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Human Serum/Plasma Glycoprotein Analysis by 1H-NMR, an Emerging Method of Inflammatory Assessment

Identifieur interne : 000E80 ( Ncbi/Merge ); précédent : 000E79; suivant : 000E81

Human Serum/Plasma Glycoprotein Analysis by 1H-NMR, an Emerging Method of Inflammatory Assessment

Auteurs : Rocío Fuertes-Martín [Espagne] ; Xavier Correig [Espagne] ; Joan-Carles Vallvé [Espagne] ; Núria Amig [Espagne]

Source :

RBID : PMC:7073769

Abstract

Several studies suggest that variations in the concentration of plasma glycoproteins can influence cellular changes in a large number of diseases. In recent years, proton nuclear magnetic resonance (1H-NMR) has played a major role as an analytical tool for serum and plasma samples. In recent years, there is an increasing interest in the characterization of glycoproteins through 1H-NMR in order to search for reliable and robust biomarkers of disease. The objective of this review was to examine the existing studies in the literature related to the study of glycoproteins from an analytical and clinical point of view. There are currently several techniques to characterize circulating glycoproteins in serum or plasma, but in this review, we focus on 1H-NMR due to its great robustness and recent interest in its translation to the clinical setting. In fact, there is already a marker in H-NMR representing the acetyl groups of the glycoproteins, GlycA, which has been increasingly studied in clinical studies. A broad search of the literature was performed showing a general consensus that GlycA is a robust marker of systemic inflammation. The results also suggested that GlycA better captures systemic inflammation even more than C-reactive protein (CRP), a widely used classical inflammatory marker. The applications reviewed here demonstrated that GlycA was potentially a key biomarker in a wide range of diseases such as cancer, metabolic diseases, cardiovascular risk, and chronic inflammatory diseases among others. The profiling of glycoproteins through 1H-NMR launches an encouraging new paradigm for its future incorporation in clinical diagnosis.


Url:
DOI: 10.3390/jcm9020354
PubMed: 32012794
PubMed Central: 7073769

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PMC:7073769

Le document en format XML

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<p>Several studies suggest that variations in the concentration of plasma glycoproteins can influence cellular changes in a large number of diseases. In recent years, proton nuclear magnetic resonance (
<sup>1</sup>
H-NMR) has played a major role as an analytical tool for serum and plasma samples. In recent years, there is an increasing interest in the characterization of glycoproteins through
<sup>1</sup>
H-NMR in order to search for reliable and robust biomarkers of disease. The objective of this review was to examine the existing studies in the literature related to the study of glycoproteins from an analytical and clinical point of view. There are currently several techniques to characterize circulating glycoproteins in serum or plasma, but in this review, we focus on
<sup>1</sup>
H-NMR due to its great robustness and recent interest in its translation to the clinical setting. In fact, there is already a marker in H-NMR representing the acetyl groups of the glycoproteins, GlycA, which has been increasingly studied in clinical studies. A broad search of the literature was performed showing a general consensus that GlycA is a robust marker of systemic inflammation. The results also suggested that GlycA better captures systemic inflammation even more than C-reactive protein (CRP), a widely used classical inflammatory marker. The applications reviewed here demonstrated that GlycA was potentially a key biomarker in a wide range of diseases such as cancer, metabolic diseases, cardiovascular risk, and chronic inflammatory diseases among others. The profiling of glycoproteins through
<sup>1</sup>
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</TEI>
<pmc article-type="review-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">J Clin Med</journal-id>
<journal-id journal-id-type="iso-abbrev">J Clin Med</journal-id>
<journal-id journal-id-type="publisher-id">jcm</journal-id>
<journal-title-group>
<journal-title>Journal of Clinical Medicine</journal-title>
</journal-title-group>
<issn pub-type="epub">2077-0383</issn>
<publisher>
<publisher-name>MDPI</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">32012794</article-id>
<article-id pub-id-type="pmc">7073769</article-id>
<article-id pub-id-type="doi">10.3390/jcm9020354</article-id>
<article-id pub-id-type="publisher-id">jcm-09-00354</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Review</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Human Serum/Plasma Glycoprotein Analysis by
