vasculitis: Vasculitis represents a clinically heterogenous group of diseases of multifactorial etiology characterized by inflammation of either large-sized vessels (large-vessel vasculitis, e.g. Giant-cell arteritis and Takayasu arteritis; see these terms), medium-sized vessels (medium-vessel vasculitis e.g. polyarteritis nodosa and Kawasaki disease; see these terms), or small-sized vessels (small-vessel vasculitis, e.g. granulomatosis with polyangiitis, microscopic polyangiitis, immunoglobulin A vasculitis, and cutaneous leukocytoclastic angiitis; see these terms). Vasculitis occurs at any age, may be acute or chronic, and manifests with general symptoms such as fever, weight loss and fatigue, as well as more specific clinical signs depending on the type of vessels and organs affected. The degree of severity is variable, ranging from life or sight threatening disease (e.g. BehC'et disease, see this term) to relatively minor skin disease.
Endpoint definition
↥
Endpoint definition steps |
FinnGen |
---|---|
Phenotype data |
473681 |
1. Apply sex-specific ruleNone |
473681 |
2. Check conditionsNone |
473681 |
3. Check pre-conditions, main-only, mode, registry filtersNone 0 out of 7 registries used, show all original rules. |
0 |
4. Check minimum number of eventsNone |
0 |
5. Include endpoints |
2047 |
6. Filter based on genotype QC (FinnGen only) |
1995 |
Control definitions (FinnGen only)
Extra metadata
Similar endpoints
↥List of similar endpoints to Other necrotizing vasculopathies (FG) based on the number of shared cases.
Similar with more cases:
- Other necrotizing vasculopathies
- Systemic connective tissue disorders
- Autoimmune diseases related-to ILD
- Finngen Rheumatological endpoints
- Diseases of the musculoskeletal system and connective tissue
Similar with less cases:
Case counts by codes
↥Summary Statistics
↥-FinRegistry-
Key figures
All | Female | Male | |
---|---|---|---|
Number of individuals | |||
Whole population | 13908 | 8486 | 5320 |
Only index persons | 11799 | 7333 | 4466 |
Unadjusted period prevalence (%) | |||
Whole population | 0.21 | 0.24 | 0.15 |
Only index persons | 0.23 | 0.27 | 0.17 |
Median age at first event (years) | |||
Whole population | 68.50 | 69.79 | 66.41 |
Only index persons | 68.01 | 69.21 | 66.04 |
-FinnGen-
Key figures
All | Female | Male | |
---|---|---|---|
Number of individuals | 1995 | 1153 | 842 |
Unadjusted period prevalence (%) | 0.44 | 0.45 | 0.42 |
Median age at first event (years) | 65.32 | 64.88 | 65.92 |
-FinRegistry-
Age distribution of first events
-FinnGen-
Age distribution of first events
-FinRegistry-
Year distribution of first events
-FinnGen-
Year distribution of first events
-FinRegistry-
Cumulative Incidence Function
-FinnGen-
Cumulative Incidence Function
Mortality – FinRegistry
↥Association
Association between endpoint NECROVASC_FG and mortality.
Females
Parameter | HR [95% CI] | p-value |
---|---|---|
NECROVASC_FG | 1.505 [1.37, 1.65] | < 0.001 |
Birth year | 0.996 [0.99, 1.0] | 0.346 |
During the follow-up period (1.1.1998 — 31.12.2019), 2254 out of 6574 females with NECROVASC_FG died.
Males
Parameter | HR [95% CI] | p-value |
---|---|---|
NECROVASC_FG | 1.727 [1.51, 1.97] | < 0.001 |
Birth year | 0.987 [0.98, 1.0] | 0.007 |
During the follow-up period (1.1.1998 — 31.12.2019), 1461 out of 3883 males with NECROVASC_FG died.
Mortality risk
Mortality risk for people of age
years, who have NECROVASC_FG.N-year risk | Females | Males |
---|---|---|
1 | 0.134% | 0.259% |
5 | 0.835% | 1.848% |
10 | 1.974% | 5.055% |
15 | 4.086% | 9.363% |
20 | 7.268% | 15.733% |
Relationships between endpoints
↥Index endpoint: NECROVASC_FG – Other necrotizing vasculopathies (FG)
GWS hits: 1