<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJRA</journal-id><journal-title-group><journal-title>Open Journal of Rheumatology and Autoimmune Diseases</journal-title></journal-title-group><issn pub-type="epub">2163-9914</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojra.2024.141002</article-id><article-id pub-id-type="publisher-id">OJRA-131032</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Interleukin 6 and Bone Erosions in Rheumatoid Arthritis in an African Hospital
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Paul</surname><given-names>Eloundou</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Aly</surname><given-names>Kamissoko</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Fernando</surname><given-names>Kempta</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Francine</surname><given-names>Same Bebey</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>William</surname><given-names>Beko’o</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ange</surname><given-names>Ngeuleu</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>William</surname><given-names>Nguekouo</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Estelle</surname><given-names>Megne</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Suzy</surname><given-names>Manizou</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Madeleine</surname><given-names>Singwe</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref></contrib></contrib-group><aff id="aff5"><addr-line>Faculty of Medicine and Biomedical Sciences Yaoundé, University of Yaoundé I, Yaounde, Cameroon</addr-line></aff><aff id="aff1"><addr-line>Faculty of Medicine and Pharmaceutical Sciences, University of Douala, Douala, Cameroon</addr-line></aff><aff id="aff3"><addr-line>Faculty of Medicine, University of Dschang, Dschang, Cameroon</addr-line></aff><aff id="aff2"><addr-line>Cameroon CHU Ignace Deen, Conakry, Guinea</addr-line></aff><aff id="aff4"><addr-line>Department of Internal Medicine, Cité Verte District Hospital, Yaounde, Cameroon</addr-line></aff><pub-date pub-type="epub"><day>09</day><month>01</month><year>2024</year></pub-date><volume>14</volume><issue>01</issue><fpage>13</fpage><lpage>19</lpage><history><date date-type="received"><day>31,</day>	<month>October</month>	<year>2023</year></date><date date-type="rev-recd"><day>1,</day>	<month>February</month>	<year>2024</year>	</date><date date-type="accepted"><day>4,</day>	<month>February</month>	<year>2024</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  <b>Introduction:</b>
   Rheumatoid arthritis (RA) is a chronic, erosive and deforming inflammatory rheumatic disease. In the era of biotherapies and the arrival of biosimilars in sub-Saharan Africa, the objective of this study was to describe plasma IL-6 variations in RA patients at Cit&#233; Verte District Hospital (Cameroon). <b>Material and Methods:</b> Descriptive and analytical cross-sectional study from December 1, 2021 to May 31, 2022. We included patients over 18 years old suffering from RA (ACR/EULAR 2010). Patients with an infection were not included. The data collected were age, sex, smoking status, family history, disease duration, disease activity by DAS28, CRP, rheumatoid factor, and plasma level of IL-6. Bone erosion was sought on radiography and ultrasound. <b>Result:</b> We included 31 patients, 25 of whom were women (80.6%). The mean age was 47.27
   
  &#177;
   
  17.97 years. Disease activity was predominantly moderate (32.3%) and severe (32.3%). Mean IL-6 level was 15.29 &#177; 2.36 pg/ml (extremes: 11.26 pg/ml and 20.15 pg/ml). IL-6 levels were higher in patients with a history of smoking. Similarly, IL-6 levels were higher in patients with mildly active RA in remission than in moderately and severely active RA. Mean IL-6 levels were significantly higher in patients with erosive RA (16.3 pg/ml VS 14.6 pg/ml). <b>Conclusion:</b> IL-6 levels were significantly elevated in men, weaned smokers and patients with bone erosions.
