Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/54273
Title: Quality of life scores differs between genotypic groups of patients with suspected hereditary hemochromatosis
Authors: Silva Fonseca, Paula Fernanda
Cancado, Rodolfo Delfini
Naoum, Flavio Augusto
Dinardo, Carla Luana
Hencklain Fonseca, Guilherme Henrique
Menosi Gualandro, Sandra Fatima
Krieger, Jose Eduardo
Pereira, Alexandre Costa
Brissot, Pierre
Junior Lima Santos, Paulo Caleb [UNIFESP]
Keywords: Hereditary hemochromatosis
Quality of life
Short form health survey
SF-36
Issue Date: 2018
Publisher: Biomed Central Ltd
Citation: Bmc Medical Genetics. London, v. 19, p. -, 2018.
Abstract: Background: Hereditary hemochromatosis (HH) encompasses a group of autosomal recessive disorders mainly characterized by enhanced intestinal absorption of iron and its accumulation in parenchymal organs. HH diagnosis is based on iron biochemical and magnetic resonance imaging (MRI) assessment, and genetic testing. Questionnaires, such as SF-36 (short form health survey), have been increasingly used to assess the impact of diseases on the patient's quality of life (QL). In addition, different genotypes are identified as results of genetic tests in patients with suspected primary iron overload. In the present study, our aim was to evaluate whether domains of QL are different according to genotypic groups in patients suspected of HH. Methods: Seventy-nine patients with primary iron overload were included and two genotypic groups were formed (group 1: homozygous genotype for the HFE p.Cys282Tyr mutation
group 2: other genotypes). Results: Group 1 had higher means of plasma transferrin saturation (86 +/- 19%) and serum ferritin (1669 +/- 1209 ng/mL) compared to group 2 (71 +/- 12%, 1252 +/- 750 ng/mL, respectively
p = 0.001). Four domains were significantly different among groups 1 and 2: physical functioning (p = 0.03), bodily pain (p = 0.03), vitality (p = 0.02) and social functioning (p = 0.01). Conclusions: Our main finding was that patients with p. Cys282Tyr homozygosity had a worse QL scenario assessed by SF-36, compared with patients with iron overload without the same genotype. Being aware of this relationship between genotypes and QL might be helpful in the overall management of patients suspected of hereditary hemochromatosis.
URI: https://repositorio.unifesp.br/handle/11600/54273
ISSN: 1471-2350
Other Identifiers: http://dx.doi.org/10.1186/s12881-017-0513-5
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