β-Thalassemia heterozygote state detrimentally affects health expectation.

Abstract:

BACKGROUND:Thalassemia minor (Tm) individuals, are generally considered healthy. However, the prognosis of Tm individuals has not been extensively studied. The aim of this study was to evaluate the prognosis of Tm versus controls without β-thalassemia carrier state. METHODS:A total of 26,006 individuals seeking thalassemia screening at the AOOR Villa Sofia-V. Cervello, Palermo (Italy) were retrospectively studied. Logistic penalised regression model was used to estimate risk of potential complications and survival techniques were used to study mortality. RESULTS:We identified a total of 4943 Tm and 21,063 controls. Tm was associated with significantly higher risks of hospitalisation for cirrhosis (OR 1·94, 95% CI 1·30 to 2·90, p = 0·001), kidney disorders (OR 2·11, 95% CI 1·27 to 3·51, p = 0·004), cholelithiatis (OR 1·39, 95% CI 1·08 to 1·79, p = 0·010), and mood disorders (OR 2·08, 95% CI 1·15 to 3·75, p = 0·015). No statistically difference in life expectancy between thalassemia minor and control group was found (HR 1·090, 95% CI 0·777 to 1·555, p < 0·590; log-rank test p = .426). CONCLUSION:This study shows that Tm affects the prognosis of Tm carriers regarding health expectation. Probably, iron overload and anaemia for several years may be at the basis of these effects.

journal_name

Eur J Intern Med

authors

Graffeo L,Vitrano A,Scondotto S,Dardanoni G,Pollina Addario WS,Giambona A,Sacco M,Di Maggio R,Renda D,Taormina F,Triveri A,Attanasio M,Gluud C,Maggio A

doi

10.1016/j.ejim.2018.06.009

subject

Has Abstract

pub_date

2018-08-01 00:00:00

pages

76-80

eissn

0953-6205

issn

1879-0828

pii

S0953-6205(18)30241-3

journal_volume

54

pub_type

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