Race, Income, and Disease Outcomes in Juvenile Dermatomyositis

To determine the relationships among race, income, and disease outcomes in children with juvenile dermatomyositis (JDM). Data from 438 subjects with JDM enrolled in the Childhood Arthritis and Rheumatology Research Alliance (CARRA) Legacy Registry were analyzed. Demographic data included age, sex, r...

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Published inThe Journal of pediatrics Vol. 184; pp. 38 - 44.e1
Main Authors Phillippi, Kathryn, Hoeltzel, Mark, Byun Robinson, Angela, Kim, Susan, Abramson, Leslie S., Anderson, Eleanor S., Becker, Mara L., Benham, Heather, Beukelman, Timothy, Blier, Peter R., Brunner, Hermine I., Dean, Joni, Dedeoglu, Fatma, Feldman, Brian M., Ferguson, Polly I., Goldsmith, Donald P., Gottlieb, Beth S., Graham, Thomas B., Griffin, Thomas A., Haftel, Hilary M., Higgins, Gloria C., Hollister, J.R., Hsu, Joyce J., Huttenlocher, Anna, Ilowite, Norman T., Imundo, Lisa F., Jerath, Rita S., Jung, Lawrence K., Kahn, Philip J., Kingsbury, Daniel J., Klein, Kristin E., Klein-Gitelman, Marisa S., Lapidus, Sivia K., Lehman, Thomas J.A., Lindsley, Carol B., Malloy, Michael A., McCurdy, Deborah K., Muscal, Eyal, Olson, Judyann C., O'Neil, Kathleen M., Onel, Karen, Prahalad, Sampath, Punaro, Marilynn G., Rabinovich, C. Egla, Reed, Ann M., Ringold, Sarah, Riordan, Mary Ellen, Robinson, Angela B., Rothman, Deborah, Ruth, Natasha M., Schikler, Kenneth N., Singer, Nora G., Spalding, Steven, Syed, Reema H., Torok, Kathryn S., Tress, Jenna, Vehe, Richard K., Von Scheven, Emily, Walters, Lydia M., Weiss, Jennifer E., Weiss, Pamela, White, Andrew J., Woo, Jennifer M., Yalcindag, Ali, Zemel, Lawrence S.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.05.2017
Subjects
Online AccessGet full text
ISSN0022-3476
1097-6833
1097-6833
DOI10.1016/j.jpeds.2017.01.046

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Abstract To determine the relationships among race, income, and disease outcomes in children with juvenile dermatomyositis (JDM). Data from 438 subjects with JDM enrolled in the Childhood Arthritis and Rheumatology Research Alliance (CARRA) Legacy Registry were analyzed. Demographic data included age, sex, race, annual family income, and insurance status. Clinical outcomes included muscle strength, presence of rash, calcinosis, weakness, physical function, and quality of life measures. Disease outcomes were compared based on race and income. Minority subjects were significantly more likely to have low annual family income and significantly worse scores on measures of physical function, disease activity, and quality of life measures. Subjects with lower annual family income had worse scores on measures of physical function, disease activity, and quality of life scores, as well as weakness. Black subjects were more likely to have calcinosis. Despite these differences in outcome measures, there were no significant differences among the racial groups in time to diagnosis or duration of disease. Using calcinosis as a marker of disease morbidity, black race, annual family income <$50 000 per year, negative antinuclear antibody, and delay in diagnosis >12 months were associated with calcinosis. Minority race and lower family income are associated with worse morbidity and outcomes in subjects with JDM. Calcinosis was more common in black subjects. Further studies are needed to examine these associations in more detail, to support efforts to address health disparities in subjects with JDM and improve disease outcomes.
AbstractList To determine the relationships among race, income, and disease outcomes in children with juvenile dermatomyositis (JDM). Data from 438 subjects with JDM enrolled in the Childhood Arthritis and Rheumatology Research Alliance (CARRA) Legacy Registry were analyzed. Demographic data included age, sex, race, annual family income, and insurance status. Clinical outcomes included muscle strength, presence of rash, calcinosis, weakness, physical function, and quality of life measures. Disease outcomes were compared based on race and income. Minority subjects were significantly more likely to have low annual family income and significantly worse scores on measures of physical function, disease activity, and quality of life measures. Subjects with lower annual family income had worse scores on measures of physical function, disease activity, and quality of life scores, as well as weakness. Black subjects were more likely to have calcinosis. Despite these differences in outcome measures, there were no significant differences among the racial groups in time to diagnosis or duration of disease. Using calcinosis as a marker of disease morbidity, black race, annual family income <$50 000 per year, negative antinuclear antibody, and delay in diagnosis >12 months were associated with calcinosis. Minority race and lower family income are associated with worse morbidity and outcomes in subjects with JDM. Calcinosis was more common in black subjects. Further studies are needed to examine these associations in more detail, to support efforts to address health disparities in subjects with JDM and improve disease outcomes.
