Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function

D3_CVID_BCELL

obsolete_common variable immunodeficiency: ['A hypogammaglobulinemia that is results in insufficient production of antibodies needed to respond to exposure of pathogens and is characterized by low Ig levels with phenotypically normal B cells that can proliferate but do not develop into Ig-producing cells. Patients with common variable immunodeficiency have marked reduction in serum levels of both immunoglobulin G (IgG) and immunoglobulin A (IgA); about half of these patients also have reduced immunoglobulin M (IgM).', 'A primary immunodeficiency characterized by low levels or absence of all the immunoglobulin classes and lack of B-lymphocytes or plasma cells. It results in recurrent bacterial infections. Complications include autoimmune phenomena and cancer development.', 'Heterogeneous group of immunodeficiency syndromes characterized by hypogammaglobulinemia of most isotypes, variable B-cell defects, and the presence of recurrent bacterial infections.']

Endpoint definition

FinnGen phenotype data

392423 individuals

diagram downward connector

Apply sex-specific rule None

392423

diagram downward connector

Check conditions None

392423

diagram downward connector
diagram bullet

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

Hospital Discharge: ICD-10 D83.0
Cause of death: ICD-10 D83.0

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

71

diagram downward connector

Check minimum number of events None

71

diagram downward connector

Include endpoints None

71

diagram downward connector
diagram bullet diagram downward connector

Remove individuals based on genotype QC

69

diagram downward connector
D3_CVID_BCELL

Control definitions

Control exclude D3_IMMUNEMECHANISM

Extra metadata

Level in the ICD hierarchy 4
First used in FinnGen datafreeze DF2
Parent code in ICD-10 D83
Name in latin Deficientia immunalis variabilis communis praecipue cum abnormalitatibus numeri et functionis cellularum B

Similar endpoints

List of similar endpoints to Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function based on the number of shared cases.

Venn diagram with an highlighted set fully inside another set Broader endpoints:

Venn diagram with a set fully inside an highlighted set Narrower endpoints:

None

Show all endpoint correlations

Summary Statistics

Key figures

All Female Male
Number of individuals 69 42 27
Unadjusted prevalence (%) 0.02 0.02 0.02
Mean age at first event (years) 46.49 46.45 46.54

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

Index endpoint: D3_CVID_BCELL – Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
GWS hits:

Survival analyses between endpoints

Plot

before Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
after Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function

Endpoint not on priority list, no data to show.