Evidence map›Paper›PMID 39489760›Full record

ArticleScientific reports2024

Dyslipidemia in Juvenile Dermatomyositis.

Amer Khojah, Gabrielle Morgan, Arya Kadakia, Marisa S Klein-Gitelman, Lauren M Pachman

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Amer KhojahDepartment of Pediatrics, College of Medicine, Umm Al-Qura University, Makkah, Saudi Arabia.
Gabrielle MorganDivision of Rheumatology, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.
Arya KadakiaDivision of Rheumatology, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.
Marisa S Klein-GitelmanNorthwestern University Feinberg School of Medicine, Chicago, IL, USA.
Lauren M PachmanNorthwestern University Feinberg School of Medicine, Chicago, IL, USA. Pachman.lab@gmail.com.

Funding

Mitochondrial calcification in juvenile dermatomyositisR21AR077565 · NIAMS · UNIVERSITY OF WASHINGTON · PI LOOD, JAN CHRISTIAN · 2020 to 2021
$432k
NIAMS NIH HHS R21 AR077565NIH HHS AR077565
6 · The paper itself

Abstract

This study investigates the prevalence of dyslipidemia and its association with disease activity in children with Juvenile Dermatomyositis (JDM). A retrospective chart review of 142 JDM patients who had fasting lipid profiles was conducted. Clinical, and laboratory indicators of disease activity at the time of lipid assessment were obtained. JDM patients displayed a high prevalence (72%) of abnormal or borderline fasting lipid profiles, particularly involving HDL and triglycerides. Treatment-naïve patients exhibited the most significant dyslipidemia, with significantly lower median HDL levels compared to those on medication (30 vs. 49 mg/dL, p < 0.0001). HDL levels inversely correlated with various disease activity measures, including disease activity score (DAS) total (r= -0.38, p < 0.001), DAS muscle weakness (r= -0.5, p < 0.001), DAS skin (r= -0.25, p = 0.003), neopterin (r= -0.41, p < 0.001), ESR (r= -0.25, p = 0.006), and vWF Ag (r= -0.21, p = 0.02). In conclusion, JDM patients have a high prevalence of dyslipidemia, especially low HDL and elevated triglycerides. The severity of dyslipidemia (low HDL) correlates with disease activity, with treatment-naïve patients demonstrating the lowest HDL levels. These findings suggest the importance of annual lipid profile monitoring in JDM patients, potentially followed by early interventions such as dietary adjustments and exercise programs.

Indexed as

DermatomyositisDyslipidemiasAdolescentChildChild, PreschoolFemaleHumansLipidsMalePrevalenceRetrospective StudiesSeverity of Illness IndexTriglyceridesLipidsTriglyceridesDisease Activity scoresDyslipidemiaHDLJuvenile DermatomyositisNeopterin

Identifiers

PMID39489760
PMCPMC11532421

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.