Evidence map›Paper›PMID 39695766›Full record

ArticleHuman genomics2024

Nationwide survey on awareness of consanguinity and genetic diseases in Saudi Arabia: challenges and potential solutions to reduce the national healthcare burden.

Nura A Yousef, Ashraf A ElHarouni, Noor Ahmad Shaik, Babajan Banaganapalli, Asayil Faisal Al Ghamdi, Amani H Galal, Turki Saad Alahmadi, Taghreed Shuaib, Deema Aljeaid, Dalal S Alshaer and 2 more

Abstract read
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Article in Human genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

19 citing papers in PubMed.

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  7. Journal of the Endocrine Society · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Nura A YousefGenetic Medicine Department, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Ashraf A ElHarouniGenetic Medicine Department, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Noor Ahmad ShaikGenetic Medicine Department, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Babajan BanaganapalliGenetic Medicine Department, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Asayil Faisal Al GhamdiBiology Department, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.
Amani H GalalOphthalmogenetics Department, Research Institute of Ophthalmology, Cairo, Egypt.
Turki Saad AlahmadiPediatrics Department, King Abdulaziz University, Jeddah, Saudi Arabia.
Taghreed ShuaibPrincess Al-Jawhara Centre of Excellence in Research of Hereditary Disorders (PACER-HD), Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Deema AljeaidGenetic Medicine Department, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Dalal S AlshaerGenetic Medicine Department, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Mahmoud AlmutadaresGenetic Medicine Department, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia. malmutadares@kau.edu.sa.
Ramu ElangoGenetic Medicine Department, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia. relango305@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundConsanguineous marriage is a major contributing factor for many genetic diseases and a burden to the healthcare system and national economy due to costly long-term care. Earlier studies highlighted the significantly limited awareness of the higher prevalence of genetic disease due to consanguinity even among the educated Arabs. In Saudi Arabia, more than 50% of marriages are between first cousins. This national study aims to gauge the level of the public awareness regarding the consanguinity and its impact on prevalence of genetic diseases across the Saudi Arabia.

methodsA cross-sectional bilingual online survey was conducted across Saudi Arabia, distributed through a variety of social media platforms for all residents. Pooled summary data was used from the participants.

resultsMajority of the 9191 participants are < 30 years of age (72.85%), single (61.35%), women (74.12%) and college educated (77.16%). Consanguineous marriages are common in the extended family of 61.24% of participants. Though majority of them (85.45%) recognise the higher genetic disease risk associated with consanguinity, low awareness among men was observed (76.61 vs 88.53%). Sickle cell anaemia and thalassemia were not considered as genetic diseases by 60.68% of males and 48.39% of females, though they are the most common genetic diseases in Saudi Arabia. More women are aware of the carrier screening tests than men (42.62 vs 34.56%). Only 6.87% know the rationale behind the national mandatory premarital screening tests and the diseases screened. Although almost all (99.18%) are active users of the social media, 47.77% of men and 57.17% of women use them to search for health-related information.

conclusionThe present study, one of the largest national surveys in highly consanguineous society, highlights that even the young and college-educated participants have low awareness of the genetic disease burden, which is strikingly high in all corners of the country. Social media platforms can be used by genetic professionals and national organizations to disseminate the reliable educational material to the public to reduce the national healthcare and economic burden in the future.

Indexed as

ConsanguinityGenetic Diseases, InbornAdolescentAdultCross-Sectional StudiesDelivery of Health CareFemaleHealth Knowledge, Attitudes, PracticeHumansMaleMiddle AgedSaudi ArabiaSurveys and QuestionnairesYoung AdultArabsConsanguinityGenetic diseasesPremarital screeningPublic awarenessSaudi ArabiaSocial media

Identifiers

PMID39695766
PMCPMC11657206

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.