Psychological impact of genetic testing for familial hypercholesterolemia within a previously aware population: A randomized controlled trial

This trial tests the hypothesis that confirming a clinical diagnosis of familial hypercholesterolemia (FH) by finding a genetic mutation reduces patients' perceptions of control over the disease and adherence to risk‐reducing behaviors. Three hundred forty‐one families, comprising 341 hyperchol...

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Published inAmerican journal of medical genetics. Part A Vol. 128A; no. 3; pp. 285 - 293
Main Authors Marteau, Theresa, Senior, Victoria, Humphries, Steve E., Bobrow, Martin, Cranston, Treena, Crook, Martin A., Day, Lorna, Fernandez, Maryam, Horne, Rob, Iversen, Andrew, Jackson, Zoe, Lynas, Jacqui, Middleton-Price, Helen, Savine, Richard, Sikorski, Jim, Watson, Melanie, Weinman, John, Wierzbicki, Anthony S., Wray, Richard
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 30.07.2004
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Online AccessGet full text
ISSN1552-4825
1552-4833
DOI10.1002/ajmg.a.30102

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Abstract This trial tests the hypothesis that confirming a clinical diagnosis of familial hypercholesterolemia (FH) by finding a genetic mutation reduces patients' perceptions of control over the disease and adherence to risk‐reducing behaviors. Three hundred forty‐one families, comprising 341 hypercholesterolemia probands and 128 adult relatives, were randomized to one of two groups: (a) routine clinical diagnosis; (b) routine clinical diagnosis plus genetic testing (mutation searching in probands and direct gene testing in relatives). The main outcome measures were perceptions of control over hypercholesterolemia, adherence to cholesterol‐lowering medication, diet, physical activity, and smoking. There was no support for the main hypothesis: finding a mutation had no impact on perceived control or adherence to risk‐reducing behavior (all P‐values > 0.10). While all groups believed that lowering cholesterol was an effective way of reducing the risk of a heart attack, participants in whom a mutation was found believed less strongly in the efficacy of diet in reducing their cholesterol level (P = 0.02 at 6 months) and showed a trend in believing more strongly in the efficacy of cholesterol‐lowering medication (P = 0.06 at 6 months). In conclusion, finding a mutation to confirm a clinical diagnosis of FH in a previously aware population does not reduce perceptions of control or adherence to risk‐reducing behaviors. The pattern of findings leads to the new hypothesis that genetic testing does not affect the extent to which people feel they have control over a condition, but does affect their perceptions of how control is most effectively achieved. Further work is needed to determine whether similar results will be obtained in populations with little previous awareness of their risks. © 2004 Wiley‐Liss, Inc.
AbstractList This trial tests the hypothesis that confirming a clinical diagnosis of familial hypercholesterolemia (FH) by finding a genetic mutation reduces patients' perceptions of control over the disease and adherence to risk-reducing behaviors. Three hundred forty-one families, comprising 341 hypercholesterolemia probands and 128 adult relatives, were randomized to one of two groups: (a) routine clinical diagnosis; (b) routine clinical diagnosis plus genetic testing (mutation searching in probands and direct gene testing in relatives). The main outcome measures were perceptions of control over hypercholesterolemia, adherence to cholesterol-lowering medication, diet, physical activity, and smoking. There was no support for the main hypothesis: finding a mutation had no impact on perceived control or adherence to risk-reducing behavior (all P-values > 0.10). While all groups believed that lowering cholesterol was an effective way of reducing the risk of a heart attack, participants in whom a mutation was found believed less strongly in the efficacy of diet in reducing their cholesterol level (P = 0.02 at 6 months) and showed a trend in believing more strongly in the efficacy of cholesterol-lowering medication (P = 0.06 at 6 months). In conclusion, finding a mutation to confirm a clinical diagnosis of FH in a previously aware population does not reduce perceptions of control or adherence to risk-reducing behaviors. The pattern of findings leads to the new hypothesis that genetic testing does not affect the extent to which people feel they have control over a condition, but does affect their perceptions of how control is most effectively achieved. Further work is needed to determine whether similar results will be obtained in populations with little previous awareness of their risks.
This trial tests the hypothesis that confirming a clinical diagnosis of familial hypercholesterolemia (FH) by finding a genetic mutation reduces patients' perceptions of control over the disease and adherence to risk‐reducing behaviors. Three hundred forty‐one families, comprising 341 hypercholesterolemia probands and 128 adult relatives, were randomized to one of two groups: (a) routine clinical diagnosis; (b) routine clinical diagnosis plus genetic testing (mutation searching in probands and direct gene testing in relatives). The main outcome measures were perceptions of control over hypercholesterolemia, adherence to cholesterol‐lowering medication, diet, physical activity, and smoking. There was no support for the main hypothesis: finding a mutation had no impact on perceived control or adherence to risk‐reducing behavior (all P ‐values > 0.10). While all groups believed that lowering cholesterol was an effective way of reducing the risk of a heart attack, participants in whom a mutation was found believed less strongly in the efficacy of diet in reducing their cholesterol level ( P  = 0.02 at 6 months) and showed a trend in believing more strongly in the efficacy of cholesterol‐lowering medication ( P  = 0.06 at 6 months). In conclusion, finding a mutation to confirm a clinical diagnosis of FH in a previously aware population does not reduce perceptions of control or adherence to risk‐reducing behaviors. The pattern of findings leads to the new hypothesis that genetic testing does not affect the extent to which people feel they have control over a condition, but does affect their perceptions of how control is most effectively achieved. Further work is needed to determine whether similar results will be obtained in populations with little previous awareness of their risks. © 2004 Wiley‐Liss, Inc.
