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Physical Growth Dynamics of Children With Juvenile Dermatomyositis
Krishna Soni1, Harvinder Kaur1, Anju Gupta1
1Pediatrics, Postgraduate Institute of Medical Education and Research, Chandigarh, IND.
Insights
Juvenile dermatomyositis (JDMS) can impact adolescent growth, with boys showing compromised physical development compared to girls. Disease activity significantly affects JDMS boys
Area of Science:
- Pediatric Endocrinology
- Rheumatology
- Growth and Development
Background:
- Juvenile dermatomyositis (JDMS) is an autoimmune disease that can lead to growth failure in adolescents.
- Auxological status, including height and weight, is crucial for monitoring the long-term health of JDMS patients.
Purpose of the Study:
- To analyze the auxological status of adolescent patients diagnosed with juvenile dermatomyositis.
- To investigate the relationship between disease activity and physical growth in JDMS patients.
Main Methods:
- A mixed-longitudinal growth study design was employed.
- Sixty serial observations of height, weight, and skinfold thicknesses were collected from 35 JDMS children (aged 10-17).
- Disease duration and activity (MMT-8 score) were recorded for correlation analysis.
Main Results:
- JDMS patients exhibited regular increases in height and weight, but BMI showed an undulating pattern.
- JDMS boys were taller, weighed less, and had less subcutaneous fat than JDMS girls.
- Compared to healthy peers, JDMS children were shorter and lighter, though girls showed catch-up growth after age 12-14.
Conclusions:
- JDMS boys demonstrated compromised growth, potentially linked to disease activity.
- JDMS girls exhibited a better auxological prognosis beyond ages 12-13, suggesting protective mechanisms against adverse disease effects.
Abstract:
Objective Growth failure is an often overlooked complication of juvenile dermatomyositis (JDMS) hence, the present study analyses the auxological status of adolescent JDMS patients. Methods Sixty serial observations with respect to height, weight, and skinfold thicknesses were made on 35 JDMS children aged 10 to 17 years in the Growth Laboratory/Clinic of the Department following a mixed-longitudinal growth research design. Information with regard to disease duration and disease activity (MMT-8 score) was recorded. Results The mean height and weight of JDMS patients showed a regular increase from 10 to 17 years while BMI depicted an undulating pattern. JDMS boys were taller yet weighed lighter and had lesser sub-cutaneous fat deposition than girls. As compared to their normal counterparts, JDMS children were lighter and shorter, however, JDMS girls caught up and became heavier and taller beyond 12 and 14 years, respectively. Only 4 (6.6%) and 5 (8.33%) of our study subjects were short-statured and underweight, respectively. Disease activity had a significant positive correlation with the physical growth of JDMS boys. Conclusion JDMS boys depicted compromised growth when contrasted with their unaffected counterparts; this may be due to the influence of disease activity on their physical growth. However, better auxological prognosis recorded for JDMS girls beyond 12-13 years reveals that there must be some protective mechanism favoring girls making them resistant to adverse effects of the disease.
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