A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä

The rare disease neurofibromatosis 1 as a source of hereditary economic inequality: evidence from Finland




TekijätJohansson Edvard, Kallionpää Roope A, Böckerman Petri, Peltonen Sirkku, Peltonen Juha

KustantajaElsevier

Julkaisuvuosi2022

JournalGenetics in Medicine

Vuosikerta24

Numero4

Aloitussivu870

Lopetussivu879

eISSN1530-0366

DOIhttps://doi.org/10.1016/j.gim.2021.11.024

Verkko-osoitehttps://doi.org/10.1016/j.gim.2021.11.024


Tiivistelmä

Purpose

This study investigated whether individuals with neurofibromatosis 1 (NF1) fare worse than individuals without NF1 in terms of economic well-being. NF1 is relatively common in the population and provides an informative case of a rare hereditary disease.

Methods

We examined a subset of 692 individuals with verified NF1 from the Finnish total population-based NF1 cohort and compared that with 7407 control individuals matched for age, sex, and municipality during 1997-2014. Economic well-being was operationalized with annual work earnings and total income, including social income transfers.

Results

NF1 significantly worsened economic well-being. Low education, increased morbidity, and reduced labor market participation partly explained the effect of NF1. Yet, NF1 was independently associated with lower income even after adjusting for these factors. Furthermore, NF1 had a larger negative effect on income from work than it had on total income, which indicated that the Finnish social security system partly compensated the labor market losses suffered by individuals with NF1. NF1 had a larger impact on economic inequality for men than for women.

Conclusion

NF1 contributes to economic inequality. A hereditary disease may convey worse economic well-being over several generations.



Last updated on 2024-26-11 at 17:32