AB0630 Clinical spectrum time course comparison between PL-7, PL-12 and EJ positive antisynthetase syndrome. (15th June 2017)
- Record Type:
- Journal Article
- Title:
- AB0630 Clinical spectrum time course comparison between PL-7, PL-12 and EJ positive antisynthetase syndrome. (15th June 2017)
- Main Title:
- AB0630 Clinical spectrum time course comparison between PL-7, PL-12 and EJ positive antisynthetase syndrome
- Authors:
- Araguas, E Trallero
Selva, A O'Callaghan
Scire, CA
Codullo, V
Castaneda, S
Centeno, N Ortego
Silva, JA Pereira da
Fiehn, C
Schwarting, A
Manfredi, A
Emmi, G
Barsotti, S
Molberg, O
Doria, A
Parisi, S
Scarpato, S
Pipitone, N
Piga, M
Cavazzana, I
Lopez-Longo, FJ
Bachiller-Corral, J
Benucci, M
Rojas-Serrano, J
Triantafyllias, K
Perez-Gomez, N
Cagnotto, G
Maurier, F
Quartuccio, L
Bocci, E Bartoloni
Tomietto, P
Caporali, R
Iannone, F
Gonzalez-Gay, MA
Cavagna, L
… (more) - Abstract:
- Abstract : Background: Arthritis, myositis and Interstital lung disease (ILD) represent the classic clinical triad of antisynthetase syndrome (ASSD). In anti Jo-1 positive patients, these findings may appear also during the follow-up. Even if a similar cumulative trend has been showed also in non anti Jo-1 positive ASSD, a head to head comparison of clinical spectrum time course in these patients is still lacking Objectives: To assess the clinical spectrum time course in non anti Jo-1 positive ASSD, according to different underlying non anti Jo-1 specificities Methods: Clinical, laboratory and instrumental data collection of anti PL-7, PL-12, and EJ positive patients from an international database of ASSD Results: We identified 63 (42%) anti PL-7, 66 (44%) anti PL-12 and 20 (14%) anti EJ positive patients, reporting their characteristics in table 1 (disease onset) and 2 (last follow-up). At disease onset, no substantial differences were observed. At the end of follow-up, we observed some differences between anti PL-12 and both anti PL-7 and anti-EJ positive patients. In particular, anti PL-12 positive patients presented less frequently ex-novo triad findings and had a reduced prevalence of myositis. From the clinical point of view, the main pattern of disease presentation was an isolated ILD in all groups at the onset and only in anti-PL12 positive ASSD at last follow-up. Conclusions: Our study seems to indicate that clinical spectrum time course of anti PL-12 positive ASSDAbstract : Background: Arthritis, myositis and Interstital lung disease (ILD) represent the classic clinical triad of antisynthetase syndrome (ASSD). In anti Jo-1 positive patients, these findings may appear also during the follow-up. Even if a similar cumulative trend has been showed also in non anti Jo-1 positive ASSD, a head to head comparison of clinical spectrum time course in these patients is still lacking Objectives: To assess the clinical spectrum time course in non anti Jo-1 positive ASSD, according to different underlying non anti Jo-1 specificities Methods: Clinical, laboratory and instrumental data collection of anti PL-7, PL-12, and EJ positive patients from an international database of ASSD Results: We identified 63 (42%) anti PL-7, 66 (44%) anti PL-12 and 20 (14%) anti EJ positive patients, reporting their characteristics in table 1 (disease onset) and 2 (last follow-up). At disease onset, no substantial differences were observed. At the end of follow-up, we observed some differences between anti PL-12 and both anti PL-7 and anti-EJ positive patients. In particular, anti PL-12 positive patients presented less frequently ex-novo triad findings and had a reduced prevalence of myositis. From the clinical point of view, the main pattern of disease presentation was an isolated ILD in all groups at the onset and only in anti-PL12 positive ASSD at last follow-up. Conclusions: Our study seems to indicate that clinical spectrum time course of anti PL-12 positive ASSD is different from that of anti PL7 and of anti EJ positive ASSD. The clinical pattern associated with these two latter antibodies was very similar. Furthermore, anti PL-12 positive patients seems to have a more stable disease, with a less common occurrence of ex-novo triad findings during the follow-up References: Cavagna L. Medicine 2015. Cavagna L. CRAI 2016. Cavagna L. ARD 2016 (Abstract). Trallero Araguas E. Scand J Rheumatol 2016. Acknowledgements: To all members of the AENEAS collaborative group. Disclosure of Interest: None declared … (more)
- Is Part Of:
- Annals of the rheumatic diseases. Volume 76(2017)Supplement 2
- Journal:
- Annals of the rheumatic diseases
- Issue:
- Volume 76(2017)Supplement 2
- Issue Display:
- Volume 76, Issue 2 (2017)
- Year:
- 2017
- Volume:
- 76
- Issue:
- 2
- Issue Sort Value:
- 2017-0076-0002-0000
- Page Start:
- 1272
- Page End:
- 1273
- Publication Date:
- 2017-06-15
- Subjects:
- Rheumatism -- Periodicals
616.723005 - Journal URLs:
- http://ard.bmjjournals.com/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=149&action=archive ↗
http://www.bmj.com/archive ↗
http://gateway.ovid.com/server3/ovidweb.cgi?T=JS&MODE=ovid&D=ovft&PAGE=titles&SEARCH=annals+of+the+rheumatic+diseases.tj&NEWS=N ↗ - DOI:
- 10.1136/annrheumdis-2017-eular.2592 ↗
- Languages:
- English
- ISSNs:
- 0003-4967
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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