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Screening for amyloid in subcutaneous fat tissue of Egyptian patients with rheumatoid arthritis: clinical and laboratory characteristics
Objective: To screen for amyloid and to assess associated clinical and laboratory characteristics in Egyptian patients with rheumatoid arthritis (RA). Methods: Abdominal subcutaneous fat aspirates were consecutively collected from 112 patients (103 women, nine men) having RA for five years or more....
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Published in: | Annals of the rheumatic diseases 2002-01, Vol.61 (1), p.42-47 |
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description | Objective: To screen for amyloid and to assess associated clinical and laboratory characteristics in Egyptian patients with rheumatoid arthritis (RA). Methods: Abdominal subcutaneous fat aspirates were consecutively collected from 112 patients (103 women, nine men) having RA for five years or more. To detect amyloid, fat smears were stained with Congo red and the concentration of amyloid A protein in fat tissue was measured. Clinical, radiological, and laboratory characteristics of the patients were assessed. Results: Amyloid was detected in eight (7%) of the fat smears stained with Congo red. Compared with the Congo red stain, the sensitivity for detecting amyloid by measurement of amyloid A protein in fat tissue was 75% and the specificity was 100%. The amount of amyloid found was small for both methods. The median disease duration of the eight amyloid patients was significantly longer (17 years) than that of the non-amyloid patients (10 years). Bronchopulmonary disease and constipation were more common, whereas proteinuria and chronic renal insufficiency were not. The number of swollen joints and the number of red blood cells were significantly lower in the amyloid group. Conclusions: Quantification of amyloid A protein and staining with Congo red are strongly concordant methods of screening for amyloid in fat tissue. The prevalence of amyloid in Egyptian patients with RA is 7%. Proteinuria is not a discriminating feature, whereas long disease duration, constipation, bronchopulmonary symptoms, and a moderate to low number of red blood cells may help to identify the arthritic patients with amyloid. |
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Methods: Abdominal subcutaneous fat aspirates were consecutively collected from 112 patients (103 women, nine men) having RA for five years or more. To detect amyloid, fat smears were stained with Congo red and the concentration of amyloid A protein in fat tissue was measured. Clinical, radiological, and laboratory characteristics of the patients were assessed. Results: Amyloid was detected in eight (7%) of the fat smears stained with Congo red. Compared with the Congo red stain, the sensitivity for detecting amyloid by measurement of amyloid A protein in fat tissue was 75% and the specificity was 100%. The amount of amyloid found was small for both methods. The median disease duration of the eight amyloid patients was significantly longer (17 years) than that of the non-amyloid patients (10 years). Bronchopulmonary disease and constipation were more common, whereas proteinuria and chronic renal insufficiency were not. The number of swollen joints and the number of red blood cells were significantly lower in the amyloid group. Conclusions: Quantification of amyloid A protein and staining with Congo red are strongly concordant methods of screening for amyloid in fat tissue. The prevalence of amyloid in Egyptian patients with RA is 7%. Proteinuria is not a discriminating feature, whereas long disease duration, constipation, bronchopulmonary symptoms, and a moderate to low number of red blood cells may help to identify the arthritic patients with amyloid.