US incidence of juvenile dermatomyositis, 1995–1998: Results from the National Institute of Arthritis and Musculoskeletal and Skin Diseases Registry

Objective To estimate the incidence of juvenile dermatomyositis (juvenile DM) in the United States between 1995 and 1998. Methods Physician referrals to the National Institute of Arthritis and Musculoskeletal and Skin Diseases Juvenile Dermatomyositis Research Registry and the National Pediatric Rhe...

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Published in:Arthritis and rheumatism Vol. 49; no. 3; pp. 300 - 305
Main Authors: Mendez, Eduardo P., Lipton, Rebecca, Ramsey‐Goldman, Rosalind, Roettcher, Phil, Bowyer, Susan, Dyer, Alan, Pachman, Lauren M.
Format: Journal Article
Language:English
Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 15-06-2003
Lippincott Williams and Wilkins
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Abstract Objective To estimate the incidence of juvenile dermatomyositis (juvenile DM) in the United States between 1995 and 1998. Methods Physician referrals to the National Institute of Arthritis and Musculoskeletal and Skin Diseases Juvenile Dermatomyositis Research Registry and the National Pediatric Rheumatology Disease Registry from Indiana University were utilized for a 2‐source capture‐recapture estimation of Juvenile DM annual incidence. Results For children 2–17 years of age, the estimated annual incidence rates from 1995 to 1998 in the US ranged from 2.5 to 4.1 juvenile DM cases per million children, and the 4‐year average annual rate was 3.2 per million children (95% confidence interval 2.9–3.4). Estimated annual incidence rates by race were 3.4 for white non‐Hispanics, 3.3 for African American non‐Hispanics, and 2.7 for Hispanics. During the 4‐year period of the study, completeness of ascertainment for the combined registries ranged from 56% to 86% and girls were affected more than boys (ratio 2.3:1). Conclusion This study provides evidence for sex, and possibly racial differences in the risk of juvenile DM in the US.
AbstractList Objective To estimate the incidence of juvenile dermatomyositis (juvenile DM) in the United States between 1995 and 1998. Methods Physician referrals to the National Institute of Arthritis and Musculoskeletal and Skin Diseases Juvenile Dermatomyositis Research Registry and the National Pediatric Rheumatology Disease Registry from Indiana University were utilized for a 2‐source capture‐recapture estimation of Juvenile DM annual incidence. Results For children 2–17 years of age, the estimated annual incidence rates from 1995 to 1998 in the US ranged from 2.5 to 4.1 juvenile DM cases per million children, and the 4‐year average annual rate was 3.2 per million children (95% confidence interval 2.9–3.4). Estimated annual incidence rates by race were 3.4 for white non‐Hispanics, 3.3 for African American non‐Hispanics, and 2.7 for Hispanics. During the 4‐year period of the study, completeness of ascertainment for the combined registries ranged from 56% to 86% and girls were affected more than boys (ratio 2.3:1). Conclusion This study provides evidence for sex, and possibly racial differences in the risk of juvenile DM in the US.
OBJECTIVETo estimate the incidence of juvenile dermatomyositis (juvenile DM) in the United States between 1995 and 1998.METHODSPhysician referrals to the National Institute of Arthritis and Musculoskeletal and Skin Diseases Juvenile Dermatomyositis Research Registry and the National Pediatric Rheumatology Disease Registry from Indiana University were utilized for a 2-source capture-recapture estimation of Juvenile DM annual incidence.RESULTSFor children 2-17 years of age, the estimated annual incidence rates from 1995 to 1998 in the US ranged from 2.5 to 4.1 juvenile DM cases per million children, and the 4-year average annual rate was 3.2 per million children (95% confidence interval 2.9-3.4). Estimated annual incidence rates by race were 3.4 for white non-Hispanics, 3.3 for African American non-Hispanics, and 2.7 for Hispanics. During the 4-year period of the study, completeness of ascertainment for the combined registries ranged from 56% to 86% and girls were affected more than boys (ratio 2.3:1).CONCLUSIONThis study provides evidence for sex, and possibly racial differences in the risk of juvenile DM in the US.
