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市場調查報告書
商品編碼
1372035
2030 年細胞遺傳學市場預測:按產品、技術、用途、最終用戶和地區進行的全球分析Cytogenetics Market Forecasts to 2030 - Global Analysis By Product, Technique, Application, End User and By Geography |
根據 Stratistics MRC 的數據,2023 年全球細胞遺傳學市場規模為 27 億美元,預計在預測期內年複合成長率為 11.8%,到 2030 年將達到 61 億美元。
對染色體、基因及其在生物體結構中的結構和數值變異的研究屬於細胞遺傳學的廣泛範疇,其中包括廣泛的方法、設備和服務。細胞遺傳學是一個重要的領域,有助於發現遺傳異常、檢測遺傳疾病以及了解癌症等疾病的遺傳背景。其應用領域為臨床診斷、研究和個人化醫療。
根據世界衛生組織統計,2018年約有1,810萬人新診斷出癌症,960萬人死於癌症。
細胞遺傳學需求增加的原因有很多。首先,它對於了解癌症、出生缺陷和遺傳疾病至關重要。此外,隨著精準醫療的普及,基因診斷和個體化治療計畫變得越來越重要。此外,由於人們對遺傳對健康和疾病的影響以及高齡化的認知不斷加深,臨床、研究和診斷用途對細胞遺傳學檢測的需求不斷增加。因此,擴大人類基因組和疾病遺傳學研究的需求不斷增加。
細胞遺傳學檢測需要使用專門的工具、消耗品和訓練有素的人員,所有這些都是昂貴的。患者通常需要申請這些費用,並且接受基因診斷和諮詢的能力受到限制。它也可能給醫院和研究機構造成財務困難。新細胞遺傳學技術的創建和使用也受到高成本的阻礙。因此,這些方面都阻礙了市場的成長。
隨著癌症發生率的增加,許多分子細胞遺傳學技術經常用於癌症診斷。此外,隨著我們對染色體層面上癌症的了解不斷加深,在癌症研究成長的推動下,細胞遺傳學收益也不斷擴大。例如,FISH 和 CGH 技術的使用促進了該市場的開拓,這些技術提供了與癌症相關的遺傳標記的重要資訊。 FISH、染色體影像分析、流式分選和基因組原位雜合技術 (GISH) 是用於創建合成植物染色體的方法,並已用於創建遺傳、物理、分子和比較圖譜。此外,分子細胞遺傳學在作物改良中的應用領域和優勢的擴大正在支持市場的成長。
不利的薪酬做法對細胞遺傳學產業有害。由於付款不一致或不足,醫療保健提供者不太可能進行細胞遺傳學檢測和治療,從而限制了患者的訪問。此外,這也透過減少需求和降低研發的經濟誘因來影響市場。此外,關於獲得尖端細胞遺傳學檢測的衝突可能會阻止患者接受癌症和遺傳性疾病等疾病的重要基因診斷。這是市場拓展的一大障礙。
細胞遺傳學市場受到了 COVID-19大流行的負面影響。封鎖和資源重新分配擾亂了實驗室業務,導致基因檢測延遲和患者准入問題。此外,經濟不確定性限制了研究和測試項目的資金,供應鏈中斷阻礙了獲得所需的測試用品。此外,學術和臨床研究活動也受到阻礙,導致臨床和科學挫折。因此,這些要素極大地阻礙了市場的成長。
據估計,核型分析部分佔最大佔有率。它通常從血液或組織樣本中可視化並檢查一個人的整個染色體。此外,核型分析有助於檢測染色體結構和數值異常,有助於癌症、遺傳性疾病和產前檢測的診斷。此外,雖然更先進的技術(例如光譜核型分析和螢光原位雜合技術(FISH))提供了更高的解析度,但傳統的核型分析程序(包括染色體染色和顯微鏡檢查)將會出現。因此,核型分析因其對染色體異常和遺傳疾病的寶貴見解而仍然是臨床和研究細胞遺傳學的基石。
由於根據患者個人化醫療調整醫療照護的領域迅速擴大,預計個人化醫療領域在預測期內將出現最高的年複合成長率。細胞遺傳學程序,例如染色體分析和分子測試,使臨床醫生能夠發現影響藥物治療反應、疾病易感性和整體健康的遺傳差異。此外,該方法可以更準確地診斷和治療選擇,改善治療結果並減少不良反應。此外,隨著基因組學和細胞遺傳學技術的進步,個人化醫療在罕見疾病、藥物基因組學和癌症的鑒定中發揮關鍵作用,根據患者的基因圖譜提供個體化的標靶治療方案,從而徹底改變醫療保健。因此,有利於擴大市場規模。
由於世界各國政府和學術機構透過資助和配合措施積極鼓勵基因研究和診斷,亞太地區在估計期間獲得了最大的市場佔有率。例如,印度的「印度基因組計畫」正試圖創建印度基因組的綜合圖譜。此外,中國和日本等國家正在啟動基因組學配合措施,以推進基因診斷和個人化醫療。此外,亞太地區正在成為基因研究、創新和臨床應用的焦點,這些計畫得到了大量多樣化人口的支持。
由於著名的研究機構、生物技術公司和醫療設施位於該地區,支持細胞遺傳學的創新和研究,預計北美在預測期內將出現有益的成長。此外,強大的醫療保健系統和積極的政府政策促進了細胞遺傳學檢測融入臨床實踐,促進個人化醫療和精準醫療。此外,由於北美在細胞遺傳學方面的領先地位和強大的法規環境,該地區處於基因診斷和研究的前沿,推動了市場的成長和進步。
According to Stratistics MRC, the Global Cytogenetics Market is accounted for $2.7 billion in 2023 and is expected to reach $6.1 billion by 2030 growing at a CAGR of 11.8% during the forecast period. The study of chromosomes, genes, and their structural and numerical variations within an organism's genetic makeup falls under the broad category of cytogenetics, which includes a wide range of methods, instruments, and services. It helps in locating genetic anomalies, detecting genetic disorders, and comprehending the genetic underpinnings of diseases like cancer, this field is crucial. Its applications are in clinical diagnostics, research, and personalized medicine.
