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市場調査レポート
商品コード
1702365
遺伝子検査の世界市場:2025年~2033年Global Genetic Testing Market - 2025-2033 |
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カスタマイズ可能
適宜更新あり
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遺伝子検査の世界市場:2025年~2033年 |
出版日: 2025年04月10日
発行: DataM Intelligence
ページ情報: 英文 176 Pages
納期: 即日から翌営業日
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世界の遺伝子検査の市場規模は、2024年に147億2,000万米ドルに達し、2033年には542億1,000万米ドルに達すると予測され、2025年~2033年の予測期間中のCAGRは15.4%と見込まれています。
世界の遺伝子検査市場とは、遺伝的状態、遺伝性疾患、将来の健康状態のリスクを特定するためにDNA、RNA、またはタンパク質を分析する診断検査の使用を指します。この市場には、保因者検査、診断検査、予測検査、出生前検査、薬理ゲノミクスなど、さまざまな種類の遺伝子検査が含まれます。これらの検査は、疾患の診断、遺伝的素因の理解、個別化治療戦略の実現に役立ちます。
遺伝子検査は、ヘルスケアを個人の遺伝子プロファイルに合わせて調整し、個別化された治療戦略を可能にします。遺伝子検査は早期診断に役立ち、最適な治療法を特定し副作用を回避することで患者の転帰を改善します。
遺伝性疾患と慢性疾患の有病率の上昇は、遺伝子検査市場の成長を大きく促進すると予想されます。嚢胞性線維症、鎌状赤血球貧血、ハンチントン病などの遺伝性疾患の罹患率が上昇を続ける中、遺伝子検査の需要も伸びています。例えば、嚢胞性線維症財団によると、毎年約1,000例のCFが新たに診断されています。このように毎年増加していることから、早期に診断するための高度な検査方法の需要が高まっています。
遺伝子検査による早期発見は、ヘルスケアプロバイダーが個別化された治療計画を提供するのに役立ち、長期的には転帰を改善し、医療費を削減できる可能性があります。さらに、がん、糖尿病、心血管疾患などの慢性疾患の有病率が上昇していることも、遺伝子検査の必要性をさらに高めています。
慢性疾患を患っている多くの人々が、病気を正確に診断するために遺伝子検査を処方されているか、遺伝子検査に関心を示しています。例えば、2022年のシカゴ大学NORCによると、アメリカ人の17%が実際に遺伝子検査を受けたことがあり、52%がそのような検査に関心があると回答しています。したがって、上記の要因が市場の成長を促進すると予想されます。
遺伝子検査とシーケンシング技術のコストが高いことは、遺伝子検査市場の成長にとって大きな障壁になると予想されます。遺伝子検査の進歩にもかかわらず、次世代シーケンシング(NGS)などのシーケンシング技術に関連する費用は依然として比較的高く、これらの検査を集団の大部分にとって手の届かないものにしています。
この高額な費用は、特に先進国市場と新興国市場の両方において、十分なサービスを受けていない人々の遺伝子検査へのアクセスを制限する可能性があります。例えば、多くの個人は、疾病リスク評価、出生前スクリーニング、個別化医療のための検査を受ける余裕がない可能性があり、これにより、健康転帰を大幅に改善できる早期診断や個別化治療計画が妨げられる可能性があります。
その結果、遺伝子検査やシークエンシング技術の高コストが、アクセシビリティを制限し需要を減少させることで、市場の成長を阻害する可能性が高いです。したがって、上記の要因が世界の遺伝子検査市場の潜在的成長を制限している可能性があります。
当レポートでは、世界の遺伝子検査市場について調査し、市場の概要とともに、製品タイプ別、技術別、検査タイプ別、用途別、地域別動向、競合情勢、および市場に参入する企業のプロファイルなどを提供しています。
The global genetic testing market reached US$ 14.72 billion in 2024 and is expected to reach US$ 54.21 billion by 2033, growing at a CAGR of 15.4 % during the forecast period of 2025-2033.
The global genetic testing market refers to the use of diagnostic tests that analyze DNA, RNA, or proteins to identify genetic conditions, hereditary diseases, and the risk of future health conditions. This market includes various types of genetic tests, such as carrier testing, diagnostic testing, predictive testing, prenatal testing, and pharmacogenomics. These tests help in diagnosing diseases, understanding genetic predispositions, and enabling personalized treatment strategies.
Genetic testing allows for personalized treatment strategies, tailoring healthcare to individual genetic profiles. It aids in early diagnosis, improving patient outcomes by identifying the best treatment options and avoiding adverse drug reactions.
