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Antinuclear Antibody-Negative Systemic Lupus Erythematosus in an International Inception Cohort.
Choi, May Y; Clarke, Ann E; St Pierre, Yvan; Hanly, John G; Urowitz, Murray B; Romero-Diaz, Juanita; Gordon, Caroline; Bae, Sang-Cheol; Bernatsky, Sasha; Wallace, Daniel J; Merrill, Joan T; Isenberg, David A; Rahman, Anisur; Ginzler, Ellen M; Petri, Michelle; Bruce, Ian N; Dooley, Mary A; Fortin, Paul R; Gladman, Dafna D; Sanchez-Guerrero, Jorge; Steinsson, Kristjan; Ramsey-Goldman, Rosalind; Khamashta, Munther A; Aranow, Cynthia; Alarcón, Graciela S; Manzi, Susan; Nived, Ola; Zoma, Asad A; van Vollenhoven, Ronald F; Ramos-Casals, Manuel; Ruiz-Irastorza, Guillermo; Lim, S Sam; Kalunian, Kenneth C; Inanc, Murat; Kamen, Diane L; Peschken, Christine A; Jacobsen, Soren; Askanase, Anca; Stoll, Thomas; Buyon, Jill; Mahler, Michael; Fritzler, Marvin J.
Afiliación
  • Choi MY; University of Calgary, Cumming School of Medicine, Calgary, Alberta, Canada.
  • Clarke AE; University of Calgary, Cumming School of Medicine, Calgary, Alberta, Canada.
  • St Pierre Y; McGill University Health Centre, Montreal, Quebec, Canada.
  • Hanly JG; Queen Elizabeth II Health Sciences Centre and Dalhousie University, Halifax, Nova Scotia, Canada.
  • Urowitz MB; Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada.
  • Romero-Diaz J; Instituto Nacional de Ciencias Médicas y Nutrición, Mexico City, Mexico.
  • Gordon C; University of Birmingham, Birmingham, UK.
  • Bae SC; Hanyang University Hospital for Rheumatic Diseases, Seoul, Korea.
  • Bernatsky S; McGill University Health Centre, Montreal, Quebec, Canada.
  • Wallace DJ; Cedars-Sinai/David Geffen School of Medicine at University of California Los Angeles.
  • Merrill JT; Oklahoma Medical Research Foundation, Oklahoma City.
  • Isenberg DA; University College London, London, UK.
  • Rahman A; University College London, London, UK.
  • Ginzler EM; State University of New York Downstate Medical Center, Brooklyn.
  • Petri M; Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Bruce IN; Arthritis Research UK, University of Manchester, NIHR Manchester Biomedical Research Centre, Central Manchester University Hospitals NHS Foundation Trust, and Manchester Academic Health Science Centre, Manchester, UK.
  • Dooley MA; University of North Carolina, Chapel Hill.
  • Fortin PR; CHU de Québec-Université Laval, Quebec City, Quebec, Canada.
  • Gladman DD; Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada.
  • Sanchez-Guerrero J; Mount Sinai Hospital and University Health Network, University of Toronto, Toronto, Ontario, Canada.
  • Steinsson K; Landspitali University Hospital, Reykjavik, Iceland.
  • Ramsey-Goldman R; Northwestern University and Feinberg School of Medicine, Chicago, Illinois.
  • Khamashta MA; St Thomas' Hospital and King's College, London School of Medicine, London, UK.
  • Aranow C; Feinstein Institute for Medical Research, Manhasset, New York.
  • Alarcón GS; University of Alabama at Birmingham.
  • Manzi S; Allegheny Health Network, Pittsburgh, Pennsylvania.
  • Nived O; University Hospital Lund, Lund, Sweden.
  • Zoma AA; Hairmyres Hospital, East Kilbride, Scotland, UK.
  • van Vollenhoven RF; University of Amsterdam, Amsterdam, The Netherlands.
  • Ramos-Casals M; Hospital Clínic, Barcelona, Spain.
  • Ruiz-Irastorza G; Hospital Universitario Cruces, University of the Basque Country, Barakaldo, Spain.
  • Lim SS; Emory University School of Medicine, Atlanta, Georgia.
  • Kalunian KC; University of California San Diego School of Medicine, La Jolla.
  • Inanc M; Istanbul University, Istanbul, Turkey.
  • Kamen DL; Medical University of South Carolina, Charleston.
  • Peschken CA; University of Manitoba, Winnipeg, Manitoba, Canada.
  • Jacobsen S; Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
  • Askanase A; Hospital for Joint Diseases and New York University, New York.
  • Stoll T; Kantousspital, Schaffhausen, Switzerland.
  • Buyon J; New York University School of Medicine, New York.
  • Mahler M; Inova Diagnostics Inc., San Diego, California.
  • Fritzler MJ; University of Calgary, Cumming School of Medicine, Calgary, Alberta, Canada.
Arthritis Care Res (Hoboken) ; 71(7): 893-902, 2019 07.
Article en En | MEDLINE | ID: mdl-30044551
ABSTRACT