 
</p></abstract><kwd-group><kwd>Rheumatoid Arthritis</kwd><kwd> Interleukin 6</kwd><kwd> Bone Erosion-DAS28</kwd><kwd> Sub-Saharan Africa</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Rheumatoid arthritis (RA) is a chronic, non-organ-specific autoimmune disease characterized by joint and extra-articular involvement. It is the most common chronic inflammatory rheumatic disease [<xref ref-type="bibr" rid="scirp.131032-ref1">1</xref>] . In Africa, prevalence varies between 0.1% and 0.9% depending on the region [<xref ref-type="bibr" rid="scirp.131032-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.131032-ref2">2</xref>] . The pathophysiology of RA involves a complex network of various cytokines (IL-1, IL-6, TNFα, IL-17) and cells that trigger the proliferation of synovial cells and damage cartilage and bone [<xref ref-type="bibr" rid="scirp.131032-ref3">3</xref>] . Smoking is a preventable risk factor for RA. The increased risk due to smoking is dependent on the amount of smoking and genotype [<xref ref-type="bibr" rid="scirp.131032-ref4">4</xref>] . The specificity of ACPA increases in the years just before the onset of RA and is higher in patients who have smoked compared to patients who have never smoked [<xref ref-type="bibr" rid="scirp.131032-ref5">5</xref>] . Biotherapies targeting these cytokines in the treatment of RA are rarely used in sub-Saharan Africa [<xref ref-type="bibr" rid="scirp.131032-ref6">6</xref>] where RA is often diagnosed in the erosive and deforming phase. In the era of biotherapies and the arrival of biosimilars in sub-Saharan Africa, the objective of this study was to describe plasma variations in Il-6 in RA patients at Cit&#233; Verte District Hospital (Cameroon).</p></sec><sec id="s2"><title>2. Patients and Methods</title><p>This was a descriptive and analytical cross-sectional study in the rheumatology department of Cit&#233; Verte District Hospital between December 1, 2021, and May 31, 2022. We included patients over 18 years of age with rheumatoid arthritis according to ACR/EULAR 2010 criteria [<xref ref-type="bibr" rid="scirp.131032-ref7">7</xref>] . Patients with infections were not included. Qualitative and quantitative data were collected: socio-demographic data (age, sex); and clinical and paraclinical data (smoking, family history, disease duration, disease activity, CRP, rheumatoid factor, IL-6 levels. Latex CRP was positive if &gt; 6 mg/L. Rheumatoid factor was determined by latex and Waaler-Rose reaction. IL-6 was assayed using an automated sandwich ELISA. Radiographic bone erosion was assessed using the SHARP/van der HEIJDE evaluation method and the Simple Erosion Narrowing Score (SENS) [<xref ref-type="bibr" rid="scirp.131032-ref8">8</xref>] . Bone erosion on osteoarticular ultrasound was assessed according to the criteria of the Outcome Measures in Rheumatology (OMERACT) group [<xref ref-type="bibr" rid="scirp.131032-ref9">9</xref>] . Disease activity was assessed by DAS28. Statistical analyses were performed using SPSS 28.0.1.1 software. Comparisons between two groups were made using Pearson’s (or Spearman’s) test for continuous variables, Student’s (or Wilcoxon’s) t-test between a continuous and a qualitative variable, and Chi2 test (or Fisher’s exact method) for qualitative variables. The significance threshold was set at 5%.</p><p>The study was conducted with the approval of the Institutional Ethics Committee of the Faculty of Medicine and Pharmaceutical Sciences of Douala (Cameroon). Patient consent was required after an explanation of the study procedure and objective.</p><sec id="s2_1"><title>2.1. Data Analysis</title><p>The results were analysed using Microsoft Excel 2019 and Epi Info 7.2.3.1. Qualitative variables were summarised by frequency and percentage, and quantitative variables by mean and standard deviation (SD). Comparisons were made by using the Pearson correlation test. All tests were two-tailed; the significance level was set at 5%.</p></sec><sec id="s2_2"><title>2.2. Ethical Considerations</title><p>Informed consent was obtained from the patients and the research protocol was accepted by the ethics committee of the Ignace Deen national hospital in Conakry.</p></sec></sec><sec id="s3"><title>3. Results</title><p>We collected 31 patients with RA, 25 of whom were women. Mean age was 47.3 &#177; 17.9 years. Mean disease duration was 6.5 &#177; 6.2 years. Disease activity was predominantly moderate (32.3%) and severe (32.3%) (<xref ref-type="table" rid="table1">Table 1</xref>, <xref ref-type="fig" rid="fig1">Figure 1</xref>).