According to WHO, in the year 2018 around 18.1 million new cases were diagnosed and 9.6 million individuals died out of cancer.
Numerous reasons have contributed to the rise in cytogenetic demand. First of all, it is essential to comprehending cancer, birth deformities, and hereditary diseases. Moreover, genetic diagnosis and individualized treatment plans are becoming more and more important as precision medicine becomes more and more popular, cytogenetic testing is now more widely available, precise, and economical thanks to technological improvements. Furthermore, the demand for cytogenetics in clinical, research, and diagnostic applications keeps rising as a result of expanding understanding of the genetic contributions to health and illness as well as an aging population. Therefore, the expansion of research into the human genome and the genetics of diseases have increased demand.
Cytogenetic testing necessitates the use of specialized tools, consumables, and trained workers, all of which can be expensive. Patients are frequently charged for these costs, which restricts their ability to get genetic diagnostics and counseling. They can present financial difficulties for hospitals and research facilities. The creation and use of new cytogenetic technologies are also hampered by high costs. Hence, these aspects hinder the market growth.
Numerous molecular cytogenetics techniques are being employed more frequently for cancer diagnosis as the incidence of the disease rises. In addition, as more is understood about cancer at the chromosomal level, this is causing the cytogenetics revenue to expand, which is being fueled by the growth of cancer research. For instance, the development of the market is facilitated by the use of FISH and CGH procedures, which offer vital information on cancer-related genetic markers. FISH, chromosomal image analysis, flow sorting, and genomic in-situ hybridization (GISH), methods used for the creation of synthetic plant chromosomes, are employed in the creation of genetic, physical, molecular, and comparative maps. Moreover, the rising application field and advantages of molecular cytogenetics in crop improvement are therefore assisting the market's growth.
Unfavourable reimbursement practices have been detrimental to the cytogenetics industry. Healthcare providers are less likely to give cytogenetic testing and treatments as a result of inconsistent or insufficient payment, which restricts patient access. Moreover, in turn, this has an impact on the market by decreasing demand and the financial incentives for R&D. Additionally, it may result in disagreements over access to cutting-edge cytogenetic testing, preventing patients from receiving vital genetic diagnostics for diseases like cancer and genetic disorders. Therefore, it is significantly hindering market expansion.
