Volume 17, Issue 8 (August 2019)                   IJRM 2019, 17(8): 543-550 | Back to browse issues page


XML Persian Abstract Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Hashemi-Soteh M B, Vali Nejad A, Ataei G, Tafazoli A, Ghasemi D, Siamy R. Knowledge and attitude toward genetic diseases and genetic tests among pre-marriage individuals: A cross-sectional study in northern Iran . IJRM 2019; 17 (8) :543-550
URL: http://ijrm.ir/article-1-1615-en.html
1- 1. Immunogenetic Research Center, Molecular and Cell Biology Research Center, Medical Faculty, Mazandaran University of Medical Sciences, Sari, Mazandaran, Iran
2- Ghaemshahr Health Center, Mazandaran University of Medical Sciences, Mazandaran, Iran.
3- Department of Medical Physics, Faculty of Paramedicine, Babol University of Medical Sciences, Babol, Iran
4- Department of Biochemistry, Biophysics and Genetics, School of Medicine, Mazandaran University of Medical Sciences, Mazandaran, Iran.
5- Department of Biostatistics, Faculty of Healthcare Sciences, Mazandaran University of Medical Sciences, Mazandaran, Iran.
Abstract:   (2934 Views)
Background: Genetic testing has been widely introduced for many hereditary disorders. While the attitudes towards these facilities have been evaluated in many countries, there are only a few reports on the knowledge of and the orientation among Iranians.
Objective: The current study assesses the attitudes and knowledge of pre-marriage individuals toward the availability and use of genetic tests.
Materials and Methods: A comprehensive questionnaire was distributed among 408 marrying individuals. The questions addressed the demographic characteristics along the registration of participant's knowledge, education, and attitude toward genetic testing. The individuals were divided into three groups based on their knowledge: 1) Scored above 80 to 100 were defined as "good" 2) 60 to 80 as "average" 3) less than 60 as "poor" knowledge.
Result: Most participants (86%) believed consanguineous marriages increase the risk of genetic diseases; 82.3% knew that thalassemia is a type of genetic disease, only 33.3% could distinguish prenatal diagnosis (PND) from other laboratory tests. The relationship between the participants' knowledge and their level of education was significant (r= 0.78, p< 0.001), age (r= -0.16, p< 0.01), and urbanity (p< 0.01). A prominent relationship was observed between the knowledge (r= 0.64, p< 0.001) or education (r= 0.62, p< 0.001) and people’s desire to use the genetic tests before the wedding ceremony. No significant correlations were found between the participant’s attitude and their ages/urbanity. Most of the individuals agreed to arrange a genetic counseling before marriage (0.94%).

Conclusion: This study revealed that most individuals were interested in using genetic counseling services and genetic tests before marriage.
 
 
Full-Text [PDF 469 kb]   (890 Downloads) |   |   Full-Text (HTML)  (445 Views)  
Type of Study: Original Article |

