Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Abnormalities in Bone Mineral Density and Bone Histology in Thalassemia

View through CrossRef
Abstract This study demonstrated that there was extensive iron staining on trabecular surface and marked reduction in trabecular bone volume without significant alteration in bone formation and bone resorption rates as well as significant reduction in bone mineral density in 18 thalassemic patients. Serum IGF-I was reduced and may modulate the reduction of bone mass. Introduction: Bone histomorphometric studies in thalassemia to show alterations in bone histology and their relationship to biochemical parameters are very limited. Therefore, this study was systematically conducted to determine the alterations in thalassemia patients. Methods: Serum biochemical parameters, trans-iliac crest bone biopsy, and determination of bone mineral density of femur and lumbar spine were done in 18 thalassemic patients (10 females and 8 males). Results: Serum osteocalcin, carboxy terminal teleopeptide fragment of type I collagen, and parathyroid hormone levels were within normal limits, but serum 25(OH) vitamin D (19.3 ± 1.6 ng/ml) and 1,25(OH)2 vitamin D (33.77 ± 1.51 pg/ml) levels were decreased. Serum insulin-like growth factor I (IGF-I; 145.2 ± 20 ng/ml) was suppressed, whereas serum ferritin (1366.6 ± 253.9 ng/ml) was markedly elevated. Reduced bone mineral density was found in all studied areas. Trabecular bone volume was significantly decreased (16.65 ± 1.12%), whereas bone formation rate, eroded surface, and other bone histomorphometric parameters were within normal limits. The trabecular bone volume varied significantly with bone mineral density of total femur (r = 0.48, p = 0.04). There was an extensive stainable iron surface on the mineral front (9–60%). Significant correlation between serum IGF-I, serum ferritin, stainable iron surface, and bone mineral density, lumbar spine, and total femur were found. Serum IGF-I correlated with trabecular bone volume (r = 0.6, p = 0.03), inversely with both serum ferritin level (r = −0.6, p < 0.01), and inversely with stainable iron surface (r = −0.53, p = 0.02). Multiple regression analysis demonstrated that IGF-I was the only independent variable that determined bone mineral density of lumbar spine and total femur. Conclusion: Low bone mineral density and reduced trabecular bone volume with extensive iron deposition are the predominant findings in thalassemic patients. There was no evidence of increased bone resorption or mineralization defect. A reduction in circulatory IGF-I may modulate the reduction of bone mass.
Title: Abnormalities in Bone Mineral Density and Bone Histology in Thalassemia
Description:
Abstract This study demonstrated that there was extensive iron staining on trabecular surface and marked reduction in trabecular bone volume without significant alteration in bone formation and bone resorption rates as well as significant reduction in bone mineral density in 18 thalassemic patients.
Serum IGF-I was reduced and may modulate the reduction of bone mass.
Introduction: Bone histomorphometric studies in thalassemia to show alterations in bone histology and their relationship to biochemical parameters are very limited.
Therefore, this study was systematically conducted to determine the alterations in thalassemia patients.
Methods: Serum biochemical parameters, trans-iliac crest bone biopsy, and determination of bone mineral density of femur and lumbar spine were done in 18 thalassemic patients (10 females and 8 males).
Results: Serum osteocalcin, carboxy terminal teleopeptide fragment of type I collagen, and parathyroid hormone levels were within normal limits, but serum 25(OH) vitamin D (19.
3 ± 1.
6 ng/ml) and 1,25(OH)2 vitamin D (33.
77 ± 1.
51 pg/ml) levels were decreased.
Serum insulin-like growth factor I (IGF-I; 145.
2 ± 20 ng/ml) was suppressed, whereas serum ferritin (1366.
6 ± 253.
9 ng/ml) was markedly elevated.
Reduced bone mineral density was found in all studied areas.
Trabecular bone volume was significantly decreased (16.
65 ± 1.
12%), whereas bone formation rate, eroded surface, and other bone histomorphometric parameters were within normal limits.
The trabecular bone volume varied significantly with bone mineral density of total femur (r = 0.
48, p = 0.
04).
There was an extensive stainable iron surface on the mineral front (9–60%).
Significant correlation between serum IGF-I, serum ferritin, stainable iron surface, and bone mineral density, lumbar spine, and total femur were found.
Serum IGF-I correlated with trabecular bone volume (r = 0.
6, p = 0.
03), inversely with both serum ferritin level (r = −0.
6, p < 0.
01), and inversely with stainable iron surface (r = −0.
53, p = 0.
02).
Multiple regression analysis demonstrated that IGF-I was the only independent variable that determined bone mineral density of lumbar spine and total femur.
Conclusion: Low bone mineral density and reduced trabecular bone volume with extensive iron deposition are the predominant findings in thalassemic patients.
There was no evidence of increased bone resorption or mineralization defect.
A reduction in circulatory IGF-I may modulate the reduction of bone mass.