</p><p>The mean interleukin-6 level was 15.13 pg/ml, with patients aged between 40 and 60 having the highest mean Il-6 level (15.97 &#177; 2.33 pg/ml) compared with younger patients aged between 18 and 21 (14.01 &#177; 0.79 pg/ml) (<xref ref-type="table" rid="table2">Table 2</xref>).</p><p>IL-6 levels were higher in patients with a history of smoking. Similarly, IL-6 levels were higher in patients with mildly active RA in remission than in moderately and severely active RA (<xref ref-type="table" rid="table3">Table 3</xref>).</p><p>Bone erosion was present in 12 patients (38.7%). Mean IL-6 levels were significantly higher in this group (16.3 pg/mL) compared with patients without bone erosion (14.6 pg/mL) (<xref ref-type="table" rid="table4">Table 4</xref>).</p></sec><sec id="s4"><title>4. Discussion</title><p>We conducted a cross-sectional study of plasma IL-6 levels according to RA characteristics. The small sample size of this cohort was related to the level of attendance at this district hospital which is a limitation of the study, as well as the absence of non-smoking control patients. However, we described the variations of IL-6 in RA. Elevated mean IL-6 levels in patients followed for RA corroborated chronic inflammatory disease data [<xref ref-type="bibr" rid="scirp.131032-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.131032-ref12">12</xref>] . IL-6 levels were highest in patients aged 40 to 60, followed by those aged 60 and over, as described in the literature. [<xref ref-type="bibr" rid="scirp.131032-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.131032-ref14">14</xref>] .</p><p>The elevation of this IL-6 level in patients with a history of smoking differed from the data of Aldaham et al. where IL-6 levels were lower in weaned smokers (0.86 &#177; 0.13 VS 0.44 &#177; 0.14) [<xref ref-type="bibr" rid="scirp.131032-ref15">15</xref>] . This is because, on one hand, tobacco has the ability to potentiate rheumatoid arthritis through ACPA [<xref ref-type="bibr" rid="scirp.131032-ref5">5</xref>] , while on the other hand, cigarette smoking alone is able to have direct effects on immune cells, inducing chronic inflammation depending on the dose, the type of cigarette and the duration of exposure [<xref ref-type="bibr" rid="scirp.131032-ref16">16</xref>] ; this can explain why stopping smoking or reducing exposure helps to improve the chronic inflammation induced by it. Mean IL-6 was high in patients with low activity Unlike the data of Cheng et al. [<xref ref-type="bibr" rid="scirp.131032-ref14">14</xref>] , where IL-6 levels were higher in patients with severe activity; Some studies showed no significant correlation between IL-6 levels and DAS 28; according to Meguid et al., IL-6 was correlated with pain, SR and anti-PCC but not with</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Socio-demographic, clinical and therapeutic characteristics of 31 rheumatoid arthritis patients</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Frequency (%)</th><th align="center" valign="middle" >Means</th></tr></thead><tr><td align="center" valign="middle" >Woman</td><td align="center" valign="middle" >25 (80.6)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Age (years)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >47.3 &#177; 17.9</td></tr><tr><td align="center" valign="middle" >Active smoking</td><td align="center" valign="middle" >6 (19)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Duration of illness (years)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >6.5 &#177; 6.2</td></tr><tr><td align="center" valign="middle" >1st degree family history of rheumatoid arthritis</td><td align="center" valign="middle" >14 (45)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >C-Reactive Protein</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >7.8 &#177; 1.1</td></tr><tr><td align="center" valign="middle" >Positive rheumatoid factors</td><td align="center" valign="middle" >21 (67.7)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Anticorps anti-cyclic citrullinated peptide</td><td align="center" valign="middle" >19 (63.1)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Disease activity score 28</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >4.3 &#177; 1.8</td></tr><tr><td