Ocular findings in patients with systemic sclerosis

Detalhes bibliográficos
Autor(a) principal: Gomes, Beatriz de A. F
Data de Publicação: 2011
Outros Autores: Santhiago, Marcony R, Magalhães, Priscilla, Kara-Junior, Newton, Azevedo, Mário N. L. de, Moraes Jr, Haroldo V
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinics
DOI: 10.1590/S1807-59322011000300003
Texto Completo: https://www.revistas.usp.br/clinics/article/view/19224
Resumo: OBJECTIVE: To evaluate the frequency and characteristics of ocular manifestations in outpatients with systemic sclerosis. METHODS: In this cross-sectional study, 45 patients with systemic sclerosis were enrolled. Data regarding demographics, disease duration and subtype, age at diagnosis, nailfold capillaroscopic pattern and autoantibody profile were collected, and a full ophthalmic examination was conducted. Parametric (Student's t-test) and nonparametric (Mann-Whitney U test) tests were used to compare continuous variables. Fisher's exact test was used to compare categorical data. P values < 0.05 were considered significant. RESULTS: Twenty-three subjects (51.1%) had eyelid skin changes; 22 (48.9%) had keratoconjunctivitis sicca, 19 (42.2%) had cataracts, 13 (28.9%) had retinal microvascular abnormalities and 6 (13.3%) had glaucoma. Eyelid skin changes were more frequent in patients with the diffuse subtype of systemic sclerosis and were associated with a younger age and an earlier age at diagnosis. Cataracts were presumed to be age-related and secondary to corticosteroid treatment. There was no association between demographic, clinical or serological data and keratoconjunctivitis sicca. The retinal microvascular abnormalities were indistinguishable from those related to systemic hypertension and were associated with an older age and a severe capillaroscopic pattern. CONCLUSIONS: Eyelid skin abnormalities and keratoconjunctivitis sicca were the most common ocular findings related to systemic sclerosis. Some demographic and clinical data were associated with some ophthalmic features and not with others, showing that the ocular manifestations of systemic sclerosis are characterized by heterogeneity and reflect the differences in the implicated pathophysiological mechanisms.
id USP-19_8720c471449f1d3033c37bf3bfe209ef
oai_identifier_str oai:revistas.usp.br:article/19224
network_acronym_str USP-19
network_name_str Clinics
spelling Ocular findings in patients with systemic sclerosis Systemic sclerodermasystemic sclerosisocular findingsocular manifestationsophthalmologic findings OBJECTIVE: To evaluate the frequency and characteristics of ocular manifestations in outpatients with systemic sclerosis. METHODS: In this cross-sectional study, 45 patients with systemic sclerosis were enrolled. Data regarding demographics, disease duration and subtype, age at diagnosis, nailfold capillaroscopic pattern and autoantibody profile were collected, and a full ophthalmic examination was conducted. Parametric (Student's t-test) and nonparametric (Mann-Whitney U test) tests were used to compare continuous variables. Fisher's exact test was used to compare categorical data. P values < 0.05 were considered significant. RESULTS: Twenty-three subjects (51.1%) had eyelid skin changes; 22 (48.9%) had keratoconjunctivitis sicca, 19 (42.2%) had cataracts, 13 (28.9%) had retinal microvascular abnormalities and 6 (13.3%) had glaucoma. Eyelid skin changes were more frequent in patients with the diffuse subtype of systemic sclerosis and were associated with a younger age and an earlier age at diagnosis. Cataracts were presumed to be age-related and secondary to corticosteroid treatment. There was no association between demographic, clinical or serological data and keratoconjunctivitis sicca. The retinal microvascular abnormalities were indistinguishable from those related to systemic hypertension and were associated with an older age and a severe capillaroscopic pattern. CONCLUSIONS: Eyelid skin abnormalities and keratoconjunctivitis sicca were the most common ocular findings related to systemic sclerosis. Some demographic and clinical data were associated with some ophthalmic features and not with others, showing that the ocular manifestations of systemic sclerosis are characterized by heterogeneity and reflect the differences in the implicated pathophysiological mechanisms. Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2011-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/1922410.1590/S1807-59322011000300003Clinics; Vol. 66 No. 3 (2011); 379-385 Clinics; v. 66 n. 3 (2011); 379-385 Clinics; Vol. 66 Núm. 3 (2011); 379-385 1980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/19224/21287Gomes, Beatriz de A. FSanthiago, Marcony RMagalhães, PriscillaKara-Junior, NewtonAzevedo, Mário N. L. deMoraes Jr, Haroldo Vinfo:eu-repo/semantics/openAccess2012-05-23T16:28:12Zoai:revistas.usp.br:article/19224Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2012-05-23T16:28:12Clinics - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Ocular findings in patients with systemic sclerosis
