Academic Journal
Reduced Serum Glucagon Like Peptide-1 In Children with Osteoporosis of Chronic Liver Diseases: A Single Center Trial
العنوان: | Reduced Serum Glucagon Like Peptide-1 In Children with Osteoporosis of Chronic Liver Diseases: A Single Center Trial |
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المؤلفون: | Nashwa F. Mohamed Elmetwaly, Ola G. Behairy, Manal S. EL-Defrawy, Ola E. Seleim, Dina S. Abdelmotaleb |
المصدر: | Pediatric Sciences Journal, Vol 5, Iss 1, Pp 1-11 (2025) |
بيانات النشر: | Cairo University, Faculty of Medicine, Department of Pediatrics, 2025. |
سنة النشر: | 2025 |
المجموعة: | LCC:Pediatrics |
مصطلحات موضوعية: | children, glp-1, chronic liver disease, liver fibrosis, bone density dual-energy x-ray absorptiometry, dexa scan, bone mineral density, Pediatrics, RJ1-570 |
الوصف: | Background: Chronic liver disease (CLD) in children is associated with reduction of bone mineral density. Glucagon like peptide- 1 (GLP-1) is essential for bone metabolism and bone turnover. GLP-1 role in bone disease associated with CLD remains to be studied. Aim of the work: to study the relationship between GLP- 1 and osteoporosis among children with CLD. Subjects and Methods: This cross-sectional study included 60 children with CLD as a study group and 60 healthy participants as a control group. GLP- 1 was measured using ELISA technique and compared between groups. All children with CLD underwent liver biopsy and bone density dual-energy X-ray absorptiometry (DEXA) scan. The study was conducted at Benha University Hospital, Egypt. Results: The mean ± SD age of the included children with CLD and control group was 9.3 ± 5.1 years and 10.43 ± 5.54 years (p=0.130). Females and males comprised 33 (55%) and 27(45%) of the CLD group and 41 (68.3%) and 19 (31.7%) of the control group (p=0.133). The mean ± SD duration of liver diseases was 7.14 ± 4.51 years. Osteoporosis was encountered among 53 (88.3%) children with CLD. Their mean ± SD age was 9.51 ± 5.27 and their mean ± SD disease duration was 7.22 ± 4.65 compared to 7.71 ± 3.13 SD and 6.60 ± 3.52 SD of those who did not have osteoporosis (p=0.498) and (p=0.910) respectively. The mean± SD bone mineral density (BMD) and Z-score for lumber spine in children with CLD was 0.46 ± 0.14 g/cm2 and mean± SD Z- score was -2.7 ± 0.38. BMD correlated negatively with liver disease duration: r: -0.135, p=0.303, histological activity index: r: -0.101, p=0.441, fibrosis: r: -0.046, p= 0.726, PELD: r= -0.46; p= 0.003; MELD: r= -0.71; p< 0.001; CHILD Pugh: r= -0.26; p= 0.04). The mean ±SD serum GLP-1 among children with CLD was 3.06 ± 1.07 pg/ml and 6.5± 2.01 pg/ml in the control group (p= 0.001). Serum GLP-1 correlated negatively with progressive fibrosis (p=0.008). Serum GLP-1 correlated with BMD (p=0.013), and at a cut-off value of 4 pg/mL, GLP- 1 had 86.7% sensitivity and 83.3% specificity in diagnosis of osteoporosis in children with CLD. Serum 25(OH) vit D less than 28 nmol/L had a 100% sensitivity and specificity for detection of osteoporosis. Conclusion: DEXA confirmed osteoporosis of lumbar vertebrae among children with CLD. Serum GLP- 1 level was reduced among children with CLD. Serum GLP- 1 correlated inversely with degree of liver fibrosis and histological activity index and positively with the progression of osteoporosis in children with CLD. Low serum 25(OH) vit D is a sensitive and specific diagnostic marker of osteoporosis in CLD. |
نوع الوثيقة: | article |
وصف الملف: | electronic resource |
اللغة: | English |
تدمد: | 2805-279X 2682-3985 |
Relation: | https://cupsj.journals.ekb.eg/article_401882_c75d34bb93e0e533336e658b129bc3bb.pdf; https://doaj.org/toc/2805-279X; https://doaj.org/toc/2682-3985 |
DOI: | 10.21608/CUPSJ.2025.316749.1141 |
URL الوصول: | https://doaj.org/article/eddc3f0b11db451da979da5984175b00 |
رقم الانضمام: | edsdoj.3f0b11db451da979da5984175b00 |
قاعدة البيانات: | Directory of Open Access Journals |
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Glucagon like peptide- 1 (GLP-1) is essential for bone metabolism and bone turnover. GLP-1 role in bone disease associated with CLD remains to be studied. Aim of the work: to study the relationship between GLP- 1 and osteoporosis among children with CLD. Subjects and Methods: This cross-sectional study included 60 children with CLD as a study group and 60 healthy participants as a control group. GLP- 1 was measured using ELISA technique and compared between groups. All children with CLD underwent liver biopsy and bone density dual-energy X-ray absorptiometry (DEXA) scan. The study was conducted at Benha University Hospital, Egypt. Results: The mean ± SD age of the included children with CLD and control group was 9.3 ± 5.1 years and 10.43 ± 5.54 years (p=0.130). Females and males comprised 33 (55%) and 27(45%) of the CLD group and 41 (68.3%) and 19 (31.7%) of the control group (p=0.133). The mean ± SD duration of liver diseases was 7.14 ± 4.51 years. Osteoporosis was encountered among 53 (88.3%) children with CLD. Their mean ± SD age was 9.51 ± 5.27 and their mean ± SD disease duration was 7.22 ± 4.65 compared to 7.71 ± 3.13 SD and 6.60 ± 3.52 SD of those who did not have osteoporosis (p=0.498) and (p=0.910) respectively. The mean± SD bone mineral density (BMD) and Z-score for lumber spine in children with CLD was 0.46 ± 0.14 g/cm2 and mean± SD Z- score was -2.7 ± 0.38. BMD correlated negatively with liver disease duration: r: -0.135, p=0.303, histological activity index: r: -0.101, p=0.441, fibrosis: r: -0.046, p= 0.726, PELD: r= -0.46; p= 0.003; MELD: r= -0.71; p< 0.001; CHILD Pugh: r= -0.26; p= 0.04). The mean ±SD serum GLP-1 among children with CLD was 3.06 ± 1.07 pg/ml and 6.5± 2.01 pg/ml in the control group (p= 0.001). Serum GLP-1 correlated negatively with progressive fibrosis (p=0.008). Serum GLP-1 correlated with BMD (p=0.013), and at a cut-off value of 4 pg/mL, GLP- 1 had 86.7% sensitivity and 83.3% specificity in diagnosis of osteoporosis in children with CLD. Serum 25(OH) vit D less than 28 nmol/L had a 100% sensitivity and specificity for detection of osteoporosis. Conclusion: DEXA confirmed osteoporosis of lumbar vertebrae among children with CLD. Serum GLP- 1 level was reduced among children with CLD. Serum GLP- 1 correlated inversely with degree of liver fibrosis and histological activity index and positively with the progression of osteoporosis in children with CLD. 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