align="center" valign="middle" >Disease activity</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Remission</td><td align="center" valign="middle" >9 (29)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Mild</td><td align="center" valign="middle" >2 (6.5)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Moderate</td><td align="center" valign="middle" >10 (32.3)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Severe</td><td align="center" valign="middle" >10 (32.3)</td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Plasma IL-6 levels according to age group</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Age (years)</th><th align="center" valign="middle" >Frequency</th><th align="center" valign="middle" >Mean IL-6 level (pg/ml)</th></tr></thead><tr><td align="center" valign="middle" >[18 - 21[</td><td align="center" valign="middle" >02</td><td align="center" valign="middle" >14.01 &#177; 0.79</td></tr><tr><td align="center" valign="middle" >[21 - 40[</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >15.38 &#177; 2.93</td></tr><tr><td align="center" valign="middle" >[40 - 60[</td><td align="center" valign="middle" >09</td><td align="center" valign="middle" >15.97 &#177; 2.33</td></tr><tr><td align="center" valign="middle" >[60 - 80]</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >14.85 &#177; 2.02</td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> IL-6 levels according to sex, history and activity of rheumatoid arthritis</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  colspan="2"  >Characteristics</th><th align="center" valign="middle" >Mean IL-6 level (pg/ml)</th><th align="center" valign="middle" >p-value</th></tr></thead><tr><td align="center" valign="middle"  rowspan="2"  >Sex</td><td align="center" valign="middle" >Female</td><td align="center" valign="middle" >15.08 &#177; 2.34</td><td align="center" valign="middle"  rowspan="2"  >0.3</td></tr><tr><td align="center" valign="middle" >Male</td><td align="center" valign="middle" >16.21 &#177; 2.46</td></tr><tr><td align="center" valign="middle"  rowspan="2"  >Smoking history (former smoker)</td><td align="center" valign="middle" >Yes</td><td align="center" valign="middle" >14.75 &#177; 1.86</td><td align="center" valign="middle"  rowspan="2"  >0.006*</td></tr><tr><td align="center" valign="middle" >No</td><td align="center" valign="middle" >17.59 &#177; 2.16</td></tr><tr><td align="center" valign="middle"  rowspan="2"  >History of rheumatoid arthritis in parents</td><td align="center" valign="middle" >Yes</td><td align="center" valign="middle" >15.13 &#177; 2.66</td><td align="center" valign="middle"  rowspan="2"  >0.67</td></tr><tr><td align="center" valign="middle" >No</td><td align="center" valign="middle" >15.50 &#177; 2.17</td></tr><tr><td align="center" valign="middle"  rowspan="4"  >Disease activity</td><td align="center" valign="middle" >Remission</td><td align="center" valign="middle" >15.63 &#177; 2.12</td><td align="center" valign="middle"  rowspan="4"  >0.02*</td></tr><tr><td align="center" valign="middle" >Mild</td><td align="center" valign="middle" >19.77 &#177; 0.54</td></tr><tr><td align="center" valign="middle" >Moderate</td><td align="center" valign="middle" >14.66 &#177; 2.18</td></tr><tr><td align="center" valign="middle" >Severe</td><td align="center" valign="middle" >14.74 &#177; 2.14</td></tr></tbody></table></table-wrap><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> IL-6 levels in patients according to the presence of bone erosion</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Bone erosion</th><th align="center" valign="middle" >Frequency</th><th align="center" valign="middle" >Mean IL-6 level (pg/ml)</th><th align="center" valign="middle" >p-value</th></tr></thead><tr><td align="center" valign="middle" >No</td><td align="center" valign="middle" >19</td><td align="center" valign="middle" >14.66 &#177; 1.90</td><td align="center" valign="middle" >0.05</td></tr><tr><td align="center" valign="middle" >Yes</td><td align="center" valign="middle" >12</td><td align="center" valign="middle" >16.30 &#177; 2.76</td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><p>DAS28 [<xref ref-type="bibr" rid="scirp.131032-ref17">17</xref>] . Concentrations of cytokines from the IL-6 family can be measured in both serum and synovium from RA patients, but these cytokines are mainly involved in the local reaction, which explains why IL-6 is not always positively correlated with disease activity at the systemic level [<xref ref-type="bibr" rid="scirp.131032-ref18">18</xref>] .