<sup>1</sup>
H-NMR, an Emerging Method of Inflammatory Assessment</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Fuertes-Martín</surname>
<given-names>Rocío</given-names>
</name>
<xref ref-type="aff" rid="af1-jcm-09-00354">1</xref>
<xref ref-type="aff" rid="af2-jcm-09-00354">2</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid" authenticated="true">https://orcid.org/0000-0002-6902-3054</contrib-id>
<name>
<surname>Correig</surname>
<given-names>Xavier</given-names>
</name>
<xref ref-type="aff" rid="af2-jcm-09-00354">2</xref>
<xref rid="c1-jcm-09-00354" ref-type="corresp">*</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid" authenticated="true">https://orcid.org/0000-0001-8711-9618</contrib-id>
<name>
<surname>Vallvé</surname>
<given-names>Joan-Carles</given-names>
</name>
<xref ref-type="aff" rid="af2-jcm-09-00354">2</xref>
<xref ref-type="aff" rid="af3-jcm-09-00354">3</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid" authenticated="true">https://orcid.org/0000-0002-0116-9145</contrib-id>
<name>
<surname>Amigó</surname>
<given-names>Núria</given-names>
</name>
<xref ref-type="aff" rid="af1-jcm-09-00354">1</xref>
<xref ref-type="aff" rid="af2-jcm-09-00354">2</xref>
</contrib>
</contrib-group>
<aff id="af1-jcm-09-00354">
<label>1</label>
Biosfer Teslab SL, 43201 Reus, Spain;
<email>rociofrtsm@gmail.com</email>
(R.F.-M.);
<email>namigo@biosferteslab.com</email>
(N.A.)</aff>
<aff id="af2-jcm-09-00354">
<label>2</label>
Metabolomic s platform, IISPV, CIBERDEM, Rovira i Virgili University, 43007 Tarragona, Spain</aff>
<aff id="af3-jcm-09-00354">
<label>3</label>
Lipids and Arteriosclerosis Research Unit, Sant Joan de Reus University Hospital, 43201 Reus, Spain</aff>
<author-notes>
<corresp id="c1-jcm-09-00354">
<label>*</label>
Correspondence:
<email>xavier.correig@urv.cat</email>
; Tel.: +34-977-559-623</corresp>
</author-notes>
<pub-date pub-type="epub">
<day>27</day>
<month>1</month>
<year>2020</year>
</pub-date>
<pub-date pub-type="collection">
<month>2</month>
<year>2020</year>
</pub-date>
<volume>9</volume>
<issue>2</issue>
<elocation-id>354</elocation-id>
<history>
<date date-type="received">
<day>19</day>
<month>12</month>
<year>2019</year>
</date>
<date date-type="accepted">
<day>17</day>
<month>1</month>
<year>2020</year>
</date>
</history>
<permissions>
<copyright-statement>© 2020 by the authors.</copyright-statement>
<copyright-year>2020</copyright-year>
<license license-type="open-access">
<license-p>Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (
<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0/">http://creativecommons.org/licenses/by/4.0/</ext-link>
).</license-p>
</license>
</permissions>
<abstract>
<p>Several studies suggest that variations in the concentration of plasma glycoproteins can influence cellular changes in a large number of diseases. In recent years, proton nuclear magnetic resonance (
<sup>1</sup>
H-NMR) has played a major role as an analytical tool for serum and plasma samples. In recent years, there is an increasing interest in the characterization of glycoproteins through
<sup>1</sup>
H-NMR in order to search for reliable and robust biomarkers of disease. The objective of this review was to examine the existing studies in the literature related to the study of glycoproteins from an analytical and clinical point of view. There are currently several techniques to characterize circulating glycoproteins in serum or plasma, but in this review, we focus on
<sup>1</sup>
H-NMR due to its great robustness and recent interest in its translation to the clinical setting. In fact, there is already a marker in H-NMR representing the acetyl groups of the glycoproteins, GlycA, which has been increasingly studied in clinical studies. A broad search of the literature was performed showing a general consensus that GlycA is a robust marker of systemic inflammation. The results also suggested that GlycA better captures systemic inflammation even more than C-reactive protein (CRP), a widely used classical inflammatory marker. The applications reviewed here demonstrated that GlycA was potentially a key biomarker in a wide range of diseases such as cancer, metabolic diseases, cardiovascular risk, and chronic inflammatory diseases among others. The profiling of glycoproteins through
<sup>1</sup>
H-NMR launches an encouraging new paradigm for its future incorporation in clinical diagnosis.</p>
</abstract>
<kwd-group>
<kwd>glycoprotein</kwd>
<kwd>GlycA</kwd>
<kwd>NAC</kwd>
<kwd>NAG</kwd>
<kwd>
<sup>1</sup>
H-NMR</kwd>
<kwd>inflammation</kwd>
</kwd-group>
</article-meta>
</front>
<floats-group>
<fig id="jcm-09-00354-f001" orientation="portrait" position="float">
<label>Figure 1</label>
<caption>
