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A pilot investigation of the prevalence of US‐detectable forefoot joint pathology and reported foot‐related disability in participants with systemic lupus erythematosus
Background The main aim of this study was to determine the prevalence of US‐detectable forefoot bursae, metatarsophalangeal (MTP) joint and metacarpophalangeal (MCP) joint synovial hypertrophy (SH), Power Doppler (PD) signal or erosion in participants with systemic lupus erythematosus (SLE). A secon...
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Published in: | Journal of foot and ankle research 2016-08, Vol.9 (1), p.27-n/a |
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description | Background
The main aim of this study was to determine the prevalence of US‐detectable forefoot bursae, metatarsophalangeal (MTP) joint and metacarpophalangeal (MCP) joint synovial hypertrophy (SH), Power Doppler (PD) signal or erosion in participants with systemic lupus erythematosus (SLE). A secondary aim was to determine the strength of potential association between patient reported foot‐related disability and US‐detected forefoot bursae, MTP joint SH, PD signal or erosion in participants with SLE.
Method
A cross‐sectional observational study of 20 participants with SLE was completed to determine the prevalence of US‐detected forefoot bursal, MTP and MCP joint pathology. Patient‐reported foot‐related impairment and activity limitation (accumulatively referred to as disability) were also recorded. Spearmans' Rank Correlation analyses were completed to determine the potential strength of association between US‐detected pathology and patient report disability.
Results
The prevalence of MTP joint SH and PD was 80 % (16/20) and 10 % (2/20), respectively. The prevalence of MCP joint SH and PD was 60 % (12/20) and 30 % (6/20) respectively. A significant association was noted between PD scores for the MTP joints and MCP joints (r = 0.556; p = 0.011) although this was not demonstrated for SH scores (r = 0.176; p = 0.459). Significant associations between forefoot bursal prevalence and MTP joint PD were noted (r = 0.467; p = 0.038). The prevalence of bursae and bursal PD (grade 2 or above) was 100 % (20/20) and 10 % (2/20), respectively. Moderate foot‐related impairment and activity limitation was reported by 95 and 85 % of participants respectively.
Conclusion
This pilot study suggests that US‐detected MTP, MCP joint and forefoot bursal abnormalities may be prevalent in participants with SLE and they may experience a moderate level of foot‐related disability. Further research is required to substantiate these preliminary findings. |
doi_str_mv | 10.1186/s13047-016-0158-1 |
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The main aim of this study was to determine the prevalence of US‐detectable forefoot bursae, metatarsophalangeal (MTP) joint and metacarpophalangeal (MCP) joint synovial hypertrophy (SH), Power Doppler (PD) signal or erosion in participants with systemic lupus erythematosus (SLE). A secondary aim was to determine the strength of potential association between patient reported foot‐related disability and US‐detected forefoot bursae, MTP joint SH, PD signal or erosion in participants with SLE.
Method
A cross‐sectional observational study of 20 participants with SLE was completed to determine the prevalence of US‐detected forefoot bursal, MTP and MCP joint pathology. Patient‐reported foot‐related impairment and activity limitation (accumulatively referred to as disability) were also recorded. Spearmans' Rank Correlation analyses were completed to determine the potential strength of association between US‐detected pathology and patient report disability.
Results
The prevalence of MTP joint SH and PD was 80 % (16/20) and 10 % (2/20), respectively. The prevalence of MCP joint SH and PD was 60 % (12/20) and 30 % (6/20) respectively. A significant association was noted between PD scores for the MTP joints and MCP joints (r = 0.556; p = 0.011) although this was not demonstrated for SH scores (r = 0.176; p = 0.459). Significant associations between forefoot bursal prevalence and MTP joint PD were noted (r = 0.467; p = 0.038). The prevalence of bursae and bursal PD (grade 2 or above) was 100 % (20/20) and 10 % (2/20), respectively. Moderate foot‐related impairment and activity limitation was reported by 95 and 85 % of participants respectively.
