TY - JOUR
T1 - Human Rhinovirus and Wheezing
T2 - Short and Long-term Associations in Children
AU - van der Gugten, Anne C
AU - van der Zalm, Marieke M
AU - Uiterwaal, Cuno S P M
AU - Wilbrink, Berry
AU - Rossen, John W A
AU - van der Ent, Cornelis K
PY - 2013/8
Y1 - 2013/8
N2 - OBJECTIVES: Human rhinoviruses (HRVs) have been suggested to play a role in the development of childhood wheezing. However, whether HRV is causally related to the development of wheezing or HRV-associated wheeze is merely an indicator of disease susceptibility is unclear. Our aim was to study the role of HRV during infancy in the development of lower respiratory disease during infancy and childhood.METHODS: In a population-based birth cohort, during the 1st year of life, nose and throat swabs were collected on a monthly basis, regardless of any symptoms. Polymerase chain reaction was used to detect an extensive panel of respiratory pathogens. Lung function was measured before 2 months of age. Information on respiratory symptoms was collected by daily questionnaires and electronic patient files.RESULTS: 1425 samples were collected in 140 infants. Both the presence of (single or multiple) pathogens (HRV equal to other pathogens) and increased respiratory system resistance were significantly associated with lower respiratory symptoms during infancy. HRV presence during infancy was not associated with the risk of wheezing at age 4, but every HRV episode with wheezing increased the risk of wheezing at age 4 (odds ratio 1.9, 1.1-3.5). This association weakened after adjustment for lung function (odds ratio 1.4, 0.7-2.9).CONCLUSIONS: HRV and other viruses are associated with lower respiratory symptoms during infancy, as well as a high presymptomatic respiratory system resistance. HRV presence during infancy is not associated with childhood wheezing, but wheeze during a HRV episode is an indicator of children at high risk for childhood wheeze, partly because of a reduced neonatal lung function.
AB - OBJECTIVES: Human rhinoviruses (HRVs) have been suggested to play a role in the development of childhood wheezing. However, whether HRV is causally related to the development of wheezing or HRV-associated wheeze is merely an indicator of disease susceptibility is unclear. Our aim was to study the role of HRV during infancy in the development of lower respiratory disease during infancy and childhood.METHODS: In a population-based birth cohort, during the 1st year of life, nose and throat swabs were collected on a monthly basis, regardless of any symptoms. Polymerase chain reaction was used to detect an extensive panel of respiratory pathogens. Lung function was measured before 2 months of age. Information on respiratory symptoms was collected by daily questionnaires and electronic patient files.RESULTS: 1425 samples were collected in 140 infants. Both the presence of (single or multiple) pathogens (HRV equal to other pathogens) and increased respiratory system resistance were significantly associated with lower respiratory symptoms during infancy. HRV presence during infancy was not associated with the risk of wheezing at age 4, but every HRV episode with wheezing increased the risk of wheezing at age 4 (odds ratio 1.9, 1.1-3.5). This association weakened after adjustment for lung function (odds ratio 1.4, 0.7-2.9).CONCLUSIONS: HRV and other viruses are associated with lower respiratory symptoms during infancy, as well as a high presymptomatic respiratory system resistance. HRV presence during infancy is not associated with childhood wheezing, but wheeze during a HRV episode is an indicator of children at high risk for childhood wheeze, partly because of a reduced neonatal lung function.
KW - respiratory function tests
KW - respiratory viruses
KW - asthma
KW - wheezing
KW - RESPIRATORY-SYNCYTIAL-VIRUS
KW - REDUCED LUNG-FUNCTION
KW - REAL-TIME PCR
KW - VIRAL-INFECTIONS
KW - BIRTH-COHORT
KW - HUMAN METAPNEUMOVIRUS
KW - TRACT INFECTION
KW - YOUNG-CHILDREN
KW - EARLY-LIFE
KW - CHILDHOOD ASTHMA
U2 - 10.1097/INF.0b013e318290620e
DO - 10.1097/INF.0b013e318290620e
M3 - Article
C2 - 23584579
SN - 0891-3668
VL - 32
SP - 827
EP - 833
JO - Pediatric infectious disease journal
JF - Pediatric infectious disease journal
IS - 8
ER -