Inflammation can predispose to myocardial infarction (MI), and mannan binding lectin (MBL) promotes phagocytic clearance of inflammatory agents, but the predictive value of MBL levels for MI is not known. MBL was analyzed in subgroups of the population-based Reykjavik study, a cohort of 19,381 participants recruited from 1967. MBL levels were very stable over time (self correlation: 0.86). In a cross-sectional group from the original cohort (n = 987), high MBL (>1,000 μg/L) was associated with a greatly lowered odds ratio for MI (0.64, P < 0.001). To verify this finding, a nested case control sample (n = 1,309) was randomly selected from the cohort. High MBL at recruitment was also associated with decreased MI risk in this follow-up group, but to a lesser extent and not significant for the whole group, smokers, or hypertensive individuals. However, high MBL was as in the cross-sectional group, associated with greatly decreased MI risk in diabetic (P = 0.02) or hypercholesterolemic individuals (P = 0.004). This also applied to raised erythrocyte sedimentation rate (P = 0.007). Diabetic patients with high MBL did not have a higher MI risk than nondiabetic individuals. Our findings indicate that high MBL may predict decreased likelihood of MI, particularly in diabetics, and are consistent with the possibility that MBL may promote clearance of atherogenic agents.
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3 January 2005
Article|
December 28 2004
Mannan binding lectin as an adjunct to risk assessment for myocardial infarction in individuals with enhanced risk
Saedis Saevarsdottir,
Saedis Saevarsdottir
1Department of Immunology, Landspitali-University Hospital, 101 Reykjavik, Iceland
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Oskar Orn Oskarsson,
Oskar Orn Oskarsson
1Department of Immunology, Landspitali-University Hospital, 101 Reykjavik, Iceland
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Thor Aspelund,
Thor Aspelund
2The Icelandic Heart Association, Heart Preventive Clinic and Research Institute, 201 Kopavogur, Iceland
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Gudny Eiriksdottir,
Gudny Eiriksdottir
2The Icelandic Heart Association, Heart Preventive Clinic and Research Institute, 201 Kopavogur, Iceland
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Thora Vikingsdottir,
Thora Vikingsdottir
1Department of Immunology, Landspitali-University Hospital, 101 Reykjavik, Iceland
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Vilmundur Gudnason,
Vilmundur Gudnason
2The Icelandic Heart Association, Heart Preventive Clinic and Research Institute, 201 Kopavogur, Iceland
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Helgi Valdimarsson
Helgi Valdimarsson
1Department of Immunology, Landspitali-University Hospital, 101 Reykjavik, Iceland
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Saedis Saevarsdottir
1Department of Immunology, Landspitali-University Hospital, 101 Reykjavik, Iceland
Oskar Orn Oskarsson
1Department of Immunology, Landspitali-University Hospital, 101 Reykjavik, Iceland
Thor Aspelund
2The Icelandic Heart Association, Heart Preventive Clinic and Research Institute, 201 Kopavogur, Iceland
Gudny Eiriksdottir
2The Icelandic Heart Association, Heart Preventive Clinic and Research Institute, 201 Kopavogur, Iceland
Thora Vikingsdottir
1Department of Immunology, Landspitali-University Hospital, 101 Reykjavik, Iceland
Vilmundur Gudnason
2The Icelandic Heart Association, Heart Preventive Clinic and Research Institute, 201 Kopavogur, Iceland
Helgi Valdimarsson
1Department of Immunology, Landspitali-University Hospital, 101 Reykjavik, Iceland
CORRESPONDENCE Helgi Valdimarsson: [email protected]
Abbreviations used: ESR, erythrocyte sedimentation rate; G1cNAc, N-acetylglucosamine; LDL, low density lipoprotein; MBL, mannan binding lectin; MI, myocardial infarction; ROC, receiver operating characteristic; SLE, systemic lupus erythematosus.
Received:
July 16 2004
Accepted:
November 22 2004
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2005
J Exp Med (2005) 201 (1): 117–125.
Article history
Received:
July 16 2004
Accepted:
November 22 2004
Citation
Saedis Saevarsdottir, Oskar Orn Oskarsson, Thor Aspelund, Gudny Eiriksdottir, Thora Vikingsdottir, Vilmundur Gudnason, Helgi Valdimarsson; Mannan binding lectin as an adjunct to risk assessment for myocardial infarction in individuals with enhanced risk . J Exp Med 3 January 2005; 201 (1): 117–125. doi: https://doi.org/10.1084/jem.20041431
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