<p>Initiation and maturation of glycoproteins in the ER–Golgi–plasma (Endoplasmic reticulum–Golgi–plasma) membrane pathway. This illustration outlines an overview of the mechanisms for initiation, trimming, and elongation of the glycoprotein in a human cell. Orange and blue spheres represent the addition of glycans chains to proteins (in green) in the Golgi apparatus. Examples of
<italic>N</italic>
-glycans structures (
<bold>a</bold>
) and
<italic>O</italic>
-Glycans structures (
<bold>b</bold>
) are also represented.</p>
</caption>
<graphic xlink:href="jcm-09-00354-g001"></graphic>
</fig>
<fig id="jcm-09-00354-f002" orientation="portrait" position="float">
<label>Figure 2</label>
<caption>
<p>
<sup>1</sup>
H-NMR (nuclear magnetic resonance) glycoprotein analysis methodology. (
<bold>A</bold>
) Sample tube and spectrometer; (
<bold>B</bold>
) examples of
<italic>N</italic>
-glycans with different residues attached to the protein chain by asparagine (Asn); (
<bold>C</bold>
)
<sup>1</sup>
H-NMR spectrum produced by the sample in which the region of the glycoproteins is marked. The chemical group producing this signal is indicated.</p>
</caption>
<graphic xlink:href="jcm-09-00354-g002"></graphic>
</fig>
<fig id="jcm-09-00354-f003" orientation="portrait" position="float">
<label>Figure 3</label>
<caption>
<p>Trend graph of the number of research articles per year in recent year.</p>
</caption>
<graphic xlink:href="jcm-09-00354-g003"></graphic>
</fig>
<table-wrap id="jcm-09-00354-t001" orientation="portrait" position="float">
<object-id pub-id-type="pii">jcm-09-00354-t001_Table 1</object-id>
<label>Table 1</label>
<caption>
<p>Examples of serum protein glycation changes and their association with disease.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" rowspan="1" colspan="1">Glycoprotein</th>
<th align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" rowspan="1" colspan="1">Glycation Change</th>
<th align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" rowspan="1" colspan="1">Related Diseases</th>
<th align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" rowspan="1" colspan="1">References</th>
</tr>
</thead>
<tbody>
<tr>
<td rowspan="4" align="center" valign="middle" style="border-bottom:solid thin" colspan="1">Alpha 1-Acid
<break></break>
Glycoprotein (AGP)</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Highly branched
<italic>N</italic>
-linked glycan</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Cirrhosis and HCC, congenital disorders, RA, SLE</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B35-jcm-09-00354" ref-type="bibr">35</xref>
,
<xref rid="B36-jcm-09-00354" ref-type="bibr">36</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Increased sialylation</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Cancer</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B37-jcm-09-00354" ref-type="bibr">37</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Decreased sialylation</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Cirrhosis and HCC</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B35-jcm-09-00354" ref-type="bibr">35</xref>
,
<xref rid="B38-jcm-09-00354" ref-type="bibr">38</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Increased fucosylation</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">liver cancer</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B39-jcm-09-00354" ref-type="bibr">39</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Alpha-Fetoprotein</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Elevated bisecting
<break></break>
<italic>N</italic>
-acetylglucosamine, decrease in sialylation and increase in fucosylation</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Cirrhosis, hepatitis and HCC</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B40-jcm-09-00354" ref-type="bibr">40</xref>
,
<xref rid="B41-jcm-09-00354" ref-type="bibr">41</xref>
,
<xref rid="B42-jcm-09-00354" ref-type="bibr">42</xref>
]</td>
</tr>
<tr>
<td rowspan="4" align="center" valign="middle" style="border-bottom:solid thin" colspan="1">Alpha -1-antitrypsin (ATT)</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Increased fucosylation alpha</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Hepatitis C, HCC</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B43-jcm-09-00354" ref-type="bibr">43</xref>
,
<xref rid="B44-jcm-09-00354" ref-type="bibr">44</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Decrease in branching, predominance of alpha 2–6 linked sialic acid and less alpha 2–3 linked sialic acid</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Breast and ovarian cancer</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B45-jcm-09-00354" ref-type="bibr">45</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Oligosaccharide branching and increased sialic acid content</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Acute general inflammation</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B46-jcm-09-00354" ref-type="bibr">46</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Increased glycan branching</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">RA</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B47-jcm-09-00354" ref-type="bibr">47</xref>