</p><p>The elevation of IL-6 in patients with bone erosion was previously reported by Yasushi et al. showing that an IL-6 level of 7.6 pg/ml or more was predictive of radiographic progression at one year. IL-6 is involved in bone destruction in RA [<xref ref-type="bibr" rid="scirp.131032-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.131032-ref20">20</xref>] .</p></sec><sec id="s5"><title>5. Conclusion</title><p>IL-6 levels were significantly elevated in men, weaned smokers and patients with bone erosions. In the era of biotherapies and similar biologics, this study shows that anti-IL-6s have a place in the therapeutic arsenal for rheumatoid arthritis in sub-Saharan Africa.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The authors declare that they have no conflicts of interest.</p></sec><sec id="s7"><title>Cite this paper</title><p>Eloundou, P., Kamissoko, A., Kempta, F., Bebey, F.S., Beko’o, W., Ngeuleu, A., Nguekouo, W., Megne, E., Manizou, S. and Singwe, M. (2024) Interleukin 6 and Bone Erosions in Rheumatoid Arthritis in an African Hospital. Open Journal of Rheumatology and Autoimmune Diseases, 14, 13-19. https://doi.org/10.4236/ojra.2024.141002</p></sec></body><back><ref-list><title>References</title><ref id="scirp.131032-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Alamanos, Y., Voulgary, P. and Drosos, A. (2006) Incidence and Prevalence of Rheumatoid Arthritis, Based on the 1987 American College of Rheumatology Criteria: A Systematic Review. Seminars in Arthritis and Rheumatism, 36, 182-188. https://doi.org/10.1016/j.semarthrit.2006.08.006</mixed-citation></ref><ref id="scirp.131032-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Jeandel, P. and Roux, H. (2002) épidémiologie des affections rhumatologiques en Afrique subsaharienne. Revue du Rhumatisme, 69, 764-776. https://doi.org/10.1016/S1169-8330(02)00389-7</mixed-citation></ref><ref id="scirp.131032-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Kondo, N., Kuroda, T. and Kobayashi, D. (2021) Cytokine Networks in the Pathogenesis of Rheumatoid Arthritis. International Journal of Molecular Sciences, 22, Article 10922. https://doi.org/10.3390/ijms222010922</mixed-citation></ref><ref id="scirp.131032-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Henrik, K., Bo, D., Leonid, P., Camilla, B., Johan, R., Lars, K., et al. (2011) Smookingis a Maorpreventablerisk Factor for Rheumatoidarthritis: Estimations of Risks after Various Exposures to Cigarette Smoke. Annals of the Rheumatic Diseases, 70, 508-511.</mixed-citation></ref><ref id="scirp.131032-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Turesson, C., Hansson, M., Bergstr&amp;#246;m, U., et al. (2012) Patterns of Circulating Antibodies in the Pre-Clinical Phase of Rheumatoid Arthritis Suggest Epitope Spreading in the Immune Reaction against Citrullinated Peptides. Annals of the Rheumatic Diseases, 71, 81-82. https://doi.org/10.1136/annrheumdis-2012-eular.1767</mixed-citation></ref><ref id="scirp.131032-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Missounga, L., Iba Ba, J., Nseng Nseng Ondo, I.R., Nziengui Madjinou, M.I.C., Mwenpindi Malekou, D., Mouendou Mouloungui, E.G. and Boguikouma, J.B. (2018) Traitement des rhumatismes inflammatoires chroniques par biothérapies au Gabon: éligibilité et suivi de 8 premiers patients en Afrique subsaharienne. Médecine et Santé Tropicales, 28, 197-200. https://doi.org/10.1684/mst.2018.0781</mixed-citation></ref><ref id="scirp.131032-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Hua, C. and Combe, B. (2017) Les nouveaux critères de classification ACR/EULAR 2010 pour un diagnostic plus précoce de la polyarthrite rhumato&amp;#239;de. Revue du Rhumatisme Monographies, 84, 337-342. https://doi.org/10.1016/j.monrhu.2017.07.001</mixed-citation></ref><ref id="scirp.131032-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Boini, S. and Guillemin, F. (2001) Radiographic Scoring Methods as Outcome Measures in Rheumatoid Arthritis: Properties and Advantages. Annals of the Rheumatic Diseases, 60, 817-827.</mixed-citation></ref><ref id="scirp.131032-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Wakefield, R., Balint, P., Szkudlarek, M., Filippucci, E., Backhaus, M., D’Agostino, M., et al. (2005) Musculoskeletal Ultrasound Including Definitions for Ultrasonographic Pathology. Journal of Rheumatology, 32, 2485-2487.