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Lower trabecular bone score is associated with an increased incidence of localized femoral periosteal thickening
Introduction Femoral localized periosteal thickening (LPT, also termed “beaking”) of the lateral cortex often precedes an atypical femoral fracture (AFF). Bisphosphonate (BP) use, glucocorticoid use, and Asian race are major risk factors for developing such fractures. The aim of this study was to de...
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Published in: | Journal of bone and mineral metabolism 2021-11, Vol.39 (6), p.952-961 |
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container_title | Journal of bone and mineral metabolism |
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creator | Sato, Hiroe Kondo, Naoki Kurosawa, Yoichi Hasegawa, Eriko Wakamatsu, Ayako Kobayashi, Daisuke Nakatsue, Takeshi Kazama, Junichiro James Kuroda, Takeshi Suzuki, Yoshiki Endo, Naoto Narita, Ichiei |
description | Introduction
Femoral localized periosteal thickening (LPT, also termed “beaking”) of the lateral cortex often precedes an atypical femoral fracture (AFF). Bisphosphonate (BP) use, glucocorticoid use, and Asian race are major risk factors for developing such fractures. The aim of this study was to determine whether the trabecular bone score (TBS) reflecting the lumbar trabecular microarchitecture was related to LPT in glucocorticoid-treated Japanese patients with autoimmune diseases.
Materials and methods
We retrospectively investigated 111 women with autoimmune diseases treated with prednisolone (PSL) who had undergone both femoral X-ray and dual-energy X-ray absorptiometry of the L1 − L4 lumbar vertebrae and for whom TBS could be evaluated for two or more of these.
Results
Femoral LPT was evident in the X-rays of 18 of 111 patients (16.2%). Higher body mass index (BMI), longer duration of PSL use and longer duration of BP use were significant in patients with LPT compared to those without. The TBS was significantly lower in patients with LPT than in those without (1.314 ± 0.092 vs. 1.365 ± 0.100,
p
= 0.044); however, the lumbar bone mineral density did not differ significantly (0.892 ± 0.141 vs. 0.897 ± 0.154 g/cm
2
,
p
= 0.897). TBS was significantly associated with LPT (odds ratio, 0.004; 95% CI, 0 − 0.96;
p
= 0.048), but not in the multivariate analysis including BMI, duration of PSL use and duration of BP use.
Conclusions
The TBS was lower in glucocorticoid-treated Japanese women with autoimmune diseases with LPT than in those without LPT, and deteriorated trabecular microarchitecture influenced by longer use of BP and glucocorticoid might be associated with the development of LPT. |
doi_str_mv | 10.1007/s00774-021-01244-z |
format | article |
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Femoral localized periosteal thickening (LPT, also termed “beaking”) of the lateral cortex often precedes an atypical femoral fracture (AFF). Bisphosphonate (BP) use, glucocorticoid use, and Asian race are major risk factors for developing such fractures. The aim of this study was to determine whether the trabecular bone score (TBS) reflecting the lumbar trabecular microarchitecture was related to LPT in glucocorticoid-treated Japanese patients with autoimmune diseases.
Materials and methods
We retrospectively investigated 111 women with autoimmune diseases treated with prednisolone (PSL) who had undergone both femoral X-ray and dual-energy X-ray absorptiometry of the L1 − L4 lumbar vertebrae and for whom TBS could be evaluated for two or more of these.
Results
Femoral LPT was evident in the X-rays of 18 of 111 patients (16.2%). Higher body mass index (BMI), longer duration of PSL use and longer duration of BP use were significant in patients with LPT compared to those without. The TBS was significantly lower in patients with LPT than in those without (1.314 ± 0.092 vs. 1.365 ± 0.100,
p
= 0.044); however, the lumbar bone mineral density did not differ significantly (0.892 ± 0.141 vs. 0.897 ± 0.154 g/cm
2
,
p
= 0.897). TBS was significantly associated with LPT (odds ratio, 0.004; 95% CI, 0 − 0.96;
p
= 0.048), but not in the multivariate analysis including BMI, duration of PSL use and duration of BP use.