Related Results

Alterations of Plasma Metabolomics Profile in Thalassemia Patients with Low Bone Mineral Density
Alterations of Plasma Metabolomics Profile in Thalassemia Patients with Low Bone Mineral Density
Background: Osteoporosis is commonly found in thalassemia patients; however, its pathogenesis is not thoroughly understood. Metabolomics is the study of metabolites in biofluids, w...
Frequency of Common Chromosomal Abnormalities in Patients with Idiopathic Acquired Aplastic Anemia
Frequency of Common Chromosomal Abnormalities in Patients with Idiopathic Acquired Aplastic Anemia
Objective: To determine the frequency of common chromosomal aberrations in local population idiopathic determine the frequency of common chromosomal aberrations in local population...
Comprehensive analysis of a-and b-thalassemia genotypes and hematologic phenotypes
Comprehensive analysis of a-and b-thalassemia genotypes and hematologic phenotypes
Background: Guizhou Province is an area with high incidence of thalassemia. However, there are few large-sample studies on the correlation between genotypes and phenotypes in Guizh...
The Molecular Basis of Alpha-Thalassemia in the Qatari Pediatric Population
The Molecular Basis of Alpha-Thalassemia in the Qatari Pediatric Population
BackgroundAnemia is the most common hematologic abnormality that a pediatrician encounters in clinical practice. Alpha-Thalassemia (a-thal) is widely reported in the Arabian Penins...
Thalassemia Phenotypes and Associated Mortality among Yemeni Patients: A Single-Center Retrospective Analysis
Thalassemia Phenotypes and Associated Mortality among Yemeni Patients: A Single-Center Retrospective Analysis
Objective: To retrospectively analyze thalassemia phenotypes and associated mortality among Yemeni patients seeking healthcare in Sana’a city, Yemen. Methods: This retrospect...
Thalassemia Phenotypes and Associated Mortality among Yemeni Patients: A Single-Center Retrospective Analysis
Thalassemia Phenotypes and Associated Mortality among Yemeni Patients: A Single-Center Retrospective Analysis
Objective: To retrospectively analyze thalassemia phenotypes and associated mortality among Yemeni patients seeking healthcare in Sana’a city, Yemen. Methods: This retrospect...
Demographics, clinical profiles and healthcare utilization of patients with beta thalassemia major: A single centered study
Demographics, clinical profiles and healthcare utilization of patients with beta thalassemia major: A single centered study
Thalassemia is an inherited autosomal recessive blood disorder that occurs due to abnormal form of hemoglobin in the blood. It is an autosomal recessive condition caused by decreas...
DIAGNOSTIC VALUE OF MENTZER INDEX FOR THALASSEMIA PREDICTION IN SUSPECTED PATIENTS OF PUNJAB
DIAGNOSTIC VALUE OF MENTZER INDEX FOR THALASSEMIA PREDICTION IN SUSPECTED PATIENTS OF PUNJAB
Thalassemia is a genetic disease and became a worldwide problem. Worldwide, about 3-8% of population are suffered from beta thalassemia. The aim of this study was to use Mentzer in...

Back to Top