</description><identifier>ISSN: 0003-4967</identifier><identifier>EISSN: 1468-2060</identifier><identifier>DOI: 10.1136/ard.61.1.42</identifier><identifier>PMID: 11779757</identifier><identifier>CODEN: ARDIAO</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and European League Against Rheumatism</publisher><subject>Abdomen ; adipose tissue ; Adipose Tissue - chemistry ; Adult ; Aged ; amyloid protein AA ; Amyloidosis - ethnology ; Amyloidosis - etiology ; Arthritis, Rheumatoid - complications ; Arthritis, Rheumatoid - ethnology ; Biological and medical sciences ; Congo Red ; Diagnosis ; Disease ; Diseases of the osteoarticular system ; Egypt ; ELISA ; Enzyme-Linked Immunosorbent Assay ; erythrocyte sedimentation rate ; ESR ; Extended Report ; Female ; HAQ ; Health Assessment Questionnaire ; Humans ; Inflammatory joint diseases ; JCA ; juvenile chronic arthritis ; Laboratories ; Male ; Medical sciences ; Methods ; Middle Aged ; Proteins ; RBC ; red blood cells ; Rheumatoid arthritis ; rheumatoid factor ; SAA ; Sensitivity and Specificity ; serum amyloid A ; Serum Amyloid A Protein - analysis ; Statistics, Nonparametric ; Studies ; Urine</subject><ispartof>Annals of the rheumatic diseases, 2002-01, Vol.61 (1), p.42-47</ispartof><rights>Copyright 2002 by Annals of the Rheumatic Diseases</rights><rights>2002 INIST-CNRS</rights><rights>COPYRIGHT 2002 BMJ Publishing Group Ltd.</rights><rights>Copyright: 2002 Copyright 2002 by Annals of the Rheumatic Diseases</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b579t-1b1a37a250fd43b09aa55d973f25e22ca8502c7d260bb99e1c9d47b487e3bbb53</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1753881/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1753881/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,4024,27923,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14122597$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11779757$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>El Mansoury, T M</creatorcontrib><creatorcontrib>Hazenberg, B P C</creatorcontrib><creatorcontrib>El Badawy, S A</creatorcontrib><creatorcontrib>Ahmed, A H</creatorcontrib><creatorcontrib>Bijzet, J</creatorcontrib><creatorcontrib>Limburg, P C</creatorcontrib><creatorcontrib>van Rijswijk, M H</creatorcontrib><title>Screening for amyloid in subcutaneous fat tissue of Egyptian patients with rheumatoid arthritis: clinical and laboratory characteristics</title><title>Annals of the rheumatic diseases</title><addtitle>Ann Rheum Dis</addtitle><description>Objective: To screen for amyloid and to assess associated clinical and laboratory characteristics in Egyptian patients with rheumatoid arthritis (RA). Methods: Abdominal subcutaneous fat aspirates were consecutively collected from 112 patients (103 women, nine men) having RA for five years or more. To detect amyloid, fat smears were stained with Congo red and the concentration of amyloid A protein in fat tissue was measured. Clinical, radiological, and laboratory characteristics of the patients were assessed. Results: Amyloid was detected in eight (7%) of the fat smears stained with Congo red. Compared with the Congo red stain, the sensitivity for detecting amyloid by measurement of amyloid A protein in fat tissue was 75% and the specificity was 100%. The amount of amyloid found was small for both methods. The median disease duration of the eight amyloid patients was significantly longer (17 years) than that of the non-amyloid patients (10 years). Bronchopulmonary disease and constipation were more common, whereas proteinuria and chronic renal insufficiency were not. The number of swollen joints and the number of red blood cells were significantly lower in the amyloid group. Conclusions: Quantification of amyloid A protein and staining with Congo red are strongly concordant methods of screening for amyloid in fat tissue. The prevalence of amyloid in Egyptian patients with RA is 7%. Proteinuria is not a discriminating feature, whereas long disease duration, constipation, bronchopulmonary symptoms, and a moderate to low number of red blood cells may help to identify the arthritic patients with amyloid.