因檢測服務市場收入及 2030 年預測(百萬美元)
歐洲基因檢測服務市場細分
歐洲基因檢測服務市場按服務類型、疾病、服務提供者和國家分類。
根據服務類型,歐洲基因檢測服務市場可細分為預測檢測、帶因者檢測、產前檢測、新生兒篩檢等。預測測試領域在 2022 年佔據最大的市場佔有率。
從疾病類型來看,歐洲基因檢測服務市場分為癌症、代謝疾病、心血管疾病和其他疾病。 2022 年,癌症細分市場佔據最大的市場。
依服務提供者分類,歐洲基因檢測服務市場分為醫院實驗室、診斷實驗室等。 2022 年,醫院實驗室細分市場佔據最大市場佔有率。
依國家/地區分類,歐洲基因檢測服務市場分為英國、德國、法國、西班牙、義大利和歐洲其他地區。 2022年,德國在歐洲基因檢測服務市場佔有率中佔據主導地位。
Eurofins Scientific SE、Exact Sciences Corp、Laboratory Corp of America Holdings、23andMe Holding Co、Quest Diagnostics Inc、Illumina Inc、F. Hoffmann-La Roche Ltd、NeoGenomics Inc 和 Centogene AG 是歐洲基因檢測領域的領先公司之一服務市場。
The Europe genetic testing services market was valued at US$ 931.11 million in 2022 and is expected to reach US$ 2,778.42 million by 2030; it is estimated to register a CAGR of 14.6% from 2022 to 2030.
Increasing Awareness and Acceptance of Personalized Medicines Drive Europe Genetic Testing Services Market
Personalized medicine is the field that utilizes patients' genetic and environmental data to deliver optimal healthcare. It is based on the principle that every patient is unique and requires individualistic pharmacological treatment. Since it is a rapidly evolving area, it is presently incorporated into several healthcare systems. The successful completion of the Human Genome Project (HGP) in 2003 and the fast-decreasing human genome sequencing costs encouraged the development of a new medical approach, which is called personalized medicine. With an expanding repository of personalized data at the molecular level, molecular diagnostics companies are exceptionally positioned to unlock value. Large-scale drug discovery is a key to increasing the viability and usefulness of personalized medicines for the diagnosis of diseases and disorders. Genomics is one of the fastest-growing divisions of medical science. It is driving a paradigm shift in the research methodology of a disease, as well as diagnosing and treating illness. Genetic testing has been extensively used in pharmacogenomics, also known as drug-gene testing. It helps in accelerating drug discovery and its development. France also developed a national plan for personalized medicine known as "Genomic Medicine France 2025." The program was presented to Prime Minister Manuel Valls by Yves Levy, President of the National Alliance for Life and Health Sciences-Aviesan and CEO of Inserm, in June 2016. It appeals to healthcare and manufacturing firms to pilot genomic sequencing platforms. The plan was supported by the government and launched with a public financing of US$ 760.8 million (€670 million) in 2020 for genomics and personalized medicine programs. It is expected to place France as a leader among countries involved in genomic medicine within the next ten years. In January 2023, The Human Genome Project is ensuring an era of personalized healthcare. Now, new research shows that precision prescribing using genetic testing has ultimately reached a global tipping point for adoption. Published by Cambridge University Press, the peer-reviewed research examines the maturation of critical factors required for the use of clinical genetics at scale. These advancements pave the way for supporting genome-informed clinical decision-making to be established as the new standard of care. Genetically informed prescribing offers one of the realistic mechanisms to successfully reduce the overall costs of the healthcare system and improve individual patient care. Genetic testing encourages the adoption of a personalized medicine approach by understanding the science behind the disease, the impact of treatment, and the development of therapies for specific individual characteristics. It also helps healthcare personnel make informed decisions about disease diagnosis, treatment, and prevention by utilizing genetic testing results, leading to improved patient outcomes.
Europe Genetic Testing Services Market Overview
European genetic testing services market is segmented into Germany, the UK, France, Italy, Spain, and the Rest of Europe. Genetic testing has been growing at an exceptional rate; a large panel of tests are now offered to screen a number of genetic diseases. Treatments are available for a number of rare genetic diseases, and the process is gaining importance in scenarios such as carrier testing, newborn screening, and predictive and pre-symptomatic testing, among others. Moreover, European countries have undertaken a number of initiatives to increase awareness among people about the benefits of genetic testing. The ultimate goal is to ensure that all aspects of genetic testing are of high quality, thereby providing accurate and reliable results for the benefit of the patients.
Europe Genetic Testing Services Market Revenue and Forecast to 2030 (US$ Million)
Europe Genetic Testing Services Market Segmentation
The Europe genetic testing services market is categorized into service type, disease, service provider, and country.
Based on service type, the Europe genetic testing services market is segmented predictive testing, carrier testing, prenatal testing, newborn screening, and others. The predictive testing segment held the largest market share in 2022.
In terms of disease, the Europe genetic testing services market is categorized into cancer, metabolic diseases, cardiovascular diseases, and other diseases. The cancer segment held the largest market share in 2022.
By service provider, the Europe genetic testing services market is segmented into hospital-based laboratories, diagnostic laboratories, and others. The hospital-based laboratories segment held the largest market share in 2022.
By country, the Europe genetic testing services market is segmented into the UK, Germany, France, Spain, Italy, and the Rest of Europe. Germany dominated the Europe genetic testing services market share in 2022.
Eurofins Scientific SE, Exact Sciences Corp, Laboratory Corp of America Holdings, 23andMe Holding Co, Quest Diagnostics Inc, Illumina Inc, F. Hoffmann-La Roche Ltd, NeoGenomics Inc, and Centogene AG are among the leading companies operating in the Europe genetic testing services market.