Skip to main content
  • Original investigation
  • Open access
  • Published:

Low mannose-binding lectin (MBL) genotype is associated with future cardiovascular events in type 2 diabetic south asians. a prospective cohort study



South Asians have a high burden of type 2 diabetes and vascular complications. Vascular inflammation is considered central in the pathophysiology of atherosclerosis, and the complement system is thought to play an important role. Mannose-Binding Lectin (MBL), which activates the lectin pathway of complement activation, has been introduced as a risk marker of vascular damage. The present study explores the association of MBL levels, genotype and cardiovascular events in type 2 diabetic South Asians.


We conducted a prospective observational study. A cohort consisting of 168 type 2 diabetic South Asians was followed for a median duration of 7.66 years. At baseline, MBL levels and genotype were determined. The association with future cardiovascular events was assessed by Cox proportional hazard regression.


During follow-up, 31 cardiovascular events occurred in 22 subjects (11 men, 11 women). The O/O genotype was significantly associated with the occurrence of cardiovascular events (hazard ratio 3.42, 95%CI 1.24-9.49, P = 0.018). However, log MBL levels were not associated with the occurrence of cardiovascular events (hazard ratio 0.93, 95% CI 0.50-1.73).


In type 2 diabetic South Asians, the O/O MBL genotype is associated with cardiovascular events, although single serum MBL levels are not.


South Asian immigrants in Western societies have a high burden of diabetes and vascular complications [1]. Traditional cardiovascular risk factors only partially explain this increased risk [2]. Hence other factors must be involved.

Atherosclerosis, the pathologic substrate of macrovascular disease, is recognized to be an inflammatory process [3]. As a player in the inflammatory response, the complement system is thought to be involved in this vascular inflammation [4] Indeed, complement activation products have been demonstrated in atherosclerotic plaques [5].

The complement system can be activated via the classical, alternative or lectin pathway, which is activated when Mannose-Binding Lectin (MBL) binds to its target molecule. MBL binds carbohydrate moieties on microorganisms. However, endogenous MBL ligands, such as glycosylated immunoglobulins or cells exposed to oxidative stress, have also been identified [6]. MBL serum levels are primarily determined by 3 polymorphisms (B,C and D genotypes, commonly referred to as O-alleles) in the MBL gene (mbl2). Subjects with wild type MBL genotype (A/A) have the highest serum MBL levels, subjects with 1 variant allele (A/O) have intermediate levels and subjects with 2 variant alleles (O/O) have the lowest levels. In addition, polymorphisms in the promoter region influence the MBL level [7]. MBL is synthesized in the liver. Although intraindividual levels are relatively stable over time [8], a two-to threefold increase occurs during acute phase reactions [9].

It has recently been suggested that MBL is involved in the pathophysiology of cardiovascular damage in high-risk populations [10]. In a group of type 1 diabetic Caucasians, MBL levels were significantly higher in subjects with either a history of cardiovascular disease or diabetic nephropathy compared to subjects without these vascular complications [10]. In type 2 diabetic Caucasians high MBL levels were associated with increased mortality [11]. However, others found an association between low MBL levels and cardiovascular events [8, 12]. Data on MBL in South Asians are lacking.

We hypothesized that MBL might be involved in the high incidence of cardiovascular complications in type 2 diabetic South Asians. The current study aims to explore the association of MBL levels and genotype with cardiovascular complications in type 2 diabetic South Asians. We demonstrate that a low MBL genotype is associated with cardiovascular events, while a single serum MBL level is not.

Research design and methods

Design of the follow-up study

We conducted a prospective cohort study. All studied subjects were recruited from a previously published study [13]. The original study population comprised 465 South Asians. At baseline, subjects that were not known with diabetes underwent a 75 g oral glucose tolerance test. Diabetes was diagnosed based on the ADA 2003 criteria. Out of 465 subjects, 168 subjects had type 2 diabetes at baseline (122 already known with diabetes, 46 newly diagnosed), and from these subjects follow-up data were collected. The study protocol was approved by the Institutional Medical Ethics Committee. All subjects provided informed consent.

