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Mesoglycan: Clinical Evidences for Use in Vascular Diseases

Identifieur interne : 004012 ( Ncbi/Merge ); précédent : 004011; suivant : 004013

Mesoglycan: Clinical Evidences for Use in Vascular Diseases

Auteurs : Antonella Tufano [Italie] ; Claudia Arturo [Italie] ; Ernesto Cimino [Italie] ; Matteo Nicola Dario Di Minno [Italie] ; Mirko Di Capua [Italie] ; Anna Maria Cerbone [Italie] ; Giovanni Di Minno [Italie]

Source :

RBID : PMC:2989756

Abstract

Vascular glycosaminoglycans (GAG) are essential components of the endothelium and vessel wall and have been shown to be involved in several biologic functions. Mesoglycan, a natural GAG preparation, is a polysaccharide complex rich in sulphur radicals with strong negative electric charge. It is extracted from porcine intestinal mucosa and is composed of heparan sulfate, dermatan sulfate, electrophoretically slow-moving heparin, and variable and minimal quantities of chondroitin sulfate. Data on antithrombotic and profibrinolytic activities of the drug show that mesoglycan, although not indicated in the treatment of acute arterial or venous thrombosis because of the low antithrombotic effect, may be useful in the management of vascular diseases, when combined with antithrombotics in the case of disease of cerebral vasculature, and with antithrombotics and vasodilator drugs in the case of chronic peripheral arterial disease. The protective effect of mesoglycan in patients with venous thrombosis and the absence of side effects, support the use of GAG in patients with chronic venous insufficiency and persistent venous ulcers, in association with compression therapy (zinc bandages, multiple layer bandages, etc.), elastic compression stockings, and local care, and in the prevention of recurrences in patients with previous DVT following the standard course of oral anticoagulation treatment.