title Ocular findings in patients with systemic sclerosis
spellingShingle Ocular findings in patients with systemic sclerosis
Ocular findings in patients with systemic sclerosis
Gomes, Beatriz de A. F
Systemic scleroderma
systemic sclerosis
ocular findings
ocular manifestations
ophthalmologic findings
Gomes, Beatriz de A. F
Systemic scleroderma
systemic sclerosis
ocular findings
ocular manifestations
ophthalmologic findings
title_short Ocular findings in patients with systemic sclerosis
title_full Ocular findings in patients with systemic sclerosis
title_fullStr Ocular findings in patients with systemic sclerosis
Ocular findings in patients with systemic sclerosis
title_full_unstemmed Ocular findings in patients with systemic sclerosis
Ocular findings in patients with systemic sclerosis
title_sort Ocular findings in patients with systemic sclerosis
author Gomes, Beatriz de A. F
author_facet Gomes, Beatriz de A. F
Gomes, Beatriz de A. F
Santhiago, Marcony R
Magalhães, Priscilla
Kara-Junior, Newton
Azevedo, Mário N. L. de
Moraes Jr, Haroldo V
Santhiago, Marcony R
Magalhães, Priscilla
Kara-Junior, Newton
Azevedo, Mário N. L. de
Moraes Jr, Haroldo V
author_role author
author2 Santhiago, Marcony R
Magalhães, Priscilla
Kara-Junior, Newton
Azevedo, Mário N. L. de
Moraes Jr, Haroldo V
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Gomes, Beatriz de A. F
Santhiago, Marcony R
Magalhães, Priscilla
Kara-Junior, Newton
Azevedo, Mário N. L. de
Moraes Jr, Haroldo V
dc.subject.por.fl_str_mv Systemic scleroderma
systemic sclerosis
ocular findings
ocular manifestations
ophthalmologic findings
topic Systemic scleroderma
systemic sclerosis
ocular findings
ocular manifestations
ophthalmologic findings
description OBJECTIVE: To evaluate the frequency and characteristics of ocular manifestations in outpatients with systemic sclerosis. METHODS: In this cross-sectional study, 45 patients with systemic sclerosis were enrolled. Data regarding demographics, disease duration and subtype, age at diagnosis, nailfold capillaroscopic pattern and autoantibody profile were collected, and a full ophthalmic examination was conducted. Parametric (Student's t-test) and nonparametric (Mann-Whitney U test) tests were used to compare continuous variables. Fisher's exact test was used to compare categorical data. P values < 0.05 were considered significant. RESULTS: Twenty-three subjects (51.1%) had eyelid skin changes; 22 (48.9%) had keratoconjunctivitis sicca, 19 (42.2%) had cataracts, 13 (28.9%) had retinal microvascular abnormalities and 6 (13.3%) had glaucoma. Eyelid skin changes were more frequent in patients with the diffuse subtype of systemic sclerosis and were associated with a younger age and an earlier age at diagnosis. Cataracts were presumed to be age-related and secondary to corticosteroid treatment. There was no association between demographic, clinical or serological data and keratoconjunctivitis sicca. The retinal microvascular abnormalities were indistinguishable from those related to systemic hypertension and were associated with an older age and a severe capillaroscopic pattern. CONCLUSIONS: Eyelid skin abnormalities and keratoconjunctivitis sicca were the most common ocular findings related to systemic sclerosis. Some demographic and clinical data were associated with some ophthalmic features and not with others, showing that the ocular manifestations of systemic sclerosis are characterized by heterogeneity and reflect the differences in the implicated pathophysiological mechanisms.
publishDate 2011
dc.date.none.fl_str_mv 2011-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/clinics/article/view/19224
10.1590/S1807-59322011000300003
url https://www.revistas.usp.br/clinics/article/view/19224
identifier_str_mv 10.1590/S1807-59322011000300003
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clinics/article/view/19224/21287
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
dc.source.none.fl_str_mv Clinics; Vol. 66 No. 3 (2011); 379-385
Clinics; v. 66 n. 3 (2011); 379-385
Clinics; Vol. 66 Núm. 3 (2011); 379-385
1980-5322
1807-5932
reponame:Clinics
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Clinics
collection Clinics
repository.name.fl_str_mv Clinics - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||clinics@hc.fm.usp.br
_version_ 1822178959142420480
dc.identifier.doi.none.fl_str_mv 10.1590/S1807-59322011000300003