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Volume 19, Issue 10, Pages 720-728 (December 2009)


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Association of human cathelicidin (hCAP-18/LL-37) gene expression with cardiovascular disease risk factors

H. Benachour1, M. ZaiouCorresponding Author Information1email address, A. Samara, B. Herbeth, M. Pfister, D. Lambert, G. Siest, S. Visvikis-Siest

Received 17 June 2008; received in revised form 7 January 2009; accepted 8 January 2009. published online 06 April 2009.

Abstract 

Background and aims

Antimicrobial peptides (AMPs) are components of the innate immune system. In addition, evidence suggests that these peptides are associated with various inflammatory diseases. We examined whether expression of the cathelicidin LL-37 in peripheral blood mononuclear cells (PBMCs) is associated with cardiovascular risk factors.

Methods and results

A total of 90 men and 87 women selected from STANISLAS cohort were studied. Expression of LL-37 mRNA isolated from PBMCs of these subjects was quantified by quantitative RT-PCR. Anthropometric measurements and biochemical profiles were assessed for each individual. In women, LL-37 mRNA expression was significantly and positively correlated with body mass index (BMI) (p0.001); waist circumference (WC) (p0.01); systolic blood pressure (SBP) (p0.05) and triglycerides (TG) level (p0.05) and negatively with plasma levels of HDL-C (p0.05). In men however, LL-37 was positively associated with waist to hip ratio (WHR) (p0.05); SBP (p0.001); TG (p0.05); fasting glucose levels (p0.01); alanine aminotransferase (ALT) activity (p0.01); neutrophils counts (p0.01) and negatively with lymphocyte counts (p0.001); serum HDL-C (p0.001) and apoA-I (p0.05) levels. After adjustment for WC and BMI, multiple regression analysis showed that LL-37 remained significantly associated with SBP; HDL-C; fasting glucose level; ALT activity; neutrophil and lymphocyte counts (p0.001 to p0.05) in men.

Conclusion

Our results suggest that LL-37 gene expression may be closely associated with cardiovascular risk factors independently of BMI and WC. However, functional studies are required to confirm these data.

Equipe “Génétique Cardiovasculaire”, Université Henri Poincaré, Faculté de Pharmacie, 30, rue Lionnois, 54000 Nancy, France

Corresponding Author InformationCorresponding author. Tel.: +33 3 8368 2159; fax: +33 3 8332 1322.

1 Authors contributed equally to this work.

PII: S0939-4753(09)00009-X

doi:10.1016/j.numecd.2009.01.001


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