The cytogenetics market was negatively impacted by the COVID-19 pandemic. Due to lockdowns and resource redistribution, it interfered with laboratory operations, causing delays in genetic testing and problems with patient access. Furthermore, economic uncertainty limited funding for research and testing projects, while supply chain interruptions hindered the accessibility of necessary testing supplies. Moreover, academic and clinical research operations were impeded, which resulted in clinical and scientific setbacks. Therefore, these factors significantly hampered the market growth.
The karyotyping segment is estimated to hold the largest share. It entails the visualization and examination of a person's whole chromosomal set, usually from a blood or tissue sample. Additionally, karyotyping aids in the detection of chromosomal structure and numerical anomalies, which aid in the diagnosis of cancer, genetic diseases, and prenatal testing. Moreover, more sophisticated techniques like spectral karyotyping and fluorescent in situ hybridization (FISH) offer higher resolution, traditional karyotyping procedures include staining and microscopic inspection of chromosomes. Therefore, with the invaluable insights into chromosomal abnormalities and genetic illnesses, karyotyping continues to be a cornerstone in clinical and research cytogenetics.
The personalized medicine segment is anticipated to have highest CAGR during the forecast period, due to a quickly expanding area that adapts medical care to a patient's genetic profile. Clinicians can find genetic differences that affect a person's response to medication, susceptibility to diseases, and general health by utilizing cytogenetic procedures such as chromosomal analysis and molecular testing. Additionally, this method allows for more exact diagnostic and treatment choices, improving therapeutic results and reducing negative effects. Moreover, with improvements in genomics and cytogenetic technology, personalized medicine is playing a crucial role in the identification of uncommon diseases, pharmacogenomics, and cancers, revolutionizing healthcare by offering patients personalized and targeted treatment plans based on their genetic profiles. Thus, helps in expanding the market size.
Asia Pacific commanded the largest market share during the extrapolated period owing to a number of initiatives, through funding and cooperative initiatives, governments and academic institutions from all around the region are actively encouraging genetic research and diagnostics. For instance, the "Genome India Project" in India attempts to produce an exhaustive map of the Indian genome. Moreover, nations like China and Japan have launched genomics efforts to advance genetic diagnoses and tailored medicine. Furthermore, the Asia-Pacific area is becoming a focus point for genetic studies, innovations, and clinical applications due to these programs, which are supported by a sizable and diversified population.
North America is expected to witness profitable growth over the projection period, owing to renowned research institutions, biotech firms, and medical facilities are located in the area, which supports cytogenetics innovation and study. Additionally, robust healthcare systems and proactive government policies have made it easier to incorporate cytogenetic testing into clinical practice, promoting personalized and precision medicine. Furthermore, the region is at the forefront of genetic diagnostics and research due to North America's leadership in cytogenetics and a strong regulatory environment, which promotes market growth and advancements.
Some of the key players in the Cytogenetics Market include: Thermo Fisher Scientific Inc., Sysmex Corporation, PerkinElmer, Inc., OPKO Health, Inc., Irvine Scientific, Abbott Laboratories, Agilent Technologies, Inc., Applied Spectrial Imaging, Inc. and Empire Genomics, LLC.
In September 2023, Abbott announced it has completed the acquisition of Bigfoot Biomedical, a leader in developing smart insulin management systems for people with diabetes.
In August 2023, Thermo Fisher Scientific Inc. the world leader in serving science, announced that it has completed the acquisition of CorEvitas, LLC ("CorEvitas"), a leading provider of regulatory-grade, real-world evidence for approved medical treatments and therapies, from Audax Private Equity ("Audax).
In August 2023, Thermo Fisher Scientific, the world leader in serving science, announced the commercial launch of the EXENT® Solution, after receiving IVDR certification*. The EXENT solution is a fully integrated and automated mass spectrometry system designed to transform diagnosis and assessment for patients with monoclonal gammopathies, including multiple myeloma.