]</td>
</tr>
<tr>
<td rowspan="2" align="center" valign="middle" style="border-bottom:solid thin" colspan="1">Transferrin</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Increased branching and fucosylation
<break></break>
of
<italic>N</italic>
-glycans. Increasing peripheral
<italic>N</italic>
-acetylglucosamine residues</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Ovarian, breast and colon cancer, HCC, Cirrhosis, hepatitis</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B48-jcm-09-00354" ref-type="bibr">48</xref>
,
<xref rid="B49-jcm-09-00354" ref-type="bibr">49</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Increased fucosylation and sialic
<break></break>
acid-linked to galactose</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Liver disease</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B50-jcm-09-00354" ref-type="bibr">50</xref>
]</td>
</tr>
<tr>
<td rowspan="3" align="center" valign="middle" style="border-bottom:solid thin" colspan="1">Haptoglobin (Hp)</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Increased fucose and
<italic>N</italic>
-acetylglucosamine</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Alcoholic liver disease</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B51-jcm-09-00354" ref-type="bibr">51</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Increased fucosylation</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Various types of cancer and RA</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B52-jcm-09-00354" ref-type="bibr">52</xref>
,
<xref rid="B53-jcm-09-00354" ref-type="bibr">53</xref>
,
<xref rid="B54-jcm-09-00354" ref-type="bibr">54</xref>
,
<xref rid="B55-jcm-09-00354" ref-type="bibr">55</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">
<italic>O</italic>
-glycans ad fucosylation</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Prostate cancer</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B56-jcm-09-00354" ref-type="bibr">56</xref>
]</td>
</tr>
<tr>
<td rowspan="2" align="center" valign="middle" style="border-bottom:solid thin" colspan="1">Inmunoglobulin G (IgG)</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Decreased galactose</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">RA, SLE, IBD, ovarian cancer, prostate cancer</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B57-jcm-09-00354" ref-type="bibr">57</xref>
,
<xref rid="B58-jcm-09-00354" ref-type="bibr">58</xref>
,
<xref rid="B59-jcm-09-00354" ref-type="bibr">59</xref>
,
<xref rid="B60-jcm-09-00354" ref-type="bibr">60</xref>
,
<xref rid="B61-jcm-09-00354" ref-type="bibr">61</xref>
,
<xref rid="B62-jcm-09-00354" ref-type="bibr">62</xref>
,
<xref rid="B63-jcm-09-00354" ref-type="bibr">63</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Increased
<italic>N</italic>
-acetylglucosamine residues (controversy)</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">RA</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B64-jcm-09-00354" ref-type="bibr">64</xref>
,
<xref rid="B65-jcm-09-00354" ref-type="bibr">65</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Inmunoglobulin A (Ig A)</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Reduced galactosylation of
<italic>O</italic>
-linked glycosylation</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Nephropathy</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B66-jcm-09-00354" ref-type="bibr">66</xref>
,
<xref rid="B67-jcm-09-00354" ref-type="bibr">67</xref>
]</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>HCC (hepatocellular carcinoma), SLE (systemic lupus erythematosus), RA (rheumatoid arthritis), IBD (inflammatory bowel disease)</p>
</fn>
</table-wrap-foot>
</table-wrap>
<table-wrap id="jcm-09-00354-t002" orientation="portrait" position="float">
<object-id pub-id-type="pii">jcm-09-00354-t002_Table 2</object-id>
<label>Table 2</label>
<caption>
<p>Summary of
<sup>1</sup>
H-NMR glycoprotein’s clinical applications. (a) Diseases.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th colspan="2" align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" rowspan="1">Clinical Study Topic</th>
<th align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" rowspan="1" colspan="1">Main Findings</th>
<th align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" rowspan="1" colspan="1">References</th>
</tr>
</thead>
<tbody>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">
<bold>Tumors and cancer</bold>
</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">OC, CSCC, BC, LC, CRC</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Increased circulating