Study-patients were followed up by letter and subsequently by phone. When subjects could not be traced by address or phone number in our database, general practitioners or participating family members were involved.

Follow-up data consisted of medical history with regard to cardiovascular events. Subjects were sent a questionnaire and were invited for a visit to our out-patient clinic. During this visit the questionnaire was reviewed by the main investigator (M.A.S.). Subjects not willing to visit the out-patient clinic were asked permission to collect medical data from their general practitioner. For subjects who had died during the follow-up period, cause of death and cardiovascular history was retrieved from the general practitioner. All (self-)reported events were verified by contacting the hospital in which the event had occurred.

Measurements at baseline

Laboratory measurements at baseline included lipids, creatinine, fasting glucose, urinary albumin/creatinine ratio, high-sensitivity C-reactive protein (hsCRP), and plasma SC5b-9, the soluble end product of complement activation. Lipids, creatinine, glucose and urinary albumin/creatinine ratio were measured according to standard methods. High-sensitivity C-reactive protein was measured with a fully automated Cobas Integra 800, according to the manufacturers proceedings (Roche, Almere, the Netherlands). The variation coefficients (VC) were below 3%. Plasma levels of SC5b-9 were measured with an ELISA as described earlier [14].

MBL genotyping

DNA was isolated routinely from peripheral blood leucocytes. MBL single nucleotide polymorphisms at codons 52, 54 and 57 of the mbl2 gene were typed by pyrosequencing. The detailed methodology has been published separately [15]. The MBL genotype of only wildtype allele carriers is designated as A/A and the presence of 1 or 2 variant alleles(s) (B, C, or D) is designated as A/O or O/O, respectively.

Serum MBL levels

At baseline, serum MBL levels were assessed by sandwich ELISA as described previously [16]. In brief, 96-well ELISA plates (Greiner, Frickenhausen, Germany) were coated with the monoclonal antibody 3E7 (mouse IgG1 anti-MBL at 2.5 mg/ml), kindly provided by Dr. T. Fujita (Fuhushima, Japan). Serum samples were diluted 1/50 and 1/500 and incubated in the coated wells. MBL was detected with Dig-conjugated 3E7. Detection of binding of Dig-conjugated antibodies was performed using HRP-conjugated sheep anti-Dig Abs (Fab fragments, Roche, Mannheim, Germany). Enzyme activity was detected using 2,2'-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) (Sigma Chemical Co., St. Louis, MO)). The optical density was measured at 415 nm using a microplate biokinetics reader (EL312e; Biotek Instruments, Winooski, VT). A calibration line was produced using human serum from a healthy donor with a known concentration of MBL. Earlier studies indicated that this assay primarily detects wild-type MBL in serum and plasma and that there is a direct association with the MBL genotype and with MBL function [17].

Definition of endpoint

Cardiovascular events were defined as the occurrence of either a myocardial infarction, Percutaneous Transluminal Coronary Angioplasty (PTCA), Coronary Artery Bypass Grafting (CABG), or sudden cardiac death. The latter was defined as a witnessed sudden circulatory arrest. The primary end-point was the time to the first cardiovascular event.

Statistical analysis

Normally distributed variables are expressed as arithmetic mean ± 1 standard deviation. Skewed distributed variables are expressed as median with interquartile range.

Differences between groups were assessed with the independent samples t-test or the Mann-Whitney-U test for normally and not-normally distributed variables respectively. Comparison between multiple groups was performed with analysis of variance. Correlations were assessed by using Pearson's correlation and Spearman's correlation as appropriate. Associations with cardiovascular events were assessed by Cox proportional hazard regression..All tests were two-sided and the level of significance was set at 0.05.

All analyses were performed using SPSS Statistical Software Package (version 17.0; SPSS, Chicago, IL)


Baseline analysis

At baseline, serum MBL levels and MBL genotype were determined in 168 diabetic subjects (122 already known with diabetes, 46 newly diagnosed). DNA was not available in 5 diabetic patients.