Objective To determine the relationships among race, income, and disease outcomes in children with juvenile dermatomyositis (JDM). Study design Data from 438 subjects with JDM enrolled in the Childhood Arthritis and Rheumatology Research Alliance (CARRA) Legacy Registry were analyzed. Demographic data included age, sex, race, annual family income, and insurance status. Clinical outcomes included muscle strength, presence of rash, calcinosis, weakness, physical function, and quality of life measures. Disease outcomes were compared based on race and income. Results Minority subjects were significantly more likely to have low annual family income and significantly worse scores on measures of physical function, disease activity, and quality of life measures. Subjects with lower annual family income had worse scores on measures of physical function, disease activity, and quality of life scores, as well as weakness. Black subjects were more likely to have calcinosis. Despite these differences in outcome measures, there were no significant differences among the racial groups in time to diagnosis or duration of disease. Using calcinosis as a marker of disease morbidity, black race, annual family income <$50 000 per year, negative antinuclear antibody, and delay in diagnosis >12 months were associated with calcinosis. Conclusion Minority race and lower family income are associated with worse morbidity and outcomes in subjects with JDM. Calcinosis was more common in black subjects. Further studies are needed to examine these associations in more detail, to support efforts to address health disparities in subjects with JDM and improve disease outcomes.
To determine the relationships among race, income, and disease outcomes in children with juvenile dermatomyositis (JDM).OBJECTIVETo determine the relationships among race, income, and disease outcomes in children with juvenile dermatomyositis (JDM).Data from 438 subjects with JDM enrolled in the Childhood Arthritis and Rheumatology Research Alliance (CARRA) Legacy Registry were analyzed. Demographic data included age, sex, race, annual family income, and insurance status. Clinical outcomes included muscle strength, presence of rash, calcinosis, weakness, physical function, and quality of life measures. Disease outcomes were compared based on race and income.STUDY DESIGNData from 438 subjects with JDM enrolled in the Childhood Arthritis and Rheumatology Research Alliance (CARRA) Legacy Registry were analyzed. Demographic data included age, sex, race, annual family income, and insurance status. Clinical outcomes included muscle strength, presence of rash, calcinosis, weakness, physical function, and quality of life measures. Disease outcomes were compared based on race and income.Minority subjects were significantly more likely to have low annual family income and significantly worse scores on measures of physical function, disease activity, and quality of life measures. Subjects with lower annual family income had worse scores on measures of physical function, disease activity, and quality of life scores, as well as weakness. Black subjects were more likely to have calcinosis. Despite these differences in outcome measures, there were no significant differences among the racial groups in time to diagnosis or duration of disease. Using calcinosis as a marker of disease morbidity, black race, annual family income <$50 000 per year, negative antinuclear antibody, and delay in diagnosis >12 months were associated with calcinosis.RESULTSMinority subjects were significantly more likely to have low annual family income and significantly worse scores on measures of physical function, disease activity, and quality of life measures. Subjects with lower annual family income had worse scores on measures of physical function, disease activity, and quality of life scores, as well as weakness. Black subjects were more likely to have calcinosis. Despite these differences in outcome measures, there were no significant differences among the racial groups in time to diagnosis or duration of disease. Using calcinosis as a marker of disease morbidity, black race, annual family income <$50 000 per year, negative antinuclear antibody, and delay in diagnosis >12 months were associated with calcinosis.Minority race and lower family income are associated with worse morbidity and outcomes in subjects with JDM. Calcinosis was more common in black subjects. Further studies are needed to examine these associations in more detail, to support efforts to address health disparities in subjects with JDM and improve disease outcomes.CONCLUSIONMinority race and lower family income are associated with worse morbidity and outcomes in subjects with JDM. Calcinosis was more common in black subjects. Further studies are needed to examine these associations in more detail, to support efforts to address health disparities in subjects with JDM and improve disease outcomes.
Author Huttenlocher, Anna
Byun Robinson, Angela
Torok, Kathryn S.
Anderson, Eleanor S.
White, Andrew J.
Griffin, Thomas A.
Robinson, Angela B.
Vehe, Richard K.
Prahalad, Sampath
Woo, Jennifer M.
Ferguson, Polly I.
Abramson, Leslie S.
Higgins, Gloria C.
Ruth, Natasha M.
Brunner, Hermine I.
Blier, Peter R.
Jerath, Rita S.
Feldman, Brian M.
Reed, Ann M.
Tress, Jenna
Kahn, Philip J.
Schikler, Kenneth N.
Muscal, Eyal
Kingsbury, Daniel J.
Goldsmith, Donald P.
Phillippi, Kathryn
Walters, Lydia M.
Riordan, Mary Ellen
Graham, Thomas B.
Beukelman, Timothy
Lehman, Thomas J.A.
Olson, Judyann C.
Singer, Nora G.
Gottlieb, Beth S.
Zemel, Lawrence S.
Klein-Gitelman, Marisa S.
Lapidus, Sivia K.
Weiss, Pamela
Malloy, Michael A.
Hoeltzel, Mark
Jung, Lawrence K.
Lindsley, Carol B.
Klein, Kristin E.
McCurdy, Deborah K.
Punaro, Marilynn G.
Rabinovich, C. Egla
Onel, Karen
Ilowite, Norman T.
Hollister, J.R.
Rothman, Deborah
Becker, Mara L.
O'Neil, Kathleen M.