<italic>N</italic>
-acetyl glycoproteins levels and increased GlcNAc-branching of
<italic>N</italic>
-glycans.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B24-jcm-09-00354" ref-type="bibr">24</xref>
,
<xref rid="B89-jcm-09-00354" ref-type="bibr">89</xref>
,
<xref rid="B90-jcm-09-00354" ref-type="bibr">90</xref>
,
<xref rid="B91-jcm-09-00354" ref-type="bibr">91</xref>
,
<xref rid="B92-jcm-09-00354" ref-type="bibr">92</xref>
,
<xref rid="B93-jcm-09-00354" ref-type="bibr">93</xref>
]</td>
</tr>
<tr>
<td rowspan="9" align="center" valign="middle" style="border-bottom:solid thin" colspan="1">
<bold>Metabolic diseases</bold>
</td>
<td rowspan="4" align="center" valign="middle" style="border-bottom:solid thin" colspan="1">Obesity</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Association between GlycA and the leptin/adiponectin ratio</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B94-jcm-09-00354" ref-type="bibr">94</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Correlation between GlycA and TG and lipids</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B95-jcm-09-00354" ref-type="bibr">95</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Correlation GlycA and branched chain amino acids</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B96-jcm-09-00354" ref-type="bibr">96</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Strong relationship of CRP, GlycA, and GlycB and insulin resistance</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B97-jcm-09-00354" ref-type="bibr">97</xref>
]</td>
</tr>
<tr>
<td rowspan="4" align="center" valign="middle" style="border-bottom:solid thin" colspan="1">Diabetes Mellitus</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">α1-acid glycoprotein as a predictor of future glycemia</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B98-jcm-09-00354" ref-type="bibr">98</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Associations of GlycA with higher IL-6 and CRP</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B99-jcm-09-00354" ref-type="bibr">99</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Associations of GlycA with future T2DM</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B100-jcm-09-00354" ref-type="bibr">100</xref>
,
<xref rid="B101-jcm-09-00354" ref-type="bibr">101</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">GlycA had a more robust correlation with CRP, plasma glucose, and measures
<break></break>
of adiposity and insulin resistance than GlycB</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B97-jcm-09-00354" ref-type="bibr">97</xref>
,
<xref rid="B102-jcm-09-00354" ref-type="bibr">102</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">MetS</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Increased levels of glycosylated acute-phase proteins (GlycA) associated with MetS</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B94-jcm-09-00354" ref-type="bibr">94</xref>
,
<xref rid="B103-jcm-09-00354" ref-type="bibr">103</xref>
,
<xref rid="B104-jcm-09-00354" ref-type="bibr">104</xref>
]</td>
</tr>
<tr>
<td rowspan="7" align="center" valign="middle" style="border-bottom:solid thin" colspan="1">
<bold>Cardiovascular risk</bold>
</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Healthy individuals</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">GlycA/alpha1-acid glycoproteins or baseline circulating glycoprotein
<italic>N</italic>
-acetyl methyl groups are associated with CVD and longitudinal risk of all-cause mortality.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B101-jcm-09-00354" ref-type="bibr">101</xref>
,
<xref rid="B105-jcm-09-00354" ref-type="bibr">105</xref>
,
<xref rid="B106-jcm-09-00354" ref-type="bibr">106</xref>
,
<xref rid="B107-jcm-09-00354" ref-type="bibr">107</xref>
,
<xref rid="B108-jcm-09-00354" ref-type="bibr">108</xref>
,
<xref rid="B109-jcm-09-00354" ref-type="bibr">109</xref>
,
<xref rid="B110-jcm-09-00354" ref-type="bibr">110</xref>
]</td>
</tr>
<tr>
<td rowspan="3" align="center" valign="middle" style="border-bottom:solid thin" colspan="1">High-risk individuals</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">GlycA and GlycB strongly associated with future major adverse CVE</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B109-jcm-09-00354" ref-type="bibr">109</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">GlycA and hsCRP was statistically significant for the outcome of death</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B111-jcm-09-00354" ref-type="bibr">111</xref>
,
<xref rid="B112-jcm-09-00354" ref-type="bibr">112</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">GlycA, and small and medium-size HDL particles proved to be independent predictors of cardiac death.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B113-jcm-09-00354" ref-type="bibr">113</xref>
