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Abstract Number: 414

Performance of the Adult Systemic Sclerosis Classification in Juvenile Systemic Sclerosis Patients. Results from the Juvenile Systemic Sclerosis Inception Cohorte Www.Juvenile-Scleroderma.Com

Ivan Foeldvari1, Jens Klotsche2, Valda Stanevicha3, Ekaterina Alexeeva4, Maria M. Katsicas5, Maria Teresa Terreri6, Ana Paula Sakamoto7, Rolando Cimaz8, Mikhail Kostik9, Tadey Avcin10, Maria Jose Santos11, Monika Moll12, Dana Nemkova13, Flavio Sztajnbok14, Cristina Battagliotti15, Juergen Brunner16, Despina Eleftheriou17, Alberto Sifuentes Giraldo18, Liora Harel19, Mahesh Janarthanan20, Tilmann Kallinich21, Kirsten Minden22, Susan Mary Nielsen23, Kathryn S. Torok24, Yosef Uziel25 and Nicola Helmus26, 1Hamburger Zentrum für Kinder-und Jugendrheumatologie, Hamburg, Germany, 2Epidemiology unit, German Rheumatism Research Center, Berlin, Germany, 3University Childrens Hospital, Riga, Latvia, 4Rheumatology, Scientific Center of Children's Health, Moscow, Russia, 5Hospital de Pediatria, Buenos Aires, Argentina, 6Pediatrics, Universidade Federal de Sao Paulo, São Paulo, Brazil, 7Assistant doctor, Pediatric Rheumatology Unit, Universidade Federal de São Paulo, São Paulo, Brazil, 8Pediatric Rheumatology, Anna Meyer Children's Hospital, Florence, Italy, 9State Pediatric Medical University, Saint-Petersburg, Russia, 10University Children's Hospital, Ljubljana, Slovenia, 11Rheumatology, Hospital Garcia de Orta, Almada, Portugal, 12Pediatric Rheumatology, University Childrenhospital, Tübingen, Germany, 13Pediatric Rheumatology Unit, Department of Pediatrics and Adolescent Medicine, General University Hospital in Prague, Prague, Czech Republic, 14Pediatric Rheumatology Division, Adolescent Health Care Unit, Universida de do Estado do Rio de Janeiro., Rio de Janeiro, Brazil, 15Hospital de Niños Dr Orlando Alasia, Santa Fé, Argentina, 16Universitätsklinik für Kinder- u. Jugendheilkunde, Innsbruck, Austria, 17Paediatric Rheumatology Department, Great Ormond Street Hospital for Children NHS Trust, London, United Kingdom, 18Department of Rheumatology, University Hospital Ramón y Cajal, Madrid, Spain, 19Pediatric Rheumatology Unit, Schneider Children's Medical Center,Tel Aviv University, Petach Tikvah, Israel, 20Pediatric Rheumatology, Chennai, India, 21Charite, University Medicine Berlin, Berlin, Germany, 22Epidemiology, Charite, DRFZ, Berlin, Germany, 23Rigshospitalet, Copenhagen, Denmark, 24Pediatric Rheumatology, Scleroderma Center of Pittsburgh, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, 25Meir Medical Center, Kfar Saba, Israel, 26Hamburg Centre for Pediatric and Adolescent Rheumatology, Hamburg, Germany

Meeting: 2015 ACR/ARHP Annual Meeting

Date of first publication: September 29, 2015

Keywords: Systemic sclerosis

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Session Information

Date: Sunday, November 8, 2015

Title: Pediatric Rheumatology – Clinical and Therapeutic Aspects Poster I: Lupus, Scleroderma, JDMS

Session Type: ACR Poster Session A

Session Time: 9:00AM-11:00AM

Background/Purpose:

The new adult classifiction criteria (1) for Systemic Sclerosis (SSc) were recently published and the pediatric criteria were published in 2007 (2). None of these criteria were validated in a pediatric cohort of patients.

Methods:

We validated the adult SSc criteria in the juvenile SSc inception cohort stratified by the disease duration of the patients. We performed a latent class analysis on the adult SSc criteria for investigating the pattern of presentation of juvenile patients adjusted for disease duration.

