Serum Levels of Lipoprotein Lipase Are Increased in Patients with Inflammatory Bowel Disease

Author:

Rodríguez-Hernández Orvelindo1,Carrillo-Palau Marta2ORCID,Hernández-Camba Alejandro3ORCID,Alonso-Abreu Inmaculada2ORCID,Ramos Laura2,de Armas-Rillo Laura4ORCID,Martín-González Candelaria56ORCID,López-Mejías Raquel7ORCID,González-Gay Miguel Á.8910ORCID,Ferraz-Amaro Iván611ORCID

Affiliation:

1. Division of Endocrinology, Hospital Universitario de Canarias, 38320 Tenerife, Spain

2. Division of Gastroenterology, Hospital Universitario de Canarias,38320 Tenerife, Spain

3. Division of Gastroenterology, Hospital Universitario de Nuestra Señora de la Candelaria, 38010 Tenerife, Spain

4. Division of Health Sciences, Universidad Europea de Canarias, 38300 Tenerife, Spain

5. Division of Internal Medicine, Hospital Universitario de Canarias, 38320 Tenerife, Spain

6. Department of Internal Medicine, University of La Laguna (ULL), 38200 Tenerife, Spain

7. Epidemiology, Genetics and Atherosclerosis Research Group on Systemic Inflammatory Diseases, IDIVAL, 39011 Santander, Spain

8. Division of Rheumatology, IIS-Fundación Jiménez Díaz, 28040 Madrid, Spain

9. Department of Medicine, University of Cantabria, 39005 Santander, Spain

10. Cardiovascular Pathophysiology and Genomics Research Unit, School of Physiology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg 2000, South Africa

11. Division of Rheumatology, Hospital Universitario de Canarias, 38320 Tenerife, Spain

Abstract

Disruption of the lipid profile is commonly found in patients with inflammatory bowel disease (IBD). Lipoprotein lipase (LPL) is a key molecule involved in triglyceride metabolism that plays a significant role in the progression of atherosclerosis. In this study, our aim was to study whether serum LPL levels are different in IBD patients and controls and whether IBD features are related to LPL. This was a cross-sectional study that encompassed 405 individuals; 197 IBD patients with a median disease duration of 12 years and 208 age- and sex-matched controls. LPL levels and a complete lipid profile were assessed in all individuals. A multivariable analysis was performed to determine whether LPL serum levels were altered in IBD and to study their relationship with IBD characteristics. After the fully multivariable analysis, including cardiovascular risk factors and the changes in lipid profile that the disease causes itself, patients with IBD showed significantly higher levels of circulating LPL (beta coefficient 196 (95% confidence interval from 113 to 259) ng/mL, p < 0.001). LPL serum levels did not differ between Crohn’s disease and ulcerative colitis. However, serum C-reactive protein levels, disease duration, and the presence of an ileocolonic Crohn’s disease phenotype were found to be significantly and independently positively related to LPL. In contrast, LPL was not associated with subclinical carotid atherosclerosis. In conclusion, serum LPL levels were independently upregulated in patients with IBD. Inflammatory markers, disease duration and disease phenotype were responsible for this upregulation.

Funder

Spanish Ministry of Health

Fondo Europeo de Desarrollo Regional—FEDER

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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