Conclusions
The TBS was lower in glucocorticoid-treated Japanese women with autoimmune diseases with LPT than in those without LPT, and deteriorated trabecular microarchitecture influenced by longer use of BP and glucocorticoid might be associated with the development of LPT.</description><identifier>ISSN: 0914-8779</identifier><identifier>EISSN: 1435-5604</identifier><identifier>DOI: 10.1007/s00774-021-01244-z</identifier><language>eng</language><publisher>Singapore: Springer Singapore</publisher><subject>Autoimmune diseases ; Body mass index ; Bone mineral density ; Cancellous bone ; Dual energy X-ray absorptiometry ; Femur ; Fractures ; Glucocorticoids ; Medicine ; Medicine & Public Health ; Metabolic Diseases ; Multivariate analysis ; Original Article ; Orthopedics ; Prednisolone ; Risk factors ; Vertebrae ; X-rays</subject><ispartof>Journal of bone and mineral metabolism, 2021-11, Vol.39 (6), p.952-961</ispartof><rights>The Japanese Society Bone and Mineral Research 2021</rights><rights>The Japanese Society Bone and Mineral Research 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c376t-4a3926e4561960273a5cabf58343366447bf5613d1b80efa1fba55a538f43ffd3</citedby><cites>FETCH-LOGICAL-c376t-4a3926e4561960273a5cabf58343366447bf5613d1b80efa1fba55a538f43ffd3</cites><orcidid>0000-0002-3952-7163</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Sato, Hiroe</creatorcontrib><creatorcontrib>Kondo, Naoki</creatorcontrib><creatorcontrib>Kurosawa, Yoichi</creatorcontrib><creatorcontrib>Hasegawa, Eriko</creatorcontrib><creatorcontrib>Wakamatsu, Ayako</creatorcontrib><creatorcontrib>Kobayashi, Daisuke</creatorcontrib><creatorcontrib>Nakatsue, Takeshi</creatorcontrib><creatorcontrib>Kazama, Junichiro James</creatorcontrib><creatorcontrib>Kuroda, Takeshi</creatorcontrib><creatorcontrib>Suzuki, Yoshiki</creatorcontrib><creatorcontrib>Endo, Naoto</creatorcontrib><creatorcontrib>Narita, Ichiei</creatorcontrib><title>Lower trabecular bone score is associated with an increased incidence of localized femoral periosteal thickening</title><title>Journal of bone and mineral metabolism</title><addtitle>J Bone Miner Metab</addtitle><description>Introduction
Femoral localized periosteal thickening (LPT, also termed “beaking”) of the lateral cortex often precedes an atypical femoral fracture (AFF). Bisphosphonate (BP) use, glucocorticoid use, and Asian race are major risk factors for developing such fractures. The aim of this study was to determine whether the trabecular bone score (TBS) reflecting the lumbar trabecular microarchitecture was related to LPT in glucocorticoid-treated Japanese patients with autoimmune diseases.
Materials and methods
We retrospectively investigated 111 women with autoimmune diseases treated with prednisolone (PSL) who had undergone both femoral X-ray and dual-energy X-ray absorptiometry of the L1 − L4 lumbar vertebrae and for whom TBS could be evaluated for two or more of these.
Results
Femoral LPT was evident in the X-rays of 18 of 111 patients (16.2%). Higher body mass index (BMI), longer duration of PSL use and longer duration of BP use were significant in patients with LPT compared to those without. The TBS was significantly lower in patients with LPT than in those without (1.314 ± 0.092 vs. 1.365 ± 0.100,
p
= 0.044); however, the lumbar bone mineral density did not differ significantly (0.892 ± 0.141 vs. 0.897 ± 0.154 g/cm
2
,
p
= 0.897). TBS was significantly associated with LPT (odds ratio, 0.004; 95% CI, 0 − 0.96;
p
= 0.048), but not in the multivariate analysis including BMI, duration of PSL use and duration of BP use.
