The Changing Epidemiology of β-Thalassemia in the Greek-Cypriot Population. (October 2013)
- Record Type:
- Journal Article
- Title:
- The Changing Epidemiology of β-Thalassemia in the Greek-Cypriot Population. (October 2013)
- Main Title:
- The Changing Epidemiology of β-Thalassemia in the Greek-Cypriot Population
- Authors:
- Kyrri, Andreani R.
Kalogerou, Eleni
Loizidou, Dena
Ioannou, Christina
Makariou, Christina
Kythreotis, Loukas
Phylactides, Marios
Kountouris, Petros
Angastiniotis, Michael
Modell, Bernadette
Kleanthous, Marina - Abstract:
- <abstract> <title> <x xml:space="preserve">Abstract</x> </title> <p>The first epidemiological study for thalassemia in Cyprus was performed by Fawdry in 1946. The study determined that the frequency of β-thalassemia (β-thal) carriers was around 18.0% and that of α<sup>0</sup>-thal carriers (individuals with both <italic>cis</italic> α-globin genes inactive) at around 2.0%. In 1998, another study concluded that Cyprus had one of the highest frequencies of β-thal carriers worldwide (17.2%). Based on Haldane's hypothesis that malaria might be the selective agent responsible for the maintenance of high levels of thalassemia and sickle cell disease in many populations around the world, it is expected that following the eradication of the disease in Cyprus in 1948, the carriers of β-thal should decline with each generation. In order to determine whether this has been the case, we compiled frequency data for β-thal carriers from three separate surveys performed as part of the Cyprus National Thalassaemia Screening Programme (NTSP). The surveys were carried out in 1986, 2003 and 2010 involving 9622, 6711 and 5228 subjects, respectively. The expected drop in the prevalence of β-thal carriers for each successive generation following the eradication of malaria, <italic>i.e., </italic> in the absence of selection pressure, was calculated using the Hardy-Weinberg equation and the mathematical model of Hartl and Clark. The surveys provide supporting evidence for the decrease of the<abstract> <title> <x xml:space="preserve">Abstract</x> </title> <p>The first epidemiological study for thalassemia in Cyprus was performed by Fawdry in 1946. The study determined that the frequency of β-thalassemia (β-thal) carriers was around 18.0% and that of α<sup>0</sup>-thal carriers (individuals with both <italic>cis</italic> α-globin genes inactive) at around 2.0%. In 1998, another study concluded that Cyprus had one of the highest frequencies of β-thal carriers worldwide (17.2%). Based on Haldane's hypothesis that malaria might be the selective agent responsible for the maintenance of high levels of thalassemia and sickle cell disease in many populations around the world, it is expected that following the eradication of the disease in Cyprus in 1948, the carriers of β-thal should decline with each generation. In order to determine whether this has been the case, we compiled frequency data for β-thal carriers from three separate surveys performed as part of the Cyprus National Thalassaemia Screening Programme (NTSP). The surveys were carried out in 1986, 2003 and 2010 involving 9622, 6711 and 5228 subjects, respectively. The expected drop in the prevalence of β-thal carriers for each successive generation following the eradication of malaria, <italic>i.e., </italic> in the absence of selection pressure, was calculated using the Hardy-Weinberg equation and the mathematical model of Hartl and Clark. The surveys provide supporting evidence for the decrease of the frequency of the β-thal carriers in the Greek Cypriot population, with a drop of 1.89% in 24 years.</p> </abstract> … (more)
- Is Part Of:
- Hemoglobin. Volume 37:Number 5(2013)
- Journal:
- Hemoglobin
- Issue:
- Volume 37:Number 5(2013)
- Issue Display:
- Volume 37, Issue 5 (2013)
- Year:
- 2013
- Volume:
- 37
- Issue:
- 5
- Issue Sort Value:
- 2013-0037-0005-0000
- Page Start:
- 435
- Page End:
- 443
- Publication Date:
- 2013-10
- Subjects:
- Hemoglobinopathy -- Periodicals
Hemoglobin -- Periodicals
Hematology -- Periodicals
Thalassemia -- Periodicals
Blood -- Diseases -- Periodicals
612.1111 - Journal URLs:
- http://informahealthcare.com/journal/hem ↗
http://informahealthcare.com ↗ - DOI:
- 10.3109/03630269.2013.801851 ↗
- Languages:
- English
- ISSNs:
- 0363-0269
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4295.040000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3997.xml