The Role of Collagen Abnormalities in Ultrasound and Densitometry Assessment: In Vivo Evidence

ISSN:
1432-0827
Keywords:
Key words: Quantitative ultrasound — Bone mineral density — Collagen abnormalities — Ehlers-Danlos syndrome — Systemic sclerosis.
Source:
Springer Online Journal Archives 1860-2000
Topics:
Biology
Medicine
Physics
Notes:
Abstract. There is little information concerning how the mutation of collagen affects bone mineralization and the assessment of bone properties. To estimate these influences, we performed ultrasonic assessments of the calcaneus and bone mineral density (BMD) measurements of the hip and lumbar spine. Females with diseases related to the mutation of collagen [Ehlers-Danlos syndrome (EDS) type III and systemic sclerosis (SSc)] participated in this study. We compared the broadband ultrasound attenuation (BUA and UBI-4), the average transit time through the heel (TTH), and a multiple factor index (UBI-4T) with control subjects matched on age, race, and menstrual status. Both groups of patients had BMD of the spine (L2–L4) within the normal range for their age and sex (for EDS: n = 23, 1.14 ± 0.14 g/cm2 and z-score = 0.37; for SSc: n = 15, 0.98 ± 0.15 g/cm2 and z-score = 0.20). EDS and SSc subjects had lower BMD of the femoral neck (FN) compared with controls (for EDS: 0.91 ± 0.13 g/cm2, z-score =−0.41, P= 0.025; for SSc 0.67 ± 0.13 g/cm2, z-score =−0.92, P= 0.006). Subjects with EDS and SSc also had lower BUA values (P= 0.051–0.001) compared with controls. After adjusting for body weight, height, and the level of physical activity, the difference in FN BMD between EDS or SSc and controls became marginal (EDS: P= 0.072; SSc: P= 0.086). However, the significant difference for BUA between subjects and controls remained for EDS (P= 0.008), and disappeared for SSc (0.70) after adjusting for weight, height, level of physical activity, and BMD. These results suggest that the abnormalities of collagen may impact on bone mass measurements differently depending on skeletal site, modality of the assessment, and the source and nature of collagen defects. To determine whether collagen properties influence QUS, proper models in vivo and in vitro should be used.
Type of Medium:
Electronic Resource
URL:
_version_ 1798295522267627521
autor Cheng, S.
Tylavsky, F. A.
Orwoll, E. S.
Rho, J.-Y.
Carbone, L. D.
autorsonst Cheng, S.
Tylavsky, F. A.
Orwoll, E. S.
Rho, J.-Y.
Carbone, L. D.
book_url http://dx.doi.org/10.1007/s002239900635
datenlieferant nat_lic_papers
hauptsatz hsatz_simple
identnr NLM20703088X
issn 1432-0827
journal_name Calcified tissue international
materialart 1
notes Abstract. There is little information concerning how the mutation of collagen affects bone mineralization and the assessment of bone properties. To estimate these influences, we performed ultrasonic assessments of the calcaneus and bone mineral density (BMD) measurements of the hip and lumbar spine. Females with diseases related to the mutation of collagen [Ehlers-Danlos syndrome (EDS) type III and systemic sclerosis (SSc)] participated in this study. We compared the broadband ultrasound attenuation (BUA and UBI-4), the average transit time through the heel (TTH), and a multiple factor index (UBI-4T) with control subjects matched on age, race, and menstrual status. Both groups of patients had BMD of the spine (L2–L4) within the normal range for their age and sex (for EDS: n = 23, 1.14 ± 0.14 g/cm2 and z-score = 0.37; for SSc: n = 15, 0.98 ± 0.15 g/cm2 and z-score = 0.20). EDS and SSc subjects had lower BMD of the femoral neck (FN) compared with controls (for EDS: 0.91 ± 0.13 g/cm2, z-score =−0.41, P= 0.025; for SSc 0.67 ± 0.13 g/cm2, z-score =−0.92, P= 0.006). Subjects with EDS and SSc also had lower BUA values (P= 0.051–0.001) compared with controls. After adjusting for body weight, height, and the level of physical activity, the difference in FN BMD between EDS or SSc and controls became marginal (EDS: P= 0.072; SSc: P= 0.086). However, the significant difference for BUA between subjects and controls remained for EDS (P= 0.008), and disappeared for SSc (0.70) after adjusting for weight, height, level of physical activity, and BMD. These results suggest that the abnormalities of collagen may impact on bone mass measurements differently depending on skeletal site, modality of the assessment, and the source and nature of collagen defects. To determine whether collagen properties influence QUS, proper models in vivo and in vitro should be used.
