A single-center study of bone mineral density in adult patients with severe hemophilia A in correlation with markers of bone metabolism
Introduction: Osteopenia and osteoporosis are well-known hemophilia A comorbidities. The pathogenesis of bone turnover alteration resulting in reduced bone mass includes impaired osteoblastic differentiation and disinhibition of RANKL-induced osteoclastogenesis as a result of a low FVIII level. Aim:...
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Published in | Folia Medica Vol. 65; no. 1; pp. 87 - 92 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Bulgaria
MEDICAL UNIVERSITY- PLOVDIV
28.02.2023
Pensoft Publishers |
Subjects | |
Online Access | Get full text |
ISSN | 0204-8043 1314-2143 1314-2143 |
DOI | 10.3897/folmed.65.e75414 |
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Abstract | Introduction:
Osteopenia and osteoporosis are well-known hemophilia A comorbidities. The pathogenesis of bone turnover alteration resulting in reduced bone mass includes impaired osteoblastic differentiation and disinhibition of RANKL-induced osteoclastogenesis as a result of a low FVIII level.
Aim:
To evaluate the bone mineral density (BMD) in adult patients with severe hemophilia A and assess a possible correlation with the bone remodeling biomarkers OPG/RANKL, CTX-1, osteocalcin, and Vit D.
Materials and methods:
28 male subjects with severe hemophilia A and 33 age-matched controls were recruited. The biomarkers were tested with the ELISA assay and BMD with DEXA of the lumbar spine (LS) and total hip (TH).
Results:
The patients had lower LS-BMD (−0.955±0.145 vs. 1.118±0.079, p=0.05) and TH-BMD (−0.840±0.147 vs. 0.951±0.075, p=0.05) than those of the controls. The TH T-scores were −1.41±0.91 vs. 0.4±0.49 (p=0.05) and the LS T-scores −1.16±1.046 vs. 0.14±0.72 (p=0.05). 66.6% of patients under 50 years had osteopenia and 8.3% had osteoporosis. Fifty percent of those over 50 years old had osteopenia and 20% had osteoporosis. We found significantly higher OPG levels (123.69±107.05 vs. 41.98±18.95, p=0.05) than that in controls and lower sRANKL levels (23.49±29.39 vs. 131.32±201.27, p=0.05) and sRANKL/OPG ratio (0.27±0.35 vs. 5.28±10.01, p=0.05) than those in controls. A positive correlation was found between sRANKL and the BMD T-score of lumbar spine (p=0.001) in the patient group.
Conclusions:
sRANKL level and ratio can be used as predictors of low BMD. |
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AbstractList | Osteopenia and osteoporosis are well-known hemophilia A comorbidities. The pathogenesis of bone turnover alteration resulting in reduced bone mass includes impaired osteoblastic differentiation and disinhibition of RANKL-induced osteoclastogenesis as a result of a low FVIII level.
To evaluate the bone mineral density (BMD) in adult patients with severe hemophilia A and assess a possible correlation with the bone remodeling biomarkers OPG/RANKL, CTX-1, osteocalcin, and Vit D.
28 male subjects with severe hemophilia A and 33 age-matched controls were recruited. The biomarkers were tested with the ELISA assay and BMD with DEXA of the lumbar spine (LS) and total hip (TH).
The patients had lower LS-BMD (-0.955±0.145 vs. 1.118±0.079, p=0.05) and TH-BMD (-0.840±0.147 vs. 0.951±0.075, p=0.05) than those of the controls. The TH T-scores were -1.41±0.91 vs. 0.4±0.49 (p=0.05) and the LS T-scores -1.16±1.046 vs. 0.14±0.72 (p=0.05). 66.6% of patients under 50 years had osteopenia and 8.3% had osteoporosis. Fifty percent of those over 50 years old had osteopenia and 20% had osteoporosis. We found significantly higher OPG levels (123.69±107.05 vs. 41.98±18.95, p=0.05) than that in controls and lower sRANKL levels (23.49±29.39 vs. 131.32±201.27, p=0.05) and sRANKL/OPG ratio (0.27±0.35 vs. 5.28±10.01, p=0.05) than those in controls. A positive correlation was found between sRANKL and the BMD T-score of lumbar spine (p=0.001) in the patient group.