OBJECTIVE:

The spectrum of antinuclear antibodies (ANAs) is changing to include both nuclear staining as well as cytoplasmic and mitotic cell patterns (CMPs) and accordingly a change is occurring in terminology to anticellular antibodies. This study examined the prevalence of indirect immunofluorescence (IIF) anticellular antibody staining using the Systemic Lupus International Collaborating Clinics inception cohort.

METHODS:

Anticellular antibodies were detected by IIF on HEp-2000 substrate using the baseline serum. Three serologic subsets were examined ANA positive (presence of either nuclear or mixed nuclear/CMP staining), anticellular antibody negative (absence of any intracellular staining), and isolated CMP staining. The odds of being anticellular antibody negative versus ANA or isolated CMP positive was assessed by multivariable analysis.

RESULTS:

A total of 1,137 patients were included; 1,049 (92.3%) were ANA positive, 71 (6.2%) were anticellular antibody negative, and 17 (1.5%) had an isolated CMP. The isolated CMP-positive group did not differ from the ANA-positive or anticellular antibody-negative groups in clinical, demographic, or serologic features. Patients who were older (odds ratio [OR] 1.02 [95% confidence interval (95% CI) 1.00, 1.04]), of white race/ethnicity (OR 3.53 [95% CI 1.77, 7.03]), or receiving high-dose glucocorticoids at or prior to enrollment (OR 2.39 [95% CI 1.39, 4.12]) were more likely to be anticellular antibody negative. Patients on immunosuppressants (OR 0.35 [95% CI 0.19, 0.64]) or with anti-SSA/Ro 60 (OR 0.41 [95% CI 0.23, 0.74]) or anti-U1 RNP (OR 0.43 [95% CI 0.20, 0.93]) were less likely to be anticellular antibody negative.

CONCLUSION:

In newly diagnosed systemic lupus erythematosus, 6.2% of patients were anticellular antibody negative, and 1.5% had an isolated CMP. The prevalence of anticellular antibody-negative systemic lupus erythematosus will likely decrease as emerging nomenclature guidelines recommend that non-nuclear patterns should also be reported as a positive ANA.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pruebas Serológicas / Anticuerpos Antinucleares / Técnica del Anticuerpo Fluorescente Indirecta / Lupus Eritematoso Sistémico Tipo de estudio: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male Idioma: En Revista: Arthritis Care Res (Hoboken) Asunto de la revista: REUMATOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pruebas Serológicas / Anticuerpos Antinucleares / Técnica del Anticuerpo Fluorescente Indirecta / Lupus Eritematoso Sistémico Tipo de estudio: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male Idioma: En Revista: Arthritis Care Res (Hoboken) Asunto de la revista: REUMATOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Canadá