Results:

All pediatric patients in the cohort fulfilled the adult classification criteria of proximal skin sclerosis from MCP joint. It is the main criteria of the pediatric classification system and it already gives sufficient points to be classified as SSc. Raynauds’ phenomena (73%) and nail fold changes (57%) were the most common items fulfilled by the juveniles. The pediatric patients had a mean score of 15.3 at <6 months (n=16), 15.5 at <12 months (n=31), 16.5 at < 24 months (n=62) and 17.1 at  <48 months (n=86). The latent class analysis on the adult SSc criteria resulted in 3 groups of juvenile SSc patients (table 1). All patients in the first severely affected group had proximal skin sclerosis, fingertip pitting scars, nail fold changes and raynauds’ phenomena. In the mild third group (n=33), the item skin sclerosis was most important, the other criteria played a minor role in that group.

Table 1. Results of the latent class analysis on the adult SSc criteria in the inception cohort of juvenile systemic sclerosis.

 

 

 

 

 

 

 

Class I

Class II

Class III

n=16

n=37

n=33

 

%

%

%

Proximal skin sclerosis

100.0

100.0

100.0

Puffy Fingers

0.0

0.0

0.0

Sclerodactyly

100.0

100.0

100.0

Digital tip ulcers

81.3

0.0

0.0

Fingertip pitting scars

100.0

44.4

36.4

Telangiectasia

0.0

0.0

0.0

Nailfold changes

100.0

78.4

12.1

PH

12.5

13.5

0.0

ISL

81.3

29.7

39.4

Raynauds

100.0

94.6

36.4

SSc AB

18.8

74.3

3.2

Conclusion:

All pediatric patients fulfilled the adult classification criteria. The cumulative score increased continuously with an increasing disease duration. The latent class analysis revealed 3 groups of jSSc patients regarding the performance of adult SSc criteria. An adaption of jSSc criteria, that patients without skin involvement can be included, would be important, to increase the number of patients with early diagnosis.

References

1.         van den Hoogen F, Khanna D, Fransen J, Johnson SR, Baron M, Tyndall A, et al. 2013 classification criteria for systemic sclerosis: an American college of rheumatology/European league against rheumatism collaborative initiative. Ann Rheum Dis. 2013;72(11):1747-55.

2.         Zulian F, Woo P, Athreya BH, Laxer RM, Medsger TA, Jr., Lehman TJ, et al. The Pediatric Rheumatology European Society/American College of Rheumatology/European League against Rheumatism provisional classification criteria for juvenile systemic sclerosis. Arthritis Rheum. 2007;57(2):203-12.


Disclosure: I. Foeldvari, None; J. Klotsche, None; V. Stanevicha, None; E. Alexeeva, None; M. M. Katsicas, None; M. T. Terreri, None; A. P. Sakamoto, None; R. Cimaz, None; M. Kostik, None; T. Avcin, None; M. J. Santos, None; M. Moll, None; D. Nemkova, None; F. Sztajnbok, None; C. Battagliotti, None; J. Brunner, None; D. Eleftheriou, None; A. Sifuentes Giraldo, None; L. Harel, None; M. Janarthanan, None; T. Kallinich, None; K. Minden, None; S. M. Nielsen, None; K. S. Torok, None; Y. Uziel, None; N. Helmus, None.

To cite this abstract in AMA style:

Foeldvari I, Klotsche J, Stanevicha V, Alexeeva E, Katsicas MM, Terreri MT, Sakamoto AP, Cimaz R, Kostik M, Avcin T, Santos MJ, Moll M, Nemkova D, Sztajnbok F, Battagliotti C, Brunner J, Eleftheriou D, Sifuentes Giraldo A, Harel L, Janarthanan M, Kallinich T, Minden K, Nielsen SM, Torok KS, Uziel Y, Helmus N. Performance of the Adult Systemic Sclerosis Classification in Juvenile Systemic Sclerosis Patients. Results from the Juvenile Systemic Sclerosis Inception Cohorte Www.Juvenile-Scleroderma.Com [abstract]. Arthritis Rheumatol. 2015; 67 (suppl 10). https://acrabstracts.org/abstract/performance-of-the-adult-systemic-sclerosis-classification-in-juvenile-systemic-sclerosis-patients-results-from-the-juvenile-systemic-sclerosis-inception-cohorte-www-juvenile-scleroderma-com/. Accessed .
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