To estimate the incidence of juvenile dermatomyositis (juvenile DM) in the United States between 1995 and 1998. Physician referrals to the National Institute of Arthritis and Musculoskeletal and Skin Diseases Juvenile Dermatomyositis Research Registry and the National Pediatric Rheumatology Disease Registry from Indiana University were utilized for a 2-source capture-recapture estimation of Juvenile DM annual incidence. For children 2-17 years of age, the estimated annual incidence rates from 1995 to 1998 in the US ranged from 2.5 to 4.1 juvenile DM cases per million children, and the 4-year average annual rate was 3.2 per million children (95% confidence interval 2.9-3.4). Estimated annual incidence rates by race were 3.4 for white non-Hispanics, 3.3 for African American non-Hispanics, and 2.7 for Hispanics. During the 4-year period of the study, completeness of ascertainment for the combined registries ranged from 56% to 86% and girls were affected more than boys (ratio 2.3:1). This study provides evidence for sex, and possibly racial differences in the risk of juvenile DM in the US.
Author Dyer, Alan
Mendez, Eduardo P.
Bowyer, Susan
Pachman, Lauren M.
Roettcher, Phil
Lipton, Rebecca
Ramsey‐Goldman, Rosalind
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  givenname: Rebecca
  surname: Lipton
  fullname: Lipton, Rebecca
– sequence: 3
  givenname: Rosalind
  surname: Ramsey‐Goldman
  fullname: Ramsey‐Goldman, Rosalind
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  givenname: Phil
  surname: Roettcher
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  givenname: Susan
  surname: Bowyer
  fullname: Bowyer, Susan
– sequence: 6
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  surname: Dyer
  fullname: Dyer, Alan
– sequence: 7
  givenname: Lauren M.
  surname: Pachman
  fullname: Pachman, Lauren M.
  email: pachman@northwestern.edu
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https://www.ncbi.nlm.nih.gov/pubmed/12794783$$D View this record in MEDLINE/PubMed
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Issue 3
Keywords Human
Immunopathology
Connective tissue disease
Skin disease
Methodology
Dermatomyositis
Autoimmune disease
Registry
Epidemiology
Incidence
Juvenile dermatomyositis
Striated muscle disease
Capture recapture method
Capture-recapture
Register
Systemic disease
Adolescent
Child
Public health
Language English
License CC BY 4.0
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  day: 15
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PublicationTitle Arthritis and rheumatism
PublicationTitleAlternate Arthritis Rheum
PublicationYear 2003
Publisher Wiley Subscription Services, Inc., A Wiley Company
Lippincott Williams and Wilkins
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1975; 292
1998; 41
1999; 149
1970; 48
1998; 25
1996; 23
1999
Shehata R (e_1_2_6_3_2) 1999; 17
Andersson Gare B (e_1_2_6_20_2) 1996; 23
See Y (e_1_2_6_23_2) 1997; 26
Cassidy JT (e_1_2_6_22_2) 2001
Oddis CV (e_1_2_6_5_2) 1990; 17
e_1_2_6_8_2
Pachman LM (e_1_2_6_2_2) 1998; 25
e_1_2_6_7_2
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e_1_2_6_15_2
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Snippet Objective To estimate the incidence of juvenile dermatomyositis (juvenile DM) in the United States between 1995 and 1998. Methods Physician referrals to the...
To estimate the incidence of juvenile dermatomyositis (juvenile DM) in the United States between 1995 and 1998. Physician referrals to the National Institute...
OBJECTIVETo estimate the incidence of juvenile dermatomyositis (juvenile DM) in the United States between 1995 and 1998.METHODSPhysician referrals to the...
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SubjectTerms Adolescent
Biological and medical sciences
Capture‐recapture
Child
Child, Preschool
Dermatomyositis - epidemiology
Dermatomyositis - ethnology
Epidemiology
Female
Humans
Incidence
Juvenile dermatomyositis
Male
Medical sciences
National Institutes of Health (U.S.)
Registries
Registry
Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis
Sex Distribution
United States - epidemiology
Title US incidence of juvenile dermatomyositis, 1995–1998: Results from the National Institute of Arthritis and Musculoskeletal and Skin Diseases Registry
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fart.11122
https://www.ncbi.nlm.nih.gov/pubmed/12794783
https://search.proquest.com/docview/73335854
Volume 49
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