Dry eyes and mouth syndrome—a subgroup of patients presenting with sicca symptoms

Objective. To evaluate the characteristics of patients presenting with symptoms suggestive of Sjögren's syndrome (SS) but failing to satisfy diagnostic criteria. Methods. Clinical, serological and histological data were collected on 34 patients presenting with dry eyes and/or mouth who did not...

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Veröffentlicht in:British journal of rheumatology 2002-04, Vol.41 (4), p.416-422
Hauptverfasser: Price, E. J., Venables, P. J. W.
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Venables, P. J. W.
description Objective. To evaluate the characteristics of patients presenting with symptoms suggestive of Sjögren's syndrome (SS) but failing to satisfy diagnostic criteria. Methods. Clinical, serological and histological data were collected on 34 patients presenting with dry eyes and/or mouth who did not satisfy the Vitali criteria for the diagnosis of SS. They were compared with 136 patients with primary SS, 38 patients with secondary SS, and 13 patients without SS. Questionnaires on symptoms from each group were compared with 43 healthy controls. Results. The 34 patients who did not satisfy the diagnostic criteria for SS or any other connective tissue disease were designated dry eyes and mouth syndrome (DEMS). Their demography including age was similar to that of a primary SS group and there was no more atrophy seen on their biopsies compared with SS and non‐SS controls. They scored highly on visual analogue scales of symptoms but had few objective signs. All were negative for anti‐Ro and anti‐La although the prevalence of antinuclear antibodies (19%) was increased compared with a normal population. There was no excess of SS‐associated tissue types. Conclusion. There was no evidence that age, salivary gland atrophy or subclinical SS accounted for the symptoms in DEMS. Most of the patients fitted into a spectrum of disease which tended more towards fibromyalgia and/or chronic fatigue syndrome.
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J. ; Venables, P. J. W.</creator><creatorcontrib>Price, E. J. ; Venables, P. J. W.</creatorcontrib><description>Objective. To evaluate the characteristics of patients presenting with symptoms suggestive of Sjögren's syndrome (SS) but failing to satisfy diagnostic criteria. Methods. Clinical, serological and histological data were collected on 34 patients presenting with dry eyes and/or mouth who did not satisfy the Vitali criteria for the diagnosis of SS. They were compared with 136 patients with primary SS, 38 patients with secondary SS, and 13 patients without SS. Questionnaires on symptoms from each group were compared with 43 healthy controls. Results. The 34 patients who did not satisfy the diagnostic criteria for SS or any other connective tissue disease were designated dry eyes and mouth syndrome (DEMS). Their demography including age was similar to that of a primary SS group and there was no more atrophy seen on their biopsies compared with SS and non‐SS controls. They scored highly on visual analogue scales of symptoms but had few objective signs. All were negative for anti‐Ro and anti‐La although the prevalence of antinuclear antibodies (19%) was increased compared with a normal population. There was no excess of SS‐associated tissue types. Conclusion. There was no evidence that age, salivary gland atrophy or subclinical SS accounted for the symptoms in DEMS. Most of the patients fitted into a spectrum of disease which tended more towards fibromyalgia and/or chronic fatigue syndrome.