sRANKL level and ratio can be used as predictors of low BMD. Введение: Остеопения и остеопороз являются хорошо известными сопутствующими заболеваниями гемофилии А. Патогенез изменения костного метаболизма, приводящего к уменьшению костной массы, включает нарушение дифференцировки остеобластов и растормаживание RANKL-индуцированного остеокластогенеза в результате низкого уровня FVIII. Цель: Оценить минеральную плотность костной ткани (МПКТ) у пожилых пациентов с тяжёлой формой гемофилии А и оценить возможную корреляцию с биомаркерами костного ремоделирования OPG/RANKL, CTX-1, остеокальцином и витамином D. Материалы и методы: Было набрано 28 лиц мужского пола с тяжёлой формой гемофилии А и 33 лица соответствоваших по возрасту в качестве контрольной группы. Биомаркеры были проверены с помощью анализа ELISA и BMD с DEXA поясничного отдела позвоночника (LS) и всего бедра (TH). Результаты: У больных была более низкая LS-BMD (-0.955±0.145 против 1.118±0.079, p=0.05) и TH-BMD (-0.840 ± 0.147 против 0.951 ± 0.075, p=0.05), чем у контрольной группы. T-показатели TH были -1.41 ± 0.91 против 0.4 ± 0.49 (p=0.05), а T-показатели тели LS -1.16 ± 1.046 против 0.14 ± 0.72 (p=0.05). У 66.6 % больных до 50 лет была остеопения, у 8.3% - остеопороз. У 50% лиц старше 50 лет была остеопения, а у 20% - остеопороз. Мы обнаружили значительно более высокие уровни OPG (123.69±107.05 против 41.98±18.95, p=0.05), чем в контрольной группе, и более низкие уровни sRANKL (23.49±29.39 против 131.32±201.27, p=0.05) и отношение sRANKL/OPG (0.27±0.05). 0.35 против 5.28±10.01, р=0.05), чем в контроле. Выявлена положительная корреляция между sRANKL и Т-баллом BMD поясничного отдела позвоночника (р=0.001) в группе больных. Заключение: Уровень и соотношение sRANKL можно использовать в качестве предикторов низкой BMD Introduction: Osteopenia and osteoporosis are well-known hemophilia A comorbidities. The pathogenesis of bone turnover alteration resulting in reduced bone mass includes impaired osteoblastic differentiation and disinhibition of RANKL-induced osteoclastogenesis as a result of a low FVIII level.Aim: To evaluate the bone mineral density (BMD) in adult patients with severe hemophilia A and assess a possible correlation with the bone remodeling biomarkers OPG/RANKL, CTX-1, osteocalcin, and Vit D.Materials and methods: 28 male subjects with severe hemophilia A and 33 age-matched controls were recruited. The biomarkers were tested with the ELISA assay and BMD with DEXA of the lumbar spine (LS) and total hip (TH).Results: The patients had lower LS-BMD (−0.955±0.145 vs. 1.118±0.079, p=0.05) and TH-BMD (−0.840±0.147 vs. 0.951±0.075, p=0.05) than those of the controls. The TH T-scores were −1.41±0.91 vs. 0.4±0.49 (p=0.05) and the LS T-scores −1.16±1.046 vs. 0.14±0.72 (p=0.05). 66.6% of patients under 50 years had osteopenia and 8.3% had osteoporosis. Fifty percent of those over 50 years old had osteopenia and 20% had osteoporosis. We found significantly higher OPG levels (123.69±107.05 vs. 41.98±18.95, p=0.05) than that in controls and lower sRANKL levels (23.49±29.39 vs. 131.32±201.27, p=0.05) and sRANKL/OPG ratio (0.27±0.35 vs. 5.28±10.01, p=0.05) than those in controls. A positive correlation was found between sRANKL and the BMD T-score of lumbar spine (p=0.001) in the patient group.Conclusions: sRANKL level and ratio can be used as predictors of low BMD. Introduction: Osteopenia and osteoporosis are well-known hemophilia A comorbidities. The pathogenesis of bone turnover alteration resulting in reduced bone mass includes impaired osteoblastic differentiation and disinhibition of RANKL-induced osteoclastogenesis as a result of a low FVIII level. Aim: To evaluate the bone mineral density (BMD) in adult patients with severe hemophilia A and assess a possible correlation with the bone remodeling biomarkers OPG/RANKL, CTX-1, osteocalcin, and Vit D. Materials and methods: 28 male subjects with severe hemophilia A and 33 age-matched controls were recruited. The biomarkers were tested with the ELISA assay and BMD with DEXA of the lumbar spine (LS) and total hip (TH). Results: The patients had lower LS-BMD (−0.955±0.145 vs. 1.118±0.079, p=0.05) and TH-BMD (−0.840±0.147 vs. 0.951±0.075, p=0.05) than those of the controls. The TH T-scores were −1.41±0.91 vs. 0.4±0.49 (p=0.05) and the LS T-scores −1.16±1.046 vs. 0.14±0.72 (p=0.05). 66.6% of patients under 50 years had osteopenia and 8.3% had osteoporosis. Fifty percent of those over 50 years old had osteopenia and 20% had osteoporosis. We found significantly higher OPG levels (123.69±107.05 vs. 41.98±18.95, p=0.05) than that in controls and lower sRANKL levels (23.49±29.39 vs. 131.32±201.27, p=0.05) and sRANKL/OPG ratio (0.27±0.35 vs. 5.28±10.01, p=0.05) than those in controls. A positive correlation was found between sRANKL and the BMD T-score of lumbar spine (p=0.001) in the patient group. Conclusions: sRANKL level and ratio can be used as predictors of low BMD. |
Author | Deneva, Tanya Mateva, Nonka Tsvetkova, Silvia Grudeva-Popova, Zhanet Ivanova, Hristina A. |
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Snippet | Introduction:
Osteopenia and osteoporosis are well-known hemophilia A comorbidities. The pathogenesis of bone turnover alteration resulting in reduced bone... Osteopenia and osteoporosis are well-known hemophilia A comorbidities. The pathogenesis of bone turnover alteration resulting in reduced bone mass includes... Введение: Остеопения и остеопороз являются хорошо известными сопутствующими заболеваниями гемофилии А. Патогенез изменения костного метаболизма, приводящего к... Introduction: Osteopenia and osteoporosis are well-known hemophilia A comorbidities. The pathogenesis of bone turnover alteration resulting in reduced bone... |
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SubjectTerms | Adult Age Biomarkers Bone Density Bone Diseases, Metabolic - epidemiology Bone Diseases, Metabolic - etiology FVIII deficiency Hemophilia Hemophilia A - complications HIV Human immunodeficiency virus Humans Lumbar Vertebrae - diagnostic imaging Male Middle Aged OPG Osteoporosis Osteoporosis - etiology Patients RANKL Statistical analysis |
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Title | A single-center study of bone mineral density in adult patients with severe hemophilia A in correlation with markers of bone metabolism |
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