The median MBL level was 476 μg/L (IQR 143-1536 μg/L). Genotype distribution in South Asians was the same as the reported genotype distribution in Caucasians [7]. MBL levels differed significantly per genotype (P < 0.001): subjects with the A/A genotype had the highest MBL levels (median 1300 μg/L, IQR 535-2258) with the A/O genotype had intermediate MBL levels (median 160 μg/L, IQR 75-295) and subjects with the O/O genotype had the lowest MBL levels (median 74 μg/L, IQR 38-101).

MBL levels correlated weakly with BMI (r = -0.155, P = 0.014), HbA1c (r = 0.165, P = 0.034) and hip circumference (-0.169, P = 0.030), but not with sex, age, blood pressure, high-sensitivity C-reactive protein (hsCRP), smoking status, total cholesterol, fasting triglycerides, and plasma SC5b-9.

Longitudinal analysis

Out of 168 type 2 diabetic subjects at baseline, 21 could not be traced and 13 subjects refused to participate and thus were excluded from analysis. Eighty-six subjects visited the out-patient clinic, 31 subjects did not visit the out-patient clinic but medical information was retrieved from the general practitioner, and 17 subjects had died (see below). The median duration of follow-up was 7.66 (IQR 7.48-8.10) years. Participants lost to follow-up did not differ in baseline characteristics from participants for whom follow-up data were available (table 1).

Table 1 Baseline characteristics of the type 2 diabetic South Asian study population

During follow-up, 31 cardiovascular events occurred in 22 subjects (11 men, 11 women): 3 sudden cardiac deaths, 2 fatal and 5 non-fatal myocardial infarction, 13 percutaneous coronary interventions, and 8 coronary artery bypass graft procedures. Eight of these 22 subjects had already experienced a cardiovascular event at baseline.

Twelve subjects died due to non-cardiovascular causes. These patients were censored, none of them reached the primary end-point before dying.

Compared to the wild-type genotype, the O/O genotype was significantly associated with the occurrence of a cardiovascular event (hazard ratio 3.43, 95%CI 1.24-9.49, P = 0.005) (table 2 and table 3 Figure 1). Subjects with the O/O genotype did not differ in lipid parameters or blood pressure compared to subjects with the A/A or A/O genotype. The A/O genotype was not associated with cardiovascular events (HR 0.65, 95% CI 0.20-2.07). Cardiovascular events were also associated with a previous cardiovascular events (HR 4.3, 95% CI 1.2-10.3) and log urinary albumin/creatinine ratio (HR 1.58, 95% CI 1.0-2.48).

Table 2 Median MBL level (interquartile range in brackets) and genotype distribution in study subjects according to ethnicity and cardiovascular complications
Table 3 Association with cardiovascular events of the MBL genotype and serum MBL level
Figure 1
figure 1

Unadjusted Kaplan-Meier survival curves according to MBL genotype (black line = A/A (wild type), grey line = O/O genotype). The O/O genotype has a worse event-free survival compared to the A/A genotype (Log rank test P = 0.011).

There was no statistically significant difference in baseline median MBL level between subjects experiencing a cardiovascular event during follow-up and subjects without a cardiovascular event (390 μg/L (IQR 77-1348 μg/L) versus 466 μg/L (IQR 139-1545 μg/L), P = 0.674). Log-transformed MBL levels were not associated with the occurrence of cardiovascular events (hazard ratio 0.93, 95% CI 0.50-1.73). MBL levels above the median were not associated with cardiovascular events (hazard ratio 0.94, 95% CI 0.40-2.20). Using other MBL cut-off levels also failed to show an association with cardiovascular events (data not shown).


From different parts of the world, South Asian ethnicity has been reported to be an independent risk factor for cardiovascular events [1, 18], although survival thereafter does not seem to be worse compared to Caucasians [19, 20]. We studied the effect of MBL genotype and level in a group of type 2 diabetic subjects of South Asians descent.

The main finding of the present study is that in type 2 diabetic South Asians, the O/O MBL genotype was significantly associated with the occurrence of cardiovascular events compared to wild-type.