</description><identifier>ISSN: 1462-0324</identifier><identifier>ISSN: 1460-2172</identifier><identifier>EISSN: 1462-0332</identifier><identifier>EISSN: 1460-2172</identifier><identifier>DOI: 10.1093/rheumatology/41.4.416</identifier><identifier>PMID: 11961172</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adult ; Aged ; Atrophy - pathology ; Biological and medical sciences ; Biopsy ; Diagnosis, Differential ; Dry Eye Syndromes - classification ; Dry Eye Syndromes - pathology ; Dry Eye Syndromes - physiopathology ; Dry eyes and mouth syndrome (DEMS) ; Female ; Humans ; Male ; Medical sciences ; Middle Aged ; Salivary Glands, Minor - metabolism ; Salivary Glands, Minor - pathology ; Salivation - physiology ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis ; Sicca ; Sjögren's syndrome ; Surveys and Questionnaires ; Xerostomia - classification ; Xerostomia - pathology ; Xerostomia - physiopathology</subject><ispartof>British journal of rheumatology, 2002-04, Vol.41 (4), p.416-422</ispartof><rights>2002 INIST-CNRS</rights><rights>Copyright Oxford University Press(England) Apr 2002</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c447t-90ef58ef7e70c5e3d764fc6554b03b4f8a5499adb12373f67c0dd67e58b67a6f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=13647656$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11961172$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Price, E. J.</creatorcontrib><creatorcontrib>Venables, P. J. W.</creatorcontrib><title>Dry eyes and mouth syndrome—a subgroup of patients presenting with sicca symptoms</title><title>British journal of rheumatology</title><addtitle>Rheumatology</addtitle><description>Objective. To evaluate the characteristics of patients presenting with symptoms suggestive of Sjögren's syndrome (SS) but failing to satisfy diagnostic criteria. Methods. Clinical, serological and histological data were collected on 34 patients presenting with dry eyes and/or mouth who did not satisfy the Vitali criteria for the diagnosis of SS. They were compared with 136 patients with primary SS, 38 patients with secondary SS, and 13 patients without SS. Questionnaires on symptoms from each group were compared with 43 healthy controls. Results. The 34 patients who did not satisfy the diagnostic criteria for SS or any other connective tissue disease were designated dry eyes and mouth syndrome (DEMS). Their demography including age was similar to that of a primary SS group and there was no more atrophy seen on their biopsies compared with SS and non‐SS controls. They scored highly on visual analogue scales of symptoms but had few objective signs. All were negative for anti‐Ro and anti‐La although the prevalence of antinuclear antibodies (19%) was increased compared with a normal population. There was no excess of SS‐associated tissue types. Conclusion. There was no evidence that age, salivary gland atrophy or subclinical SS accounted for the symptoms in DEMS. Most of the patients fitted into a spectrum of disease which tended more towards fibromyalgia and/or chronic fatigue syndrome.</description><subject>Adult</subject><subject>Aged</subject><subject>Atrophy - pathology</subject><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>Diagnosis, Differential</subject><subject>Dry Eye Syndromes - classification</subject><subject>Dry Eye Syndromes - pathology</subject><subject>Dry Eye Syndromes - physiopathology</subject><subject>Dry eyes and mouth syndrome (DEMS)</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Salivary Glands, Minor - metabolism</subject><subject>Salivary Glands, Minor - pathology</subject><subject>Salivation - physiology</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</subject><subject>Sicca</subject><subject>Sjögren's syndrome</subject><subject>Surveys and Questionnaires</subject><subject>Xerostomia - classification</subject><subject>Xerostomia - pathology</subject><subject>Xerostomia - physiopathology</subject><issn>1462-0324</issn><issn>1460-2172</issn><issn>1462-0332</issn><issn>1460-2172</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkN1q1UAUhQdR7I8-gjII7V1OZzJ_yaXU1goFW_ylN8Nksuc0NcnE2QmaOx_CJ_RJzOEcWvFm7wX7W4vNIuQFZyvOSnGSbmHq3BjbuJ5PJF_JleT6EdnnUucZEyJ_fK9zuUcOEO8YY4qL4inZ47zUnJt8n3x4k2YKMyB1fU27OI23FOe-TrGDP79-O4pTtU5xGmgMdHBjA_2IdEiAi2j6Nf3RbByN9ws6d8MYO3xGngTXIjzf7UPy6fzs4-lFdvn-7bvT15eZl9KMWckgqAKCAcO8AlEbLYPXSsmKiUqGwilZlq6ueC6MCNp4VtfagCoqbZwO4pAcb3OHFL9PgKPtGvTQtq6HOKE1XPPcSL6Ar_4D7-KU-uU3y0uldVHocoHUFvIpIiYIdkhN59JsObObyu2_lVvJrVyGXnwvd-FT1UH94Np1vABHO8Chd21IrvcNPnBCS6PVJijbcg2O8PP-7tI3q40wyl58vbE35-L6S1l8tlfiL7Igntg</recordid><startdate>20020401</startdate><enddate>20020401</enddate><creator>Price, E. J.</creator><creator>Venables, P. J. W.