package_name Springer
publikationsjahr_anzeige 1999
publikationsjahr_facette 1999
publikationsjahr_intervall 8004:1995-1999
publikationsjahr_sort 1999
publisher Springer
reference 64 (1999), S. 470-476
schlagwort Key words: Quantitative ultrasound — Bone mineral density — Collagen abnormalities — Ehlers-Danlos syndrome — Systemic sclerosis.
search_space articles
shingle_author_1 Cheng, S.
Tylavsky, F. A.
Orwoll, E. S.
Rho, J.-Y.
Carbone, L. D.
shingle_author_2 Cheng, S.
Tylavsky, F. A.
Orwoll, E. S.
Rho, J.-Y.
Carbone, L. D.
shingle_author_3 Cheng, S.
Tylavsky, F. A.
Orwoll, E. S.
Rho, J.-Y.
Carbone, L. D.
shingle_author_4 Cheng, S.
Tylavsky, F. A.
Orwoll, E. S.
Rho, J.-Y.
Carbone, L. D.
shingle_catch_all_1 Cheng, S.
Tylavsky, F. A.
Orwoll, E. S.
Rho, J.-Y.
Carbone, L. D.
The Role of Collagen Abnormalities in Ultrasound and Densitometry Assessment: In Vivo Evidence
Key words: Quantitative ultrasound — Bone mineral density — Collagen abnormalities — Ehlers-Danlos syndrome — Systemic sclerosis.
Key words: Quantitative ultrasound — Bone mineral density — Collagen abnormalities — Ehlers-Danlos syndrome — Systemic sclerosis.
Abstract. There is little information concerning how the mutation of collagen affects bone mineralization and the assessment of bone properties. To estimate these influences, we performed ultrasonic assessments of the calcaneus and bone mineral density (BMD) measurements of the hip and lumbar spine. Females with diseases related to the mutation of collagen [Ehlers-Danlos syndrome (EDS) type III and systemic sclerosis (SSc)] participated in this study. We compared the broadband ultrasound attenuation (BUA and UBI-4), the average transit time through the heel (TTH), and a multiple factor index (UBI-4T) with control subjects matched on age, race, and menstrual status. Both groups of patients had BMD of the spine (L2–L4) within the normal range for their age and sex (for EDS: n = 23, 1.14 ± 0.14 g/cm2 and z-score = 0.37; for SSc: n = 15, 0.98 ± 0.15 g/cm2 and z-score = 0.20). EDS and SSc subjects had lower BMD of the femoral neck (FN) compared with controls (for EDS: 0.91 ± 0.13 g/cm2, z-score =−0.41, P= 0.025; for SSc 0.67 ± 0.13 g/cm2, z-score =−0.92, P= 0.006). Subjects with EDS and SSc also had lower BUA values (P= 0.051–0.001) compared with controls. After adjusting for body weight, height, and the level of physical activity, the difference in FN BMD between EDS or SSc and controls became marginal (EDS: P= 0.072; SSc: P= 0.086). However, the significant difference for BUA between subjects and controls remained for EDS (P= 0.008), and disappeared for SSc (0.70) after adjusting for weight, height, level of physical activity, and BMD. These results suggest that the abnormalities of collagen may impact on bone mass measurements differently depending on skeletal site, modality of the assessment, and the source and nature of collagen defects. To determine whether collagen properties influence QUS, proper models in vivo and in vitro should be used.
