Genetic susceptibility to acute lung injury

被引:27
作者
Villar, J [1 ]
Flores, C
Méndez-Alvarez, S
机构
[1] Hosp Univ NS Candelaria, Res Inst, Tenerife, Canary Isl, Spain
[2] Mt Sinai Hosp, Dept Med, Toronto, ON M5G 1X5, Canada
[3] Mercer Univ, Macon, GA 31207 USA
[4] Univ La Laguna, Dept Microbiol, Tenerife, Canary Isl, Spain
关键词
acute lung injury; acute respiratory distress syndrome; cytokine; functional genomics; gene expression; microarray; polymorphism; sepsis;
D O I
10.1097/01.CCM.0000057903.11528.6D
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: To review the complex interactions of markers of genetic susceptibility for critical illness and acute lung injury. These may affect the responses of critically ill patients to acute lung injury and acute respiratory distress syndrome and may affect outcome. Data Sources and Study Selection: Published research and review articles related to genetic factors associated with susceptibility to critical illnesses and pulmonary disease. Data Extraction and Synthesis: Critical illness in adults often is followed by acute lung injury, a phenomenon of acute diffuse lung inflammation. Physicians have long known that each patient responds differently to drugs and has a different risk for a particular event or outcome. Now, there is some evidence that cellular and humoral immune responses are subject to polymorphic genetic control, which explains the well-known diversity of clinical manifestations and outcomes in critically ill patients with the same disease. By revealing altered expression of relatively few genes involved in the responses to lung injury and repair, some investigators have found that these responses, and susceptibility to acute lung injury, are heritable. In the last 5 yrs, we have discovered that an individual's risks and cellular responses can be related to his or her Own unique DNA. Conclusions: The search for an association between functional variants of a gene and clinical phenotype may help to identify key pathophysiological processes of disease. In the future, we will know much about which therapy is best for each individual patient in the intensive care unit.
引用
收藏
页码:S272 / S275
页数:4
相关论文
共 21 条
[1]   Relative production of tumour necrosis factor a and interleukin 10 in adult respiratory distress syndrome [J].
Armstrong, L ;
Millar, AB .
THORAX, 1997, 52 (05) :442-446
[2]   Cytokine gene polymorphism in human disease: on-line databases [J].
Bidwell, J ;
Keen, L ;
Gallagher, G ;
Kimberly, R ;
Huizinga, T ;
McDermott, MF ;
Oksenberg, J ;
McNicholl, J ;
Pociot, F ;
Hardt, C ;
D'Alfonso, S .
GENES AND IMMUNITY, 1999, 1 (01) :3-19
[3]   Functional genomics of critical illness and injury [J].
Chung, TP ;
Laramie, JM ;
Province, M ;
Cobb, JP .
CRITICAL CARE MEDICINE, 2002, 30 (01) :S51-S57
[4]   WHOLE-GENOME RANDOM SEQUENCING AND ASSEMBLY OF HAEMOPHILUS-INFLUENZAE RD [J].
FLEISCHMANN, RD ;
ADAMS, MD ;
WHITE, O ;
CLAYTON, RA ;
KIRKNESS, EF ;
KERLAVAGE, AR ;
BULT, CJ ;
TOMB, JF ;
DOUGHERTY, BA ;
MERRICK, JM ;
MCKENNEY, K ;
SUTTON, G ;
FITZHUGH, W ;
FIELDS, C ;
GOCAYNE, JD ;
SCOTT, J ;
SHIRLEY, R ;
LIU, LI ;
GLODEK, A ;
KELLEY, JM ;
WEIDMAN, JF ;
PHILLIPS, CA ;
SPRIGGS, T ;
HEDBLOM, E ;
COTTON, MD ;
UTTERBACK, TR ;
HANNA, MC ;
NGUYEN, DT ;
SAUDEK, DM ;
BRANDON, RC ;
FINE, LD ;
FRITCHMAN, JL ;
FUHRMANN, JL ;
GEOGHAGEN, NSM ;
GNEHM, CL ;
MCDONALD, LA ;
SMALL, KV ;
FRASER, CM ;
SMITH, HO ;
VENTER, JC .
SCIENCE, 1995, 269 (5223) :496-512
[5]   Genomic medicine - A primer [J].
Guttmacher, AE ;
Collins, FS .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (19) :1512-1520
[6]   Genetic polymorphisms in lung disease: bandwagon or breakthrough? [J].
Iannuzzi, MC ;
Maliarik, M ;
Rybicki, B .
RESPIRATORY RESEARCH, 2002, 3 (01)
[7]   Measured haplotype analysis of the angiotensin-I converting enzyme gene [J].
Keavney, B ;
McKenzie, CA ;
Connell, JMC ;
Julier, C ;
Ratcliffe, PJ ;
Sobel, E ;
Lathrop, M ;
Farrall, M .
HUMAN MOLECULAR GENETICS, 1998, 7 (11) :1745-1751
[8]   Acute lung injury - Functional genomics and genetic susceptibility [J].
Leikauf, GD ;
McDowell, SA ;
Wesselkamper, SC ;
Hardie, WD ;
Leikauf, JE ;
Korfhagen, TR ;
Prows, DR .
CHEST, 2002, 121 (03) :70S-75S
[9]  
LEIKAUF GD, 2001, PATHOGENOMIC MECH PA
[10]   Polymorphisms of human SP-A, SP-B, and SP-D genes:: association of SP-B Thr131Ile with ARDS [J].
Lin, Z ;
Pearson, C ;
Chinchilli, V ;
Pietschmann, SM ;
Luo, J ;
Pison, U ;
Floros, J .
CLINICAL GENETICS, 2000, 58 (03) :181-191