Connections Between Clonal Hematopoiesis, Cardiovascular Disease, and Cancer A Review

被引:55
作者
Calvillo-Arguelles, Oscar [1 ,2 ]
Jaiswal, Siddhartha [3 ]
Shlush, Liran I. [4 ]
Moslehi, Javid J. [5 ,6 ]
Schimmer, Aaron [7 ]
Barac, Ana [8 ]
Thavendiranathan, Paaladinesh [1 ]
机构
[1] Toronto Gen Hosp, Ted Rogers Program Cardiotox Prevent, Toronto, ON, Canada
[2] Inst Nacl Cancerol, Mexico City, DF, Mexico
[3] Stanford Univ, Dept Pathol, Sch Med, Stanford, CA 94305 USA
[4] Weizmann Inst Sci, Dept Immunol, Rehovot, Israel
[5] Vanderbilt Univ, Med Ctr, Div Cardiovasc Med, Cardiooncol Program, Nashville, TN USA
[6] Vanderbilt Ingram Canc Ctr, Nashville, TN USA
[7] Princess Margaret Canc Ctr, Toronto, ON, Canada
[8] Georgetown Univ, MedStar Heart & Vasc Inst, Washington, DC USA
基金
美国国家卫生研究院;
关键词
CHRONIC MYELOID-LEUKEMIA; TYROSINE KINASE INHIBITORS; SOMATIC MUTATIONS; HEART-FAILURE; DRIVER MUTATIONS; THERAPY; RISK; DNMT3A; TET2; BLOOD;
D O I
10.1001/jamacardio.2019.0302
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IMPORTANCE Clonal hematopoiesis (CH) has been recently described as a novel driver for cancer and cardiovascular disease (CVD). Clonal hematopoiesis is a common, age-associated disorder marked by expansion of hematopoietic clones carrying recurrent somatic mutations. Current literature suggests that patients with CH have a higher risk of subsequent hematological malignant conditions and mortality attributable to excess CVD. This review discusses the association of cancer with CVD with CH as a potential unifying factor. OBSERVATIONS The prevalence of CH varies based on the sequencing depth, diagnostic criteria, and patient age and ranges from less than 1% in those younger than 40 years to more than 15% to 20% in those 90 years and older. Clonal hematopoiesis is associated with a 0.5% to 1.0% absolute annual risk of hematological malignant condition and a 2-fold to 4-fold higher risk of coronary artery disease, stroke, and CVD deaths, independent of traditional cardiovascular risk factors. In fact, CH appears to have a relative risk similar to that of traditional cardiovascular risk factors for CVD. Experimental studies suggest that the link between CVD and CH is causal, with inflammation as 1 potential mechanism. There may be also a link between CH and CVD in survivors of cancer; however, data to support this association are currently limited. CONCLUSIONS AND RELEVANCE Clonal hematopoiesis represents a premalignant state, with carriers having an increased risk of hematological malignant conditions. Although most carriers will not develop a malignant condition, CH confers an increased risk of CVD, possibly via inflammation. Clonal hematopoiesis may also contribute to CVD in survivors of cancer, although this hypothesis requires validation. Clinically, as advanced sequencing techniques become available, CH may pave the way for precision medicine in the field of cardio-oncology.
引用
收藏
页码:380 / 387
页数:8
相关论文
共 67 条
[1]   A Population-Based Study of Cardiovascular Mortality Following Early-Stage Breast Cancer [J].
Abdel-Qadir, Husam ;
Austin, Peter C. ;
Lee, Douglas S. ;
Amir, Eitan ;
Tu, Jack V. ;
Thavendiranathan, Paaladinesh ;
Fung, Kinwah ;
Anderson, Geoffrey M. .
JAMA CARDIOLOGY, 2017, 2 (01) :88-93
[2]   Prediction of acute myeloid leukaemia risk in healthy individuals [J].
Abelson, Sagi ;
Collord, Grace ;
Ng, Stanley W. K. ;
Weissbrod, Omer ;
Cohen, Netta Mendelson ;
Niemeyer, Elisabeth ;
Barda, Noam ;
Zuzarte, Philip C. ;
Heisler, Lawrence ;
Sundaravadanam, Yogi ;
Luben, Robert ;
Hayat, Shabina ;
Wang, Ting Ting ;
Zhao, Zhen ;
Cirlan, Julia ;
Pugh, Trevor J. ;
Soave, David ;
Ng, Karen ;
Latimer, Calli ;
Hardy, Claire ;
Raine, Keiran ;
Jones, David ;
Hoult, Diana ;
Britten, Abigail ;
McPherson, John D. ;
Johansson, Mattias ;
Mbabaali, Faridah ;
Eagles, Jenna ;
Millers, Jessica K. ;
Pasternack, Danielle ;
Timms, Lee ;
Krzyzanowski, Paul ;
Awadalla, Philip ;
Costa, Rui ;
Segal, Eran ;
Bratman, Scott, V ;
Beer, Philip ;
Behjati, Sam ;
Martincorena, Inigo ;
Wang, Jean C. Y. ;
Bowles, Kristian M. ;
Ramon Quiros, J. ;
Karakatsani, Anna ;
La Vecchia, Carlo ;
Trichopoulou, Antonia ;
Salamanca-Fernandez, Elena ;
Huerta, Jose M. ;
Barricarte, Aurelio ;
Travis, Ruth C. ;
Tumino, Rosario .
