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Anamnestic risk factor questionnaire as reliable diagnostic instrument for osteoporosis (reduced bone morphogenic density)
BACKGROUND: Osteoporosis is a major health problem worldwide, and is included in the WHO list of the top 10 major diseases. However, it is often undiagnosed until the first fracture occurs, due to inadequate patient education and lack of insurance coverage for screening tests. Anamnestic risk factor...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3176487/ https://www.ncbi.nlm.nih.gov/pubmed/21849030 http://dx.doi.org/10.1186/1471-2474-12-187 |
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author | Kolios, Leila Takur, Caner Moghaddam, Arash Hitzler, Mirjam Schmidt-Gayk, Heinrich Suda, Arnold J Höner, Bernd Grützner, Paul A Wölfl, Christoph |
author_facet | Kolios, Leila Takur, Caner Moghaddam, Arash Hitzler, Mirjam Schmidt-Gayk, Heinrich Suda, Arnold J Höner, Bernd Grützner, Paul A Wölfl, Christoph |
author_sort | Kolios, Leila |
collection | PubMed |
description | BACKGROUND: Osteoporosis is a major health problem worldwide, and is included in the WHO list of the top 10 major diseases. However, it is often undiagnosed until the first fracture occurs, due to inadequate patient education and lack of insurance coverage for screening tests. Anamnestic risk factors like positive family anamnesis or early menopause are assumed to correlate with reduced BMD. METHODS: In our study of 78 patients with metaphyseal long bone fractures, we searched for a correlation between anamnestic risk factors, bone specific laboratory values, and the bone morphogenic density (BMD). Each indicator was examined as a possible diagnostic instrument for osteoporosis. The secondary aim of this study was to demonstrate the high prevalence of osteoporosis in patients with metaphyseal fractures. RESULTS: 76.9% of our fracture patients had decreased bone density and 43.6% showed manifest osteoporosis in DXA (densitometry) measurements. Our questionnaire, identifying anamnestic risk factors, correlated highly significantly (p = 0.01) with reduced BMD, whereas seven bone-specific laboratory values (p = 0.046) correlated significantly. CONCLUSIONS: Anamnestic risk factors correlate with pathological BMD. The medical questionnaire used in this study would therefore function as a cost-effective primary diagnostic instrument for identification of osteoporosis patients. |
format | Online Article Text |
id | pubmed-3176487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31764872011-09-21 Anamnestic risk factor questionnaire as reliable diagnostic instrument for osteoporosis (reduced bone morphogenic density) Kolios, Leila Takur, Caner Moghaddam, Arash Hitzler, Mirjam Schmidt-Gayk, Heinrich Suda, Arnold J Höner, Bernd Grützner, Paul A Wölfl, Christoph BMC Musculoskelet Disord Research Article BACKGROUND: Osteoporosis is a major health problem worldwide, and is included in the WHO list of the top 10 major diseases. However, it is often undiagnosed until the first fracture occurs, due to inadequate patient education and lack of insurance coverage for screening tests. Anamnestic risk factors like positive family anamnesis or early menopause are assumed to correlate with reduced BMD. METHODS: In our study of 78 patients with metaphyseal long bone fractures, we searched for a correlation between anamnestic risk factors, bone specific laboratory values, and the bone morphogenic density (BMD). Each indicator was examined as a possible diagnostic instrument for osteoporosis. The secondary aim of this study was to demonstrate the high prevalence of osteoporosis in patients with metaphyseal fractures. RESULTS: 76.9% of our fracture patients had decreased bone density and 43.6% showed manifest osteoporosis in DXA (densitometry) measurements. Our questionnaire, identifying anamnestic risk factors, correlated highly significantly (p = 0.01) with reduced BMD, whereas seven bone-specific laboratory values (p = 0.046) correlated significantly. CONCLUSIONS: Anamnestic risk factors correlate with pathological BMD. The medical questionnaire used in this study would therefore function as a cost-effective primary diagnostic instrument for identification of osteoporosis patients. BioMed Central 2011-08-17 /pmc/articles/PMC3176487/ /pubmed/21849030 http://dx.doi.org/10.1186/1471-2474-12-187 Text en Copyright ©2011 Kolios et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Kolios, Leila Takur, Caner Moghaddam, Arash Hitzler, Mirjam Schmidt-Gayk, Heinrich Suda, Arnold J Höner, Bernd Grützner, Paul A Wölfl, Christoph Anamnestic risk factor questionnaire as reliable diagnostic instrument for osteoporosis (reduced bone morphogenic density) |
title | Anamnestic risk factor questionnaire as reliable diagnostic instrument for osteoporosis (reduced bone morphogenic density) |
title_full | Anamnestic risk factor questionnaire as reliable diagnostic instrument for osteoporosis (reduced bone morphogenic density) |
title_fullStr | Anamnestic risk factor questionnaire as reliable diagnostic instrument for osteoporosis (reduced bone morphogenic density) |
title_full_unstemmed | Anamnestic risk factor questionnaire as reliable diagnostic instrument for osteoporosis (reduced bone morphogenic density) |
title_short | Anamnestic risk factor questionnaire as reliable diagnostic instrument for osteoporosis (reduced bone morphogenic density) |
title_sort | anamnestic risk factor questionnaire as reliable diagnostic instrument for osteoporosis (reduced bone morphogenic density) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3176487/ https://www.ncbi.nlm.nih.gov/pubmed/21849030 http://dx.doi.org/10.1186/1471-2474-12-187 |
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