Essential (haemorrhagic) thrombocythaemia

THROMBOCYTAEMIA

primary myelofibrosis: Myelofibrosis with myeloid metaplasia is a myeloproliferative disease with annual incidence of approximately 1 case per 100,000 individuals and age at diagnosis around 60 (an increased prevalence is noted in Ashkenazi Jews). Clinical manifestations depend on the type of blood cell affected and may include anemia, pallor, splenomegaly, hypermetabolic state, petechiae, ecchymosis, bleeding, lymphadenopathy, hepatomegaly, portal hypertension.

Endpoint definition

FinnGen phenotype data

321302 individuals

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Apply sex-specific rule None

321302

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Check conditions None

321302

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Filter registries

Hospital Discharge: ICD-10 D47.3
Hospital discharge: ICD-9 2387B
Hospital discharge: ICD-8 2872
Cause of death: ICD-10 D47.3
Cause of death: ICD-9 2387B
Cause of death: ICD-8 2872

669

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Check pre-conditions, main-only, mode, ICD version

Look only at ICD versions H.D: 10, 8, 9 ; C.O.D: 10, 8, 9

657

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Check minimum number of events None

657

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Include endpoints None

657

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THROMBOCYTAEMIA

Extra metadata

First used in FinnGen datafreeze DF2, additional

Summary Statistics

Key figures

All Female Male
Number of individuals 640 388 252
Unadjusted prevalence (%) 0.21 0.22 0.19
Mean age at first event (years) 60.51 59.42 62.18

Mortality

Follow-up Absolute risk HR [95% CI] p N
1998–2019 0.05 4.12 [2.54, 6.69] 1.0e-8 80
15 years 0.01 2.07 [1.22, 3.50] 6.7e-3 38
5 years 0.00 3.60 [2.18, 5.96] 6.3e-7 26
1 year 0.00 7.55 [3.79, 15.04] 9.2e-9 11

Age distribution of first events

Year distribution of first events

Cumulative Incidence

Correlations

Index endpoint: THROMBOCYTAEMIA – Essential (haemorrhagic) thrombocythaemia
GWS hits: 5

Survival analyses between endpoints

Plot

before Essential (haemorrhagic) thrombocythaemia
after Essential (haemorrhagic) thrombocythaemia

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Drugs most likely to be purchased after Essential (haemorrhagic) thrombocythaemia