Accelerated epigenetic aging and myopenia in young adult cancer survivors

被引:11
作者
Gehle, Stephanie C. [1 ]
Kleissler, Daniel [2 ]
Heiling, Hillary [3 ]
Deal, Allison [2 ]
Xu, Zongli [4 ]
Ayer Miller, Vanessa L. [5 ]
Taylor, Jack A. [4 ]
Smitherman, Andrew B. [1 ,2 ,6 ]
机构
[1] Univ North Carolina Chapel Hill, UNC Sch Med, Dept Pediat, Chapel Hill, NC USA
[2] Univ North Carolina Chapel Hill, Lineberger Comprehens Canc Ctr, Chapel Hill, NC USA
[3] Univ North Carolina Chapel Hill, Gillings Sch Global Publ Hlth, Dept Biostat, Chapel Hill, NC USA
[4] Natl Inst Environm Hlth Sci, Epidemiol Branch, Durham, NC USA
[5] Campbell Univ, Coll Pharm & Hlth Sci, Buies Creek, NC USA
[6] Campus Box 7236,170 Manning Dr,1185A Phys Off Bldg, Chapel Hill, NC 27599 USA
关键词
aging; cancer survivorship; DNA methylation; epigenetic age; BIAS CORRECTION METHOD; SKELETAL-MUSCLE MASS; CHILDHOOD-CANCER; DNA METHYLATION; OLDER-ADULTS; AGE; FRAILTY; HEALTH; SENESCENCE; SARCOPENIA;
D O I
10.1002/cam4.5908
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Young adult cancer survivors experience early aging-related morbidities and mortality. Biological aging biomarkers may identify at-risk survivors and increase our understanding of mechanisms underlying this accelerated aging.Methods: Using an observational study design, we cross-sectionally measured DNA methylation-based epigenetic age in young adult cancer survivors at a tertiary, academic state cancer hospital. Participants were a convenience sample of consecutively enrolled survivors of childhood, adolescent, and young adult cancers treated with either an anthracycline or alkylating agent, and who were at least 3 months post-treatment. Similarly aged healthy comparators were consecutively enrolled. Cancer treatment and treatment intensity were compared to DNA methylation-based epigenetic age and pace of aging.Results: Sixty survivors (58 completing assessments, mean age 20.5 years, range 18-29) and 27 comparators (mean age 20 years, range 17-29) underwent DNA methylation measurement. Survivors were predominantly female (62%) and white (60%) and averaged nearly 6 years post-treatment (range 0.2-25 years). Both epigenetic age (AgeAccelGrim: 1.5 vs. -2.4, p < 0.0001; AgeAccelPheno 2.3 vs. -3.8, p = 0.0013) and pace of aging (DunedinPACE 0.99 vs. 0.83, p < 0.0001) were greater in survivors versus comparators. In case-case adjusted analysis, compared to survivors with normal muscle mass, myopenic survivors had higher AgeAccelGrim (2.2 years, 95% CI 0.02-4.33, p = 0.02), AgeAccelPheno (6.2 years, 2.36-10.09, p < 0.001), and DunedinPACE (0.11, 0.05-0.17, p < 0.001).Conclusions: Epigenetic age is older and pace of aging is faster in young adult cancer survivors compared to noncancer peers, which is evident in the early post-therapy period. Survivors with physiological impairment demonstrate greater epigenetic age advancement. Measures of epigenetic age may identify young adult survivors at higher risk for poor functional and health outcomes.
引用
收藏
页码:12149 / 12160
页数:12
相关论文
共 55 条
[1]   Breast Carcinomas Arising at a Young Age: Unique Biology or a Surrogate for Aggressive Intrinsic Subtypes? [J].
Anders, Carey K. ;
Fan, Cheng ;
Parker, Joel S. ;
Carey, Lisa A. ;
Blackwell, Kimberly L. ;
Klauber-DeMore, Nancy ;
Perou, Charles M. .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (01) :E18-E20
[2]   Noncancer mortality among adolescents and young adults with cancer [J].
Anderson, Chelsea ;
Lund, Jennifer L. ;
Weaver, Mark A. ;
Wood, William A. ;
Olshan, Andrew F. ;
Nichols, Hazel B. .
CANCER, 2019, 125 (12) :2107-2114
[3]   Conditional relative survival among long-term survivors of adolescent and young adult cancers [J].
Anderson, Chelsea ;
Smitherman, Andrew B. ;
Nichols, Hazel B. .
CANCER, 2018, 124 (14) :3037-3043
[4]  
[Anonymous], CANC TREATM SURV FAC
[5]   Cause-specific mortality in survivors of adolescent and young adult cancer [J].
Armenian, Saro H. ;
Xu, Lanfang ;
Cannavale, Kimberly L. ;
Wong, F. Lennie ;
Bhatia, Smita ;
Chao, Chun .
CANCER, 2020, 126 (10) :2305-2316
[6]   Premature Aging in Young Cancer Survivors [J].
Armenian, Saro H. ;
Gibson, Christopher J. ;
Rockne, Russell C. ;
Ness, Kirsten K. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2019, 111 (03) :226-232
[7]   Aging and Risk of Severe, Disabling, Life-Threatening, and Fatal Events in the Childhood Cancer Survivor Study [J].
Armstrong, Gregory T. ;
Kawashima, Toana ;
Leisenring, Wendy ;
Stratton, Kayla ;
Stovall, Marilyn ;
Hudson, Melissa M. ;
Sklar, Charles A. ;
Robison, Leslie L. ;
Oeffinger, Kevin C. .
JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (12) :1218-+
[8]   Late Mortality Among 5-Year Survivors of Childhood Cancer: A Summary From the Childhood Cancer Survivor Study [J].
Armstrong, Gregory T. ;
Liu, Qi ;
Yasui, Yutaka ;
Neglia, Joseph P. ;
Leisenring, Wendy ;
Robison, Leslie L. ;
Mertens, Ann C. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (14) :2328-2338
[9]   DNA methylation aging clocks: challenges and recommendations [J].
Bell, Christopher G. ;
Lowe, Robert ;
Adams, Peter D. ;
Baccarelli, Andrea A. ;
Beck, Stephan ;
Bell, Jordana T. ;
Christensen, Brock C. ;
Gladyshev, Vadim N. ;
Heijmans, Bastiaan T. ;
Horvath, Steve ;
Ideker, Trey ;
Issa, Jean-Pierre J. ;
Kelsey, Karl T. ;
Marioni, Riccardo E. ;
Reik, Wolf ;
Relton, Caroline L. ;
Schalkwyk, Leonard C. ;
Teschendorff, Andrew E. ;
Wagner, Wolfgang ;
Zhang, Kang ;
Rakyan, Vardhman K. .
GENOME BIOLOGY, 2019, 20 (01)
[10]  
Belsky DW, 2022, ELIFE, V11, DOI [10.7554/eLife.73420, 10.7554/eLife.73420.sa0, 10.7554/eLife.73420.sa1, 10.7554/eLife.73420.sa2]