Dean, Joni
Yalcindag, Ali
Weiss, Jennifer E.
Spalding, Steven
Hsu, Joyce J.
Benham, Heather
Kim, Susan
Syed, Reema H
AuthorAffiliation 2 Assistant Professor, Division of Pediatric Rheumatology, C. S. Mott Children’s Hospital, University of Michigan, Ann Arbor, MI
3 Assistant Professor, Division of Pediatric Infectious Diseases and Rheumatology, Rainbow Babies and Children’s Hospital / Case Medical Center, Cleveland, OH
1 Fellow, Division of Pediatric Infectious Diseases and Rheumatology, Rainbow Babies and Children’s Hospital / Case Medical Center, Cleveland, OH
4 Associate Clinical Professor, Division of Rheumatology, University of California at San Francisco, Benioff Children’s Hospital, San Francisco, CA
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/28410093$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Contributor Huttenlocher, Anna
Hollister, J R
Olson, Judyann C
Prahalad, Sampath
Robinson, Angela B
Lindsley, Carol B
O'Neil, Kathleen M
Zemel, Lawrence S
Lapidus, Sivia K
Graham, Thomas B
Syed, Reema H
Abramson, Leslie S
Hsu, Joyce J
Vehe, Richard K
Tress, Jenna
Klein, Kristin E
Lehman, Thomas J A
Schikler, Kenneth N
Gottlieb, Beth S
Muscal, Eyal
Jung, Lawrence K
Goldsmith, Donald P
Brunner, Hermine I
Malloy, Michael A
Imundo, Lisa F
White, Andrew J
Woo, Jennifer M
Riordan, Mary Ellen
Becker, Mara L
Higgins, Gloria C
Beukelman, Timothy
Anderson, Eleanor S
Ferguson, Polly I
Weiss, Pamela
Haftel, Hilary M
Kahn, Philip J
Torok, Kathryn S
Feldman, Brian M
Onel, Karen
Ruth, Natasha M
Rothman, Deborah
Weiss, Jennifer E
Dean, Joni
Singer, Nora G
Yalcindag, Ali
Jerath, Rita S
Klein-Gitelman, Marisa S
Spalding, Steven
Griffin, Thomas A
Reed, Ann M
Benham, Heather
Kingsbury, Daniel J
McCurdy, Deborah K
Walters, Lydia M
Punaro, Marilynn G
Von Scheven, Emily
Dedeoglu, Fatma
Rabinovich, C Egla
Blier, Peter R
Ringold, Sarah
Ilowite, Norman T
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  organization: Permanente Medical Group, Union City, CA
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  organization: Children's Mercy Hospitals and Clinics, Kansas City, MO
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  surname: Benham
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  organization: Texas Scottish Rite Hospital, Dallas, TX
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  organization: University of Alabama-Birmingham, AL
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  organization: American Family Children's Hospital, Madison, WI
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  organization: The Hospital for Sick Children, Toronto, ON
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  organization: University of Iowa Carver College of Medicine, Iowa City, IA
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  organization: St. Christopher's Hospital for Children, Philadelphia, PA
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  organization: Nationwide Children's Hospital, Columbus, OH
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  organization: University of Colorado, Colorado Springs, CO
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  organization: University of Wisconsin School of Medicine, Madison, WI
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  organization: Children's Hospital of Montefiore, Bronx, NY
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  organization: Columbia University Medical Center, New York, NY
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  organization: Children's Hospital of Georgia, Augusta, GA
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  organization: Children's National Medical Center, Washington, DC
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  organization: New York University, New York, NY
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Keywords ACR
JDM
health disparities
calcinosis
CMAS
ANA
MRI
juvenile dermatomyositis
HRQoL
CHAQ
CARRA
EMG
Health-related quality of life
Childhood Health Assessment Questionnaire
Childhood Arthritis and Rheumatology Research Alliance
Magnetic resonance imaging
Electromyography
American College of Rheumatology
Antinuclear antibody
Childhood Myositis Assessment Scale
Language English
License Copyright © 2017 Elsevier Inc. All rights reserved.
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content type line 23
List of members of the CARRA Legacy Registry is available at www.jpeds.com (Appendix)
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Snippet To determine the relationships among race, income, and disease outcomes in children with juvenile dermatomyositis (JDM). Data from 438 subjects with JDM...
Objective To determine the relationships among race, income, and disease outcomes in children with juvenile dermatomyositis (JDM). Study design Data from 438...
To determine the relationships among race, income, and disease outcomes in children with juvenile dermatomyositis (JDM).OBJECTIVETo determine the relationships...
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StartPage 38
SubjectTerms calcinosis
Child
Child, Preschool
Dermatomyositis - complications
Dermatomyositis - epidemiology
Female
health disparities
Humans
Income
JDM
juvenile dermatomyositis
Male
Pediatrics
Racial Groups
Retrospective Studies
Title Race, Income, and Disease Outcomes in Juvenile Dermatomyositis
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https://www.ncbi.nlm.nih.gov/pubmed/28410093
https://www.proquest.com/docview/1888680727
https://pubmed.ncbi.nlm.nih.gov/PMC5410644
Volume 184
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