The association between low MBL genotype and cardiovascular events has previously been reported in different populations [12, 21, 22]. For instance, the Strong Heart Study included American Indians [12], which - like South Asians-have a high burden of diabetes and subsequent vascular complications. A low MBL genotype was associated with a threefold increased risk for coronary heart disease.

With respect to serum MBL levels and cardiovascular events, data are more controversial. Cross sectional studies found higher MBL levels in type 1 and type 2 diabetic Caucasians with a previous cardiovascular event compared to diabetic subjects without cardiovascular disease [10, 11]. In non-diabetic Caucasian males but not in females, high MBL levels were associated with future cardiovascular events [23]. In type 2 diabetic Caucasians high MBL levels were associated with increased all cause mortality, although data with respect to cardiovascular events were not reported [11]. In contrast, the prospective Reykjavik study found that in type 2 diabetic subjects low rather than high MBL levels were associated with increased incidence of myocardial infarction [8]. Recently, the Strong Heart Study provided data on MBL levels, confirming that low baseline MBL levels indeed were associated with future cardiovascular events [24]. In our study, MBL levels were not associated with future cardiovascular events.

A possible explanation for an association between low MBL levels and cardiovascular events might be a defective clearance of atherogenic particles. MBL binds N-acetylglucosamine moieties, which are expressed on several lipoproteins and oxidized LDL [25], and this may facilitate their phagocytic clearance. This hypothesis is supported by a recently published study showing that MBL deficient subjects have impaired clearance of triglyceride-rich lipoproteins [26]. Additionally, MBL deficiency might influence the susceptibility and course of infection with Chlamydia pneumoniae, which is associated with coronary artery disease [27]. On the other hand, MBL levels may increase in the setting of an inflammatory response [9]. Experimental studies show that in the setting of ischemia/reperfusion high MBL levels are detrimental rather than protective [28]. Oxidative stress induces a change on the cellular surface [29], which results in binding of MBL leading to enhanced complement mediated injury. However, since MBL levels were not correlated with plasma SC5-9 levels in our study, we found no evidence that high MBL levels result in increased complement activation.

Summarizing the above, whereas most cross sectional studies found an association between cardiovascular disease and high MBL levels, most prospective studies show an association between low MBL levels and cardiovascular events.

In our study, low MBL genotype was associated with cardiovascular events and MBL genotype corresponds with MBL level. One would therefore expect low MBL levels to be associated with cardiovascular events, which however was not the case in our study. MBL genotype probably is a more accurate estimate of cumulative MBL exposure than a single serum MBL level. The contribution of MBL to vascular disease might differ according to the pathophysiologic phase: early in the course low MBL levels might promote atherosclerosis, and once a vascular inflammatory response is established MBL levels might secondarily become increased and - perhaps - subsequently promote vascular inflammation. A recent experimental study demonstrated local MBL synthesis in early atherosclerotic plaques [30], supporting the hypothesis that MBL levels might become increased due to atherogenesis. Based on the assumption of time-dependency of the association between MBL and cardiovascular disease, our single baseline sample might have been too late in the pathophysiologic course to detect the effect of low MBL level on cardiovascular outcome. In addition, intra-individual variation in MBL level and variations of the MBL assay might contribute to the discordant findings between MBL genotype and MBL level. Finally, at least theoretically, the association of low MBL genotype with cardiovascular events might be based on an association with other susceptibility genes for cardiovascular events.

Noteworthy, although the O/O genotype was associated with cardiovascular events, the A/0 genotype was not, although the difference in median MBL level between the O/O and the A/O genotype was relatively small. However, it has previously been shown that although MBL concentration in A/O and O/O genotype is rather similar, functional capacity of MBL in carriers of the O/O genotype is less compared to MBL of A/O carriers. Functional MBL consists of polymers of 3 to 6 subunits. The number of structural variants influences the assembly of the MBL subunits, and lower polymerization grade results in loss of function [31].

We do want to point out that the results of our study may not apply to South Asians in general as the ancestors of the South Asians included in our study originally came from a circumscriptive area in North India called Uttar Pradesh, Uttarakhand and West-Bihar.

