The MBL2 'LYQA secretor' haplotype is an independent predictor of postoperative myocardial infarction in whites undergoing coronary artery bypass graft surgery

被引:29
作者
Collard, Charles D.
Shernan, Stanton K.
Fox, Amanda A.
Bernig, Toralf
Chanock, Stephen J.
Vaughn, William K.
Takahashi, Kazue
Ezekowitz, Alan B.
Jarolim, Petr
Body, Simon C.
机构
[1] St Lukes Episcopal Hosp, Texas Heart Inst, Baylor Coll Med, Div Cardiovasc Anesthesiol, Houston, TX 77030 USA
[2] Harvard Univ, Brigham & Womens Hosp, Dept Anesthesiol Perioperat & Pain Med, Boston, MA 02115 USA
[3] NCI, Canc Res Ctr, Bethesda, MD 20892 USA
[4] St Lukes Episcopal Hosp, Texas Heart Inst, Div Biostat & Epidemiol, Houston, TX 77030 USA
[5] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Pediat,Lab Dev Immunol, Boston, MA USA
[6] Merck Res Labs, Rahway, NJ USA
[7] Harvard Univ, Sch Med, Brigham & Womens Hosp, Boston, MA USA
关键词
genetics; myocardial infarction; immunology; inflammation; surgery;
D O I
10.1161/CIRCULATIONAHA.106.679530
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background - Mannose-binding lectin (MBL) is an important component of innate immunity and activator of the lectin complement pathway. Within the MBL2 gene are seven 5' "secretor" haplotypes that code for altered serum MBL levels and complement activation. However, recent evidence suggests that 3' MBL2 haplotypes may also modify MBL function and circulating levels. Because MBL and the lectin complement pathway have been implicated in cardiovascular injury, we investigated whether MBL2 haplotypes are independently associated with an increased risk of postoperative myocardial infarction (PMI) in patients undergoing coronary artery bypass graft surgery. Methods and Results - Genotyping of 18 polymorphic sites within the MBL2 gene was performed in a prospective, longitudinal multi-institutional study of 978 patients undergoing primary coronary artery bypass graft-only surgery with cardiopulmonary bypass between August 2001 and May 2005. After adjustment for multiple comparisons by permutation testing, multivariate, stepwise logistic regression, including a score test, was performed controlling for patient demographics, preoperative risk factors, medications, and intraoperative variables to determine if MBL2 secretor haplotypes are independent predictors of PMI in whites undergoing primary coronary artery bypass graft surgery. Neither the 5' nor 3' MBL2 haplotypes alone were associated with an increased incidence of PMI. However, the incidence of PMI in whites (n = 843) expressing the combined MBL2 5' LYQA secretor haplotype (CGTCGG) and 3' haplotype (CGGGT) was significantly higher than in whites not expressing the haplotype (38% versus 10%; P < 0.007). Moreover, the combined MBL2 LYQA secretor haplotype was an independent predictor of PMI in whites after primary coronary artery bypass graft surgery after adjustment for other covariates (P < 0.02; adjusted OR: 3.97; 95% CI: 1.30 to 12.07). The combined MBL2 LYQA secretor haplotype in whites was also an independent predictor of postoperative CKMB levels exceeding 60 ng/mL (P < 0.02; adjusted OR: 4.48; 95% CI: 1.95 to 16.80). Inclusion of the combined MBL2 LYQA secretor haplotype improved prediction models for PMI based on traditional risk factors alone (C-statistic 0.715 versus 0.705). Conclusions - The combined MBL2 LYQA secretor haplotype is a novel independent predictor of PMI and may aid in preoperative risk stratification of whites undergoing primary coronary artery bypass graft surgery.
引用
收藏
页码:I106 / I112
页数:7
相关论文
共 33 条
[1]   The effect of mannan-binding lectin variant alleles on coronary artery reactivity in healthy young men [J].
Aittoniemi, J ;
Fan, YM ;
Laaksonen, R ;
Janatuinen, T ;
Vesalainer, R ;
Nuutila, P ;
Knuuti, J ;
Hulkkonen, J ;
Hurme, M ;
Lehtimäki, T .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2004, 97 (02) :317-318
[2]  
ARAI T, 1993, Q J MED, V86, P575
[3]   Mannose-binding lectin-2 genetic variation and stomach cancer risk [J].
Baccarelli, Andrea ;
Hou, Lifang ;
Chen, Jinbo ;
Lissowska, Jolanta ;
El-Omar, Emad M. ;
Grillo, Paolo ;
Giacomini, Sara M. ;
Yaeger, Meredith ;
Bernig, Toralf ;
Zatonski, Witold ;
Fraumeni, Joseph F., Jr. ;
Chanock, Stephen J. ;
Chow, Wong-Ho .
INTERNATIONAL JOURNAL OF CANCER, 2006, 119 (08) :1970-1975
[4]   An analysis of genetic variation across the MBL2 locus in Dutch Caucasians indicates that 3′ haplotypes could modify circulating levels of mannose-binding lectin [J].
Bernig, T ;
Breunis, W ;
Brouwer, N ;
Hutchinson, A ;
Welch, R ;
Roos, D ;
Kuijpers, T ;
Chanock, S .
HUMAN GENETICS, 2005, 118 (3-4) :404-415
[5]   Sequence analysis of the mannose-binding lectin (MBL2) gene reveals a high degree of heterozygosity with evidence of selection [J].
Bernig, T ;
Taylor, JG ;
Foster, CB ;
Staats, B ;
Yeager, M ;
Chanock, SJ .
GENES AND IMMUNITY, 2004, 5 (06) :461-476
[6]   The mannose-binding lectin (MBL2) haplotype and breast cancer:: an association study in African-American and Caucasian women [J].
Bernig, Toralf ;
Boersma, Brenda J. ;
Howe, Tiffany M. ;
Welch, Robert ;
Yadavalli, Sunita ;
Staats, Brian ;
Mechanic, Leah E. ;
Chanock, Stephen J. ;
Ambs, Stefan .
CARCINOGENESIS, 2007, 28 (04) :828-836
[7]   Prospective analysis of mannose-binding lectin genotypes and coronary artery disease in American Indians - The Strong Heart Study [J].
Best, LG ;
Davidson, M ;
North, KE ;
MacCluer, JW ;
Zhang, Y ;
Lee, ET ;
Howard, BV ;
DeCroo, S ;
Ferrell, RE .
CIRCULATION, 2004, 109 (04) :471-475
[8]   Elevated levels of mannose-binding lectin at clinical manifestation of type 1 diabetes in juveniles [J].
Bouwman, LH ;
Eerligh, P ;
Terpstra, OT ;
Daha, MR ;
de Knijff, P ;
Ballieux, BEPB ;
Bruining, GJ ;
van der Slik, AR ;
Roos, A ;
Roep, BO .
DIABETES, 2005, 54 (10) :3002-3006
[9]   Human mannose-binding lectin in immunity: Friend, foe, or both? [J].
Casanova, JL ;
Abel, L .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 199 (10) :1295-1299
[10]   Complement activation after oxidative stress -: Role of the lectin complement pathway [J].
Collard, CD ;
Väkevä, A ;
Morrissey, MA ;
Agah, A ;
Rollins, SA ;
Reenstra, WR ;
Buras, JA ;
Meri, S ;
Stahl, GL .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 156 (05) :1549-1556