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 inFolia Medica Vol. 65; no. 1; pp. 87 - 92
Main Authors Ivanova, Hristina A., Grudeva-Popova, Zhanet, Deneva, Tanya, Tsvetkova, Silvia, Mateva, Nonka
Format Journal Article
LanguageEnglish
Published Bulgaria MEDICAL UNIVERSITY- PLOVDIV 28.02.2023
Pensoft Publishers
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ISSN0204-8043
1314-2143
1314-2143
DOI10.3897/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.
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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BackLink https://www.ncbi.nlm.nih.gov/pubmed/36855979$$D View this record in MEDLINE/PubMed
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Keywords RANKL
osteoporosis
OPG
FVIII deficiency
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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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StartPage 87
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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