,
<xref rid="B114-jcm-09-00354" ref-type="bibr">114</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Life expectancy</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Higher GlycA levels had lower life expectancy.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B115-jcm-09-00354" ref-type="bibr">115</xref>
]</td>
</tr>
<tr>
<td rowspan="2" align="center" valign="middle" style="border-bottom:solid thin" colspan="1">All-cause mortality</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Positive association between α1-antitrypsin and increased risk of liver diseases, heart failure, and COPD, and significant association between α1-acid glycoprotein and heart failure and chronic lower respiratory diseases</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B85-jcm-09-00354" ref-type="bibr">85</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">GlycA related to increased risk of alcoholic liver disease, chronic renal failure, glomerular diseases, COPD, inflammatory polyarthropathies, and hypertension</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B116-jcm-09-00354" ref-type="bibr">116</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">
<bold>HIV-infection</bold>
</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1"></td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Higher GlycA levels in HIV-infected patients</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B117-jcm-09-00354" ref-type="bibr">117</xref>
]</td>
</tr>
<tr>
<td rowspan="7" align="center" valign="middle" style="border-bottom:solid thin" colspan="1">
<bold>Chronic inflammatory diseases</bold>
</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">RA</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">GlycA is higher in RA patients than in controls.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B83-jcm-09-00354" ref-type="bibr">83</xref>
,
<xref rid="B118-jcm-09-00354" ref-type="bibr">118</xref>
,
<xref rid="B119-jcm-09-00354" ref-type="bibr">119</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">SLE</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">GlycA levels increased with each unit increase in SELDAI.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B120-jcm-09-00354" ref-type="bibr">120</xref>
,
<xref rid="B121-jcm-09-00354" ref-type="bibr">121</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1"></td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">GlycA has been shown to be a good marker of systemic inflammation in lupus-nephritis.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B122-jcm-09-00354" ref-type="bibr">122</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Psoriasis</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">GlycA is increased in psoriasis.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B123-jcm-09-00354" ref-type="bibr">123</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">IBD</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">GlycA in populations with ulcerative colitis and Chron’s disease better reflects
<break></break>
inflammatory status than other classical markers.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B124-jcm-09-00354" ref-type="bibr">124</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">CKD</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">GlycA was independently associated with albuminuria and inversely related to eGFR.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B125-jcm-09-00354" ref-type="bibr">125</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">CHC</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Increased severity of fibrosis has been associated with higher NAC plasma levels.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B126-jcm-09-00354" ref-type="bibr">126</xref>
]</td>
</tr>
<tr>
<td rowspan="2" align="center" valign="middle" style="border-bottom:solid thin" colspan="1">
<bold>Cognitive function and</bold>
<break></break>
<bold>psychological health</bold>
</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Global cognitive function</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">GlycA is inversely related to global cognition, information processing speed and memory domains.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B127-jcm-09-00354" ref-type="bibr">127</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">AD</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Elevated circulating glycoproteins were associated with the risk for AD and MCI.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B128-jcm-09-00354" ref-type="bibr">128</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">
<bold>Rare vascular diseases</bold>
</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Takayasu arteritis</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">
