TY - JOUR
T1 - Influence of the factor V Leiden mutation on infectious disease susceptibility and outcome
T2 - A population-based study
AU - Benfield, Thomas L.
AU - Dahl, Mortens
AU - Nordestgaard, Børge G.
AU - Tybjærg-Hansen, Anne
PY - 2005/11/15
Y1 - 2005/11/15
N2 - Background. The effect of the coagulation factor V Leiden mutation on infectious disease susceptibility and outcome is controversial. Methods. We genotyped 9253 individuals from the Copenhagen City Heart Study for the factor V Leiden mutation. The risk of hospitalization for any infectious disease during a follow-up period of 7.2 years and subsequent risk of disease progression to death were estimated by Cox proportional-hazards regression analysis. Results. During 66,789 person-years of follow-up, 1093 persons were hospitalized because of infection. The risk of urinary-tract infection was decreased in factor V Leiden heterozygotes, compared with that in noncarriers (adjusted relative risk [aRR], 0.55 [95% confidence interval {CI}, 0.31-0.99]), whereas the risk of skin infection was increased (aRR, 1.68 [95% CI, 1.07-2.66]). No associations between carrier status and risk of diarrheal disease, other viral infections, parasitic infections, pneumonia, sepsis, or upper respiratory-tract infection were detected. However, in subjects hospitalized for sepsis, factor V Leiden carriers were at an increased risk of mortality 28 days after admission, compared with noncarriers (aRR, 4.41; 95% CI, 1.42-13.67]). Conclusion. In the Danish general population, the factor V Leiden mutation may be associated with infectious disease susceptibility and an increased risk of mortality from sepsis.
AB - Background. The effect of the coagulation factor V Leiden mutation on infectious disease susceptibility and outcome is controversial. Methods. We genotyped 9253 individuals from the Copenhagen City Heart Study for the factor V Leiden mutation. The risk of hospitalization for any infectious disease during a follow-up period of 7.2 years and subsequent risk of disease progression to death were estimated by Cox proportional-hazards regression analysis. Results. During 66,789 person-years of follow-up, 1093 persons were hospitalized because of infection. The risk of urinary-tract infection was decreased in factor V Leiden heterozygotes, compared with that in noncarriers (adjusted relative risk [aRR], 0.55 [95% confidence interval {CI}, 0.31-0.99]), whereas the risk of skin infection was increased (aRR, 1.68 [95% CI, 1.07-2.66]). No associations between carrier status and risk of diarrheal disease, other viral infections, parasitic infections, pneumonia, sepsis, or upper respiratory-tract infection were detected. However, in subjects hospitalized for sepsis, factor V Leiden carriers were at an increased risk of mortality 28 days after admission, compared with noncarriers (aRR, 4.41; 95% CI, 1.42-13.67]). Conclusion. In the Danish general population, the factor V Leiden mutation may be associated with infectious disease susceptibility and an increased risk of mortality from sepsis.
UR - https://www.scopus.com/pages/publications/27744590529
U2 - 10.1086/497167
DO - 10.1086/497167
M3 - Article
C2 - 16235188
AN - SCOPUS:27744590529
SN - 0022-1899
VL - 192
SP - 1851
EP - 1857
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 10
ER -