Conclusion
This pilot study suggests that US‐detected MTP, MCP joint and forefoot bursal abnormalities may be prevalent in participants with SLE and they may experience a moderate level of foot‐related disability. Further research is required to substantiate these preliminary findings.</description><identifier>ISSN: 1757-1146</identifier><identifier>EISSN: 1757-1146</identifier><identifier>DOI: 10.1186/s13047-016-0158-1</identifier><identifier>PMID: 27486482</identifier><language>eng</language><publisher>London: BioMed Central</publisher><subject>Activities of Daily Living ; Adult ; Aged ; Bursa ; Bursa (Anatomy) ; Bursa, Synovial - diagnostic imaging ; Disability Evaluation ; Distribution ; Female ; Foot Diseases - diagnostic imaging ; Foot Diseases - etiology ; Forefoot ; Forefoot, Human - diagnostic imaging ; Human ; Humans ; Joint diseases ; Joints ; Lupus erythematosus ; Lupus Erythematosus, Systemic - complications ; Male ; Metacarpophalangeal Joint - diagnostic imaging ; Metatarsophalangeal Joint - diagnostic imaging ; Middle Aged ; Physiological aspects ; Pilot Projects ; Prevalence ; Severity of Illness Index ; Synovial ; Synovitis - diagnostic imaging ; Synovitis - etiology ; Systemic ; Systemic lupus erythematosus ; Ultrasonography ; Ultrasonography, Doppler - methods</subject><ispartof>Journal of foot and ankle research, 2016-08, Vol.9 (1), p.27-n/a</ispartof><rights>2016 The Authors</rights><rights>COPYRIGHT 2016 John Wiley & Sons, Inc.</rights><rights>Copyright BioMed Central 2016</rights><rights>The Author(s). 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5767-f92d0e40844818736f5574620880274098d622e079ed4d7cb3559ccec70316903</citedby><cites>FETCH-LOGICAL-c5767-f92d0e40844818736f5574620880274098d622e079ed4d7cb3559ccec70316903</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4969688/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1816896861?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11562,25753,27924,27925,37012,37013,44590,46052,46476,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27486482$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mukherjee, Sandeep</creatorcontrib><creatorcontrib>Cherry, Lindsey</creatorcontrib><creatorcontrib>Zarroug, Jalaa</creatorcontrib><creatorcontrib>Culliford, David</creatorcontrib><creatorcontrib>Bowen, Catherine</creatorcontrib><creatorcontrib>Arden, Nigel</creatorcontrib><creatorcontrib>Edwards, Christopher</creatorcontrib><title>A pilot investigation of the prevalence of US‐detectable forefoot joint pathology and reported foot‐related disability in participants with systemic lupus erythematosus</title><title>Journal of foot and ankle research</title><addtitle>J Foot Ankle Res</addtitle><description>Background
The main aim of this study was to determine the prevalence of US‐detectable forefoot bursae, metatarsophalangeal (MTP) joint and metacarpophalangeal (MCP) joint synovial hypertrophy (SH), Power Doppler (PD) signal or erosion in participants with systemic lupus erythematosus (SLE). A secondary aim was to determine the strength of potential association between patient reported foot‐related disability and US‐detected forefoot bursae, MTP joint SH, PD signal or erosion in participants with SLE.
Method
A cross‐sectional observational study of 20 participants with SLE was completed to determine the prevalence of US‐detected forefoot bursal, MTP and MCP joint pathology. Patient‐reported foot‐related impairment and activity limitation (accumulatively referred to as disability) were also recorded. Spearmans' Rank Correlation analyses were completed to determine the potential strength of association between US‐detected pathology and patient report disability.
Results
The prevalence of MTP joint SH and PD was 80 % (16/20) and 10 % (2/20), respectively. The prevalence of MCP joint SH and PD was 60 % (12/20) and 30 % (6/20) respectively. A significant association was noted between PD scores for the MTP joints and MCP joints (r = 0.556; p = 0.011) although this was not demonstrated for SH scores (r = 0.176; p = 0.459). Significant associations between forefoot bursal prevalence and MTP joint PD were noted (r = 0.467; p = 0.038). The prevalence of bursae and bursal PD (grade 2 or above) was 100 % (20/20) and 10 % (2/20), respectively. Moderate foot‐related impairment and activity limitation was reported by 95 and 85 % of participants respectively.
