<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>0872-8178</journal-id>
<journal-title><![CDATA[Jornal Português de Gastrenterologia ]]></journal-title>
<abbrev-journal-title><![CDATA[J Port Gastrenterol.]]></abbrev-journal-title>
<issn>0872-8178</issn>
<publisher>
<publisher-name><![CDATA[Sociedade Portuguesa de Gastrenterologia]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0872-81782007000100002</article-id>
<title-group>
<article-title xml:lang="pt"><![CDATA[Elastografia hepática transitória: um método não invasivo para avaliação da fibrose em doentes com hepatite C crónica]]></article-title>
<article-title xml:lang="en"><![CDATA[Transitory hepatic elastography: A non invasive method to evaluate fibrosis in chronic HCV patients]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Serejo]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Marinho]]></surname>
<given-names><![CDATA[R.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Velosa]]></surname>
<given-names><![CDATA[J.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Costa]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Moura]]></surname>
<given-names><![CDATA[M. Carneiro de]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
<xref ref-type="aff" rid="A02"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Universidade de Lisboa Faculdade de Medicina de Lisboa Departamento de Anatomia Patológica]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="A02">
<institution><![CDATA[,Hospital de Santa Maria  ]]></institution>
<addr-line><![CDATA[Lisboa ]]></addr-line>
<country>Portugal</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>01</month>
<year>2007</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>01</month>
<year>2007</year>
</pub-date>
<volume>14</volume>
<numero>1</numero>
<fpage>8</fpage>
<lpage>15</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_arttext&amp;pid=S0872-81782007000100002&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_abstract&amp;pid=S0872-81782007000100002&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_pdf&amp;pid=S0872-81782007000100002&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="pt"><p><![CDATA[A biopsia hepática é o melhor método para avaliar a fibrose, mas é invasivo e não isento de complicações. Objectivos: Verificar o interesse da elastografia hepática transitória na monitorização da gravidade histológica em doentes com hepatite C crónica. Métodos: Foram estudados 214 doentes com hepatite C crónica, 134 homens e 70 mulheres, idade média 47,4 ± 11,6 anos e 26 indivíduos considerados saudáveis, com provas hepáticas normais, serviram de controlos. Nas biopsias hepáticas foi utilizado o Índice de Actividade Histológico (IAH) de Knodell / Peter Scheuer: 154 com estádio F0/F2; 50 com F3/F4. O valor normal da elastografia hepática transitória (Fibroscan®, Echosens, Paris, França) foi de 4,5 kPa (3,30 - 5,69). Resultados: A elastografia hepática diferenciou os diversos estádios de fibrose: F0/1 - 4,92 kPa (4,21-6,17) vs F2/3/4 - 6,81 kPa (5,14-15,95), p =0,006; F0,1,2 - 5.90 kPa (4,85 - 7,25) vs F3/F4 - 12,55 kPa (9,10-16,24), p =0,001; na cirrose hepática (F4) - 13.75 kPa (11,44-27,05), p =0,001.Utilizando as curvas de ROC foram optimizados os pontos de corte para diferenciar os estádios de fibrose em 60 doentes com biopsia hepática concomitante e com mais de 10 espaços porta estudados: F&#8805;2 - 5,43 (AUC- 0,79; Se- 0,78; esp- 0,67; VPP- 0,98; VPN- 0,25); F&#8805;3 - 8,18 (AUC- 0,96; se- 0,95; esp- 0,93; VPP- 0,87; VPN- 0,97); F4- 10,08 (AUC- 0,98; se- 0,93; esp- 0,93; VPP- 0,82; VPN- 0,98). Verificou-se uma correlação significativa entre a elastografia hepática e o IAH (P <0,003), assim como com a fibrose (p <0,0005), mas não com a actividade inflamatória (p =0,28). Por análise multivariada confirmou-se uma relação entre a elastografia hepática e a idade do doente (p =0,009) e o valor do ferro sérico (p =0,035). Conclusões: A elastografia hepática revelou-se eficaz na detecção de fibrose hepática significativa e para o diagnóstico de cirrose. Verificou-se uma relação entre este meio de diagnóstico a idade do doente e o ferro sérico, parâmetros associados à progressão da doença. Como método não invasivo fácil de executar, rápido e reprodutível é útil para o seguimento dos doentes com hepatite C crónica com o objectivo de avaliar a gravidade da fibrose hepática.