</description><subject>Abdomen</subject><subject>adipose tissue</subject><subject>Adipose Tissue - chemistry</subject><subject>Adult</subject><subject>Aged</subject><subject>amyloid protein AA</subject><subject>Amyloidosis - ethnology</subject><subject>Amyloidosis - etiology</subject><subject>Arthritis, Rheumatoid - complications</subject><subject>Arthritis, Rheumatoid - ethnology</subject><subject>Biological and medical sciences</subject><subject>Congo Red</subject><subject>Diagnosis</subject><subject>Disease</subject><subject>Diseases of the osteoarticular system</subject><subject>Egypt</subject><subject>ELISA</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>erythrocyte sedimentation rate</subject><subject>ESR</subject><subject>Extended Report</subject><subject>Female</subject><subject>HAQ</subject><subject>Health Assessment Questionnaire</subject><subject>Humans</subject><subject>Inflammatory joint diseases</subject><subject>JCA</subject><subject>juvenile chronic arthritis</subject><subject>Laboratories</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Methods</subject><subject>Middle Aged</subject><subject>Proteins</subject><subject>RBC</subject><subject>red blood cells</subject><subject>Rheumatoid arthritis</subject><subject>rheumatoid factor</subject><subject>SAA</subject><subject>Sensitivity and Specificity</subject><subject>serum amyloid A</subject><subject>Serum Amyloid A Protein - analysis</subject><subject>Statistics, Nonparametric</subject><subject>Studies</subject><subject>Urine</subject><issn>0003-4967</issn><issn>1468-2060</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNp9kk2PEyEYxydG467Vk3dDYvSircAMA-PBZNOsL0mzHnbVI3lgmJY6A11g1H4DP7Y0bbar2RgOBJ7f839ei-IpwTNCyvoNhHZWkxmZVfRecUqqWkwprvH94hRjXE6rpuYnxaMY1_mJBREPixNCOG8446fF70sdjHHWLVHnA4Jh23vbIutQHJUeEzjjx4g6SCjZGEeDfIfOl9tNsuDQBpI1LkX006YVCiszDpB2_hDSKtjs8Rbp3jqroUfgWtSD8iEjYYv0CgLoZIKNyer4uHjQQR_Nk8M9Kb68P7-af5wuPn_4ND9bTBXjTZoSRaDkQBnu2qpUuAFgrG142VFmKNUgGKaat7TGSjWNIbppK64qwU2plGLlpHi3192MajCtzukH6OUm2AHCVnqw8m-Lsyu59D8k4awUgmSBlweB4K9HE5McbNSm7_etkpyUjNS0yuDzf8C1H4PLxWUtzkXFdvOZFK_31BJ6I63rfI6ql8aZHNw709n8fSYoFaKiPOPTO_B8WjNYfRf_as_r4GMMpruplGC5Wx-Z10fWRBJZ0Uw_u92cI3vYlwy8OAAQ80y7AE7beOQqQilrbqWZh2t-3dghfJc1LzmTF1_nks-rb-Ly6kIujk1Vw_q_Gf4Btk_sig</recordid><startdate>200201</startdate><enddate>200201</enddate><creator>El Mansoury, T M</creator><creator>Hazenberg, B P C</creator><creator>El Badawy, S A</creator><creator>Ahmed, A H</creator><creator>Bijzet, J</creator><creator>Limburg, P C</creator><creator>van Rijswijk, M H</creator><general>BMJ Publishing Group Ltd and European League Against Rheumatism</general><general>BMJ</general><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><scope>IQODW</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>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200201</creationdate><title>Screening for amyloid in subcutaneous fat tissue of Egyptian patients with rheumatoid arthritis: clinical and laboratory characteristics</title><author>El Mansoury, T M ; Hazenberg, B P C ; El Badawy, S A ; Ahmed, A H ; Bijzet, J ; Limburg, P C ; van Rijswijk, M H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b579t-1b1a37a250fd43b09aa55d973f25e22ca8502c7d260bb99e1c9d47b487e3bbb53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Abdomen</topic><topic>adipose tissue</topic><topic>Adipose Tissue - chemistry</topic><topic>Adult</topic><topic>Aged</topic><topic>amyloid protein AA</topic><topic>Amyloidosis - ethnology</topic><topic>Amyloidosis - etiology</topic><topic>Arthritis, Rheumatoid - complications</topic><topic>Arthritis, Rheumatoid - ethnology</topic><topic>Biological and medical sciences</topic><topic>Congo Red</topic><topic>Diagnosis</topic><topic>Disease</topic><topic>Diseases of the osteoarticular system</topic><topic>Egypt</topic><topic>ELISA</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>erythrocyte sedimentation rate</topic><topic>ESR</topic><topic>Extended Report</topic><topic>Female</topic><topic>HAQ</topic><topic>Health Assessment Questionnaire</topic><topic>Humans</topic><topic>Inflammatory joint diseases</topic><topic>JCA</topic><topic>juvenile chronic arthritis</topic><topic>Laboratories</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Methods</topic><topic>Middle Aged</topic><topic>Proteins</topic><topic>RBC</topic><topic>red blood cells</topic><topic>Rheumatoid arthritis</topic><topic>rheumatoid factor</topic><topic>SAA</topic><topic>Sensitivity and Specificity</topic><topic>serum amyloid A</topic><topic>Serum Amyloid A Protein - analysis</topic><topic>Statistics, Nonparametric</topic><topic>Studies</topic><topic>Urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>El Mansoury, T M</creatorcontrib><creatorcontrib>Hazenberg, B P