Dermatopolymyositis (FG)

juvenile dermatomyositis: Juvenile dermatomyositis (JDM) is the early-onset form of dermatomyositis (DM, see this term), a systemic, autoimmune inflammatory muscle disorder, characterized by proximal muscle weakness, evocative skin lesion, and systemic manifestations.

Endpoint definition

FinnGen phenotype data

Filter registries None

Check pre-conditions None

Check conditions None

Apply sex-specific rule None

diagram downward connector DERMATOPOLY_FG

Extra metadata

First used in FinnGen datafreeze DF2

Summary Statistics

Key figures

All Female Male
Number of individuals 252 166 86
Unadjusted prevalence (%) 0.10 0.11 0.08
Mean age at first event (years) 52.31 51.60 53.68

Mortality

Follow-up Absolute risk HR [95% CI] p N
1998–2019 0.05 3.46 [1.90, 6.31] 5.0e-5 44
15 years 0.02 3.67 [2.03, 6.65] 1.7e-5 37
5 years 0.01 5.65 [3.14, 10.19] 8.3e-9 17
1 year - - - -

Correlations

Index endpoint: DERMATOPOLY_FG – Dermatopolymyositis (FG)
GWS hits: 0

Survival analyses between endpoints

Plot

before Dermatopolymyositis (FG)
after Dermatopolymyositis (FG)

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Dermatopolymyositis (FG)