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Pre-transplant short telomeres are associated with high mortality risk after unrelated donor haematopoietic cell transplant for severe aplastic anaemia

  1. Author:
    Wang, Youjin [ORCID]
    McReynolds, Lisa J [ORCID]
    Dagnall,Casey
    Katki, Hormuzd A
    Spellman, Stephen R
    Wang, Tao
    Hicks,Belynda
    Freedman, Neal D
    Jones,Kristine
    Lee, Stephanie J
    Savage, Sharon A
    Gadalla, Shahinaz M [ORCID]
  2. Author Address

    Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA., Cancer Genomics Research Laboratory, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA., Leidos Biomedical Research, Inc. Frederick National Laboratory for Cancer Research, Frederick, MD, USA., Biostatistics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA., Center for International Blood and Marrow Transplant Research, Minneapolis, MN, USA., Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, WI, USA., Division of Biostatistics, Medical College of Wisconsin, Milwaukee, WI, USA., Metabolic Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA., Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.,
    1. Year: 2019
    2. Date: Aug 19
    3. Epub Date: 2019 08 19
  1. Journal: British journal of haematology
  2. Type of Article: Article
  3. ISSN: 0007-1048
  1. Abstract:

    Telomeres are essential for chromosomal stability and markers of biological age. We evaluated the effect of pre-transplant short (< 10th percentile-for-age) or very short (< 5th or < 1st percentile-for-age) leucocyte telomere length on survival after unrelated donor haematopoietic cell transplantation (HCT) for acquired severe aplastic anaemia (SAA). Patient pre-transplant blood samples and clinical data were available at the Center for International Blood and Marrow Transplant Research. We used quantitative real time polymerase chain reaction to measure relative telomere length (RTL) in 490 SAA patients who received HCT between 1990 and 2013 (median age = 20 years). One hundred and twelve patients (22·86%) had pre-HCT RTL < 10th percentile-for-age, with the majority below the 5th percentile (N = 80, 71·43%). RTL < 10th percentile-for-age was associated with a higher risk of post-HCT mortality (hazard ratio [HR] = 1·78, 95% confidence interval [CI]=1·18-2·69, P = 0·006) compared with RTL =50th percentile; no survival differences were noted in longer RTL categories (P > 0·10). Time-dependent effects for post-HCT mortality were only observed in relation to very short RTL; HR comparing RTL < 5th versus =5th percentile = 1·38, P = 0·15 for the first 12 months after HCT, and HR = 3·91, P < 0·0001, thereafter, P-heterogeneity = 0·008; the corresponding HRs for RTL < 1st versus =1st percentile = 1·29, P = 0·41, and HR = 5·18, P < 0·0001, P-heterogeneity = 0·005. The study suggests a potential role for telomere length in risk stratification of SAA patients in regard to their HCT survival. © 2019 British Society for Haematology and John Wiley & Sons Ltd.

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External Sources

  1. DOI: 10.1111/bjh.16153
  2. PMID: 31426123
  3. WOS: 000482317500001

Library Notes

  1. Fiscal Year: FY2018-2019
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