1432-0827
14320827
Springer
shingle_catch_all_2 Cheng, S.
Tylavsky, F. A.
Orwoll, E. S.
Rho, J.-Y.
Carbone, L. D.
The Role of Collagen Abnormalities in Ultrasound and Densitometry Assessment: In Vivo Evidence
Key words: Quantitative ultrasound — Bone mineral density — Collagen abnormalities — Ehlers-Danlos syndrome — Systemic sclerosis.
Key words: Quantitative ultrasound — Bone mineral density — Collagen abnormalities — Ehlers-Danlos syndrome — Systemic sclerosis.
Abstract. There is little information concerning how the mutation of collagen affects bone mineralization and the assessment of bone properties. To estimate these influences, we performed ultrasonic assessments of the calcaneus and bone mineral density (BMD) measurements of the hip and lumbar spine. Females with diseases related to the mutation of collagen [Ehlers-Danlos syndrome (EDS) type III and systemic sclerosis (SSc)] participated in this study. We compared the broadband ultrasound attenuation (BUA and UBI-4), the average transit time through the heel (TTH), and a multiple factor index (UBI-4T) with control subjects matched on age, race, and menstrual status. Both groups of patients had BMD of the spine (L2–L4) within the normal range for their age and sex (for EDS: n = 23, 1.14 ± 0.14 g/cm2 and z-score = 0.37; for SSc: n = 15, 0.98 ± 0.15 g/cm2 and z-score = 0.20). EDS and SSc subjects had lower BMD of the femoral neck (FN) compared with controls (for EDS: 0.91 ± 0.13 g/cm2, z-score =−0.41, P= 0.025; for SSc 0.67 ± 0.13 g/cm2, z-score =−0.92, P= 0.006). Subjects with EDS and SSc also had lower BUA values (P= 0.051–0.001) compared with controls. After adjusting for body weight, height, and the level of physical activity, the difference in FN BMD between EDS or SSc and controls became marginal (EDS: P= 0.072; SSc: P= 0.086). However, the significant difference for BUA between subjects and controls remained for EDS (P= 0.008), and disappeared for SSc (0.70) after adjusting for weight, height, level of physical activity, and BMD. These results suggest that the abnormalities of collagen may impact on bone mass measurements differently depending on skeletal site, modality of the assessment, and the source and nature of collagen defects. To determine whether collagen properties influence QUS, proper models in vivo and in vitro should be used.
1432-0827
14320827
Springer
shingle_catch_all_3 Cheng, S.
Tylavsky, F. A.
Orwoll, E. S.
Rho, J.-Y.
Carbone, L. D.
The Role of Collagen Abnormalities in Ultrasound and Densitometry Assessment: In Vivo Evidence
Key words: Quantitative ultrasound — Bone mineral density — Collagen abnormalities — Ehlers-Danlos syndrome — Systemic sclerosis.
Key words: Quantitative ultrasound — Bone mineral density — Collagen abnormalities — Ehlers-Danlos syndrome — Systemic sclerosis.
Abstract. There is little information concerning how the mutation of collagen affects bone mineralization and the assessment of bone properties. To estimate these influences, we performed ultrasonic assessments of the calcaneus and bone mineral density (BMD) measurements of the hip and lumbar spine. Females with diseases related to the mutation of collagen [Ehlers-Danlos syndrome (EDS) type III and systemic sclerosis (SSc)] participated in this study. We compared the broadband ultrasound attenuation (BUA and UBI-4), the average transit time through the heel (TTH), and a multiple factor index (UBI-4T) with control subjects matched on age, race, and menstrual status. Both groups of patients had BMD of the spine (L2–L4) within the normal range for their age and sex (for EDS: n = 23, 1.14 ± 0.14 g/cm2 and z-score = 0.37; for SSc: n = 15, 0.98 ± 0.15 g/cm2 and z-score = 0.20). EDS and SSc subjects had lower BMD of the femoral neck (FN) compared with controls (for EDS: 0.91 ± 0.13 g/cm2, z-score =−0.41, P= 0.025; for SSc 0.67 ± 0.13 g/cm2, z-score =−0.92, P= 0.006). Subjects with EDS and SSc also had lower BUA values (P= 0.051–0.001) compared with controls. After adjusting for body weight, height, and the level of physical activity, the difference in FN BMD between EDS or SSc and controls became marginal (EDS: P= 0.072; SSc: P= 0.086). However, the significant difference for BUA between subjects and controls remained for EDS (P= 0.008), and disappeared for SSc (0.70) after adjusting for weight, height, level of physical activity, and BMD. These results suggest that the abnormalities of collagen may impact on bone mass measurements differently depending on skeletal site, modality of the assessment, and the source and nature of collagen defects. To determine whether collagen properties influence QUS, proper models in vivo and in vitro should be used.
