Public Health
Volume 122, Issue 6 , Pages 620-624, June 2008

Thalassaemia screening in a non-prevalent region of a prevalent country (Turkey): is it necessary?

  • H. Acemoglu

      Affiliations

    • Department of Medical Education, Ataturk University School of Medicine, 25240 Erzurum, Turkey
    • Corresponding Author InformationCorresponding author. Tel.: +904422361212; fax: +904422360968.
  • ,
  • N.E. Beyhun

      Affiliations

    • Department of Public Health, Ataturk University School of Medicine, 25240 Erzurum, Turkey
  • ,
  • S. Vancelik

      Affiliations

    • Department of Public Health, Ataturk University School of Medicine, 25240 Erzurum, Turkey
  • ,
  • H. Polat

      Affiliations

    • Erzurum Maternal and Family Planning Centre, 25240 Erzurum, Turkey
  • ,
  • A. Guraksin

      Affiliations

    • Department of Public Health, Ataturk University School of Medicine, 25240 Erzurum, Turkey

Received 28 March 2007; received in revised form 25 July 2007; accepted 20 September 2007.

Summary 

Objectives

Haemoglobinopathies are the most widespread inherited disorders in the world, and are also common in Turkey. Haemoglobinopathies are preventable with control programmes. Therefore, the Ministry of Health initiated a control and prevention programme in 33 provinces in Turkey. The aim of this study was to determine the frequency of haemoglobinopathies in Erzurum as part of the programme mentioned above, and to discuss the need for premarital screening in a non-prevalent region (Erzurum) of a prevalent country (Turkey) as part of a national control programme.

Study design

Epidemiological and descriptive survey.

Methods

This study was conducted between May 2005 and February 2006 in Erzurum. Subjects were couples who attended for premarital screening. All blood samples were measured by high-performance liquid chromatography (HPLC) to determine haemoglobinopathies.

Results

In total, 1610 individuals were screened. The frequency of β-thalassaemia trait was 0.68%. Haemoglobin D was the most common (0.12%) abnormal haemoglobin. Haemoglobins S, C and E were not detected. The frequency of β-thalassaemia trait and other haemoglobinopathies in Erzurum was quite low compared with other provinces in Turkey.

Conclusions

Premarital haemoglobinopathy screening should not be mandatory in a non-prevalent region of a prevalent country as part of a national control programme. If screening is mandatory, it should be performed by total blood count or enzyme-linked immunosorbent assay, which are simple, rapid and less expensive than HPLC.

Keywords: β-Thalassaemia trait, Premarital screening, National policy

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0033-3506(07)00315-0

doi:10.1016/j.puhe.2007.09.007

Public Health
Volume 122, Issue 6 , Pages 620-624, June 2008