C</creatorcontrib><creatorcontrib>El Badawy, S A</creatorcontrib><creatorcontrib>Ahmed, A H</creatorcontrib><creatorcontrib>Bijzet, J</creatorcontrib><creatorcontrib>Limburg, P C</creatorcontrib><creatorcontrib>van Rijswijk, M H</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</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>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science 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 Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>BMJ Journals</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 Central Student</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Science Journals</collection><collection>ProQuest Biological Science Journals</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Annals of the rheumatic diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>El Mansoury, T M</au><au>Hazenberg, B P C</au><au>El Badawy, S A</au><au>Ahmed, A H</au><au>Bijzet, J</au><au>Limburg, P C</au><au>van Rijswijk, M H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Screening for amyloid in subcutaneous fat tissue of Egyptian patients with rheumatoid arthritis: clinical and laboratory characteristics</atitle><jtitle>Annals of the rheumatic diseases</jtitle><addtitle>Ann Rheum Dis</addtitle><date>2002-01</date><risdate>2002</risdate><volume>61</volume><issue>1</issue><spage>42</spage><epage>47</epage><pages>42-47</pages><issn>0003-4967</issn><eissn>1468-2060</eissn><coden>ARDIAO</coden><abstract>Objective: To screen for amyloid and to assess associated clinical and laboratory characteristics in Egyptian patients with rheumatoid arthritis (RA). Methods: Abdominal subcutaneous fat aspirates were consecutively collected from 112 patients (103 women, nine men) having RA for five years or more. To detect amyloid, fat smears were stained with Congo red and the concentration of amyloid A protein in fat tissue was measured. Clinical, radiological, and laboratory characteristics of the patients were assessed. Results: Amyloid was detected in eight (7%) of the fat smears stained with Congo red. Compared with the Congo red stain, the sensitivity for detecting amyloid by measurement of amyloid A protein in fat tissue was 75% and the specificity was 100%. The amount of amyloid found was small for both methods. The median disease duration of the eight amyloid patients was significantly longer (17 years) than that of the non-amyloid patients (10 years). Bronchopulmonary disease and constipation were more common, whereas proteinuria and chronic renal insufficiency were not. The number of swollen joints and the number of red blood cells were significantly lower in the amyloid group. Conclusions: Quantification of amyloid A protein and staining with Congo red are strongly concordant methods of screening for amyloid in fat tissue. The prevalence of amyloid in Egyptian patients with RA is 7%. Proteinuria is not a discriminating feature, whereas long disease duration, constipation, bronchopulmonary symptoms, and a moderate to low number of red blood cells may help to identify the arthritic patients with amyloid.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and European League Against Rheumatism</pub><pmid>11779757</pmid><doi>10.1136/ard.61.1.42</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Abdomen adipose tissue Adipose Tissue - chemistry Adult Aged amyloid protein AA Amyloidosis - ethnology Amyloidosis - etiology Arthritis, Rheumatoid - complications Arthritis, Rheumatoid - ethnology Biological and medical sciences Congo Red Diagnosis Disease Diseases of the osteoarticular system Egypt ELISA Enzyme-Linked Immunosorbent Assay erythrocyte sedimentation rate ESR Extended Report Female HAQ Health Assessment Questionnaire Humans Inflammatory joint diseases JCA juvenile chronic arthritis Laboratories Male Medical sciences Methods Middle Aged Proteins RBC red blood cells Rheumatoid arthritis rheumatoid factor SAA Sensitivity and Specificity serum amyloid A Serum Amyloid A Protein - analysis Statistics, Nonparametric Studies Urine |
title | Screening for amyloid in subcutaneous fat tissue of Egyptian patients with rheumatoid arthritis: clinical and laboratory characteristics |
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