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I. Ajzen (1991)
The theory of planned behaviorOrganizational Behavior and Human Decision Processes, 50
L Henneman, I Bramsen, L Van Kempen (2003)
Offering preconceptional cystic fibrosis carrier couple screening in the absence of established preconceptional care servicesCommunity Genet, 6
J. Bobadilla, M. Macek, J. Fine, P. Farrell (2002)
Cystic fibrosis: A worldwide analysis of CFTR mutations—correlation with incidence data and application to screeningHuman Mutation, 19
Shelli Deskins, Carole Harris, A. Bradlyn, L. Cottrell, Jessica Coffman, Julie Olexa, W. Neal (2006)
Preventive care in Appalachia: use of the theory of planned behavior to identify barriers to participation in cholesterol screenings among West Virginians.The Journal of rural health : official journal of the American Rural Health Association and the National Rural Health Care Association, 22 4
(2001)
Genetic screening for hemoglobinopathies, number 238, July 2000. Committee on GeneticsInt J Gynaecol Obstet, 74
Phillis Lakeman, L. Henneman, P. Bezemer, M. Cornel, L. Kate (2006)
Developing and optimizing a decisional instrument using self-reported ancestry for carrier screening in a multi-ethnic societyGenetics in Medicine, 8
E. Clayton, V. Hannig, Jean Pfotenhauer, R. Parker, P. Campbell, J. Phillips (1996)
Lack of interest by nonpregnant couples in population-based cystic fibrosis carrier screening.American journal of human genetics, 58 3
X. Estivill, C. Bancells, C. Ramos (1997)
Geographic distribution and regional origin of 272 cystic fibrosis mutations in European populationsHuman Mutation, 10
F. Poppelaars, L. Henneman, H. Adèr, M. Cornel, R. Hermens, G. Wal, L. Kate (2004)
How Should Preconceptional Cystic Fibrosis Carrier Screening Be Provided? Opinions of Potential Providers and the Target PopulationPublic Health Genomics, 6
Y. Koga, Atsuko Koga, R. Iwanaga, Y. Akita, Junko Tubone, T. Matsuishi, N. Takane, Yoshihiro Sato, H. Kato (2000)
Single-fiber analysis of mitochondrial A3243G mutation in four different phenotypesActa Neuropathologica, 99
J. Mitchell, Annie Capua, C. Clow, C. Scriver (1996)
Twenty-year outcome analysis of genetic screening programs for Tay-Sachs and beta-thalassemia disease carriers in high schools.American journal of human genetics, 59 4
T. Marteau (2000)
Population screening for cystic fibrosis: a research agenda for the next 10 years.American journal of medical genetics, 93 3
(2001)
ACOG (American College of Obstetricians and Gynecologists) committee opinion. Genetic screening for hemoglobinopathies, number 238, July 2000 (replaces number 168, February 1996). Committee on Genetics.International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics, 74 3
S. Orbell, M. Hagger, V. Brown, J. Tidy (2006)
Comparing two theories of health behavior: a prospective study of noncompletion of treatment following cervical cancer screening.Health psychology : official journal of the Division of Health Psychology, American Psychological Association, 25 5
E. Grasbon-Frodl, S. Kösel, M. Sprinzl, U. Eitzen, P. Mehraein, M. Graeber (1999)
Two novel point mutations of mitochondrial tRNA genes in histologically confirmed Parkinson diseaseNeurogenetics, 2
J. Green, J. Hewison, H. Bekker, L. Bryant, H. Cuckle (2004)
Psychosocial aspects of genetic screening of pregnant women and newborns: a systematic review.Health technology assessment, 8 33
E. Cardaioli, P. Pozzo, G. Gallus, A. Malandrini, S. Gambelli, C. Gaudiano, E. Malfatti, C. Viscomi, E. Zicari, G. Berti, G. Serni, M. Dotti, A. Federico (2007)
A novel heteroplasmic tRNASer(UCN) mtDNA point mutation associated with progressive external ophthalmoplegia and hearing lossNeuromuscular Disorders, 17
C. Gaff, K. Aittomäki, R. Williamson (2001)
Oncology nurse training in cancer geneticsJournal of Medical Genetics, 38
S Ahmed, H Bekker, J Hewison, S Kinsey (2002)
Thalassaemia carrier testing in Pakistani adults: behaviour, knowledge and attitudesCommunity Genet, 5
P. Sheeran, M. Conner, P. Norman (2001)
Can the theory of planned behavior explain patterns of health behavior changeHealth Psychology, 20
S. Aymé (2003)
Population genetic screening programmes: technical, social and ethical issuesEuropean Journal of Human Genetics, 11
S. Loader, P. Caldwell, A. Kozyra, J. Levenkron, C. Boehm, H. Kazazian, P. Rowley (1996)
Cystic fibrosis carrier population screening in the primary care setting.American journal of human genetics, 59 1
Michele Spagnolo, G. Tomelleri, G. Vattemi, M. Filosto, N. Rizzuto, P. Tonin (2001)
A new mutation in the mitochondrial tRNAAla gene in a patient with ophthalmoplegia and dysphagiaNeuromuscular Disorders, 11
R. Andrews, I. Kubacka, P. Chinnery, R. Lightowlers, D. Turnbull, N. Howell (1999)
Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNANature Genetics, 23
Jacklyn Pancrudo, S. Shanske, E. Bonilla, M. Daras, H. Akman, S. Krishna, Elfrida Malkin, S. Dimauro (2007)
Mitochondrial Encephalomyopathy Due to a Novel Mutation in the tRNAGlu of Mitochondrial DNAJournal of Child Neurology, 22
L. Wong, M. Liang, H. Kwon, Ren-kui Bai, O. Alper, A. Gropman (2002)
A cystic fibrosis patient with two novel mutations in mitochondrial DNA: mild disease led to delayed diagnosis of both disorders.American journal of medical genetics, 113 1
FA Poppelaars, L Henneman, HJ Ader (2003)
How should preconceptional cystic fibrosis carrier screening be provided? Opinions of potential providers and the target populationCommunity Genet, 6
E. Dormandy, S. Michie, R. Hooper, T. Marteau (2005)
Low uptake of prenatal screening for Down syndrome in minority ethnic groups and socially deprived groups: a reflection of women's attitudes or a failure to facilitate informed choices?International journal of epidemiology, 34 2
Lei-Shih Chen, P. Goodson (2007)
Factors affecting decisions to accept or decline cystic fibrosis carrier testing/screening: A theory-guided systematic reviewGenetics in Medicine, 9
Y. Kirino, Yu-ichi Goto, Y. Campos, J. Arenas, Tsutomu Suzuki (2005)
Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease.Proceedings of the National Academy of Sciences of the United States of America, 102 20
Shenaz Ahmed, H. Bekker, J. Hewison, S. Kinsey (2002)
Thalassaemia Carrier Testing in Pakistani Adults: Behaviour, Knowledge and AttitudesPublic Health Genomics, 5
R. Giegé, M. Sissler, C. Florentz (1998)
Universal rules and idiosyncratic features in tRNA identity.Nucleic acids research, 26 22
V. Ionasescu, M. Hart, S. Dimauro, C. Moraes (1994)
Clinical and morphologic features of a myopathy associated with a point mutation in the mitochondrial tRNAPro geneNeurology, 44
K Stronks, AC Ravelli, SA Reijneveld (2001)
Immigrants in the Netherlands: equal access for equal needs?J Epidemiol Community Health, 55
E. Cardaioli, P. Pozzo, E. Radi, M. Dotti, A. Federico (2005)
A novel heteroplasmic tRNALeu(CUN) mtDNA point mutation associated with chronic progressive external ophthalmoplegiaBiochemical and Biophysical Research Communications, 327
M. Bugiani, F. Invernizzi, Simona Alberio, Egill Briem, E. Lamantea, F. Carrara, I. Moroni, L. Farina, M. Spada, M. Donati, G. Uziel, M. Zeviani (2004)
Clinical and molecular findings in children with complex I deficiency.Biochimica et biophysica acta, 1659 2-3
L Henneman, I Bramsen, HM Van der Ploeg (2001)
Participation in preconceptional carrier couple screening: characteristics, attitudes, and knowledge of both partnersJ Med Genet, 38
K. Stronks, A. Ravelli, S. Reijneveld (2001)
UvA-DARE ( Digital Academic Repository ) Immigrants in the Netherlands : equal access for equal needs ?
Howard Markel (1992)
The stigma of disease: implications of genetic screening.The American journal of medicine, 93 2
E. Schon, M. Hirano, S. Dimauro (1994)
Mitochondrial encephalomyopathies: Clinical and molecular analysisJournal of Bioenergetics and Biomembranes, 26
Phillis Lakeman, Academisch Proefschrift (2008)
Preconceptional Carrier Couple Screening for Cystic fibrosis and Hemoglobinopathies : An ancestry-based offer in a multi-ethnic society
W. Grody, G. Cutting, K. Klinger, C. Richards, M. Watson, R. Desnick (2001)
Laboratory standards and guidelines for population-based cystic fibrosis carrier screeningGenetics in Medicine, 3
P. Giordano, A. Dihal, C. Harteveld (2005)
Estimating the attitude of immigrants toward primary prevention of the hemoglobinopathiesPrenatal Diagnosis, 25
P. Pozzo, E. Cardaioli, E. Radi, A. Federico (2004)
Sequence analysis of the complete mitochondrial genome in patients with mitochondrial encephaloneuromyopathies lacking the common pathogenic DNA mutations.Biochemical and biophysical research communications, 324 1
J. Newman, J. Sorenson, B. Devellis, B. Cheuvront (2002)
Gender differences in psychosocial reactions to cystic fibrosis carrier testing.American journal of medical genetics, 113 2
M. McQueen (2002)
Some ethical and design challenges of screening programs and screening tests.Clinica chimica acta; international journal of clinical chemistry, 315 1-2
T. Keränen, H. Kuusisto (2006)
NARP syndrome and adult-onset generalised seizures.Epileptic disorders : international epilepsy journal with videotape, 8 3
A. Gason, S. Metcalfe, M. Delatycki, Vicki Petrou, Edith Sheffield, A. Bankier, M. Aitken (2005)
Tay Sachs disease carrier screening in schools: Educational alternatives and cheekbrush samplingGenetics in Medicine, 7
M. Mennie, A. Gilfillan, M. Compton, L. Curtis, D. Brock, W. Liston, I. Pullen, D. Whyte (1985)
Prenatal screening for cystic fibrosisThe Lancet, 340