1432-0827
14320827
Springer
shingle_catch_all_4 Cheng, S.
Tylavsky, F. A.
Orwoll, E. S.
Rho, J.-Y.
Carbone, L. D.
The Role of Collagen Abnormalities in Ultrasound and Densitometry Assessment: In Vivo Evidence
Key words: Quantitative ultrasound — Bone mineral density — Collagen abnormalities — Ehlers-Danlos syndrome — Systemic sclerosis.
Key words: Quantitative ultrasound — Bone mineral density — Collagen abnormalities — Ehlers-Danlos syndrome — Systemic sclerosis.
Abstract. There is little information concerning how the mutation of collagen affects bone mineralization and the assessment of bone properties. To estimate these influences, we performed ultrasonic assessments of the calcaneus and bone mineral density (BMD) measurements of the hip and lumbar spine. Females with diseases related to the mutation of collagen [Ehlers-Danlos syndrome (EDS) type III and systemic sclerosis (SSc)] participated in this study. We compared the broadband ultrasound attenuation (BUA and UBI-4), the average transit time through the heel (TTH), and a multiple factor index (UBI-4T) with control subjects matched on age, race, and menstrual status. Both groups of patients had BMD of the spine (L2–L4) within the normal range for their age and sex (for EDS: n = 23, 1.14 ± 0.14 g/cm2 and z-score = 0.37; for SSc: n = 15, 0.98 ± 0.15 g/cm2 and z-score = 0.20). EDS and SSc subjects had lower BMD of the femoral neck (FN) compared with controls (for EDS: 0.91 ± 0.13 g/cm2, z-score =−0.41, P= 0.025; for SSc 0.67 ± 0.13 g/cm2, z-score =−0.92, P= 0.006). Subjects with EDS and SSc also had lower BUA values (P= 0.051–0.001) compared with controls. After adjusting for body weight, height, and the level of physical activity, the difference in FN BMD between EDS or SSc and controls became marginal (EDS: P= 0.072; SSc: P= 0.086). However, the significant difference for BUA between subjects and controls remained for EDS (P= 0.008), and disappeared for SSc (0.70) after adjusting for weight, height, level of physical activity, and BMD. These results suggest that the abnormalities of collagen may impact on bone mass measurements differently depending on skeletal site, modality of the assessment, and the source and nature of collagen defects. To determine whether collagen properties influence QUS, proper models in vivo and in vitro should be used.
1432-0827
14320827
Springer
shingle_title_1 The Role of Collagen Abnormalities in Ultrasound and Densitometry Assessment: In Vivo Evidence
shingle_title_2 The Role of Collagen Abnormalities in Ultrasound and Densitometry Assessment: In Vivo Evidence
shingle_title_3 The Role of Collagen Abnormalities in Ultrasound and Densitometry Assessment: In Vivo Evidence
shingle_title_4 The Role of Collagen Abnormalities in Ultrasound and Densitometry Assessment: In Vivo Evidence
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titel The Role of Collagen Abnormalities in Ultrasound and Densitometry Assessment: In Vivo Evidence
titel_suche The Role of Collagen Abnormalities in Ultrasound and Densitometry Assessment: In Vivo Evidence
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