Shorter leukocyte telomere length is associated with higher risk of infections: a prospective study of 75,309 individuals from the general population

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Shorter leukocyte telomere length is associated with higher risk of infections : a prospective study of 75,309 individuals from the general population. / Helby, Jens; Nordestgaard, Børge G; Benfield, Thomas; Bojesen, Stig E.

In: Haematologica, Vol. 102, No. 8, 08.2017, p. 1457-1465.

Research output: Contribution to journalJournal articlepeer-review

Harvard

Helby, J, Nordestgaard, BG, Benfield, T & Bojesen, SE 2017, 'Shorter leukocyte telomere length is associated with higher risk of infections: a prospective study of 75,309 individuals from the general population', Haematologica, vol. 102, no. 8, pp. 1457-1465. https://doi.org/10.3324/haematol.2016.161943

APA

Helby, J., Nordestgaard, B. G., Benfield, T., & Bojesen, S. E. (2017). Shorter leukocyte telomere length is associated with higher risk of infections: a prospective study of 75,309 individuals from the general population. Haematologica, 102(8), 1457-1465. https://doi.org/10.3324/haematol.2016.161943

Vancouver

Helby J, Nordestgaard BG, Benfield T, Bojesen SE. Shorter leukocyte telomere length is associated with higher risk of infections: a prospective study of 75,309 individuals from the general population. Haematologica. 2017 Aug;102(8):1457-1465. https://doi.org/10.3324/haematol.2016.161943

Author

Helby, Jens ; Nordestgaard, Børge G ; Benfield, Thomas ; Bojesen, Stig E. / Shorter leukocyte telomere length is associated with higher risk of infections : a prospective study of 75,309 individuals from the general population. In: Haematologica. 2017 ; Vol. 102, No. 8. pp. 1457-1465.

Bibtex

@article{393c52a0f46344e48d6856fd69bb38cd,
title = "Shorter leukocyte telomere length is associated with higher risk of infections: a prospective study of 75,309 individuals from the general population",
abstract = "In the general population, older age is associated with short leukocyte telomere length and with high risk of infections. In a recent study of allogeneic hematopoietic cell transplantation for severe aplastic anemia, long donor leukocyte telomere length was associated with improved survival in the recipients. These findings suggest that leukocyte telomere length could possibly be a marker of immune competence. Therefore, we tested the hypothesis that shorter leukocyte telomere length is associated with higher risk of infectious disease hospitalization and infection-related death. Relative peripheral blood leukocyte telomere length was measured using quantitative polymerase chain reaction in 75,309 individuals from the general population and the individuals were followed for up to 23 years. During follow up, 9228 individuals were hospitalized with infections and infection-related death occurred in 1508 individuals. Shorter telomere length was associated with higher risk of any infection (hazard ratio 1.05 per standard deviation shorter leukocyte telomere length; 95% confidence interval 1.03-1.07) and pneumonia (1.07; 1.03-1.10) after adjustment for conventional infectious disease risk factors. Corresponding hazard ratios for infection-related death were 1.10 (1.04-1.16) for any infection and 1.11 (1.04-1.19) for pneumonia. Telomere length was not associated with risk of skin infection, urinary tract infection, sepsis, diarrheal disease, endocarditis, meningitis or other infections. In conclusion, our findings indicate that leukocyte telomere length may be a marker of immune competence. Further studies are needed to determine whether risk of infections in allogeneic hematopoietic cell transplantation recipients can be reduced by considering donor leukocyte telomere length when selecting donors.",
author = "Jens Helby and Nordestgaard, {B{\o}rge G} and Thomas Benfield and Bojesen, {Stig E}",
note = "Copyright{\textcopyright} 2017 Ferrata Storti Foundation.",
year = "2017",
month = aug,
doi = "10.3324/haematol.2016.161943",
language = "English",
volume = "102",
pages = "1457--1465",
journal = "Haematologica",
issn = "0390-6078",
publisher = "Ferrata Storti Foundation",
number = "8",

}

RIS

TY - JOUR

T1 - Shorter leukocyte telomere length is associated with higher risk of infections

T2 - a prospective study of 75,309 individuals from the general population

AU - Helby, Jens

AU - Nordestgaard, Børge G

AU - Benfield, Thomas

AU - Bojesen, Stig E

N1 - Copyright© 2017 Ferrata Storti Foundation.

PY - 2017/8

Y1 - 2017/8

N2 - In the general population, older age is associated with short leukocyte telomere length and with high risk of infections. In a recent study of allogeneic hematopoietic cell transplantation for severe aplastic anemia, long donor leukocyte telomere length was associated with improved survival in the recipients. These findings suggest that leukocyte telomere length could possibly be a marker of immune competence. Therefore, we tested the hypothesis that shorter leukocyte telomere length is associated with higher risk of infectious disease hospitalization and infection-related death. Relative peripheral blood leukocyte telomere length was measured using quantitative polymerase chain reaction in 75,309 individuals from the general population and the individuals were followed for up to 23 years. During follow up, 9228 individuals were hospitalized with infections and infection-related death occurred in 1508 individuals. Shorter telomere length was associated with higher risk of any infection (hazard ratio 1.05 per standard deviation shorter leukocyte telomere length; 95% confidence interval 1.03-1.07) and pneumonia (1.07; 1.03-1.10) after adjustment for conventional infectious disease risk factors. Corresponding hazard ratios for infection-related death were 1.10 (1.04-1.16) for any infection and 1.11 (1.04-1.19) for pneumonia. Telomere length was not associated with risk of skin infection, urinary tract infection, sepsis, diarrheal disease, endocarditis, meningitis or other infections. In conclusion, our findings indicate that leukocyte telomere length may be a marker of immune competence. Further studies are needed to determine whether risk of infections in allogeneic hematopoietic cell transplantation recipients can be reduced by considering donor leukocyte telomere length when selecting donors.

AB - In the general population, older age is associated with short leukocyte telomere length and with high risk of infections. In a recent study of allogeneic hematopoietic cell transplantation for severe aplastic anemia, long donor leukocyte telomere length was associated with improved survival in the recipients. These findings suggest that leukocyte telomere length could possibly be a marker of immune competence. Therefore, we tested the hypothesis that shorter leukocyte telomere length is associated with higher risk of infectious disease hospitalization and infection-related death. Relative peripheral blood leukocyte telomere length was measured using quantitative polymerase chain reaction in 75,309 individuals from the general population and the individuals were followed for up to 23 years. During follow up, 9228 individuals were hospitalized with infections and infection-related death occurred in 1508 individuals. Shorter telomere length was associated with higher risk of any infection (hazard ratio 1.05 per standard deviation shorter leukocyte telomere length; 95% confidence interval 1.03-1.07) and pneumonia (1.07; 1.03-1.10) after adjustment for conventional infectious disease risk factors. Corresponding hazard ratios for infection-related death were 1.10 (1.04-1.16) for any infection and 1.11 (1.04-1.19) for pneumonia. Telomere length was not associated with risk of skin infection, urinary tract infection, sepsis, diarrheal disease, endocarditis, meningitis or other infections. In conclusion, our findings indicate that leukocyte telomere length may be a marker of immune competence. Further studies are needed to determine whether risk of infections in allogeneic hematopoietic cell transplantation recipients can be reduced by considering donor leukocyte telomere length when selecting donors.

U2 - 10.3324/haematol.2016.161943

DO - 10.3324/haematol.2016.161943

M3 - Journal article

C2 - 28522577

VL - 102

SP - 1457

EP - 1465

JO - Haematologica

JF - Haematologica

SN - 0390-6078

IS - 8

ER -

ID: 193665227