Url:
DOI: 10.1155/2010/390643
PubMed: 21152191
PubMed Central: 2989756

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PMC:2989756

Le document en format XML

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<p>Vascular glycosaminoglycans (GAG) are essential components of the endothelium and vessel wall and have been shown to be involved in several biologic functions. Mesoglycan, a natural GAG preparation, is a polysaccharide complex rich in sulphur radicals with strong negative electric charge. It is extracted from porcine intestinal mucosa and is composed of heparan sulfate, dermatan sulfate, electrophoretically slow-moving heparin, and variable and minimal quantities of chondroitin sulfate. Data on antithrombotic and profibrinolytic activities of the drug show that mesoglycan, although not indicated in the treatment of acute arterial or venous thrombosis because of the low antithrombotic effect, may be useful in the management of vascular diseases, when combined with antithrombotics in the case of disease of cerebral vasculature, and with antithrombotics and vasodilator drugs in the case of chronic peripheral arterial disease. The protective effect of mesoglycan in patients with venous thrombosis and the absence of side effects, support the use of GAG in patients with chronic venous insufficiency and persistent venous ulcers, in association with compression therapy (zinc bandages, multiple layer bandages, etc.), elastic compression stockings, and local care, and in the prevention of recurrences in patients with previous DVT following the standard course of oral anticoagulation treatment.</p>
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</back>
</TEI>
<pmc article-type="review-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Int J Vasc Med</journal-id>
<journal-id journal-id-type="iso-abbrev">Int J Vasc Med</journal-id>
<journal-id journal-id-type="publisher-id">IJVM</journal-id>
<journal-title-group>
<journal-title>International Journal of Vascular Medicine</journal-title>
</journal-title-group>
<issn pub-type="ppub">2090-2824</issn>
<issn pub-type="epub">2090-2832</issn>
<publisher>
<publisher-name>Hindawi Publishing Corporation</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">21152191</article-id>
<article-id pub-id-type="pmc">2989756</article-id>
<article-id pub-id-type="doi">10.1155/2010/390643</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Review Article</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Mesoglycan: Clinical Evidences for Use in Vascular Diseases</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Tufano</surname>
<given-names>Antonella</given-names>
</name>
<xref ref-type="aff" rid="I1"></xref>
<xref ref-type="corresp" rid="cor1">*</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Arturo</surname>
<given-names>Claudia</given-names>
</name>
<xref ref-type="aff" rid="I1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Cimino</surname>
<given-names>Ernesto</given-names>
</name>
<xref ref-type="aff" rid="I1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Di Minno</surname>
<given-names>Matteo Nicola Dario</given-names>
</name>
<xref ref-type="aff" rid="I1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Di Capua</surname>
<given-names>Mirko</given-names>
</name>
<xref ref-type="aff" rid="I1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Cerbone</surname>
<given-names>Anna Maria</given-names>
</name>
<xref ref-type="aff" rid="I1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Di Minno</surname>
<given-names>Giovanni</given-names>
</name>
<xref ref-type="aff" rid="I1"></xref>
</contrib>
</contrib-group>
<aff id="I1">Regional Reference Centre for Coagulation Disorders, Department of Clinical and Experimental Medicine, AOU “Federico II” Naples 80131, Italy</aff>
<author-notes>
<corresp id="cor1">*Antonella Tufano:
<email>atufano@unina.it</email>
</corresp>
<fn fn-type="other">
<p>Academic Editor: Alun H. Davies</p>
</fn>
</author-notes>
<pub-date pub-type="ppub">
<year>2010</year>
</pub-date>
<pub-date pub-type="epub">
<day>31</day>
<month>8</month>
<year>2010</year>
</pub-date>
<volume>2010</volume>
<elocation-id>390643</elocation-id>
<history>
<date date-type="received">
<day>1</day>
<month>3</month>
<year>2010</year>
</date>
<date date-type="rev-recd">
<day>4</day>
<month>6</month>
<year>2010</year>
</date>
<date date-type="accepted">
<day>12</day>
<month>7</month>
<year>2010</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright © 2010 Antonella Tufano et al.</copyright-statement>
<copyright-year>2010</copyright-year>
<license xlink:href="https://creativecommons.org/licenses/by/3.0/">
<license-p>This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<abstract>