Conclusions
The TBS was lower in glucocorticoid-treated Japanese women with autoimmune diseases with LPT than in those without LPT, and deteriorated trabecular microarchitecture influenced by longer use of BP and glucocorticoid might be associated with the development of LPT.</description><subject>Autoimmune diseases</subject><subject>Body mass index</subject><subject>Bone mineral density</subject><subject>Cancellous bone</subject><subject>Dual energy X-ray absorptiometry</subject><subject>Femur</subject><subject>Fractures</subject><subject>Glucocorticoids</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metabolic Diseases</subject><subject>Multivariate analysis</subject><subject>Original Article</subject><subject>Orthopedics</subject><subject>Prednisolone</subject><subject>Risk factors</subject><subject>Vertebrae</subject><subject>X-rays</subject><issn>0914-8779</issn><issn>1435-5604</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kUtLJDEUhYMo2OP4B1wFZjObcvJO1VLEUaHBjbMOt9I3Gq1O2qQasX-9cXpAmIWb--I7hwuHkDPOzjlj9ldtxaqOCd4xLpTqdgdkwZXUnTZMHZIFG7jqemuHY_Kt1ifGuNWWL8hmmV-x0LnAiH47QaFjTkirzwVprBRqzT7CjCv6GudHConG5AtCbZc2xRUmjzQHOmUPU9y1c8B1LjDRDZaY64xtnB-jf8YU08N3chRgqnj6r5-QP7-v7i9vuuXd9e3lxbLz0pq5UyAHYVBpwwfDhJWgPYxB91JJaYxSti2GyxUfe4YBeBhBa9CyD0qGsJIn5Ofed1Pyyxbr7NaxepwmSJi31QmtpRbaMtXQH_-hT3lbUvuuUYPpueRCNErsKV9yrQWD25S4hvLmOHMfIbh9CK6F4P6G4HZNJPei2uD0gOXT-gvVOzTOi3w</recordid><startdate>20211101</startdate><enddate>20211101</enddate><creator>Sato, Hiroe</creator><creator>Kondo, Naoki</creator><creator>Kurosawa, Yoichi</creator><creator>Hasegawa, Eriko</creator><creator>Wakamatsu, Ayako</creator><creator>Kobayashi, Daisuke</creator><creator>Nakatsue, Takeshi</creator><creator>Kazama, Junichiro James</creator><creator>Kuroda, Takeshi</creator><creator>Suzuki, Yoshiki</creator><creator>Endo, Naoto</creator><creator>Narita, Ichiei</creator><general>Springer Singapore</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-3952-7163</orcidid></search><sort><creationdate>20211101</creationdate><title>Lower trabecular bone score is associated with an increased incidence of localized femoral periosteal thickening</title><author>Sato, Hiroe ; Kondo, Naoki ; Kurosawa, Yoichi ; Hasegawa, Eriko ; Wakamatsu, Ayako ; Kobayashi, Daisuke ; Nakatsue, Takeshi ; Kazama, Junichiro James ; Kuroda, Takeshi ; Suzuki, Yoshiki ; Endo, Naoto ; Narita, Ichiei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c376t-4a3926e4561960273a5cabf58343366447bf5613d1b80efa1fba55a538f43ffd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Autoimmune diseases</topic><topic>Body mass index</topic><topic>Bone mineral density</topic><topic>Cancellous bone</topic><topic>Dual energy X-ray absorptiometry</topic><topic>Femur</topic><topic>Fractures</topic><topic>Glucocorticoids</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metabolic Diseases</topic><topic>Multivariate analysis</topic><topic>Original Article</topic><topic>Orthopedics</topic><topic>Prednisolone</topic><topic>Risk factors</topic><topic>Vertebrae</topic><topic>X-rays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sato, Hiroe</creatorcontrib><creatorcontrib>Kondo, Naoki</creatorcontrib><creatorcontrib>Kurosawa, Yoichi</creatorcontrib><creatorcontrib>Hasegawa, Eriko</creatorcontrib><creatorcontrib>Wakamatsu, Ayako</creatorcontrib><creatorcontrib>Kobayashi, Daisuke</creatorcontrib><creatorcontrib>Nakatsue, Takeshi</creatorcontrib><creatorcontrib>Kazama, Junichiro