Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Smoking has been identified as a key risk factor for the development of cardiovascular diseases (CVD). It was found that a persistent increase in levels of oxidative stress and prolonged inflammation play a pivotal role in the pathogenesis of smoking associated CVD. Oligomeric proanthocyanidins (OPCs) are widely known for their anti-oxidant and anti-inflammatory effects, in vitro and in vivo. However, there are hardly any studies available that systematically investigated their acute and long-term effects on vascular function as well as on established biomarkers of oxidative stress and inflammation in an "at risk" population such as smokers.
Therefore, the aim of the present study is to investigate the effects of an eight-week supplementation with OPCs on vascular function as well as biomarkers of oxidative stress and inflammation in blood of smokers.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Placebo Comparator | placebo |
|
| 2 | Active Comparator | 200 mg oligomeric proanthocyanidins (MASQUELIER'S Original OPCs) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| oligomeric proanthocyanidins (MASQUELIER'S Original OPCs) | Dietary Supplement | 200 mg oligomeric proanthocyanidins (MASQUELIER'S Original OPCs) per day over 8 weeks |
|
| Measure | Description | Time Frame |
|---|---|---|
| Vasoreactivity of conduit arteries by means of flow mediated dilation (FMD) | before start of intervention and at the end of the 8 week of intervention |
| Measure | Description | Time Frame |
|---|---|---|
| Endothelium-dependent and -independent reactivity of microvasculature by means of Laser Doppler flowmetry (LDF) | before start of intervention, after 4 and 8 weeks of intervention | |
| Plasma nitrite and nitrate levels | before start of intervention, after 4 and 8 weeks of intervention |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Antje R Weseler, PhD | Maastricht University | Principal Investigator |
| Aalt Bast, PhD, Prof. | Maastricht University | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Maastricht University | Maastricht | 6200 MD | Netherlands |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 22174811 | Derived | Weseler AR, Ruijters EJ, Drittij-Reijnders MJ, Reesink KD, Haenen GR, Bast A. Pleiotropic benefit of monomeric and oligomeric flavanols on vascular health--a randomized controlled clinical pilot study. PLoS One. 2011;6(12):e28460. doi: 10.1371/journal.pone.0028460. Epub 2011 Dec 8. |
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D012907 | Smoking |
| D007249 | Inflammation |
| ID | Term |
|---|---|
| D001519 | Behavior |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Placebo | Dietary Supplement | placebo |
|
| Systemic oxidative stress markers such as plasma levels of PGF2alpha and TEAC, GSH erythrocyte levels and gene expression of redox enzymes | before start of intervention, after 4 and 8 weeks of intervention |
| Systemic inflammation markers such as plasma levels of hsCRP, fibrinogen and cytokines, as well as gene expression levels of the latter | before start of intervention, after 4 and 8 weeks of intervention |