Clinical Value of Serum Interleukin-33 Biomarker in Infants With Neonatal Cholestasis
• 2020
معلومات البحث
المؤلفون
Ola G. Behairy,
Akram E. Elsadek, y
Eman G. Behiry, z
Ibrahim A. Elhenawy,
§
Naglaa H. Shalan, and jjKamal R. Sayied
الكلمات المفتاحية
Not Available
المجلة العلمية
Not Available
الناشر
Not Available
المجلد
Not Available
العدد
Not Available
الصفحات
Not Available
publication.type
International
رابط البحث
Not Available
المواد المرفقة
Not Available
الملخص
Objectives: The present study aimed to estimate the value of serum
interleukin-33 (IL-33) levels in infants with cholestasis, correlate serum
IL-33 levels with the clinicopathological profile of infants with cholestasis, and compare its level with that of healthy infants who served as
control.
Methods: Sixty infants with cholestasis were enrolled in the present study
and divided into biliary atresia (BA) group and non-BA group, in addition to
30 healthy infants as a control group. All infants were analyzed for their
clinical and biochemical features, histopathological profile, and serum level of
IL-33 by enzyme-linked immune sorbent assay.
Results: Serum level of IL-33 in BA group (median 48.0, interquartile
range: 28.9–106.2) was significantly higher than that of the non-BA group
(median 17.3, interquartile range: 13.7–18.8 pg/mL) and both were higher
than that of the control group. There was a positive correlation between
serum IL-33 and aspartate aminotransferase, alanine aminotransferase,
bilirubin (total and direct) levels, and fibrosis stage among the BA group.
Serum IL-33 at a cut-off value of 20.8 pg/mL can detect BA with a
specificity of 95% and a sensitivity of 96.7%.
Conclusion: The significantly higher production of IL-33 in patients with
BA compared to non-BA suggests a potential role of IL-33 for initiation and
progression of the disease process, also, IL-33 may have a diagnostic role in
infants with BA.
interleukin-33 (IL-33) levels in infants with cholestasis, correlate serum
IL-33 levels with the clinicopathological profile of infants with cholestasis, and compare its level with that of healthy infants who served as
control.
Methods: Sixty infants with cholestasis were enrolled in the present study
and divided into biliary atresia (BA) group and non-BA group, in addition to
30 healthy infants as a control group. All infants were analyzed for their
clinical and biochemical features, histopathological profile, and serum level of
IL-33 by enzyme-linked immune sorbent assay.
Results: Serum level of IL-33 in BA group (median 48.0, interquartile
range: 28.9–106.2) was significantly higher than that of the non-BA group
(median 17.3, interquartile range: 13.7–18.8 pg/mL) and both were higher
than that of the control group. There was a positive correlation between
serum IL-33 and aspartate aminotransferase, alanine aminotransferase,
bilirubin (total and direct) levels, and fibrosis stage among the BA group.
Serum IL-33 at a cut-off value of 20.8 pg/mL can detect BA with a
specificity of 95% and a sensitivity of 96.7%.
Conclusion: The significantly higher production of IL-33 in patients with
BA compared to non-BA suggests a potential role of IL-33 for initiation and
progression of the disease process, also, IL-33 may have a diagnostic role in
infants with BA.
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