Conclusion
This pilot study suggests that US‐detected MTP, MCP joint and forefoot bursal abnormalities may be prevalent in participants with SLE and they may experience a moderate level of foot‐related disability. Further research is required to substantiate these preliminary findings.</description><subject>Activities of Daily Living</subject><subject>Adult</subject><subject>Aged</subject><subject>Bursa</subject><subject>Bursa (Anatomy)</subject><subject>Bursa, Synovial - diagnostic imaging</subject><subject>Disability Evaluation</subject><subject>Distribution</subject><subject>Female</subject><subject>Foot Diseases - diagnostic imaging</subject><subject>Foot Diseases - etiology</subject><subject>Forefoot</subject><subject>Forefoot, Human - diagnostic imaging</subject><subject>Human</subject><subject>Humans</subject><subject>Joint diseases</subject><subject>Joints</subject><subject>Lupus erythematosus</subject><subject>Lupus Erythematosus, Systemic - complications</subject><subject>Male</subject><subject>Metacarpophalangeal Joint - diagnostic imaging</subject><subject>Metatarsophalangeal Joint - diagnostic imaging</subject><subject>Middle Aged</subject><subject>Physiological aspects</subject><subject>Pilot Projects</subject><subject>Prevalence</subject><subject>Severity of Illness Index</subject><subject>Synovial</subject><subject>Synovitis - diagnostic imaging</subject><subject>Synovitis - etiology</subject><subject>Systemic</subject><subject>Systemic lupus erythematosus</subject><subject>Ultrasonography</subject><subject>Ultrasonography, Doppler - methods</subject><issn>1757-1146</issn><issn>1757-1146</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><recordid>eNqFkt-K1DAUxoso7rr6AN5IQBBvuib9k6ZeLIyL4x8WvNC9Dpn0dJoh09QknaV3PoIP4lP5JJ4y6zojgpTSNv193zk5-ZLkKaPnjAn-KrCcFlVKGce7FCm7l5yyqqxSxgp-_-D9JHkUwoZSnnHOHiYnWVUIXojsNPmxIIOxLhLT7yBEs1bRuJ64lsQOyOBhpyz0GuaV688_v31vIIKOamWBtM5D61C7caaPZFCxc9atJ6L6hngYnI_QkJlAnQer5s_GBLUy1sQJS6LGR6PNoPoYyI2JHQlTiLA1mthxGAMBP2EjWxVdGMPj5EGrbIAnt8-z5Hr59svl-_Tq07sPl4urVJcVr9K2zhoKBRVFIZioct6WZVXwjApBcee0Fg3PMqBVDU3RVHqVl2WtNeiK5ozXND9LLva-w7jaQqOhj15ZOXizVX6SThl5_Kc3nVy7nSxqXnMh0ODlrYF3X0ecq9yaoMFa1YMbg2SC1nhy2B-iz_9CN270PW4PKcYF-nH2h1rjcUjTtw7r6tlULgqsyHLGcqTO_0Hh1cwTdT20BtePBC8OBB0oG7vg7DhnIByDbA9q70LAY78bBqNyzqLcZ1FiFuWcRTn3_OxwineK3-FD4PUeuMG2pv87yo_LRfZmSWnNq_wXrp3uuQ</recordid><startdate>20160802</startdate><enddate>20160802</enddate><creator>Mukherjee, Sandeep</creator><creator>Cherry, Lindsey</creator><creator>Zarroug, Jalaa</creator><creator>Culliford, David</creator><creator>Bowen, Catherine</creator><creator>Arden, Nigel</creator><creator>Edwards, Christopher</creator><general>BioMed Central</general><general>John Wiley & Sons, Inc</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160802</creationdate><title>A pilot investigation of the prevalence of US‐detectable forefoot joint pathology and reported foot‐related disability in participants with systemic lupus erythematosus</title><author>Mukherjee, Sandeep ; Cherry, Lindsey ; Zarroug, Jalaa ; Culliford, David ; Bowen, Catherine ; Arden, Nigel ; Edwards, Christopher</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5767-f92d0e40844818736f5574620880274098d622e079ed4d7cb3559ccec70316903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Activities of Daily Living</topic><topic>Adult</topic><topic>Aged</topic><topic>Bursa</topic><topic>Bursa (Anatomy)</topic><topic>Bursa, Synovial - diagnostic imaging</topic><topic>Disability Evaluation</topic><topic>Distribution</topic><topic>Female</topic><topic>Foot Diseases - diagnostic imaging</topic><topic>Foot Diseases - etiology</topic><topic>Forefoot</topic><topic>Forefoot, Human - diagnostic imaging</topic><topic>Human</topic><topic>Humans</topic><topic>Joint diseases</topic><topic>Joints</topic><topic>Lupus erythematosus</topic><topic>Lupus Erythematosus, Systemic - complications</topic><topic>Male</topic><topic>Metacarpophalangeal Joint - diagnostic imaging</topic><topic>Metatarsophalangeal Joint - diagnostic imaging</topic><topic>Middle Aged</topic><topic>Physiological aspects</topic><topic>Pilot Projects</topic><topic>Prevalence</topic><topic>Severity of Illness Index</topic><topic>Synovial</topic><topic>Synovitis - diagnostic imaging</topic><topic>Synovitis - etiology</topic><topic>Systemic</topic><topic>Systemic lupus erythematosus</topic><topic>Ultrasonography</topic><topic>Ultrasonography, Doppler - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mukherjee, Sandeep</creatorcontrib><creatorcontrib>Cherry, Lindsey</creatorcontrib><creatorcontrib>Zarroug, Jalaa</creatorcontrib><creatorcontrib>Culliford, David</creatorcontrib><creatorcontrib>Bowen, Catherine</creatorcontrib><creatorcontrib>Arden, Nigel</creatorcontrib><creatorcontrib>Edwards, Christopher</creatorcontrib><collection>Wiley Open Access</collection><collection>Wiley Online Library Free Content</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Physical Education Index</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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 Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</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 - Publicly Available Content Database</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of foot and ankle research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mukherjee, Sandeep</au><au>Cherry, Lindsey</au><au>Zarroug, Jalaa</au><au>Culliford, David</au><au>Bowen, Catherine</au><au>Arden, Nigel</au><au>Edwards, Christopher</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A pilot investigation of the prevalence of US‐detectable forefoot joint pathology and reported foot‐related disability in participants with systemic lupus erythematosus</atitle><jtitle>Journal of foot and ankle research</jtitle><addtitle>J Foot Ankle Res</addtitle><date>2016-08-02</date><risdate>2016</risdate><volume>9</volume><issue>1</issue><spage>27</spage><epage>n/a</epage><pages>27-n/a</pages><issn>1757-1146</issn><eissn>1757-1146</eissn><abstract>Background
The main aim of this study was to determine the prevalence of US‐detectable forefoot bursae, metatarsophalangeal (MTP) joint and metacarpophalangeal (MCP) joint synovial hypertrophy (SH), Power Doppler (PD) signal or erosion in participants with systemic lupus erythematosus (SLE). A secondary aim was to determine the strength of potential association between patient reported foot‐related disability and US‐detected forefoot bursae, MTP joint SH, PD signal or erosion in participants with SLE.
Method
A cross‐sectional observational study of 20 participants with SLE was completed to determine the prevalence of US‐detected forefoot bursal, MTP and MCP joint pathology. Patient‐reported foot‐related impairment and activity limitation (accumulatively referred to as disability) were also recorded. Spearmans' Rank Correlation analyses were completed to determine the potential strength of association between US‐detected pathology and patient report disability.
Results
The prevalence of MTP joint SH and PD was 80 % (16/20) and 10 % (2/20), respectively. The prevalence of MCP joint SH and PD was 60 % (12/20) and 30 % (6/20) respectively. A significant association was noted between PD scores for the MTP joints and MCP joints (r = 0.556; p = 0.011) although this was not demonstrated for SH scores (r = 0.176; p = 0.459). Significant associations between forefoot bursal prevalence and MTP joint PD were noted (r = 0.467; p = 0.038). The prevalence of bursae and bursal PD (grade 2 or above) was 100 % (20/20) and 10 % (2/20), respectively. Moderate foot‐related impairment and activity limitation was reported by 95 and 85 % of participants respectively.
Conclusion
This pilot study suggests that US‐detected MTP, MCP joint and forefoot bursal abnormalities may be prevalent in participants with SLE and they may experience a moderate level of foot‐related disability. Further research is required to substantiate these preliminary findings.</abstract><cop>London</cop><pub>BioMed Central</pub><pmid>27486482</pmid><doi>10.1186/s13047-016-0158-1</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Activities of Daily Living Adult Aged Bursa Bursa (Anatomy) Bursa, Synovial - diagnostic imaging Disability Evaluation Distribution Female Foot Diseases - diagnostic imaging Foot Diseases - etiology Forefoot Forefoot, Human - diagnostic imaging Human Humans Joint diseases Joints Lupus erythematosus Lupus Erythematosus, Systemic - complications Male Metacarpophalangeal Joint - diagnostic imaging Metatarsophalangeal Joint - diagnostic imaging Middle Aged Physiological aspects Pilot Projects Prevalence Severity of Illness Index Synovial Synovitis - diagnostic imaging Synovitis - etiology Systemic Systemic lupus erythematosus Ultrasonography Ultrasonography, Doppler - methods |
title | A pilot investigation of the prevalence of US‐detectable forefoot joint pathology and reported foot‐related disability in participants with systemic lupus erythematosus |
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