</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</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>7QP</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>20020401</creationdate><title>Dry eyes and mouth syndrome—a subgroup of patients presenting with sicca symptoms</title><author>Price, E. J. ; Venables, P. J. W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c447t-90ef58ef7e70c5e3d764fc6554b03b4f8a5499adb12373f67c0dd67e58b67a6f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Atrophy - pathology</topic><topic>Biological and medical sciences</topic><topic>Biopsy</topic><topic>Diagnosis, Differential</topic><topic>Dry Eye Syndromes - classification</topic><topic>Dry Eye Syndromes - pathology</topic><topic>Dry Eye Syndromes - physiopathology</topic><topic>Dry eyes and mouth syndrome (DEMS)</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Salivary Glands, Minor - metabolism</topic><topic>Salivary Glands, Minor - pathology</topic><topic>Salivation - physiology</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><topic>Sicca</topic><topic>Sjögren's syndrome</topic><topic>Surveys and Questionnaires</topic><topic>Xerostomia - classification</topic><topic>Xerostomia - pathology</topic><topic>Xerostomia - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Price, E. J.</creatorcontrib><creatorcontrib>Venables, P. J. W.</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>Calcium &amp; Calcified Tissue Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>British journal of rheumatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Price, E. J.</au><au>Venables, P. J. W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dry eyes and mouth syndrome—a subgroup of patients presenting with sicca symptoms</atitle><jtitle>British journal of rheumatology</jtitle><addtitle>Rheumatology</addtitle><date>2002-04-01</date><risdate>2002</risdate><volume>41</volume><issue>4</issue><spage>416</spage><epage>422</epage><pages>416-422</pages><issn>1462-0324</issn><issn>1460-2172</issn><eissn>1462-0332</eissn><eissn>1460-2172</eissn><abstract>Objective. To evaluate the characteristics of patients presenting with symptoms suggestive of Sjögren's syndrome (SS) but failing to satisfy diagnostic criteria. Methods. Clinical, serological and histological data were collected on 34 patients presenting with dry eyes and/or mouth who did not satisfy the Vitali criteria for the diagnosis of SS. They were compared with 136 patients with primary SS, 38 patients with secondary SS, and 13 patients without SS. Questionnaires on symptoms from each group were compared with 43 healthy controls. Results. The 34 patients who did not satisfy the diagnostic criteria for SS or any other connective tissue disease were designated dry eyes and mouth syndrome (DEMS). Their demography including age was similar to that of a primary SS group and there was no more atrophy seen on their biopsies compared with SS and non‐SS controls. They scored highly on visual analogue scales of symptoms but had few objective signs. All were negative for anti‐Ro and anti‐La although the prevalence of antinuclear antibodies (19%) was increased compared with a normal population. There was no excess of SS‐associated tissue types. Conclusion. There was no evidence that age, salivary gland atrophy or subclinical SS accounted for the symptoms in DEMS. 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source MEDLINE; Oxford University Press Journals All Titles (1996-Current); Alma/SFX Local Collection
subjects Adult
Aged
Atrophy - pathology
Biological and medical sciences
Biopsy
Diagnosis, Differential
Dry Eye Syndromes - classification
Dry Eye Syndromes - pathology
Dry Eye Syndromes - physiopathology
Dry eyes and mouth syndrome (DEMS)
Female
Humans
Male
Medical sciences
Middle Aged
Salivary Glands, Minor - metabolism
Salivary Glands, Minor - pathology
Salivation - physiology
Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis
Sicca
Sjögren's syndrome
Surveys and Questionnaires
Xerostomia - classification
Xerostomia - pathology
Xerostomia - physiopathology
title Dry eyes and mouth syndrome—a subgroup of patients presenting with sicca symptoms
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