NATURE, 2018, 559 (7714) :400-+
[3]   Ultra-sensitive Sequencing Identifies High Prevalence of Clonal Hematopoiesis-Associated Mutations throughout Adult Life [J].
Acuna-Hidalgo, Rocio ;
Sengul, Hilal ;
Steehouwer, Marloes ;
van de Vorst, Maartje ;
Vermeulen, Sita H. ;
Kiemeney, Lambertus A. L. M. ;
Veltman, Joris A. ;
Gilissen, Christian ;
Hoischen, Alexander .
AMERICAN JOURNAL OF HUMAN GENETICS, 2017, 101 (01) :50-64
[4]  
Aghel N, 2017, VASC HEALTH RISK MAN, V13, P293, DOI 10.2147/VHRM.S108874
[5]   Prevention and Monitoring of Cardiac Dysfunction in Survivors of Adult Cancers: American Society of Clinical Oncology Clinical Practice Guideline [J].
Armenian, Saro H. ;
Lacchetti, Christina ;
Barac, Ana ;
Carver, Joseph ;
Constine, Louis S. ;
Denduluri, Neelima ;
Dent, Susan ;
Douglas, Pamela S. ;
Durand, Jean-Bernard ;
Ewer, Michael ;
Fabian, Carol ;
Hudson, Melissa ;
Jessup, Mariell ;
Jones, Lee W. ;
Ky, Bonnie ;
Mayer, Erica L. ;
Moslehi, Javid ;
Oeffinger, Kevin ;
Ray, Katharine ;
Ruddy, Kathryn ;
Lenihan, Daniel .
JOURNAL OF CLINICAL ONCOLOGY, 2017, 35 (08) :893-U144
[6]   Managing Clonal Hematopoiesis in Patients With Solid Tumors [J].
Bolton, Kelly L. ;
Gillis, Nancy K. ;
Coombs, Catherine C. ;
Takahashi, Koichi ;
Zehir, Ahmet ;
Bejar, Rafael ;
Garcia-Manero, Guillermo ;
Futreal, Andrew ;
Jensen, Brian C. ;
Diaz, Luis A., Jr. ;
Gupta, Dipti ;
Mantha, Simon ;
Klimek, Virginia ;
Papaemmanuil, Elli ;
Levine, Ross ;
Padron, Eric .
JOURNAL OF CLINICAL ONCOLOGY, 2019, 37 (01) :7-+
[7]   Association between large detectable clonal mosaicism and type 2 diabetes with vascular complications [J].
Bonnefond, Amelie ;
Skrobek, Boris ;
Lobbens, Stephane ;
Eury, Elodie ;
Thuillier, Dorothee ;
Cauchi, Stephane ;
Lantieri, Olivier ;
Balkau, Beverley ;
Riboli, Elio ;
Marre, Michel ;
Charpentier, Guillaume ;
Yengo, Loic ;
Froguel, Philippe .
NATURE GENETICS, 2013, 45 (09) :1040-+
[8]   DNMT3A and TET2 dominate clonal hematopoiesis and demonstrate benign phenotypes and different genetic predispositions [J].
Buscarlet, Manuel ;
Provost, Sylvie ;
Zada, Yassamin Feroz ;
Barhdadi, Amina ;
Bourgoin, Vincent ;
Lepine, Guylaine ;
Mollica, Luigina ;
Szuber, Natasha ;
Dube, Marie-Pierre ;
Busque, Lambert .
BLOOD, 2017, 130 (06) :753-762
[9]   Therapy-Related Clonal Hematopoiesis in Patients with Non-hematologic Cancers Is Common and Associated with Adverse Clinical Outcomes [J].
Coombs, Catherine C. ;
Zehir, Ahmet ;
Devlin, Sean M. ;
Kishtagari, Ashwin ;
Syed, Aijazuddin ;
Jonsson, Philip ;
Hyman, David M. ;
Solit, David B. ;
Robson, Mark E. ;
Baselga, Jose ;
Arcila, Maria E. ;
Ladanyi, Marc ;
Tallman, Martin S. ;
Levine, Ross L. ;
Berger, Michael F. .
CELL STEM CELL, 2017, 21 (03) :374-+
[10]   Somatic mutations precede myeloid leukemia years before diagnosis [J].
Desai, Pinkal ;
Mencia-Trinchant, Nuria ;
Savenkov, Oleksandr ;
Simon, Michael S. ;
Cheang, Gloria ;
Lee, Sangmin ;
Samuel, Michael ;
Ritchie, Ellen K. ;
Guzman, Monica L. ;
Ballman, Karla V. ;
Roboz, Gail J. ;
Hassane, Duane C. .
NATURE MEDICINE, 2018, 24 (07) :1015-+