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| ID | Type | Description | Link |
|---|---|---|---|
| C26A12BPZN | Other Identifier | Sapienza University |
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Peripheral arterial disease (PAD) is a clinical setting characterized by an exceptionally high risk for cardiovascular events. Oxidative stress seems to play a role in impairing flow-mediated dilation (FMD) and contributing to atherosclerosis in patients with PAD. Cocoa seems to exert artery dilatation via oxidative stress inhibition.
OBJECTIVES: To investigate whether in PAD patients, dark chocolate elicits artery dilatation via down-regulation of NOX2, the catalytic core of NADPH oxidase.
Atherosclerosis represents the major cause of worldwide death; it is a complex phenomenon that encompasses the intricate interplay of classic cardiovascular risk factors, oxidative stress and inflammation.
Peripheral artery disease (PAD) is a clinical setting that well represents the model of widespread atherosclerosis. PAD affects 20% of patients over the age of 75. Furthermore, PAD patients are at an exceptionally high risk for cardiovascular events and the majority will eventually die of a cardiac or cerebrovascular etiology.
Polyphenol could represent a novel therapeutic strategy to counteract atherosclerosis. During the last decades, a growing interest in polyphenols resulted from prospective and epidemiological studies that showed the beneficial effects of these substances on human health. In particular, polyphenols exert their beneficial effect by inhibition of NADPH oxidase (NOX2), an enzyme directly involved in atherosclerosis; thus, the activation of this enzyme leads to an enhanced production of oxidative stress and inflammatory processes.
The objective of this study is to evaluate the effect of polyphenols on oxidative stress and inflammation and on surrogate markers of atherosclerosis in PAD patients. Polyphenols, inhibiting NOX2-mediated oxidative stress and immune-mediated process, could represent a novel therapy to reduce the high risk of cardiovascular events in PAD.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| milk chocolate | Placebo Comparator | dosage form: orally given dosage:40 g milk chocolate (≤35% cocoa) frequency and duration: 40 g/day for one month |
|
| dark chocolate | Active Comparator | dosage form: orally given dosage:40 g dark chocolate (≥85% cocoa) frequency and duration: 40 g/day for one month |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| dark chocolate with crossover to milk chocolate | Dietary Supplement | 40 g/d of dark chocolate for 4 weeks followed by wash-out (1 week) and by 40 g/d of milk chocolate for 4 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| endothelial function assessed by flow mediated dilation (FMD) | 2 hours after (dark or milk) chocolate ingestion | |
| endothelial function assessed by flow mediated dilation (FMD) | after 30 days of (dark or milk) chocolate ingestion |
| Measure | Description | Time Frame |
|---|---|---|
| Oxidative stress markers | Oxidative stress markers: sNOX2dp, Isoprostanes, NOx | 2 hours after (dark or milk) chocolate ingestion |
| Maximal walking distance | 2 hours after (dark or milk) chocolate ingestion |
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Inclusion Criteria:
Every PAD patient to be enrolled in the study had:
Patients had to be in stable conditions without abrupt changes of ABI (>20%) in the last month before the enrolment.
Exclusion Criteria:
Subjects were excluded from the study if they had liver insufficiency, serious renal disorders (serum creatinine>2.8 mg/dL), acute stroke, acute myocardial infarction, deep venous thrombosis or if they were current smokers or were taking antioxidants.
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| Name | Affiliation | Role |
|---|---|---|
| Francesco Violi, MD | Sapienza University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Sapienza University of Rome, I Clinica Medica, Research Tower | Rome | 00161 | Italy |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 22336250 | Background | Loffredo L, Carnevale R, Cangemi R, Angelico F, Augelletti T, Di Santo S, Calabrese CM, Della Volpe L, Pignatelli P, Perri L, Basili S, Violi F. NOX2 up-regulation is associated with artery dysfunction in patients with peripheral artery disease. Int J Cardiol. 2013 Apr 30;165(1):184-92. doi: 10.1016/j.ijcard.2012.01.069. Epub 2012 Feb 14. | |
| 22066819 |
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| ID | Term |
|---|---|
| D058729 | Peripheral Arterial Disease |
| ID | Term |
|---|---|
| D050197 | Atherosclerosis |
| D001161 | Arteriosclerosis |
| D001157 | Arterial Occlusive Diseases |
| D014652 | Vascular Diseases |
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| milk chocolate with crossover to dark chocolate | Dietary Supplement | 40 g/d of milk chocolate for 4 weeks followed by wash-out (1 week) and by 40 g/d of dark chocolate for 4 weeks. |
|
| Ankle Brachial Index (ABI) | 2 hours after (dark or milk) chocolate ingestion |
| Oxidative stress markers | Oxidative stress markers: sNOX2dp, Isoprostanes, NOx | after 30 days of (dark or milk) chocolate ingestion |
| Maximal walking distance | after 30 days of (dark or milk) chocolate ingestion |
| Ankle Brachial Index (ABI) | after 30 days of (dark or milk) chocolate ingestion |
| Carnevale R, Loffredo L, Pignatelli P, Nocella C, Bartimoccia S, Di Santo S, Martino F, Catasca E, Perri L, Violi F. Dark chocolate inhibits platelet isoprostanes via NOX2 down-regulation in smokers. J Thromb Haemost. 2012 Jan;10(1):125-32. doi: 10.1111/j.1538-7836.2011.04558.x. |
| 21807659 | Background | Loffredo L, Carnevale R, Perri L, Catasca E, Augelletti T, Cangemi R, Albanese F, Piccheri C, Nocella C, Pignatelli P, Violi F. NOX2-mediated arterial dysfunction in smokers: acute effect of dark chocolate. Heart. 2011 Nov;97(21):1776-81. doi: 10.1136/heartjnl-2011-300304. Epub 2011 Jul 31. |
| 24990275 | Derived | Loffredo L, Perri L, Catasca E, Pignatelli P, Brancorsini M, Nocella C, De Falco E, Bartimoccia S, Frati G, Carnevale R, Violi F. Dark chocolate acutely improves walking autonomy in patients with peripheral artery disease. J Am Heart Assoc. 2014 Jul 2;3(4):e001072. doi: 10.1161/JAHA.114.001072. |
| D002318 |
| Cardiovascular Diseases |
| D016491 | Peripheral Vascular Diseases |