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Liver biopsy is the current "gold standard" for evaluating liver fibrosis but it is an invasive procedure, unsuitable for monitoring disease progression. Aims: To evaluate the interest of hepatic elastography for assessment and monitoring of liver fibrosis in chronic HCV patients. Methods: 214 chronic hepatitis C patients, 134 male and 70 female, mean age 47.4 ± 11.6 years and 26 healthy individuals with normal liver function tests served as controls, were included in the study. Histological activity index (HAI) was graded according Knodell / Peter Scheuer: 154 patients F0/2; 50 patients F3/4. Liver stiffness was measured using Fibroscan® (Echosens, Paris, France). The median in 25 controls was 4.5 kPa (3.30 - 5.69) and was correlated with clinical and laboratorial data. Results: A significant correlation was found between liver stiffness and HAI (p< 0.003). Median liver stiffness was 12.55 kPa (9.10 - 16.24), and corresponded to the different stages: F0.1 - 4.92 kPa (4.21-6.17) vs F2.3.4 - 6.81 kPa (5.14- 15.95), P =0.006; F0.1.2 - 5.90 kPa (4.85 - 7.25) vs F3/F4 - 12.55 kPa (9.10-16.24), P =0.001. The median liver stiffness for detection of cirrhosis was 13.75 KPa (11.44-27.05), p=0.001. Optimal stiffness cut-off values for fibrosis stage assessment were determined by ROC curve analysis in 60 patients with concomitant liver biopsy specimens that contain more then 10 portal tracts. Optimized cut-off values: F&#8805; 2 - 5.43 (AUC- 0.79; Se- 0.78; sp- 0.67; PPV- 0.98; PNV-0.25); F&#8805;3 - 8.18 (AUC- 0.96; se- 0.95; sp- 0.93; PPV- 0.87; PNV- 0.97); F4- 10.08 (AUC- 0.98; se- 0.93; sp- 0.93; PPV-0.82; PNV- 0.98). A significant correlation with liver stiffness was seen with age of the patient (p= 0.009) and serum iron levels (p =0.035) by multivariate analysis. Conclusions: These preliminary results suggest that Fibroscan® is able to differenciate between the different stages of fibrosis and correlates with other parameters of progressive liver fibrosis (age and iron). Being a non-invasive method, easy and quick to perform and providing reproducible results Fibroscan® may become a useful and reliable method for the follow-up of HCV patients.]]></p></abstract>
</article-meta>
</front><body><![CDATA[ <p><b>Elastografia hep&aacute;tica transit&oacute;ria, um m&eacute;todo n&atilde;o    invasivo para avalia&ccedil;&atilde;o da fibrose em doentes com hepatite C cr&oacute;nica</b></p>      <p>F. Serejo<a href="#1">*</a><a name="top1"></a>, R. Marinho<a href="#1">*</a>,    J. Velosa<a href="#1">*</a>, A. Costa<a href="#1">*</a>, M. Carneiro de Moura<a href="#1">*</a></p>      <p>&nbsp;</p>      <p><b>Resumo</b></p>      <p>A biopsia hepática é o melhor método para avaliar a fibrose, mas é invasivo e não isento de complicações. <i>Objectivos: </i>Verificar o interesse da elastografia hepática transitória na monitorização da gravidade histológica em doentes com hepatite C crónica. <i>Métodos: </i>Foram estudados 214 doentes com hepatite C crónica, 134 homens e 70 mulheres, idade média 47,4 ± 11,6 anos e 26 indivíduos considerados saudáveis, com provas hepáticas normais, serviram de controlos. Nas biopsias hepáticas foi utilizado o Índice de Actividade Histológico (IAH) de Knodell / Peter Scheuer: 154 com estádio F0/F2; 50 com F3/F4. O valor normal da elastografia hepática transitória (Fibroscan®, Echosens, Paris, França) foi de 4,5 kPa (3,30 - 5,69). <i>Resultados: </i>A elastografia hepática diferenciou os diversos estádios de fibrose: F0/1 - 4,92 kPa (4,21-6,17) <i>vs</i><i> </i>F2/3/4 - 6,81 kPa (5,14-15,95), p =0,006; F0,1,2 - 5.90 kPa (4,85 - 