In conclusion, low MBL genotype is associated with cardiovascular events in type 2 diabetic South Asians, suggesting that MBL is involved in the pathogenesis of cardiovascular events. However, single serum MBL concentrations were not associated with cardiovascular events and therefore a single MBL level is not a clinically useful risk marker for cardiovascular events in type 2 diabetic South Asians.


A/A genotype:

Wild type MBL genotype

A/O genotype:

1 structural variant


Hazard Ratio


Mannose-binding Lectin

O/O genotype:

2 structural variants.


  1. Anand SS, Yusuf S: Risk factors for cardiovascular disease in Canadians of South Asian and European origin: a pilot study of the Study of Heart Assessment and Risk in Ethnic Groups (SHARE). Clin Invest Med. 1997, 20: 204-210.

    CAS  PubMed  Google Scholar 

  2. Forouhi NG, Sattar N, Tillin T, McKeigue PM, Chaturvedi N: Do known risk factors explain the higher coronary heart disease mortality in South Asians compared with European men? Prospective follow-up of the Southall and Brent studies, UK. Diabetologia. 2006, 49: 2580-2588. 10.1007/s00125-006-0393-2.

    Article  CAS  PubMed  Google Scholar 

  3. Ross R: Atherosclerosis--an inflammatory disease. N Engl J Med. 1999, 115-126. 340

  4. Ostergaard J, Hansen TK, Thiel S, Flyvbjerg A: Complement activation and diabetic vascular complications. Clin Chim Acta. 2005, 361: 10-19. 10.1016/j.cccn.2005.04.028.

    Article  CAS  PubMed  Google Scholar 

  5. Rus HG, Niculescu F, Vlaicu R: Co-localization of terminal C5b-9 complement complexes and macrophages in human atherosclerotic arterial walls. Immunol Lett. 1988, 19: 27-32. 10.1016/0165-2478(88)90115-0.

    Article  CAS  PubMed  Google Scholar 

  6. Takahashi K, Ip WE, Michelow IC, Ezekowitz RA: The mannose-binding lectin: a prototypic pattern recognition molecule. Curr Opin Immunol. 2006, 18: 16-23. 10.1016/j.coi.2005.11.014.

    Article  CAS  PubMed  Google Scholar 

  7. Garred P, Larsen F, Seyfarth J, Fujita R, Madsen HO: Mannose-binding lectin and its genetic variants. Genes Immun. 2006, 7: 85-94. 10.1038/sj.gene.6364283.

    Article  CAS  PubMed  Google Scholar 

  8. Saevarsdottir S, Oskarsson OO, Aspelund T, Eiriksdottir G, Vikingsdottir T, Gudnason V, Valdimarsson H: Mannan binding lectin as an adjunct to risk assessment for myocardial infarction in individuals with enhanced risk. J Exp Med. 2005, 201: 117-125. 10.1084/jem.20041431.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  9. Thiel S, Holmskov U, Hviid L, Laursen SB, Jensenius JC: The Concentration of the C-Type Lectin, Mannan-Binding Protein, in Human Plasma Increases During An Acute Phase Response. Clin Exp Immunol. 1992, 90: 31-35.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  10. Hansen TK, Tarnow L, Thiel S, Steffensen R, Stehouwer CD, Schalkwijk CG, Parving HH, Flyvbjerg A: Association between mannose-binding lectin and vascular complications in type 1 diabetes. Diabetes. 2004, 53: 1570-1576. 10.2337/diabetes.53.6.1570.

    Article  CAS  PubMed  Google Scholar 

  11. Hansen TK, Gall MA, Tarnow L, Thiel S, Stehouwer CD, Schalkwijk CG, Parving HH, Flyvbjerg A: Mannose-binding lectin and mortality in type 2 diabetes. Arch Intern Med. 2006, 166: 2007-2013. 10.1001/archinte.166.18.2007.

    Article  CAS  PubMed  Google Scholar 

  12. Best LG, Davidson M, North KE, MacCluer JW, Zhang Y, Lee ET, Howard BV, DeCroo S, Ferrell RE: Prospective analysis of mannose-binding lectin genotypes and coronary artery disease in American Indians: the Strong Heart Study. Circulation. 2004, 109: 471-475. 10.1161/01.CIR.0000109757.95461.10.