References
1. Swanson A, Ramos E, Snyder H. Next generation sequencing is the impetus for the next generation of laboratory-based genetic counselors. J Genet Couns 2014; 23: 647-654. [DOI:10.1007/s10897-013-9684-1]
2. Henneman L, Timmermans DR, Van Der Wal G. Public attitudes toward genetic testing: perceived benefits and objections. Genet Test 2006; 10: 139-145. [DOI:10.1089/gte.2006.10.139]
3. Senior V, Marteau TM, Peters TJ. Will genetic testing for predisposition for disease result in fatalism? A qualitative study of parents responses to neonatal screening for familial hypercholesterolaemia. Soc Sci Med 1999; 48: 1857-1860. [DOI:10.1016/S0277-9536(99)00099-4]
4. Lesko LJ, Schmidt S. Clinical implementation of genetic testing in medicine: a US regulatory science perspective. Br J Clin Pharmacol 2014; 77: 606-611. [DOI:10.1111/bcp.12299]
5. Aro AR, Hakonen A, Hietala M, Lonnqvist J, Niemela P, Peltonen L, et al. Acceptance of genetic testing in a general population: age, education and gender differences. Patient Educ Couns 1997; 32: 41-49. [DOI:10.1016/S0738-3991(97)00061-X]
6. Levitt DM. Let the consumer decide? The regulation of commercial genetic testing. J Med Ethics 2001; 27: 398-403. [DOI:10.1136/jme.27.6.398]
7. Gaskell G, Bauer MW, Durant J, Allum NC. Worlds apart? The reception of genetically modified foods in Europe and the U.S. Science 1999; 285: 384-387. [DOI:10.1126/science.285.5426.384]
8. Gaskell G, Allum N, Bauer M, Durant J, Allansdottir A, Bonfadelli H, et al. Biotechnology and the European public. Nat Bbiotechnol 2000; 18: 935-938. [DOI:10.1038/79403]
9. Etchegary H. Public attitudes toward genetic risk testing and its role in healthcare. Per Med 2014; 11: 509-522. [DOI:10.2217/pme.14.35]
10. Haga SB, Barry WT, Mills R, Ginsburg GS, Svetkey L, Sullivan J, et al. Public knowledge of and attitudes toward genetics and genetic testing. Genet Test Mol Biomarkers 2013; 17: 327-335. [DOI:10.1089/gtmb.2012.0350]
11. Henneman L, Vermeulen E, van El CG, Claassen L, Timmermans DR, Cornel MC. Public attitudes towards genetic testing revisited: comparing opinions between 2002 and 2010. Eur J Hum Genet 2013; 21: 793-799. [DOI:10.1038/ejhg.2012.271]
12. Mokhtari R, Bagga A. Consanguinity, genetic disorders and malformations in the Iranian population. Acta Biologica Szegediensis 2003; 47: 47-50.
13. Najmabadi H, Karimi-Nejad R, Sahebjam S, Pourfarzad F, Teimourian S, Sahebjam F, et al. The beta-thalassemia mutation spectrum in the Iranian population. Hemoglobin 2001; 25: 285-296. [DOI:10.1081/HEM-100105221]
14. Hosseini SH, Gaffari Saravi W, Hashemi Soteh SMB, Zarghami M, Saljughian A. Evaluation of co-segregation between bipolar mood disorder and heterozygous beta thalassemia in patients originated from Iran. Res J Biol Sci 2008; 3: 798-800.
15. Najmabadi H, Ghamari A, Sahebjam F, Kariminejad R, Hadavi V, Khatibi T, et al. Fourteen-year experience of prenatal diagnosis of thalassemia in Iran. Community Genet 2006; 9: 93-97. [DOI:10.1159/000091486]
16. Abolghasemi H, Amid A, Zeinali S, Radfar MH, Eshghi P, Rahiminejad MS, et al. Thalassemia in Iran: epidemiology, prevention, and management. J Pediatr Hematol Oncol 2007; 29: 233-238. [DOI:10.1097/MPH.0b013e3180437e02]
17. Ihaka R, Gentleman R. R: A Language for data analysis and graphics. Journal of Computational and Graphical Statistics 1996; 5: 299-314 [DOI:10.1080/10618600.1996.10474713]
18. Walter H, Farhud DD, Danker-Hopfe H, Amirshahi P. Investigations on the ethnic variability of the ABO blood group polymorphism in Iran. Z Morphol Anthropol 1991; 78: 289-306.
19. Grugni V, Battaglia V, Hooshiar Kashani B, Parolo S, Al-Zahery N, Achilli A, et al. Ancient migratory events in the Middle East: new clues from the Y-chromosome variation of modern Iranians. PLoS One 2012; 7: e41252. [DOI:10.1371/journal.pone.0041252]
20. Saadat M, Ansari-Lari M, Farhud DD. Consanguineous marriage in Iran. Ann Hum Biol 2004; 31: 263-269. [DOI:10.1080/03014460310001652211]
21. Samavat A, Modell B. Iranian national thalassaemia screening programme. BMJ 2004; 329: 1134-1137. [DOI:10.1136/bmj.329.7475.1134]
22. Khorasani G, Kosaryan M, Vahidshahi K, Shakeri S, Nasehi MM. Results of the national program for prevention of beta-thalassemia major in the Iranian Province of Mazandaran. Hemoglobin 2008; 32: 263-271. [DOI:10.1080/03630260802004269]
23. Olwi D, Merdad L, Ramadan E. Knowledge of Genetics and Attitudes toward Genetic Testing among College Students in Saudi Arabia. Public Health Genomics 2016; 19: 260-268. [DOI:10.1159/000446511]
24. Jallinoja P, Hakonen A, Aro AR, Niemela P, Hietala M, Lonnqvist J, et al. Attitudes towards genetic testing: analysis of contradictions. Soc Sci Med 1998; 46: 1367-1374. [DOI:10.1016/S0277-9536(98)00017-3]
25. Roberts CD, Stough LD, Parrish LH. The role of genetic counseling in the elective termination of pregnancies involving fetuses with disabilities. J Spec Educ 2002; 36: 48-55. [DOI:10.1177/00224669020360010501]
26. Oliveri S, Masiero M, Arnaboldi P, Cutica I, Fioretti C, Pravettoni G. Health orientation, knowledge, and attitudes toward genetic testing and personalized genomic services: preliminary data from an italian sample. Biomed Res Int 2016; 2016: 6824581. [DOI:10.1155/2016/6824581]
27. Karimi M, Bonyadi M, Galehdari Mr, Zareifar S. Termination of pregnancy due to Thalassemia major, Hemophilia, and Down's syndrome: the views of Iranian physicians. BMC Med Ethics 2008; 9: 19. [DOI:10.1186/1472-6939-9-19]
28. Bryant LD, Green JM, Hewison J. Prenatal screening for down's syndrome: some psychosocial implications of a 'screening for all' policy. Public Health 2001; 115: 356-358. [DOI:10.1016/S0033-3506(01)00475-9]

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Designed & Developed by : Yektaweb