H. Nishimura et al., Relationship between bronchial hyperresponsiveness and development of asthma in children with chronic cough, PEDIAT PULM, 31(6), 2001, pp. 412-418
To evaluate the relationship between bronchial hyperresponsiveness (BHR) an
d the development of asthma in children with chronic cough, we performed me
thacholine inhalation challenges and transcutaneous oxygen pressure (tcPO(2
)) measurements in 92 children with chronic cough aged from 1-13 years (55
boys and 37 girls; mean, 5.3 years) and followed them for greater than or e
qual to 10 years. Forty-four age-matched children with asthma (24 males and
20 females; mean, 6.5 years) and 44 age-matched children without cough or
asthma served as controls (18 males and 26 females; mean, 4.6 years). Conse
cutive doubling doses of methacholine were inhaled until a 10% decrease in
tcPO(2) from baseline was observed. The cumulative dose of methacholine at
the inflection point of the tcPO(2) record (Dmin-PO2) was considered to rep
resent hyperresponsiveness to inhaled methacholine.
After 10 years or more of follow-up, 60 of the 92 subjects with cough answe
red our questionnaire, and 27/60 had been diagnosed with asthma. There was
a statistical difference in Dmin-PO2 between the children who presented wit
h chronic cough originally and who developed asthma (asthma-developed group
) and those who did not develop asthma (asthma-free group). There was no di
fference in the value of Dmin-PO2 between the asthma-developed group and th
e asthma group, or between the asthma-free group and the age-matched contro
l group. Among the children with chronic cough, there was no difference in
Dmin-PO2 between girls and boys, either in the asthma-developed group or in
the asthma-group.
We conclude that 45% of the children with a chronic cough in early life dev
eloped asthma, and that BHR in children with chronic cough during the child
hood period is a strong risk factor for the development of asthma. (C) 2001
Wiley-Liss, Inc.