<p>Vascular glycosaminoglycans (GAG) are essential components of the endothelium and vessel wall and have been shown to be involved in several biologic functions. Mesoglycan, a natural GAG preparation, is a polysaccharide complex rich in sulphur radicals with strong negative electric charge. It is extracted from porcine intestinal mucosa and is composed of heparan sulfate, dermatan sulfate, electrophoretically slow-moving heparin, and variable and minimal quantities of chondroitin sulfate. Data on antithrombotic and profibrinolytic activities of the drug show that mesoglycan, although not indicated in the treatment of acute arterial or venous thrombosis because of the low antithrombotic effect, may be useful in the management of vascular diseases, when combined with antithrombotics in the case of disease of cerebral vasculature, and with antithrombotics and vasodilator drugs in the case of chronic peripheral arterial disease. The protective effect of mesoglycan in patients with venous thrombosis and the absence of side effects, support the use of GAG in patients with chronic venous insufficiency and persistent venous ulcers, in association with compression therapy (zinc bandages, multiple layer bandages, etc.), elastic compression stockings, and local care, and in the prevention of recurrences in patients with previous DVT following the standard course of oral anticoagulation treatment.</p>
</abstract>
</article-meta>
</front>
<floats-group>
<table-wrap id="tab1" position="float">
<label>Table 1</label>
<caption>
<p>Mesoglycan in ischemic stroke. Clinical studies.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" rowspan="1" colspan="1">Author</th>
<th align="center" rowspan="1" colspan="1">Study design</th>
<th align="left" rowspan="1" colspan="1">Pathology</th>
<th align="center" rowspan="1" colspan="1">Patients (
<italic>n</italic>
)</th>
<th align="left" rowspan="1" colspan="1">Doses/route</th>
<th align="left" rowspan="1" colspan="1">Results</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" rowspan="1" colspan="1">Orefice [
<xref rid="B13" ref-type="bibr">12</xref>
]</td>
<td align="center" rowspan="1" colspan="1">Prospective</td>
<td align="left" rowspan="1" colspan="1">Stroke
<break></break>
(1–3 mo before)</td>
<td align="center" rowspan="1" colspan="1">30</td>
<td align="left" rowspan="1" colspan="1">Mesoglycan 50 mg twice daily orally for 3 months</td>
<td align="left" rowspan="1" colspan="1">Mesoglycan: safe and effective in reducing FBR without interfering with other coagulative parameters</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Orefice [
<xref rid="B12" ref-type="bibr">11</xref>
]</td>
<td align="center" rowspan="1" colspan="1">Randomized Controlled</td>
<td align="left" rowspan="1" colspan="1">Stroke
<break></break>
(2-3 mo before)</td>
<td align="center" rowspan="1" colspan="1">46</td>
<td align="left" rowspan="1" colspan="1">Mesoglycan 50 mg twice daily orally versus Ticlopidine 250 mg twice daily, for 2 months</td>
<td align="left" rowspan="1" colspan="1">Mesoglycan and ticlopidine: both safe and effective in reducing FBR without interfering with other coagulative parameters</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Vecchio [
<xref rid="B15" ref-type="bibr">13</xref>
]</td>
<td align="center" rowspan="1" colspan="1">Prospective</td>
<td align="left" rowspan="1" colspan="1">Stroke
<break></break>
(within 2 mo)</td>
<td align="center" rowspan="1" colspan="1">20</td>
<td align="left" rowspan="1" colspan="1">Mesoglycan 30 mg twice daily intramuscular, for 15 days</td>
<td align="left" rowspan="1" colspan="1">Mesoglycan: significant reduction in FBR, cholesterol, triglycerides, improved erythrocyte filterability without interfering with other coagulative parameters</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Mansi [
<xref rid="B16" ref-type="bibr">14</xref>
]</td>
<td align="center" rowspan="1" colspan="1">Prospective</td>
<td align="left" rowspan="1" colspan="1">TIA or stroke (within 3 mo)</td>
<td align="center" rowspan="1" colspan="1">30</td>
<td align="left" rowspan="1" colspan="1">Mesoglycan 50 mg twice daily orally</td>
<td align="left" rowspan="1" colspan="1">Mesoglycan decreases neurologic deficits</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Forconi [
<xref rid="B17" ref-type="bibr">15</xref>
]</td>
<td align="center" rowspan="1" colspan="1">Multicenter clinical trial</td>
<td align="left" rowspan="1" colspan="1">History of stroke, TIA, RIND or minor stroke</td>
<td align="center" rowspan="1" colspan="1">1,398</td>
<td align="left" rowspan="1" colspan="1">Mesoglycan 30 mg twice daily i.m., then 100 mg daily orally, versus ASA 300 mg daily</td>
<td align="left" rowspan="1" colspan="1">No differences. ASA: higher incidence of side effects</td>
</tr>
</tbody>
</table>
</table-wrap>
<table-wrap id="tab2" position="float">
<label>Table 2</label>
<caption>
<p>Mesoglycan in peripheral obstructive arterial disease (POAD). Clinical studies.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" rowspan="1" colspan="1">Author</th>
<th align="left" rowspan="1" colspan="1">Study design</th>
<th align="left" rowspan="1" colspan="1">Pathology</th>
<th align="center" rowspan="1" colspan="1">Patients (
<italic>n</italic>
)</th>
<th align="left" rowspan="1" colspan="1">Doses/route</th>
<th align="left" rowspan="1" colspan="1">Results</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" rowspan="1" colspan="1">Andreozzi [
<xref rid="B18" ref-type="bibr">18</xref>
]</td>
<td align="left" rowspan="1" colspan="1">Prospective</td>
<td align="left" rowspan="1" colspan="1">POAD in stages I-II Fontaine</td>
<td align="center" rowspan="1" colspan="1">10</td>
<td align="left" rowspan="1" colspan="1">Mesoglycan 60 mg daily
<break></break>
for 20 days</td>
<td align="left" rowspan="1" colspan="1">Mesoglycan: safe and effective in improving the wall response to vasodilator stimulus</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Raso [
<xref rid="B21" ref-type="bibr">19</xref>
]</td>
<td align="left" rowspan="1" colspan="1">Prospective</td>