</mixed-citation></ref><ref id="scirp.131032-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Ridker, P., Stampfer, J., Rifai, N. and Hennekens, C. (2000) Plasma Concentration of Interleukin-6 and the Risk of Future Myocardial Infarction among Apparently Healthy Men. Circulation, 101, 1767-1772. https://www.ahajournals.org/doi/epub/10.1161/01.CIR.101.15.1767</mixed-citation></ref><ref id="scirp.131032-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">https://doi.org/10.1161/01.CIR.101.15.1767</mixed-citation></ref><ref id="scirp.131032-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Reimund, J., Wittersheim, C., Dumont, S., Muller, C., Kenney, J., Baumann, R., et al. (1996) Increased Production of Tumor Necrosis Factor-Alpha Interleukin-1 Beta, and Interleukin-6 by Morphologically Normal Intestinal Biopsies from Patients with Crohn’s Disease. BMJ Journals, 39, 684-689. https://doi.org/10.1136/gut.39.5.684</mixed-citation></ref><ref id="scirp.131032-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Hirano, T., Matsuda, T., Turner, M., Miyasaka, N., Buchan, G., Tang, B., et al. (1988) Excessive Production of Interleukin 6/B Cell Stimulatory Factor-2 in Rheumatoid Arthritis. European Journal of Immunology, 18, 1797-1801. https://doi.org/10.1002/eji.1830181122</mixed-citation></ref><ref id="scirp.131032-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Wei, J., Xu, H., Davies, J. and Hemmings, G. (1992) Increase of Plasma IL-6 Concentration with Age in Healthy Subjects. Life Sciences, 51, 1953-1956. https://doi.org/10.1016/0024-3205(92)90112-3</mixed-citation></ref><ref id="scirp.131032-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Chen, D.Y., Hsieh, T.Y., Chen, Y.M., Hsieh, C.W., Lan, J.L. and Lin, F.J. (2009) Proinflammatory Cytokine Profiles of Patients with Elderly-Onset Rheumatoid Arthritis: A Comparison with Younger-Onset Disease. Gerontology, 55, 250-258. https://doi.org/10.1159/000164393</mixed-citation></ref><ref id="scirp.131032-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Aldaham, S., Foote, J.A., Chow, H.H. and Hakim, I.A. (2015) Smoking Status Effect on Inflammatory Markers in a Randomized Trial of Current and Former Heavy Smokers. International Journal of Inflammation, 2015, Article ID: 439396. https://doi.org/10.1155/2015/439396</mixed-citation></ref><ref id="scirp.131032-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Lee, J., Taneja, V. and Vassallo, R. (2012) Cigarette Smoking and Inflammation: Cellular and Molecular Mechanisms. Journal of Dental Research, 91, 142-149 https://doi.org/10.1177/0022034511421200</mixed-citation></ref><ref id="scirp.131032-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Abdel Meguid, M.H., Hamad, Y.H., Swilam, R.S. and Barakat, M.S. (2013) Relation of Interleukin-6 in Rheumatoid Arthritis Patients to Systemic Bone Loss and Structural Bone Damage. Rheumatology International, 33, 697-703. https://doi.org/10.1007/s00296-012-2375-7</mixed-citation></ref><ref id="scirp.131032-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Okamoto, H., Yamamura, M., Morita, Y., Harada, S., Makino, H. and Ota, Z. (1997) The Synovial Expression and Serum Levels of Interleukin-6, Interleukin-11, Leukemia Inhibitory Factor, and Oncostatin M in Rheumatoid Arthritis. Arthritis &amp; Rheumatology, 40, 1096-1105. https://doi.org/10.1002/art.1780400614</mixed-citation></ref><ref id="scirp.131032-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Yasushi, K., Yuko, K., Hiroaki, S., Shunsuke, M., Naoshi, N., Masataka, K., et al. (2017) Pre-Treatment Interleukin-6 Levels Strongly Affect Bone Erosion Progression and Repair Detected by Magnetic Resonance Imaging in Rheumatoid Arthritis Patients. Rheumatology, 56, 1089-1094. https://doi.org/10.1093/rheumatology/kex046</mixed-citation></ref><ref id="scirp.131032-ref21"><label>21</label><mixed-citation publication-type="other" xlink:type="simple">de Lima, C.A.D., Rushansky, E., Adelino, J.E., de Oliveira Souza, A.P., d’Emery Alves Santos, P., de Araújo Mariano, M.H.Q., Crovella, S., de Azevêdo Silva, J. and Sandrin-Garcia, P. (2020) Are Key Cytokines Genetic and Serum Levels Variations Related to Rheumatoid Arthritis Clinical Severity? Gene, 722, Article 144098. https://doi.org/10.1016/j.gene.2019.144098</mixed-citation></ref></ref-list></back></article>