THE RELATIONSHIP BETWEEN ATOPY AND NONSPECIFIC BRONCHIAL RESPONSIVENESS

被引:26
作者
GRAINGER, DN [1 ]
STENTON, SC [1 ]
AVERY, AJ [1 ]
DUDDRIDGE, M [1 ]
WALTERS, EH [1 ]
HENDRICK, DJ [1 ]
机构
[1] UNIV NEWCASTLE UPON TYNE,NEWCASTLE GEN HOSP,CHEST UNIT,WESTGATE RD,NEWCASTLE TYNE NE4 6BE,ENGLAND
关键词
D O I
10.1111/j.1365-2222.1990.tb02665.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Atopy is often regarded as a risk factor for the development of asthma, particularly childhood asthma and occupational asthma. This could reflect an association with nonspecific bronchial responsiveness (NSBR), though atopy could influence asthma independently. We have evaluated the possible relationship between atopy and NSBR (PD20FEV1 to methacholine) in the siblings of 59 probands with atopic asthma. Thirty‐four (58%) were atopic ( 1 prick test with weal diameter that of a 0.1% histamine control) and 28 (47%) showed NSBR. Atopy and NSBR occurred together more frequently than would be expected by chance (P<0.05); both variables being observed in 20 subjects, neither in 17, and only one in 22. A significant association was also noted when atopy was defined by a serum total IgE > 150IU (or >50IU), but when atopy was defined by other commonly used criteria ( 2 prick tests with weal diameter histamine control; or weal diameter 2 mm or more > than a saline control), no significant association was demonstrated. Furthermore, linear logistic regression and multiple regression analyses showed that both the presence and the degree of NSBR were influenced much more by the baseline level of FEV1 than by atopic status. At best, atopy accounted for 10% of the variance of the PD20 measurements. We conclude that atopy is associated with NSBR but not strongly; that the relationship may be readily obscured according to the defining criteria used for atopy: and that atopy should not be used as a marker for NSBR. Copyright © 1990, Wiley Blackwell. All rights reserved
引用
收藏
页码:181 / 187
页数:7
相关论文
共 22 条
  • [1] ALVEY NG, 1983, GENSTAT 404 GENERAL
  • [2] DISTRIBUTION OF IGE IN A COMMUNITY POPULATION-SAMPLE - CORRELATIONS WITH AGE, SEX, AND ALLERGEN SKIN-TEST REACTIVITY
    BARBEE, RA
    HALONEN, M
    LEBOWITZ, M
    BURROWS, B
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1981, 68 (02) : 106 - 111
  • [3] BRYANT D H, 1975, Clinical Allergy, V5, P145, DOI 10.1111/j.1365-2222.1975.tb01847.x
  • [4] DESCRIPTIVE EPIDEMIOLOGY OF BRONCHIAL REACTIVITY IN AN ADULT-POPULATION - RESULTS FROM A COMMUNITY STUDY
    BURNEY, PGJ
    BRITTON, JR
    CHINN, S
    TATTERSFIELD, AE
    PAPACOSTA, AO
    KELSON, MC
    ANDERSON, F
    CORFIELD, DR
    [J]. THORAX, 1987, 42 (01) : 38 - 44
  • [5] CLINICAL-FEATURES AND NATURAL-HISTORY OF OCCUPATIONAL ASTHMA DUE TO WESTERN RED CEDAR (THUJA-PLICATA)
    CHANYEUNG, M
    LAM, S
    KOENER, S
    [J]. AMERICAN JOURNAL OF MEDICINE, 1982, 72 (03) : 411 - 415
  • [6] BRONCHIAL REACTIVITY TO INHALED HISTAMINE - METHOD AND CLINICAL SURVEY
    COCKCROFT, DW
    KILLIAN, DN
    MELLON, JJA
    HARGREAVE, FE
    [J]. CLINICAL ALLERGY, 1977, 7 (03): : 235 - 243
  • [7] COCKCROFT DW, 1984, ANN ALLERGY, V53, P26
  • [8] Connolly M J, 1988, Pulm Pharmacol, V1, P53, DOI 10.1016/0952-0600(88)90011-7
  • [9] ASSOCIATIONS BETWEEN ASTHMA HISTORY, ATOPY, AND NONSPECIFIC BRONCHIAL RESPONSIVENESS IN YOUNG-ADULTS
    COOKSON, WOCM
    MUSK, AW
    RYAN, G
    [J]. CLINICAL ALLERGY, 1986, 16 (05): : 425 - 432
  • [10] GART JJ, 1962, J ROY STAT SOC B, V24, P454