E. Singer, T. Antonucci, John Hoewyk (2004)
Racial and ethnic variations in knowledge and attitudes about genetic testing.Genetic testing, 8 1
Melanie Honnor, Melanie Honnor, S. Zubrick, S. Zubrick, I. Walpole, C. Bower, C. Bower, J. Goldblatt (2000)
Population screening for cystic fibrosis in Western Australia: community response.American journal of medical genetics, 93 3
Mark Conner, Brian McMillan (2004)
The Theory of Planned Behaviour
S. Seneca, W. Lissens, C. Groote, R. Coster, L. Meirleir (2000)
A novel mitochondrial transfer RNA proline mutationJournal of Inherited Metabolic Disease, 23
X Estivill, C Bancells, C Ramos (1997)
Geographic distribution and regional origin of 272 cystic fibrosis mutations in European populations. The Biomed CF mutation analysis consortiumHum Mutat, 10
L. Henneman, I. Bramsen, L. Kempen, M. Acker, G. Pals, H. Horst, H. Adèr, H. Ploeg, L. Kate (2003)
Offering Preconceptional Cystic Fibrosis Carrier Couple Screening in the Absence of Established Preconceptional Care ServicesPublic Health Genomics, 6
M Angastiniotis, B Modell (1998)
Global epidemiology of hemoglobin disordersAnn NY Acad Sci, 850
Shenaz Ahmed, J. Green, J. Hewison (2006)
Attitudes towards prenatal diagnosis and termination of pregnancy for thalassaemia in pregnant Pakistani women in the North of EnglandPrenatal Diagnosis, 26
P. Chinnery, D. Taylor, Denise Brown, D. Manners, P. Styles, R. Lodi (2000)
Very low levels of the mtDNA A3243G mutation associated with mitochondrial dysfunction in vivoAnnals of Neurology, 47
F. Poppelaars, L. Henneman, H. Adèr, M. Cornel, R. Hermens, G. Wal, L. Kate (2004)
Preconceptional cystic fibrosis carrier screening: attitudes and intentions of the target population.Genetic testing, 8 2
M. Angastiniotis, B. Modell (1998)
Global Epidemiology of Hemoglobin DisordersAnnals of the New York Academy of Sciences, 850
E. Zifa, Stamatina Giannouli, Paschalis Theotokis, C. Stamatis, Z. Mamuris, C. Stathopoulos (2007)
Mitochondrial tRNA Mutations: Clinical and Functional PerturbationsRNA Biology, 4
S. Shiloh, S. Ilan (2005)
To Test or Not To Test? Moderators of the Relationship Between Risk Perceptions and Interest in Predictive Genetic TestingJournal of Behavioral Medicine, 28
E. Tambor, B. Bernhardt, Gary Chase, R. Faden, G. Geller, K. Hofman, N. Holtzman (1994)
Offering cystic fibrosis carrier screening to an HMO population: factors associated with utilization.American journal of human genetics, 55 4
J. Leib, Sarah Gollust, S. Hull, B. Wilfond (2005)
Carrier screening panels for Ashkenazi Jews: Is more better?Genetics in Medicine, 7
D. Weatherall, J. Clegg (2001)
Inherited haemoglobin disorders: an increasing global health problem.Bulletin of the World Health Organization, 79 8
This paper explores determinants of the intention to participate or not and of actual participation in preconceptional ancestry-based carrier couple screening for cystic fibrosis (CF) and haemoglobinopathies (HbPs). In total, 9453 individuals from a multi-ethnic population were invited. Invitees who had a partner and who were planning a pregnancy were the target population (33–36%). Test participation was conditional on survey participation. Those who refrained from test participation were asked to participate in the survey only. The questionnaire was based on the Theory of Planned Behaviour, which explains behaviour through intention. It was completed by 418 survey participants: 171 who intended to participate in the testing, and 247 who refrained from test participation. Both test intenders and offer decliners generally had a positive attitude towards test participation, and perceived high behavioural control. This applied to Western and non-Western survey participants equally. Offer decliners, however, perceived less control in terms of the time and effort needed for participation. Still, 68% of them intended to participate in the future if the screening would be offered routinely. Test intenders more often would draw reproductive consequences from test results, perceived a higher risk of being a carrier, more benefits and less adverse psychological outcomes. Feelings of stigmatisation were not an important issue, but 14% thought that there would be discrimination against carriers: among them more were non-Western survey participants. Preconceptional ancestry-based CF and HbPs carrier screening was evaluated as positive and desirable among Western and non-Western survey participants. The effort and time needed for participation were important reasons for declining participation, which might be overcome by improving access to the screening.
European Journal of Human Genetics – Springer Journals
Published: Feb 18, 2009
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