James</creatorcontrib><creatorcontrib>Kuroda, Takeshi</creatorcontrib><creatorcontrib>Suzuki, Yoshiki</creatorcontrib><creatorcontrib>Endo, Naoto</creatorcontrib><creatorcontrib>Narita, Ichiei</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of bone and mineral metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sato, Hiroe</au><au>Kondo, Naoki</au><au>Kurosawa, Yoichi</au><au>Hasegawa, Eriko</au><au>Wakamatsu, Ayako</au><au>Kobayashi, Daisuke</au><au>Nakatsue, Takeshi</au><au>Kazama, Junichiro James</au><au>Kuroda, Takeshi</au><au>Suzuki, Yoshiki</au><au>Endo, Naoto</au><au>Narita, Ichiei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lower trabecular bone score is associated with an increased incidence of localized femoral periosteal thickening</atitle><jtitle>Journal of bone and mineral metabolism</jtitle><stitle>J Bone Miner Metab</stitle><date>2021-11-01</date><risdate>2021</risdate><volume>39</volume><issue>6</issue><spage>952</spage><epage>961</epage><pages>952-961</pages><issn>0914-8779</issn><eissn>1435-5604</eissn><abstract>Introduction
Femoral localized periosteal thickening (LPT, also termed “beaking”) of the lateral cortex often precedes an atypical femoral fracture (AFF). Bisphosphonate (BP) use, glucocorticoid use, and Asian race are major risk factors for developing such fractures. The aim of this study was to determine whether the trabecular bone score (TBS) reflecting the lumbar trabecular microarchitecture was related to LPT in glucocorticoid-treated Japanese patients with autoimmune diseases.
Materials and methods
We retrospectively investigated 111 women with autoimmune diseases treated with prednisolone (PSL) who had undergone both femoral X-ray and dual-energy X-ray absorptiometry of the L1 − L4 lumbar vertebrae and for whom TBS could be evaluated for two or more of these.
Results
Femoral LPT was evident in the X-rays of 18 of 111 patients (16.2%). Higher body mass index (BMI), longer duration of PSL use and longer duration of BP use were significant in patients with LPT compared to those without. The TBS was significantly lower in patients with LPT than in those without (1.314 ± 0.092 vs. 1.365 ± 0.100,
p
= 0.044); however, the lumbar bone mineral density did not differ significantly (0.892 ± 0.141 vs. 0.897 ± 0.154 g/cm
2
,
p
= 0.897). TBS was significantly associated with LPT (odds ratio, 0.004; 95% CI, 0 − 0.96;
p
= 0.048), but not in the multivariate analysis including BMI, duration of PSL use and duration of BP use.
Conclusions
The TBS was lower in glucocorticoid-treated Japanese women with autoimmune diseases with LPT than in those without LPT, and deteriorated trabecular microarchitecture influenced by longer use of BP and glucocorticoid might be associated with the development of LPT.</abstract><cop>Singapore</cop><pub>Springer Singapore</pub><doi>10.1007/s00774-021-01244-z</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-3952-7163</orcidid></addata></record> |
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subjects | Autoimmune diseases Body mass index Bone mineral density Cancellous bone Dual energy X-ray absorptiometry Femur Fractures Glucocorticoids Medicine Medicine & Public Health Metabolic Diseases Multivariate analysis Original Article Orthopedics Prednisolone Risk factors Vertebrae X-rays |
title | Lower trabecular bone score is associated with an increased incidence of localized femoral periosteal thickening |
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