7,25) <i>vs</i><i> </i>F3/F4 - 12,55 kPa (9,10-16,24), p =0,001; na cirrose hepática (F4) - 13.75 kPa (11,44-27,05), p =0,001.Utilizando as curvas de ROC foram optimizados os pontos de corte para diferenciar os estádios de fibrose em 60 doentes com biopsia hepática concomitante e com mais de 10 espaços porta estudados: F&#8805;2 - 5,43 (AUC- 0,79; Se- 0,78; esp- 0,67; VPP- 0,98; VPN- 0,25); F&#8805;3 - 8,18 (AUC- 0,96; se- 0,95; esp- 0,93; VPP- 0,87; VPN- 0,97); F4- 10,08 (AUC- 0,98; se- 0,93; esp- 0,93; VPP- 0,82; VPN- 0,98). Verificou-se uma correlação significativa entre a elastografia hepática e o IAH (P &lt;0,003), assim como com a fibrose (p &lt;0,0005), mas não com a actividade inflamatória (p =0,28). Por análise multivariada confirmou-se uma relação entre a elastografia hepática e a idade do doente (p =0,009) e o valor do ferro sérico (p =0,035). <i>Conclusões: </i>A elastografia hepática revelou-se eficaz na detecção de fibrose hepática significativa e para o diagnóstico de cirrose. Verificou-se uma relação entre este meio de diagnóstico a idade do doente e o ferro sérico, parâmetros associados à progressão da doença. Como método não invasivo fácil de executar, rápido e reprodutível é útil para o seguimento dos doentes com hepatite C crónica com o objectivo de avaliar a gravidade da fibrose hepática.</p>      <p>&nbsp;</p>     <p><b>Transitory hepatic elastography. A non invasive method to evaluate fibrosis    in chronic HCV patients</b></p>      <p><b>Summary</b></p>      <p>Liver biopsy is the current &quot;gold standard&quot; for evaluating liver    fibrosis but it is an invasive procedure, unsuitable for monitoring disease    progression. Aims: To evaluate the interest of hepatic elastography for assessment    and monitoring of liver fibrosis in chronic HCV patients. Methods: 214 chronic    hepatitis C patients, 134 male and 70 female, mean age 47.4 ± 11.6 years and    26 healthy individuals with normal liver function tests served as controls,    were included in the study. Histological activity index (HAI) was graded according    Knodell / Peter Scheuer: 154 patients F0/2; 50 patients F3/4. Liver stiffness    was measured using Fibroscan® (Echosens, Paris, France). The median in 25 controls    was 4.5 kPa (3.30 - 5.69) and was correlated with clinical and laboratorial    data. Results: A significant correlation was found between liver stiffness and    HAI (p&lt; 0.003). Median liver stiffness was 12.55 kPa (9.10 - 16.24), and    corresponded to the different stages: F0.1 - 4.92 kPa (4.21-6.17) vs F2.3.4    - 6.81 kPa (5.14- 15.95), P =0.006; F0.1.2 - 5.90 kPa (4.85 - 7.25) vs F3/F4    - 12.55 kPa (9.10-16.24), P =0.001. The median liver stiffness for detection    of cirrhosis was 13.75 KPa (11.44-27.05), p=0.001. Optimal stiffness cut-off    values for fibrosis stage assessment were determined by ROC curve analysis in    60 patients with concomitant liver biopsy specimens that contain more then 10    portal tracts. Optimized cut-off values: F&#8805; 2 - 5.43 (AUC- 0.79; Se- 0.78;    sp- 0.67; PPV- 0.98; PNV-0.25); F&#8805;3 - 8.18 (AUC- 0.96; se- 0.95; sp- 0.93;    PPV- 0.87; PNV- 0.97); F4- 10.08 (AUC- 0.98; se- 0.93; sp- 0.93; PPV-0.82; PNV-    0.98). A significant correlation with liver stiffness was seen with age of the    patient (p= 0.009) and serum iron levels (p =0.035) by multivariate analysis.    Conclusions: These preliminary results suggest that Fibroscan® is able to differenciate    between the different stages of fibrosis and correlates with other parameters    of progressive liver fibrosis (age and iron). Being a non-invasive method, easy    and quick to perform and providing reproducible results Fibroscan® may become    a useful and reliable method for the follow-up of HCV patients.</p>      <p>&nbsp;</p>      ]]></body>
