Patterns and significance of exhaled-breath biomarkers in lung transplant recipients with acute allograft rejection

被引:103
作者
Studer, SM
Orens, JB
Rosas, I
Krishnan, JA
Cope, KA
Yang, S
Conte, JV
Becker, PB
Risby, TH
机构
[1] Johns Hopkins Med Inst, Dept Med, Div Pulm & Crit Care Med, Baltimore, MD 21205 USA
[2] Johns Hopkins Med Inst, Dept Surg, Baltimore, MD 21205 USA
[3] Johns Hopkins Med Inst, Dept Environm Hlth Sci, Baltimore, MD 21205 USA
[4] NHLBI, Bethesda, MD 20892 USA
关键词
D O I
10.1016/S1053-2498(01)00343-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Obliterative bronchiolitis (OB) remains one of the leading causes of death in lung transplant recipients after 2 years, and acute rejection (AR) of lung allograft is a major risk factor for OB. Treatment of AR may reduce the incidence of OB, although diagnosis of AR often requires bronchoscopic lung biopsy. In this study, we evaluated the utility of exhaled-breath biomarkers for the non-invasive diagnosis of AR. Methods: We obtained breath samples from 44 consecutive lung transplant recipients who attended ambulatory follow-up visits for the Johns Hopkins Lung Transplant Program. Bronchoscopy within 7 days of their breath samples showed histopathology in 21of these patients, and we included them in our analysis. We measured hydrocarbon markers of pro-oxidant events (ethane and 1-pentane), isoprene, acetone, and sulfur-containing compounds (hydrogen sulfide and carbonyl sulfide) in exhaled breath and compared their levels to the lung histopathology, graded as stable (non-rejection) or AR. None of the study subjects were diagnosed with OB or infection at the time of the clinical bronchoscopy. Results: We found no significant difference in exhaled levels of hydrocarbons, acetone, or hydrogen sulfide between the stable and AR groups. However, we did find significant increase in exhaled carbonyl sulfide (COS) levels in AR subjects compared with stable subjects. We also observed a trend in 7 of 8 patients who had serial sets of breath and histopathology data that supported a role for COS as a breath biomarker of AR. Conclusions: This study demonstrated elevations in exhaled COS levels in subjects with AR compared with stable subjects, suggesting a diagnostic role for this non-invasive Z biomarker. Further exploration of breath analysis in lung transplant recipients is warranted to complement fiberoptic bronchoscopy and obviate the need for this procedure in some patients.
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页码:1158 / 1166
页数:9
相关论文
共 28 条
[1]   Ethane: A marker of lipid peroxidation during cardiopulmonary bypass in humans [J].
Andreoni, KA ;
Kazui, M ;
Cameron, DE ;
Nyhan, D ;
Sehnert, SS ;
Rohde, CA ;
Bulkley, GB ;
Risby, TH .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 26 (3-4) :439-445
[2]   OBLITERATIVE BRONCHIOLITIS AFTER LUNG AND HEART-LUNG TRANSPLANTATION - AN ANALYSIS OF RISK-FACTORS AND MANAGEMENT [J].
BANDO, K ;
PARADIS, IL ;
SIMILO, S ;
KONISHI, H ;
KOMATSU, K ;
ZULLO, TG ;
YOUSEM, SA ;
CLOSE, JM ;
ZEEVI, A ;
DUQUESNOY, RJ ;
MANZETTI, J ;
KEENAN, RJ ;
ARMITAGE, JM ;
HARDESTY, RL ;
GRIFFITH, BP .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1995, 110 (01) :4-14
[3]   Diagnostic yield of bronchoscopies after isolated lung transplantation [J].
Baz, MA ;
Layish, DT ;
Govert, JA ;
Howell, DN ;
Lawerence, CM ;
Davis, RD ;
Tapson, VF .
CHEST, 1996, 110 (01) :84-88
[4]   STUDIES OF CARBONYL SULFIDE TOXICITY - METABOLISM BY CARBONIC-ANHYDRASE [J].
CHENGELIS, CP ;
NEAL, RA .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1980, 55 (01) :198-202
[5]   OXIDATIVE-METABOLISM OF CARBON-DISULFIDE BY ISOLATED RAT HEPATOCYTES AND MICROSOMES [J].
CHENGELIS, CP ;
NEAL, RA .
BIOCHEMICAL PHARMACOLOGY, 1987, 36 (03) :363-368
[6]  
CHENGELIS CP, 1979, BIOCHEM BIOPH RES CO, P995
[7]  
CLELLAND C, 1990, J HEART TRANSPLANT, V9, P177
[8]   Prophylaxis post-transplant: The role of monitoring surveillance bronchoscopy and antimicrobials [J].
Corris, PA .
CLINICS IN CHEST MEDICINE, 1997, 18 (02) :311-&
[9]  
DALVI RR, 1975, CHEM-BIOL INTERACT, V10, P347, DOI 10.1016/0009-2797(75)90057-5
[10]   In stable lung transplant recipients, exhaled nitric oxide levels positively correlate with airway neutrophilia and bronchial epithelial iNOS [J].
Gabbay, E ;
Walters, EH ;
Orsida, B ;
Whitford, H ;
Ward, C ;
Kotsimbos, TC ;
Snell, GI ;
Williams, TJ .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1999, 160 (06) :2093-2099