<italic>N</italic>
-Acetyl glycoproteins are significantly up-regulated in TA patients</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B129-jcm-09-00354" ref-type="bibr">129</xref>
,
<xref rid="B130-jcm-09-00354" ref-type="bibr">130</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1"></td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Kawasaki disease</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">High levels of GlycA were confirmed in paediatric population with acute KD disease</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B110-jcm-09-00354" ref-type="bibr">110</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">
<bold>Primary aldosteronism</bold>
</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1"></td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">GlycA levels significantly increased in PA population.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B131-jcm-09-00354" ref-type="bibr">131</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">
<bold>Sickle cell disease</bold>
</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1"></td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">GlycA levels are decreased in SCL.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B132-jcm-09-00354" ref-type="bibr">132</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">
<bold>Human African</bold>
<break></break>
<bold>Trypanosomiasis</bold>
</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1"></td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Significant increase of
<italic>N</italic>
-acetyl glycoprotein in HAT patients.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B133-jcm-09-00354" ref-type="bibr">133</xref>
]</td>
</tr>
</tbody>
</table>
</table-wrap>
<table-wrap id="jcm-09-00354-t003" orientation="portrait" position="float">
<object-id pub-id-type="pii">jcm-09-00354-t003_Table 3</object-id>
<label>Table 3</label>
<caption>
<p>Summary of
<sup>1</sup>
H-NMR glycoprotein’s clinical applications. (b) Treatment effects and lifestyle.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th colspan="2" align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" rowspan="1">Clicical Study Topic</th>
<th align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" rowspan="1" colspan="1">Main Findings</th>
<th align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" rowspan="1" colspan="1">References</th>
</tr>
</thead>
<tbody>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">
<bold>Tobacco smoking</bold>
</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1"></td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Similar significant associations between different measures of smoking behaviour and
<break></break>
higher GlycA and hsCRP levels.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B134-jcm-09-00354" ref-type="bibr">134</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">
<bold>Effect of exercise</bold>
</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1"></td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Regular exercise significantly reduced plasma GlycA.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B135-jcm-09-00354" ref-type="bibr">135</xref>
,
<xref rid="B136-jcm-09-00354" ref-type="bibr">136</xref>
,
<xref rid="B137-jcm-09-00354" ref-type="bibr">137</xref>
]</td>
</tr>
<tr>
<td rowspan="5" align="center" valign="middle" style="border-bottom:solid thin" colspan="1">
<bold>Effect of treatments</bold>
</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Anti-TNF and
<break></break>
monoclonal antibodies</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Decrease in GlycA levels.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B122-jcm-09-00354" ref-type="bibr">122</xref>
,
<xref rid="B123-jcm-09-00354" ref-type="bibr">123</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Antirretroviral treatment</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">GlycA was the only marker of inflammation, among hsCRP, IL-6 and D-dimer, that decreased.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B138-jcm-09-00354" ref-type="bibr">138</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Statins</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Do not affect GlycA levels.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B114-jcm-09-00354" ref-type="bibr">114</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Metformin</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Lower NAC serum levels in T2DM patients treated in metformin than in untreated patients.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B139-jcm-09-00354" ref-type="bibr">139</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Probiotics</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Greater gut microbiota richness is negatively linked with low-grade inflammation marker GlycA.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B86-jcm-09-00354" ref-type="bibr">86</xref>
