Increased DNA levels in bronchoalveolar lavage fluid obtained from infants with cystic fibrosis

被引:102
作者
Kirchner, KK [1 ]
Wagener, JS [1 ]
Khan, TZ [1 ]
Copenhaver, SC [1 ]
Accurso, FJ [1 ]
机构
[1] UNIV COLORADO,CHILDRENS HOSP,SCH MED,DEPT PEDIAT,DENVER,CO 80218
关键词
D O I
10.1164/ajrccm.154.5.8912759
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Airway inflammation in children younger than 5 yr of age is difficult to assess, particularly in patients with cystic fibrosis (CF). Furthermore, determining responses to therapies is often subjective in infants, especially those with CF. To determine whether airway DNA levels could be used as an index of airway inflammation, we measured DNA levels in bronchoalveolar lavage fluid (BALF), using a Hoechst dye-binding assay. BALF DNA levels and neutrophils from 16 infants with CF were compared with levels obtained from seven older CF patients and nine control children who underwent bronchoalveolar lavage for evaluation of other pulmonary diseases. BALF DNA was increased in both infants (3.2 +/- 0.7 mu g/ml) and older patients with CF (5.4 +/- 0.9 mu g/ml) compared with the controls (0.7 +/- 0.2 mu g/ml) (mean +/- SEM). BALF DNA levels were not significantly different between infants and older patients with CF. BALF neutrophil counts in CF patients were significantly higher than in controls, Furthermore, BALF DNA levels and total neutrophil counts in infants with CF correlated positively with one another. We conclude that: (1) DNA levels were easily quantifiable in BALF of young children; (2) DNA levels in BALF from CF patients were greater than in a group of children with other pulmonary diseases, and that in some infants with CF, BALF DNA levels were equivalent to those of much order patients with CF; (3) DNA levels in BALF correlate with BALF neutrophil number, an index of inflammation; and (4) some infants with CF have increased levels of DNA in BALF, which may justify a clinical trial of aerosolized rhDNase in this population.
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页码:1426 / 1429
页数:4
相关论文
共 16 条
[1]  
*AB CONC INC, 1988, STATSV V102
[2]   PROTEASE-ANTIPROTEASE IMBALANCE IN THE LUNGS OF CHILDREN WITH CYSTIC-FIBROSIS [J].
BIRRER, P ;
MCELVANEY, NG ;
RUDEBERG, A ;
SOMMER, CW ;
LIECHTIGALLATI, S ;
KRAEMER, R ;
HUBBARD, R ;
CRYSTAL, RG .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1994, 150 (01) :207-213
[3]  
BRASFIELD D, 1979, PEDIATRICS, V63, P24
[4]  
CANTIN A, 1995, AM J RESP CRIT CARE, V151, P939
[5]   MARKERS OF MUCUS SECRETION AND DNA LEVELS IN INDUCED SPUTUM FROM ASTHMATIC AND FROM HEALTHY-SUBJECTS [J].
FAHY, JV ;
STEIGER, DJ ;
LIU, J ;
BASBAUM, CB ;
FINKBEINER, WE ;
BOUSHEY, HA .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1993, 147 (05) :1132-1137
[6]   PATHOGENESIS OF THE PSEUDOMONAS LUNG LESION IN CYSTIC-FIBROSIS [J].
FICK, RB .
CHEST, 1989, 96 (01) :158-164
[7]   THE CHANGING EPIDEMIOLOGY OF CYSTIC-FIBROSIS [J].
FITZSIMMONS, SC .
JOURNAL OF PEDIATRICS, 1993, 122 (01) :1-9
[8]   EFFECT OF AEROSOLIZED RECOMBINANT HUMAN DNASE ON EXACERBATIONS OF RESPIRATORY SYMPTOMS AND ON PULMONARY-FUNCTION IN PATIENTS WITH CYSTIC-FIBROSIS [J].
FUCHS, HJ ;
BOROWITZ, DS ;
CHRISTIANSEN, DH ;
MORRIS, EM ;
NASH, ML ;
RAMSEY, BW ;
ROSENSTEIN, BJ ;
SMITH, AL ;
WOHL, ME .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (10) :637-642
[9]   EFFICACY OF STATEWIDE NEONATAL SCREENING FOR CYSTIC-FIBROSIS BY ASSAY OF TRYPSINOGEN CONCENTRATIONS [J].
HAMMOND, KB ;
ABMAN, SH ;
SOKOL, RJ ;
ACCURSO, FJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (11) :769-774
[10]  
KHAN TZ, 1995, AM J RESP CRIT CARE, V151, P1075