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Effects of Interleukin-6 Inhibition on Vascular, Endothelial and Left Ventricular Function in Rheumatoid Arthritis

The Effect of Inhibition of Interleukin-6 Activity on Vascular, Endothelial and Left Ventricular Function in Patients With Rheumatoid Arthritis

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03288584
Enrollment
60
Registered
2017-09-20
Start date
2017-10-27
Completion date
2020-12-31
Last updated
2020-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inflammation, Rheumatoid Arthritis

Keywords

Arterial stiffness, Endothelial function, Endothelial glycocalyx, Left ventricular function, Apoptosis, Oxidative stress

Brief summary

Recent studies show beneficial effect of the inhibition of interleukin-6 (IL-6) activity on vascular and left ventricular (LV) function. The purpose of this study is to investigate whether anakinra, an IL-6 receptor antagonist, improves vascular, endothelial and LV function in patients with rheumatoid arthritis (RA).

Detailed description

The inflammatory processes observed in patients with rheumatoid arthritis (RA) are strongly linked to enhanced interleukin-6 (IL-6) activity. Increased IL-6 activity causes myocardial cell damage and endothelial dysfunction. The adverse effects of IL-6 on myocardial and endothelial cells are mediated by an enhanced nitrooxidative stress and the promotion of apoptotic cardiomyocyte death through increased nitrooxidative stress and inflammation. Tocilizumab, a recombinant form of human IL-6 receptor antagonist, is commonly used for the treatment of RA. However it has not been defined whether inhibition of IL-6 activity by tocilizumab shows beneficial effects on endothelial, coronary, arterial and LV systolic and diastolic function in patients with RA. For this purpose, we studied 60 patients with RA (American Rheumatism Association criteria). All the above subjects had an inadequate response to disease modifying antirheumatic drugs (DMARDs) and corticosteroids and were going to initiate treatment with IL-6 activity inhibitor (tocilizumab). All patients were on treatment with statins and cardioactive medications respectively, for the last 6 months. All patients were randomized to receive a single injection of tocilizumab (150 mg s.c.), or other biological agent (TNFa inhibitor, abatacept, rituximab, IL-1Ra) or enhanced treatment with corticosteroid and non-biological agents. Twenty asymptomatic subjects matched for age and sex as the RA patients and with a normal ECG, echocardiogram, and treadmill test were selected as healthy control subjects among subjects attending the cardiology outpatients' clinic. At baseline in all RA subjects and controls as well as 3 months after the single injection of tocilizumab in RA subjects, we assessed the following parameters a)carotid-femoral pulse wave velocity (PWV), b) the LV dimensions,fractional shortening and wall motion score index (WMSI) c) the systolic (Sm), early diastolic (Em) and late diastolic (Am) myocardial velocities of the mitral annulus by using of tissue Doppler (TDI) as well as the ratio of E wave of the mitral inflow measured by pulsed wave Doppler to the mean Em as an index of LV diastolic filling pressures d) the LV longitudinal, circumferential and radial strain and strain rate, as well as Global Longitudinal strain and Torsion using speckle tracking echocardiography e) the coronary flow reserve (CFR)after adenosine infusion to assess coronary vasomotor function f) the flow-mediated endothelial-dependent dilation of the brachial artery (FMD) to assess peripheral endothelial function g) the diameters of aorta at systole and diastole to calculate the aortic strain as an index of local aortic properties, h) perfused boundary region (PBR) of the sublingual arterial microvessels (ranged from 5-25μm) using Sideview, Darkfield imaging (Microscan, Glycocheck). Increased PBR is considered an accurate index of reduced endothelial glucocalyx thickness because of a deeper red blood cells (RBC) penetration in the glucocalyx. At the same time periods, we measured in blood samples a) nitrotyrosine (NT), protein carbonyls (PC) and malondialdehyde (MDA) to assess oxidative stress, b) soluble Fas and Fas-ligand to assess apoptosis, and c) interleukin-6 and tumor necrosis factor-a to assess inflammation.

Interventions

Inhibition of Interleukin-6 activity by tocilizumab (Actemra®) 150mg od, sc injection

Other biological agent (TNFa inhibitor, abatacept, rituximab, IL-1Ra)

DRUGCorticosteroid and non-biological agents.

Enhanced treatment with corticosteroid and non-biological agents.

Sponsors

University of Athens
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients with rheumatoid arthritis who had an inadequate response to disease modifying antirheumatic drugs (DMARDs) and corticosteroids and were going to initiate treatment with interleukin-6 inhibitor.

Exclusion criteria

* Familiar hyperlipidemia * Diabetes mellitus * Chronic obstructive pulmonary disease or asthma * Moderate or severe valvular heart disease * Primary cardiomyopathies * Malignant tumors

Design outcomes

Primary

MeasureTime frameDescription
Reduction of pulse wave velocity after treatment with tocilizumab3 months after treatmentReduction of pulse wave velocity (PWV, m/sec) using tonometry after administration of tocilizumab
Increase of global longitudinal strain after treatment with tocilizumab3 months after treatmentIncrease of left ventricular global longitudinal strain (GLS, %) using speckle tracking echocardiography after administration of tocilizumab

Secondary

MeasureTime frameDescription
Reduction of malondialdehyde after treatment with tocilizumab3 months after treatmentReduction of malondialdehyde (MDA, nmol/L) using spectrophotometry after treatment with tocilizumab
Reduction of protein carbonyls after treatment with tocilizumab3 months after treatmentReduction of protein carbonyls (PCs, nmol/mg protein) using spectrophotometry after treatment with tocilizumab
Increased of endothelial glycocalyx thickness after treatment with tocilizumab3 months after treatmentIncreased of endothelial glycocalyx thickness as assessed by perfused boundary region (PBR, micrometers) of the sublingual arterial microvessels after treatment with tocilizumab

Countries

Greece

Contacts

Primary ContactIgnatios Ikonomidis, MD
ignoik@otenet.gr00302105832187
Backup ContactJohn Lekakis, MD
lekakisster@gmail.com00302105832187

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026