]</td>
</tr>
</tbody>
</table>
</table-wrap>
<table-wrap id="jcm-09-00354-t004" orientation="portrait" position="float">
<object-id pub-id-type="pii">jcm-09-00354-t004_Table 4</object-id>
<label>Table 4</label>
<caption>
<p>Summary of
<sup>1</sup>
H-NMR glycoprotein’s clinical applications. (c) Other conditions.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th colspan="2" align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" rowspan="1">Clinical Study Topic</th>
<th align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" rowspan="1" colspan="1">Main Findings</th>
<th align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" rowspan="1" colspan="1">References</th>
</tr>
</thead>
<tbody>
<tr>
<td colspan="2" align="center" valign="middle" style="border-bottom:solid thin" rowspan="1">
<bold>Sodium intake</bold>
</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Lower GlycA and hsCRP concentrations were both associated with higher 24-h sodium excretion.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B140-jcm-09-00354" ref-type="bibr">140</xref>
]</td>
</tr>
<tr>
<td rowspan="3" colspan="2" align="center" valign="middle" style="border-bottom:solid thin">
<bold>Pregnancy</bold>
</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Gradual increase in
<italic>N</italic>
-acetyl glycoproteins during pregnancy.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B141-jcm-09-00354" ref-type="bibr">141</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Multiple nutrient intake correlates with GlycA including fibre, LC-PUFA and w-3 LC-PUFA and several vitamins and minerals.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B86-jcm-09-00354" ref-type="bibr">86</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">GlycA and hsCRP were statistically significantly higher in obese than in overweight pregnant women.</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B142-jcm-09-00354" ref-type="bibr">142</xref>
]</td>
</tr>
<tr>
<td rowspan="2" align="center" valign="middle" style="border-bottom:solid thin" colspan="1">
<bold>Toxicity</bold>
</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Sodium valproate</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">
<italic>N</italic>
-acetyl moieties of glycoprotein significantly increased (
<italic>p</italic>
< 0.01) in valproate sodium induced hepatotoxicity</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B143-jcm-09-00354" ref-type="bibr">143</xref>
]</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Oncologic toxicity</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">The high acute radiation sequelae were associated with increased signals of
<italic>N</italic>
-acetyl glycoproteins</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">[
<xref rid="B144-jcm-09-00354" ref-type="bibr">144</xref>
]</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>OC (ovarian cancer), CSCC (cervical squamous cell carcinoma), BC (breast cancer), LC (lung cancer), CRC (colorectal cancer), GlcNAc (
<italic>N</italic>
-Acetyl glucosamine), TG (total triglycerides), CRP (C-reactive protein), IL-6 (interleukin-6), T2DM (type 2 diabetes mellitus), MetS (metabolic syndrome), CVD (cardiovascular disease), CVE (cardiovascular event), COPD (chronic obstructive pulmonary disease), RA (rheumatoid arthritis), SLE (systemic lupus erythematosus), SELDAI (Systemic Lupus Erythematosus Disease Activity Index), IBD (inflammatory bowel disease), CKD (chronic kidney disease), CHC (chronic hepatitis C), AD (Alzheimer disease), MCI (mild cognitive impairment), TA (Takayasu arteritis), KD (Kawasaki disease), PUFA (polyunsaturated fatty acids), PA (primary aldosterism), SCL (sickle cell disease).</p>
</fn>
</table-wrap-foot>
</table-wrap>
</floats-group>
</pmc>
<affiliations>
<list>
<country>
<li>Espagne</li>
</country>
<region>
<li>Catalogne</li>
</region>
</list>
<tree>
<country name="Espagne">
<region name="Catalogne">
<name sortKey="Fuertes Martin, Rocio" sort="Fuertes Martin, Rocio" uniqKey="Fuertes Martin R" first="Rocío" last="Fuertes-Martín">Rocío Fuertes-Martín</name>
</region>
<name sortKey="Amig, Nuria" sort="Amig, Nuria" uniqKey="Amig N" first="Núria" last="Amig">Núria Amig</name>
<name sortKey="Correig, Xavier" sort="Correig, Xavier" uniqKey="Correig X" first="Xavier" last="Correig">Xavier Correig</name>
<name sortKey="Vallve, Joan Carles" sort="Vallve, Joan Carles" uniqKey="Vallve J" first="Joan-Carles" last="Vallvé">Joan-Carles Vallvé</name>
<name sortKey="Vallve, Joan Carles" sort="Vallve, Joan Carles" uniqKey="Vallve J" first="Joan-Carles" last="Vallvé">Joan-Carles Vallvé</name>
</country>
</tree>
</affiliations>
</record>

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