Genetic disorder prenatal diagnosis and pregnancy termination practices among high consanguinity population, Saudi Arabia.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
21 11 2019
Historique:
received: 08 01 2019
accepted: 05 11 2019
entrez: 23 11 2019
pubmed: 23 11 2019
medline: 6 11 2020
Statut: epublish

Résumé

The prevalence of consanguineous marriage and genetic disorders are high in Saudi Arabia. There were records on the practices of Saudis toward prenatal diagnosis (PND) and termination of pregnancy (TOP), however the sample sizes are small. This study has targeted the Saudi Arabian community and family history of genetic disorders to determine the practices toward PND and TOP. The cross-sectional survey was conducted among Saudis (n = 2761) to determine their practices toward reproductive-decision making. Regression analysis was conducted to identify the association of the limiting factors, relative merits and family history on the outcomes. Total of 2507 participants returned completed questionnaire. The practice towards PND (68%) were more favorable than TOP (33%). PND was found to be a good opportunity for early diagnosis and gives parent's choice. Education, history with affected baby, prior knowledge and religious belief were significant deciding factors of PND and TOP. Down syndrome (n = 161) and sickle cell anemia (n = 152) were commonly available genetic disorder among participant's family. Respondents with autistic cases in their family have higher acceptance rate for TOP. Non-consanguineous are more willing to consider TOP than consanguineous. Participants with abnormal fetus, aged of > 36 years, married and educated Saudis were more likely consider TOP. Though, religion is the most influencing factor for not accepting TOP, comparatively willingness to PND and TOP have increased recently. Awareness campaigns about PND and TOP may increase the chances of accepting prenatal genetic diagnosis.

Identifiants

pubmed: 31754150
doi: 10.1038/s41598-019-53655-8
pii: 10.1038/s41598-019-53655-8
pmc: PMC6872573
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

17248

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Auteurs

Sayed AbdulAzeez (S)

Department of Genetic Research, Institute for Research and Medical Consultation (IRMC), Imam Abdulrahman Bin Faisal University, Dammam, 31441, Saudi Arabia.

Nourah H Al Qahtani (NH)

Department of Obstetrics and Gynaecology, College of Medicine, Imam Abdulrahman Bin Faisal University, Dammam, 31441, Saudi Arabia.

Noor B Almandil (NB)

Department of Clinical Pharmacy Research, Institute for Research and Medical Consultation (IRMC), Imam Abdulrahman Bin Faisal University, Dammam, 31441, Saudi Arabia.

Amani M Al-Amodi (AM)

Department of Genetic Research, Institute for Research and Medical Consultation (IRMC), Imam Abdulrahman Bin Faisal University, Dammam, 31441, Saudi Arabia.

Sumayh A Aldakeel (SA)

Department of Genetic Research, Institute for Research and Medical Consultation (IRMC), Imam Abdulrahman Bin Faisal University, Dammam, 31441, Saudi Arabia.

Neda Z Ghanem (NZ)

Department of Genetic Research, Institute for Research and Medical Consultation (IRMC), Imam Abdulrahman Bin Faisal University, Dammam, 31441, Saudi Arabia.

Deem N Alkuroud (DN)

Department of Genetic Research, Institute for Research and Medical Consultation (IRMC), Imam Abdulrahman Bin Faisal University, Dammam, 31441, Saudi Arabia.

Ameen AlTurki (A)

Department of Genetic Research, Institute for Research and Medical Consultation (IRMC), Imam Abdulrahman Bin Faisal University, Dammam, 31441, Saudi Arabia.

Quds Abdulhakeem AlQattan (QA)

Department of Genetic Research, Institute for Research and Medical Consultation (IRMC), Imam Abdulrahman Bin Faisal University, Dammam, 31441, Saudi Arabia.

Abdulrahman Alghamdi (A)

Department of Genetic Research, Institute for Research and Medical Consultation (IRMC), Imam Abdulrahman Bin Faisal University, Dammam, 31441, Saudi Arabia.

Norah Fahad Alhur (NF)

Department of Genetic Research, Institute for Research and Medical Consultation (IRMC), Imam Abdulrahman Bin Faisal University, Dammam, 31441, Saudi Arabia.

Hatoon Ahmed Al Taifi (HA)

Department of Obstetrics and Gynaecology, College of Medicine, Imam Abdulrahman Bin Faisal University, Dammam, 31441, Saudi Arabia.

Halah Egal Aljofi (HE)

Department of Environmental Health Research, Institute for Research and Medical Consultation (IRMC), Imam Abdulrahman Bin Faisal University, Dammam, 31441, Saudi Arabia.

B Rabindran Jermy (BR)

Department of Nano Medicine Research, Institute for Research and Medical Consultation (IRMC), Imam Abdulrahman Bin Faisal University, Dammam, 31441, Saudi Arabia.

Vinoth Raman (V)

Deanship of Quality and Academic Accreditation, Imam Abdulrahman Bin Faisal University, Dammam, 31441, Saudi Arabia.

Antonino Giambona (A)

Unit of Hematology for Rare Diseases of the Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Hospital Villa Sofia Cervello, Palermo, 90145, Italy.

Aurelio Maggio (A)

Campus of Haematology Franco and Piera Cutino, AOOR Villa Sofia-V. Cervello, Palermo, 90146, Italy.

J Francis Borgio (JF)

Department of Genetic Research, Institute for Research and Medical Consultation (IRMC), Imam Abdulrahman Bin Faisal University, Dammam, 31441, Saudi Arabia. fbalexander@iau.edu.sa.

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