ABSTRACT
INTRODUCTION: The life expectancy of ß-thalassemia patients has increased over the last 20 years. In this study, we evaluated the current health status and quality of life of these patients managed in a reference center in Marseille. METHODS: This is a single-center, descriptive study conducted between June and August 2019 in patients over 18 years of age with ß-thalassemia major or intermedia. Clinical and paraclinical data were collected retrospectively and the SF-36 health survey questionnaire was proposed to each patient. RESULTS: 43 of 64 selected patients were included and divided into 2 groups: 35 patients with transfusion-dependent ß-thalassemia and 8 patients with non-transfusion-dependent ß-thalassemia. Liver iron overload is the most frequent complication, present in 80% of transfusion-dependent and 62.5% of non-transfusion-dependent patients. Cardiac iron overload is present only in the transfusion dependent ß-thalassemia group (20%). Hypogonadotropic hypogonadism remains the most common endocrine disorder (41.9%) followed by osteoporosis (37.2%). Among the 31 patients who completed the SF-36 questionnaire, physical and mental quality of life scores were lowered in transfusion dependent (respectively 42.7 and 46.8) as in non-transfusion-dependent patients (respectively 43.8 and 28.9). CONCLUSION: Despite an improvement in medical care, our patients with ß-thalassemia show an alteration in their quality of life that will need to be characterized in the entire French cohort.
Subject(s)
Health Status , Quality of Life , beta-Thalassemia , Humans , beta-Thalassemia/therapy , beta-Thalassemia/epidemiology , beta-Thalassemia/complications , beta-Thalassemia/psychology , France/epidemiology , Male , Female , Adult , Retrospective Studies , Young Adult , Middle Aged , Blood Transfusion/statistics & numerical data , Iron Overload/epidemiology , Iron Overload/etiology , Surveys and Questionnaires , AdolescentSubject(s)
Codon/genetics , DNA Helicases/chemistry , DNA Helicases/genetics , Mental Retardation, X-Linked/genetics , Mutation/genetics , Nuclear Proteins/chemistry , Nuclear Proteins/genetics , alpha-Thalassemia/genetics , Amino Acid Sequence , Animals , Base Sequence , Family , Humans , Molecular Sequence Data , Phenotype , Protein Structure, Tertiary , Sequence Alignment , X-linked Nuclear ProteinABSTRACT
To evaluate the analytical performance of a new capillary electrophoresis instrument, the Capillarys 2 Flex piercing (Sebia, France), allowing the separation and quantitative estimation of the different haemoglobin fractions from whole blood, in capped primary tube.The analytical precision for the determination of HbA2 and HbF percentages was satisfactory and within the range of previously published results for HPLC methods. The correlation between Capillarys 2 Flex Piercing and Bio-Rad Variant II HPLC system showed a linear correlation for HbA2, HbF and HbS measurements, and the analysis interpretation was the same whatever the method used. Conversely to HPLC method, the capillary's electrophoresis technology allowed HbE and Hb Lepore fraction separation from HbA2. We showed that the Capillarys 2 Flex Piercing is suitable for haemoglobinopathies diagnosis and screening and offers an excellent alternative to HPLC techniques as a first-line method or for confirmatory analysis.