    Article  PubMed  Google Scholar 

  13. Chandie Shaw PK, van Es LA, Paul LC, Rosendaal FR, Souverijn JH, Vandenbroucke JP: Renal disease in relatives of Indo-Asian Type 2 diabetic patients with end-stage diabetic nephropathy. Diabetologia. 2003, 46: 618-624.

    CAS  PubMed  Google Scholar 

  14. Siezenga MA, Chandie Shaw PK, van der Geest RN, Mollness TE, Daha MR, Rabelink TJ, Berger SP: Enhanced complement activation is part of the unfavourable cardiovascular risk profile in South Asians. Clin Exp Immunol. 2009, 157: 98-103. 10.1111/j.1365-2249.2009.03959.x.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  15. Roos A, Dieltjes P, Vossen RH, Daha MR, de Knijff P: Detection of three single nucleotide polymorphisms in the gene encoding mannose-binding lectin in a single pyrosequencing reaction. J Immunol Methods. 2006, 309: 108-114. 10.1016/j.jim.2005.11.017.

    Article  CAS  PubMed  Google Scholar 

  16. Berger SP, Roos A, Mallat MJ, Fujita T, de Fijter JW, Daha MR: Association between mannose-binding lectin levels and graft survival in kidney transplantation. Am J Transplant. 2005, 5: 1361-1366. 10.1111/j.1600-6143.2005.00841.x.

    Article  CAS  PubMed  Google Scholar 

  17. Roos A, Garred P, Wildenberg ME, Lynch NJ, Munoz JR, Zuiverloon TC, Bouwman LH, Schlagwein N, Fallaux van der Houten FC, Faber-Krol MC, Madsen HO, Schwaeble WJ, Matsushita M, Fujita T, Daha MR: Antibody-mediated activation of the classical pathway of complement may compensate for mannose-binding lectin deficiency. Eur J Immunol. 2004, 34 (9): 2589-2598. 10.1002/eji.200324401.

    Article  CAS  PubMed  Google Scholar 

  18. Prasad GV, Vangala SK, Silver SA, Wong SC, Huang M, Rapi L, Nash MM, Zaltzman JS: South Asian ethnicity as a risk factor for major adverse cardiovascular events after renal transplantation. Clin J Am Soc Nephrol. 2011, 6 (1): 204-2011. 10.2215/CJN.03100410.

    Article  PubMed Central  PubMed  Google Scholar 

  19. Fischbacher CM, Bhopal R, Povey C, Steiner M, Chalmers J, Mueller G, Jamieson J, Knowles D: Record linked retrospective cohort study of 4.6 million people exploring ethnic variations in disease: myocardial infarction in SOuth Asians. BMC Public Health. 2007, 7: 142-10.1186/1471-2458-7-142.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  20. Nijjar AP, Wang H, Dasgupta K, Rabi DM, Quan H, Khan NA: Outcomes in a diabetic population of South Asians and whites following hospitalization for acute myocardial infarction: a retrospective cohort study. Cardiovasc Diabetol. 2010, 22 (9): 4-11.

    Article  Google Scholar 

  21. Madsen HO, Videm V, Svejgaard A, Svennevig JL, Garred P: Association of mannose-binding-lectin deficiency with severe atherosclerosis. Lancet. 1998, 352: 959-960. 10.1016/S0140-6736(05)61513-9.

    Article  CAS  PubMed  Google Scholar 

  22. Ohlenschlaeger T, Garred P, Madsen HO, Jacobsen S: Mannose-binding-lectin variant alleles and the risk of arterial thrombosis in systemic lupus erythematosus. N Engl J Med. 2004, 351 (5): 260-267.

    Article  CAS  PubMed  Google Scholar 

  23. Keller TT, van Leuven SI, Meuwese MC, Wareham NJ, Luben R, Stroes ES, Hack E, Levi M, Khaw KT, Boekholdt SM: Serum levels of mannose-binding lectin and the risk of future coronary artery disease in apparently healthy men and women. Arterioscler Thromb Vasc Biol. 2006, 26: 2345-2350. 10.1161/01.ATV.0000240517.69201.77.