<td align="left" rowspan="1" colspan="1">POAD stage IIb Fontaine</td>
<td align="center" rowspan="1" colspan="1">36</td>
<td align="left" rowspan="1" colspan="1">Mesoglycan 60 mg daily endovenous for 10 days then 100 mg daily orally for 20 days, repeated for two months then oral mesoglycan for 12 months</td>
<td align="left" rowspan="1" colspan="1">Mesoglycan: significant improvement of symptoms and signs in all patients but one</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Nenci [
<xref rid="B22" ref-type="bibr">20</xref>
]</td>
<td align="left" rowspan="1" colspan="1">Randomized, double-blinded</td>
<td align="left" rowspan="1" colspan="1">PAOD stage II Fontaine</td>
<td align="center" rowspan="1" colspan="1">242</td>
<td align="left" rowspan="1" colspan="1">Mesoglycan 30 mg daily i.m. for 3 weeks then 100 mg daily orally for two weeks, versus matching placebo All patients receive ASA</td>
<td align="left" rowspan="1" colspan="1">Mesoglycan: significant clinical improvement versus placebo. Significant improvement in quality of life scores.</td>
</tr>
</tbody>
</table>
</table-wrap>
<table-wrap id="tab3" position="float">
<label>Table 3</label>
<caption>
<p>Mesoglycan and venous disease.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" rowspan="1" colspan="1">Author</th>
<th align="left" rowspan="1" colspan="1">Study design</th>
<th align="left" rowspan="1" colspan="1">Pathology</th>
<th align="center" rowspan="1" colspan="1">Patients (
<italic>n</italic>
)</th>
<th align="left" rowspan="1" colspan="1">Doses/route</th>
<th align="left" rowspan="1" colspan="1">Results</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" rowspan="1" colspan="1">Arosio [
<xref rid="B23" ref-type="bibr">23</xref>
]</td>
<td align="left" rowspan="1" colspan="1">Randomized</td>
<td align="left" rowspan="1" colspan="1">Chronic venous ulcers</td>
<td align="center" rowspan="1" colspan="1">183</td>
<td align="left" rowspan="1" colspan="1">Mesoglycan 30 mg daily i.m. for 3 weeks then 100 mg daily orally, versus placebo, for 24 ± 1 weeks</td>
<td align="left" rowspan="1" colspan="1">Mesoglycan: significant difference in the rate of ulcer healing versus placebo</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Andreozzi [
<xref rid="B28" ref-type="bibr">24</xref>
]</td>
<td align="left" rowspan="1" colspan="1">Retrospective analysis</td>
<td align="left" rowspan="1" colspan="1">Patients with previous DVT</td>
<td align="center" rowspan="1" colspan="1">36</td>
<td align="left" rowspan="1" colspan="1">Mesoglycan 50 mg twice daily orally</td>
<td align="left" rowspan="1" colspan="1">Mesoglycan: effective in preventing thrombotic recurrences</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Viliani [
<xref rid="B32" ref-type="bibr">25</xref>
]</td>
<td align="left" rowspan="1" colspan="1">Randomized</td>
<td align="left" rowspan="1" colspan="1">Mechanical oedema (MO)</td>
<td align="center" rowspan="1" colspan="1">44</td>
<td align="left" rowspan="1" colspan="1">FKT+Mesoglycan 30 mg twice daily orally versus FKT alone</td>
<td align="left" rowspan="1" colspan="1">Mesoglycan: significant clinical improvement in objective and subjective parameters</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Prandoni [
<xref rid="B33" ref-type="bibr">26</xref>
]</td>
<td align="left" rowspan="1" colspan="1">Randomized</td>
<td align="left" rowspan="1" colspan="1">DVT venographically proved</td>
<td align="center" rowspan="1" colspan="1">90</td>
<td align="left" rowspan="1" colspan="1">Heparin and then oral anticoagulation (12 weeks), then mesoglycan 72 mg daily orally versus placebo, for 1 year</td>
<td align="left" rowspan="1" colspan="1">Recurrences of DVT and/or PE less frequent with mesoglycan versus placebo (nonsignificant difference)</td>
</tr>
</tbody>
</table>
</table-wrap>
</floats-group>
</pmc>
<affiliations>
<list>
<country>
<li>Italie</li>
</country>
</list>
<tree>
<country name="Italie">
<noRegion>
<name sortKey="Tufano, Antonella" sort="Tufano, Antonella" uniqKey="Tufano A" first="Antonella" last="Tufano">Antonella Tufano</name>
</noRegion>
<name sortKey="Arturo, Claudia" sort="Arturo, Claudia" uniqKey="Arturo C" first="Claudia" last="Arturo">Claudia Arturo</name>
<name sortKey="Cerbone, Anna Maria" sort="Cerbone, Anna Maria" uniqKey="Cerbone A" first="Anna Maria" last="Cerbone">Anna Maria Cerbone</name>
<name sortKey="Cimino, Ernesto" sort="Cimino, Ernesto" uniqKey="Cimino E" first="Ernesto" last="Cimino">Ernesto Cimino</name>
<name sortKey="Di Capua, Mirko" sort="Di Capua, Mirko" uniqKey="Di Capua M" first="Mirko" last="Di Capua">Mirko Di Capua</name>
<name sortKey="Di Minno, Giovanni" sort="Di Minno, Giovanni" uniqKey="Di Minno G" first="Giovanni" last="Di Minno">Giovanni Di Minno</name>
<name sortKey="Di Minno, Matteo Nicola Dario" sort="Di Minno, Matteo Nicola Dario" uniqKey="Di Minno M" first="Matteo Nicola Dario" last="Di Minno">Matteo Nicola Dario Di Minno</name>
</country>
</tree>
</affiliations>
</record>

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   |étape=   Merge
   |type=    RBID
   |clé=     PMC:2989756
   |texte=   Mesoglycan: Clinical Evidences for Use in Vascular Diseases
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Ncbi/Merge/RBID.i   -Sk "pubmed:21152191" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Ncbi/Merge/biblio.hfd   \
       | NlmPubMed2Wicri -a LymphedemaV1 

Wicri

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