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Acromegaly and pituitary gigantism

DOID EFO MESH SNOMED Endpoint Browser PheWeb

E4_ACROMEG

hyperpituitarism: Disease of the glandular, anterior portion of the pituitary (pituitary gland, anterior) resulting in hypersecretion of adenohypophyseal hormones such as growth hormone; prolactin; thyrotropin; luteinizing hormone; follicle stimulating hormone ; and adrenocorticotropic hormone. Hyperpituitarism usually is caused by a functional adenoma.

Endpoint definition

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FinnGen phenotype data

429209 individuals

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Apply sex-specific rule None

429209

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Check conditions None

429209

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Check pre-conditions, main-only, mode, registry filters

Hospital Discharge: ICD-10 E22.0
Hospital discharge: ICD-9 2530
Hospital discharge: ICD-8 2530
Hospital discharge: excluded ICD-8 25301
Cause of death: ICD-10 E22.0
Cause of death: ICD-9 2530
Cause of death: ICD-8 2530
Cause of death: excluded ICD-8 25301

2 out of 7 registries used, show all original rules.

201

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Check minimum number of events None

201

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Include endpoints None

201

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Remove individuals based on genotype QC

195

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E4_ACROMEG

Control definitions

Control exclude E4_ENDOGLAND

Extra metadata

Level in the ICD hierarchy 4
First used in FinnGen datafreeze DF2
Parent code in ICD-10 E22
Name in latin Acromegalia

Summary Statistics

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Key figures

All Female Male
Number of individuals 195 124 71
Unadjusted prevalence (%) 0.05 0.05 0.04
Mean age at first event (years) 45.80 44.34 48.36

Mortality

Follow-up Absolute risk HR [95% CI] p N
1998–2019 - - - -
15 years - - - -
5 years - - - -
1 year - - - -

Age distribution of first events

Year distribution of first events

Cumulative Incidence

Correlations

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Index endpoint: E4_ACROMEG – Acromegaly and pituitary gigantism
GWS hits:

Survival analyses between endpoints

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Plot

before Acromegaly and pituitary gigantism
after Acromegaly and pituitary gigantism

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Drugs most likely to be purchased after Acromegaly and pituitary gigantism

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Endpoint not on priority list, no data to show.