<body><![CDATA[<p>&nbsp;</p>      <p>Texto Completo disponível apenas em PDF</p>      <p>Full text only available in PDF format</p>      <p>&nbsp;</p>      <p>&nbsp;</p>      <p><b>Bibliografia</b><b></b></p>      <!-- ref --><p>1. Poynard T, Mathurin P, Lai CL, et al. A comparisson of fibrosis progression    in chronic liver diseases. J Hepatol. 2005;38: 257-265.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000019&pid=S0872-8178200700010000200001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><p>2. Hoofnagle J. Hepatitis C. The clinical spectrum of disease. Hepatology. 1997;26(suppl1): 15S.</p>      <p>3. Realdi G, Alberti A, Rugge M, et al. Long term follow up of acute and chronic NANB hepatitis: evidence of progress to liver cirrhosis. Gut. 1982;23: 270-275.</p>      <p>4. Serejo F, Costa A, Oliveira AG, Ramalho F, Batista A, Moura MC. Alfa Interferon improves liver fibrosis in chronic hepatitis C. Clinical significance of the serum N-terminal propeptide of procollagen</p>      ]]></body>
<body><![CDATA[<p>type III. Dig.Dis.Sci. 2001;46: 1684-1689.</p>      <p>5. Poynard T, McHutchinson J, Manns M, et al. Impact of Pegylated interferon alfa 2b and ribavirin on liver fibrosis in patients with chronic hepatitis C. Gastroenterology. 2002;122: 1303-1313.</p>      <p>6. Bedossa P, Dargere D, Paradis V. Sampling variability of liver fibrosis in chronic hepatitis C. Hepatology. 2003;38:1449-1457.</p>      <p>7. Regev A, Bertho M, Jeffers LJ, et al. Sampling error and intraobserver variation in liver biopsy in patients with chronic HCV infection. Am J Gastroenterol. 2002;97: 2614-2618.</p>      <p>8. Standish RA, Cholongitas E, Dhillon A, Burroughs A, Dhillon AP. An appraisal of the pathological assessment of liver fibrosis. Gut. 2006;55: 569-578.</p>      <p>9. Beaugrand M. How to assess liver fibrosis and for what purpose? J Hepatol. 2006;44: 444-445.</p>      <p>10. Sandrin L, Fourquet B, Hasquenoph J, et al. Transient elastography: a new noninvasive method for assessment of hepatic fibrosis. Ultrasound in Med and Biol. 2003;29:1705-1713.</p>      <p>11. Knodell RG, Ishak KG, Black WC, et al. Formulation and application of a numerical scoring system for assessing histological activity in assymptomatic chronic active hepatitis. Hepatology. 1981;1: 431-435.</p>      <p>12. Brunt EM. Nonalcoholic steatohepatitis: Definition and pathology. Sem Liv Dis. 1995;21: 3-16.</p>      <p>13. Mac Sween RN, Anthony P, Scheuer PJ, Burt AD, Portman BC. Histological assessement of hepatic iron stores. In Pathology of the liver. New York: Churchill Livingstone; 2000: 223.</p>      ]]></body>
<body><![CDATA[<p>14. Castéra L, Vergniol J, Foucher J, et al. Transient elastography (Fibroscan) a novel noninvasive sensitive method for the assessment of liver fibrosis in chronic hepatitis C: a prospective evaluation in comparison with liver fibrosis, Fibrotest and APRI. Hepatology. 2004;40:Abstract AASLD.</p>      <p>15. Ziol M, Handra-Luca A, Kettaneh C, et al. Noninvasive assessment of liver fibrosis by measurement of stiffness in patients with chronic hepatitis C. Hepatology. 2005;41:48-54.</p>      <p>16. Castéra L, Vergniol J, Foucher J, et al. Prospective comparison of transient elastography, Fibrotest, APRI and liver biopsy for the assessment of fibrosis in chronic hepatits C. Gastroenterology. 2005;128(343-350).</p>      <p>17. Beaugrand M. Le Fibroscan: mode d´emploi. Gastroenterol Clin Biol. 2006;30:513-514.</p>      <p>18. Nguyen Khac E. Résultats et place du Fibroscan dans le diagnostic non invasive de la fibrose hépatique. La revue de medicine interne. 2006;in press.</p>      <p>19. Grando-Lemaire V, Beaugrand M, Lédinghen V, et al. Liver stiffness measurement (LSM) as a tool to measure liver fibrosis in treated patients with chronic hepatitis C (CHC) (abstract). J Hepatol. 2006;44(suppl 2): A577.</p>      <p>20. Lédinghen V, Castéra L, Foucher J, et al. Evaluation of fibrosis regression using fibroscan in HCV responder patients. A prospective controlled study (abstract). J Hepatol. 2006;44 (suppl 2): A564.</p>      <p>21. Nahon P, Thabut G, Ziol M, et al. Liver stiffness measurements versus clinicians`prediction or both for the assessment of liver fibrosis in patients with chronic hepatitis C. Am J Gastroenterol. 2006;101: 2744-2751.</p>      <p>22. Foucher J, Chanteloup E, Castéra L, et al. Diagnosis of cirrhosis and its complications by transient elastography (Fbroscan): A prospective study. Gut. 2006;55: 403-408.</p>      <p>23. Kasemi F, Kettaneh A, N´Kontchou G, et al. Liver stiffness measurement selects patients with cirrhosis at risk of bearing large oesophageal varices. J Hepatol. 2006;45: 230-235.</p>      ]]></body>
<body><![CDATA[<p>24. Aubé C, Oberti F, Korali N, et al. Ultrasonographic diagnosis of hepatic fibrosis or cirrhosis. J Hepatol. 1999;30: 472-478.</p>      <p>25. Chawla Y, Santa M, R.K. D, et al. Portal Hemodynamics by duplex doppler sonograpgy in different grades of cirrhosis. Dig. Dis. Sci. 1998;43: 354-357.</p>      <p>26. Gómez-Dominguez E, Mendoza J, Rubio S, Moreno-Monteagudo JA, García-Buey L, Moreno-Otero R. Transient elastography: a valid alternative to byopsy in patients with chronic liver disease. Aliment Pharmacol Ther. 2006;24: 513-518.</p>      <p>27. Serejo F. Fibrogénese hepática e sobrecarga oxidante na hepatite C crónica. Universidade de Medicina; 2004.</p>      <p>28. Lédinghen V, Beaugrand M, Kelleher TB, et al. Prediction of liver fibrosis in non-alcoholic steatohepatitis (NASH): risk factors and diagnostic potential of elasticity using Fibroscan (abstract). J Hepatol. 2006;44(suppl 2): A87.</p>      <p>29. Castéra L, Foucher J, Bertet J, Couzigou P, Ledinghen V. Fibroscan and Fibrotest to assess fibrosis in HCV with normal aminotransferases. Hepatology. 2006;43(2): 373-374.</p>      <p>30. Colletta C, Smirne C, Fabris C, et al. Value of two non-invasive methods to detect progression of fibrosis among HCV carriers with normal aminotranderases. Hepatology. 2005;42(4): 838-845.</p>      <p>31. Foucher J, Chanteloup E, Castéra L, et al. Diagnosis of cirrhosis and its complication by transient elastography (Fibroscan): A prospective study. Gut. 2006;55: 403-408.</p>      <p>32. Lédinghen V, Douvin C, Kettaneh A, et al. Diagnosis of hepatic fibrosis and cirrhosis by transient elastography (Fibroscan) in HIVHCV co-infected patients. Journal of Acquired Immune Deficiency Syndromes. 2006;41(2): 175-179.</p>      <p>33. Foucher J, Castéra L, Bernard PH, et al. Prevalence and factors associated with failure of liver stiffness measurements using FibroScan in a prospective study of 2114 examinations. Eur J Gastroenterol Hepatol. 2006;18: 411-412.</p>      ]]></body>
<body><![CDATA[<p>34. Coco B, Oliveri F, Bonino F, et al. Liver stiffness measured by transient    elastography: the influence of biochemical activity (abstract). J Hepatol. 2006;44(suppl    2): A526.</p>     <p>&nbsp;</p>      <p><b>Correspondência:</b></p>     <p>Fátima Serejo</p>     <p>Rua Henrique António da Mota, 27 - 3º Dto.</p>     <p>2775-700 Carcavelos</p>     <p>Tel.: 214570665</p>     <p>Fax: 214570665</p>     <p><i>e-mail</i>: <a href="mailto:fatima_serejo@netcabo.pt">fátima_serejo@netcabo.pt</a></p>     <p>&nbsp;</p>      ]]></body>
<body><![CDATA[<p><a name="1"></a><a href="#top1">*</a> Serviço de Gastrenterologia, Departamento    de Anatomia Patológica, Faculdade de Medicina de Lisboa, Hospital de Santa Maria,    Lisboa, Portugal.</p>      <p>&nbsp;</p>      <p align="right">Recebido para publicação: 12/01/2007</p>     <p align="right">Aceite para publicação: 22/01/2007</p>       ]]></body><back>
<ref-list>
<ref id="B1">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Poynard]]></surname>
<given-names><![CDATA[T]]></given-names>
</name>
<name>
<surname><![CDATA[Mathurin]]></surname>
<given-names><![CDATA[P]]></given-names>
</name>
<name>
<surname><![CDATA[Lai]]></surname>
<given-names><![CDATA[CL]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[A comparisson of fibrosis progression in chronic liver diseases]]></article-title>
<source><![CDATA[J Hepatol.]]></source>
<year>2005</year>
<volume>38</volume>
<page-range>257-265</page-range></nlm-citation>
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</article>