Market Dynamics: Drivers & Restraints
Increasing Prevalence of Genetic Disorders and Chronic Diseases
The increasing prevalence of genetic disorders and chronic diseases is expected to significantly drive the growth of the genetic testing market. As the incidence of genetic conditions like cystic fibrosis, sickle cell anemia, and Huntington's disease continues to rise, the demand for genetic testing is also growing. For instance, according to the Cystic Fibrosis Foundation, approximately 1,000 new cases of CF are diagnosed each year. This increase in the number every year increases the demand for advanced testing procedures to diagnose the condition at an early stage.
Early detection through genetic testing can help healthcare providers offer personalized treatment plans, potentially improving outcomes and reducing healthcare costs in the long run. In addition, the rising prevalence of chronic diseases such as cancer, diabetes, and cardiovascular conditions is increasing the need for genetic testing even more.
A large number of individuals suffering from chronic diseases are prescribed or are showing interest in genetic testing to diagnose the disease accurately. For instance, according to the NORC at the University of Chicago in 2022, it is stated that 17 percent of Americans have actually undergone genetic testing, and 52 percent report interest in such a test. Thus, the above factors are expected to drive the market growth.
High Cost of Genetic Tests and Sequencing Technologies
The high cost of genetic tests and sequencing technologies is expected to be a significant barrier to the growth of the genetic testing market. Despite advancements in genetic testing, the expenses associated with sequencing technologies, such as next-generation sequencing (NGS), remain relatively high, making these tests unaffordable for a large portion of the population.
This high cost can limit access to genetic testing, particularly for underserved populations in both developed and emerging markets. For example, many individuals may be unable to afford tests for disease risk assessment, prenatal screening, or personalized medicine, which could prevent early diagnosis or personalized treatment plans that could significantly improve health outcomes.
As a result, the high cost of genetic tests and sequencing technologies is likely to hinder the market's growth by limiting accessibility and reducing demand. Thus, the above factors could be limiting the global genetic testing market's potential growth.
The global genetic testing market is segmented based on product type, technology, testing type, application, and region.
The next-generation sequencing (NGS) segment in technology is expected to dominate the global genetic testing market with the highest market share
Next-Generation Sequencing (NGS) is a transformative technology in the genetic testing market, enabling the rapid and cost-effective sequencing of DNA and RNA. It is widely used in various applications, including clinical diagnostics, oncology, precision medicine, biomarker discovery, and agriculture. The global NGS market is experiencing strong growth, driven by advancements in sequencing technology, decreasing costs, and increasing demand for personalized medicine and genetic research.
For instance, in February 2025, Devyser launched Devyser Thalassemia v2, a next-generation sequencing (NGS) solution aimed at improving the accuracy and efficiency of genetic testing for alpha and beta thalassemia. This new version enhances the detection of structural variants and copy number variations (CNVs), providing broader and more precise screening capabilities. This innovation aligns with the growing demand for high-accuracy genetic diagnostics, particularly in the expanding NGS segment in the market.
North America is expected to hold a significant position in the global genetic testing market, with the highest market share
North America is expected to dominate the genetic testing market due to various significant factors. The growing prevalence of chronic diseases, and genetic disorders in North America fuels the demand for genetic testing. As more individuals are diagnosed with conditions such as diabetes, cancer, and hereditary diseases, there is a growing demand for genetic testing to help in early diagnosis, risk assessment, and personalized treatment planning.
For instance, according to the report by the American Cancer Society in 2025, it is stated that approximately 1 in 8 women in the United States are diagnosed with breast cancer. Being one of the common cancers among women, the need for genetic testing is expected to increase, which is expected to drive the genetic testing market. Genetic testing detects inherited genetic mutations for various cancers.
Companies in the region are mainly focusing on developing advanced solutions for the diagnosis of genetic diseases to help in identifying the mutations in the genes and help in developing personalized medicine. For instance, in March 2024, Nucleus Genomics, a next-generation genetic testing and analysis company, launched its DNA analysis product aimed at making the benefits of personalized medicine accessible to everyone. This product is designed to empower individuals with the knowledge of their genetic makeup, helping them make informed decisions about their health.
Moreover, North America has one of the highest adoption rates of personalized medicine, where genetic tests play a crucial role in tailoring treatments to individual patients based on their genetic makeup. Thus, various factors are contributing to the region's dominant position in the global genetic testing market.
The major global players in the genetic testing market include Abbott Laboratories, Bio-Rad Laboratories Inc., Illumina Inc., Myriad Genetics Inc., Danaher Corporation, Quest Diagnostics Incorporated, MedGenome, LabCorp, 3billion, Inc., and Blueprint Genetics, among others.
The global genetic testing market report delivers a detailed analysis with 70 key tables, more than 68 visually impactful figures, and 176 pages of expert insights, providing a complete view of the market landscape.
Target Audience 2024
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