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Published on: September 6, 2017
Ethnicity study and non-selective screening for haemoglobinopathies in the antenatal population of central Manchester
M Kadkhodaei Elyaderani1, K I Cinkotai, K Hyde
1University Department of Clinical Haematology, Manchester Royal Infirmary, UK.
Insights
Non-selective screening for haemoglobinopathies is recommended for pregnant individuals in Manchester. This ensures equitable access to care, particularly for ethnic minority groups with higher carrier frequencies.
Area of Science:
- Medical Genetics
- Public Health
- Obstetrics
Background:
- Haemoglobinopathies are inherited blood disorders.
- Accurate ethnic data is crucial for targeted antenatal screening services.
- Manchester has a diverse population requiring tailored healthcare approaches.
Purpose of the Study:
- To determine the ethnic distribution of the antenatal population in central Manchester.
- To assess the effectiveness of current haemoglobinopathy screening in reaching at-risk groups.
- To inform service provision for antenatal haemoglobinopathy screening.
Main Methods:
- Analysis of ethnic data from 6718 antenatal patients over 7 months.
- Screening of 1144 patients for haemoglobinopathies over 1 month.
- Calculation of carrier frequencies across different ethnic groups.
Main Results:
- The antenatal population comprised 62.3% White, 13.2% Asian, 7.9% Black, and 3.8% other ethnic groups.
- Overall haemoglobinopathy incidence was 2.62% in the screened subset.
- Highest carrier frequencies were observed in the Black (18.2%) and 'no information' (5.6%) groups.
Conclusions:
- A significant proportion of the antenatal population belongs to ethnic minority groups.
- The high incidence of haemoglobinopathies in certain ethnic groups and the 'no information' category supports universal screening.
- Non-selective screening is recommended for all pregnant individuals in central Manchester to ensure equitable care.
Abstract:
The objective of this study was to determine the frequency of ethnic groups within the antenatal population in central Manchester and thereby ensure that the haemoglobinopathy service was targeting the correct population and their needs. Ethnic data collection records of 6718 patients were analysed over a 7 month period. Of these 62.3% stated that they were White, 13.2% Asian, 7.9% Black, 3.8% Chinese or 'other ethnic groups' and 12.7% gave no information about their ethnic background. A subset of 1144 patients were screened for haemoglobinopathies over a 1 month period. The incidence of haemoglobinopathies within the screened population was 2.62%, and comprised 0.69% beta thalassaemia trait, 1.22% sickle cell trait, 0.43% haemoglobin C trait and 0.26% haemoglobin D trait. The total incidence of haemoglobinopathies was highest within the Black population (18.2%), followed by the no information group (5.6%), Asian (3.35%) and white (0.26%). The high proportion of ethnic minorities and the significant carrier frequency in the no information group, support our view that non-selective screening should be offered to the antenatal population of central Manchester.
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