Abstract:
BACKGROUND:Hyperthyroidism is a risk factor for reduced bone mineral density (BMD) and osteoporotic fractures. Vertebral fracture assessment (VFA) by dual-energy X-ray absorptiometry (DXA) is a radiological method of visualization of the spine, which enables patient comfort and reduced radiation exposure. OBJECTIVES:This study was carried out to evaluate BMD and the prevalence of silent vertebral fractures in young men with hyperthyroidism. DESIGN:We conducted a cross-sectional study in a group of Portuguese men aged up to 50 years and matched in hyperthyroidism (n=24) and control (n=24) groups. MATERIALS AND METHODS:A group of 48 Portuguese men aged up to 50 years was divided and matched in hyperthyroidism (n=24) and control (n=24) groups. BMD (g/cm(2)) at L1-L4, hip, radius 33%, and whole body as well as the total body masses (kg) were studied by DXA. VFA was used to detect fractures and those were classified by Genant's semiquantitative method. No patient had previously been treated for hyperthyroidism, osteoporosis, or low bone mass. Adequate statistical tests were used. RESULTS:The mean age, height, and total fat mass were similar in both groups (P≥0.05). The total lean body mass and the mean BMD at lumbar spine, hip, and whole body were significantly decreased in the hyperthyroidism group. In this group, there was also a trend for an increased prevalence of reduced BMD/osteoporosis and osteoporotic vertebral fractures. CONCLUSIONS:The results obtained using VFA technology (confirmed by X-ray) suggest that the BMD changes in young men with nontreated hyperthyroidism may lead to the development of osteoporosis and vertebral fractures. This supports the pertinence of using VFA in the routine of osteoporosis assessment to detect silent fractures precociously and consider early treatment.
journal_name
Eur J Endocrinoljournal_title
European journal of endocrinologyauthors
Barbosa AP,Rui Mascarenhas M,Silva CF,Távora I,Bicho M,do Carmo I,de Oliveira AGdoi
10.1530/EJE-14-0602subject
Has Abstractpub_date
2015-02-01 00:00:00pages
189-94issue
2eissn
0804-4643issn
1479-683Xpii
172/2/189journal_volume
172pub_type
杂志文章abstract:BACKGROUND:Activating mutations of the vasopressin receptor gene on the X chromosome cause the nephrogenic syndrome of inappropriate antidiuresis (NSIAD). We describe a male child who presented with persistent hyponatraemia and whose mother was also found to be hyponatraemic. She had learnt to avoid excess fluid consum...
journal_title:European journal of endocrinology
pub_type: 杂志文章
doi:10.1530/EJE-09-0246
更新日期:2009-09-01 00:00:00
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journal_title:European journal of endocrinology
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doi:10.1530/EJE-13-0023
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journal_title:European journal of endocrinology
pub_type: 杂志文章
doi:10.1530/EJE-08-0387
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journal_title:European journal of endocrinology
pub_type: 杂志文章
doi:10.1530/eje.0.1360330
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journal_title:European journal of endocrinology
pub_type: 杂志文章,评审
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journal_title:European journal of endocrinology
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更新日期:2011-07-01 00:00:00
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更新日期:1994-12-01 00:00:00
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journal_title:European journal of endocrinology
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更新日期:2012-03-01 00:00:00
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journal_title:European journal of endocrinology
pub_type: 临床试验,杂志文章,多中心研究,随机对照试验
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更新日期:2007-04-01 00:00:00
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journal_title:European journal of endocrinology
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journal_title:European journal of endocrinology
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更新日期:2000-05-01 00:00:00
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更新日期:2015-08-01 00:00:00
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更新日期:2003-03-01 00:00:00
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更新日期:1995-11-01 00:00:00
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更新日期:2004-11-01 00:00:00
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更新日期:2001-07-01 00:00:00