    Article  CAS  PubMed  Google Scholar 

  24. Best LG, Ferrell RE, DeCroo S, North KE, MacCluer JW, Zhang Y, Lee ET, Howard BV, Umans J, Palmieri V, Garred P: Genetic and other factors determining mannose-binding lectin levels in American Indians: the Strong Heart Study. BMC Med Genet. 2009, 10 (5):

  25. Tertov VV, Sobenin IA, Tonevitsky AG, Orekhov AN, Smirnov VN: Isolation of atherogenic modified (desialylated) low density lipoprotein from blood of atherosclerotic patients: separation from native lipoprotein by affinity chromatography. Biochem Biophys Res Commun. 1990, 167: 1122-1127. 10.1016/0006-291X(90)90639-5.

    Article  CAS  PubMed  Google Scholar 

  26. Alipour A, van Oostrom AJHHM, van Wijk JPH, Verseyden C, PLokker HWM, Jukema JW, Rabelink AJ, Castro Cabezas M: Mannose binding lectin deficiency and triglyceride-rich lipoprotein metabolism in normolipidemic subjects. Atherosclerosis. 2009, 206: 444-450. 10.1016/j.atherosclerosis.2009.03.007.

    Article  CAS  PubMed  Google Scholar 

  27. Rugonfalvi-Kiss S, Endrész V, Madsen HO, Burian K, Duba J, Prohaszka Z, Karadi I, Romics L, Gönczöl E, Füst G, Garred P: Association of Chlamydia pneumonia with coronary artery disease and its progression is dependent on the modifying effect of mannose-binding lectin. Circulation. 2002, 106: 1071-1076. 10.1161/01.CIR.0000027137.96791.6A.

    Article  CAS  PubMed  Google Scholar 

  28. Walsh MC, Bourcier T, Takahashi K, Shi L, Busche MN, Rother RP, Solomon SC, Ezekowitz AB, Stahl GL: Mannose-binding lectin is a regulator of inflammation that accompanies myocardial ischemia and reperfusion injury. J Immunol. 2005, 175: 541-546.

    Article  CAS  PubMed  Google Scholar 

  29. Collard CD, Montalto MC, Reenstra WR, Buras JA, Stahl GL: Endothelial oxidative stress activates the lectin complement pathway: role of cytokeratin 1. Am J Pathol. 2001, 159: 1045-1054. 10.1016/S0002-9440(10)61779-8.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  30. Matthijsen RA, de Winther MPJ, Kuipers D, van der Made I, Weber C, Herias V, Gijbels MJJ, Buurman WA: Macrophage-specific expression of Mannose-binding lectin controls atherosclerosis in low-density lipoprotein receptor-deficient mice. Circulation. 2009, 119: 2188-2195. 10.1161/CIRCULATIONAHA.108.830661.

    Article  CAS  PubMed  Google Scholar 

  31. Garred P, Flemming Larsen, Madsen HO, Koch C: Mannose-binding lectin deficiency-revisited. Mol Immunol. 2003, 40: 73-84. 10.1016/S0161-5890(03)00104-4.

    Article  CAS  PubMed  Google Scholar 

Download references


We thank Reinier van der Geest and Nicole Schlagwein for technical assistance.

Author information

Authors and Affiliations


Corresponding author

Correspondence to Machiel A Siezenga.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

M.S. researched data and wrote manuscript, P.C.S researched data, M.D. reviewed manuscript, A.R.reviewed manuscript, S.B. contributed to discussion, reviewed manuscript. All authors read and approved the final manuscript.

Authors’ original submitted files for images

Below are the links to the authors’ original submitted files for images.

Authors’ original file for figure 1

Rights and permissions

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and permissions

About this article

Cite this article

Siezenga, M.A., Chandie Shaw, P.K., Daha, M.R. et al. Low mannose-binding lectin (MBL) genotype is associated with future cardiovascular events in type 2 diabetic south asians. a prospective cohort study. Cardiovasc Diabetol 10, 60 (2011).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: