<p>To assess the correlation between serum Golgi protein-73 (GP-73) and the degree of hepatic fibrosis in children with autoimmune liver diseases. This case–control study included 100 children. Group A involved 50 children with autoimmune hepatitis (AIH), aged 2–17&#xa0;years (mean 11.3 ± 2.7&#xa0;years), while Group B included 50 age- and sex-matched healthy controls. All participants underwent clinical assessment, abdominal ultrasonography, laboratory investigations, and measurement of serum GP-73 using enzyme-linked immunosorbent assay. Children with AIH had significantly higher serum GP-73 levels than controls (median 110.7&#xa0;ng/L vs. 21.3&#xa0;ng/L, <i>p</i> &lt; 0.001). GP-73 levels showed a strong positive correlation with both the histological activity index (r = 0.879, <i>p</i> &lt; 0.001) and the stage of fibrosis (r = 0.647, p &lt; 0.001). At a cutoff level &gt; 49&#xa0;ng/L, GP-73 distinguished AIH cases with 100% sensitivity and 100% specificity. For identifying severe fibrosis, a cutoff &gt; 124.6&#xa0;ng/L yielded 100% sensitivity and 91.7% specificity (area under the ROC curve = 0.995, <i>p</i> &lt; 0.001).</p><p><i>Conclusion</i>:&#xa0;Serum GP-73 levels are significantly elevated in children with autoimmune hepatitis and correlate strongly with both histological grading and staging. GP-73 may serve as a reliable non-invasive marker for assessing disease severity and guiding clinical management in pediatric autoimmune liver diseases.<Table Float="No" ID="Taba"> <tgroup cols="1"> <colspec align="left" colname="c1" colnum="1" /> <tbody> <row> <entry align="left" colname="c1"> <p><b>What is Known:</b></p> <p>• <i>Non-invasive biomarkers for assessing liver fibrosis in children with autoimmune hepatitis are still limited, and liver biopsy remains the gold standard despite its risks.</i></p> </entry> </row> <row> <entry align="left" colname="c1"> <p><b>What is New:</b></p> <p>• <i>Serum GP-73 is significantly elevated in pediatric AIH, strongly correlates with fibrosis severity, and may serve as a reliable non-invasive biomarker.</i></p> </entry> </row> </tbody> </tgroup> </Table></p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Serum golgi protein-73 (GP-73) in children with autoimmune hepatitis

  • Marwa Sabry Rizk,
  • Ola Galal Ali Behairy,
  • Amera Mohamed Abdel Salam Dawood,
  • Rana Atef Khashaba,
  • Walaa El Gendy,
  • Nashwa Farouk Mohamed

摘要

To assess the correlation between serum Golgi protein-73 (GP-73) and the degree of hepatic fibrosis in children with autoimmune liver diseases. This case–control study included 100 children. Group A involved 50 children with autoimmune hepatitis (AIH), aged 2–17 years (mean 11.3 ± 2.7 years), while Group B included 50 age- and sex-matched healthy controls. All participants underwent clinical assessment, abdominal ultrasonography, laboratory investigations, and measurement of serum GP-73 using enzyme-linked immunosorbent assay. Children with AIH had significantly higher serum GP-73 levels than controls (median 110.7 ng/L vs. 21.3 ng/L, p < 0.001). GP-73 levels showed a strong positive correlation with both the histological activity index (r = 0.879, p < 0.001) and the stage of fibrosis (r = 0.647, p < 0.001). At a cutoff level > 49 ng/L, GP-73 distinguished AIH cases with 100% sensitivity and 100% specificity. For identifying severe fibrosis, a cutoff > 124.6 ng/L yielded 100% sensitivity and 91.7% specificity (area under the ROC curve = 0.995, p < 0.001).

Conclusion: Serum GP-73 levels are significantly elevated in children with autoimmune hepatitis and correlate strongly with both histological grading and staging. GP-73 may serve as a reliable non-invasive marker for assessing disease severity and guiding clinical management in pediatric autoimmune liver diseases.

What is Known:

Non-invasive biomarkers for assessing liver fibrosis in children with autoimmune hepatitis are still limited, and liver biopsy remains the gold standard despite its risks.

What is New:

Serum GP-73 is significantly elevated in pediatric AIH, strongly correlates with fibrosis severity, and may serve as a reliable non-invasive biomarker.