This trial tests the hypothesis that confirming a clinical diagnosis of familial hypercholesterolemia (FH) by finding a genetic mutation reduces patients' perceptions of control over the disease and adherence to risk‐reducing behaviors. Three hundred forty‐one families, comprising 341 hypercholesterolemia probands and 128 adult relatives, were randomized to one of two groups: (a) routine clinical diagnosis; (b) routine clinical diagnosis plus genetic testing (mutation searching in probands and direct gene testing in relatives). The main outcome measures were perceptions of control over hypercholesterolemia, adherence to cholesterol‐lowering medication, diet, physical activity, and smoking. There was no support for the main hypothesis: finding a mutation had no impact on perceived control or adherence to risk‐reducing behavior (all P‐values > 0.10). While all groups believed that lowering cholesterol was an effective way of reducing the risk of a heart attack, participants in whom a mutation was found believed less strongly in the efficacy of diet in reducing their cholesterol level (P = 0.02 at 6 months) and showed a trend in believing more strongly in the efficacy of cholesterol‐lowering medication (P = 0.06 at 6 months). In conclusion, finding a mutation to confirm a clinical diagnosis of FH in a previously aware population does not reduce perceptions of control or adherence to risk‐reducing behaviors. The pattern of findings leads to the new hypothesis that genetic testing does not affect the extent to which people feel they have control over a condition, but does affect their perceptions of how control is most effectively achieved. Further work is needed to determine whether similar results will be obtained in populations with little previous awareness of their risks. © 2004 Wiley‐Liss, Inc.
Author Watson, Melanie
Jackson, Zoe
Senior, Victoria
Wray, Richard
Sikorski, Jim
Savine, Richard
Cranston, Treena
Crook, Martin A.
Weinman, John
Horne, Rob
Wierzbicki, Anthony S.
Fernandez, Maryam
Iversen, Andrew
Lynas, Jacqui
Humphries, Steve E.
Day, Lorna
Middleton-Price, Helen
Marteau, Theresa
Bobrow, Martin
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  organization: Centre for Health Care Research, University of Brighton, Brighton, United Kingdom
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  organization: Department of Chemical Pathology, Royal Sussex County Hospital, Brighton, United Kingdom
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  fullname: Wray, Richard
  organization: Cardiology Department, The Conquest Hospital, East Sussex, United Kingdom
BackLink https://www.ncbi.nlm.nih.gov/pubmed/15216550$$D View this record in MEDLINE/PubMed
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The Wellcome Trust - No. 037006
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PublicationTitle American journal of medical genetics. Part A
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References Myant NB. 1993. Familial defective apolipoprotein B-100: A review, including some comparisons with familial hypercholesterolaemia. Atherosclerosis 104: 1-18.
Godin G, Shephard RJ. 1985. A simple method to assess exercise behavior in the community. Can J Appl Sport Sci 10: 141-146.
Milne S, Sheeran P, Orbell S. 2000. Prediction and intervention in health related behavior: A meta-analytic review of protection motivation theory. J Appl Soc Psychol 30: 106-143.
Nelkin D, Lindee MS. 1995. The DNA mystique. New York: WH Freeman & Company.
Blaxter M, Paterson E. 1982. Mothers and daughters: A three generational study of health attitudes and behaviour. London: Heinemann Education Books.
Durrington PN. 2001. Rigorous detection and vigorous treatment of familial hypercholesterolaemia. Lancet 357(9256): 574-575.
Ward AJ, O'Kane M, Nicholls DP, Young IS, Nevin N, Graham CA. 1996. A novel single base deletion in the LDLR gene (211 del G). Effect on serum lipid profiles and the influence of other genetic polymorphisms in the ACE, APOE and APOB genes. Atherosclerosis 120: 83-91.
Zigmond AS, Snaith RP. 1983. The Hospital Anxiety and Depression Scale. Acta Psychiatr Scand 67: 361-370.
Wright AJ, Weinman J, Marteau TM. 2003. The impact of learning of a genetic vulnerability to nicotine addiction: An analogue study. Tob Control 12: 227-230.
Hicken B, Tucker D. 2002. Impact of genetic risk feedback: Perceived risk and motivation for health protective behaviours. Psychol Health Med 7: 725-736.
Simon Broome Steering Committee. 1999. Steering committee on behalf of the Simon Broome Register Group. Mortality in treated heterozygous familial hypercholesterolaemia: Implications for clinical management. Atherosclerosis 142: 105-112.
Stata Corporation. 2001. Stata release 7. Vol. 4. Su-Z. College Station, Texas: Stata Press. p 434-455.
Senior V, Marteau TM, Peters TJ. 1999. 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 48: 1857-1860.
Marteau TM, Bekker H. 1992. The development of a six-item short-form of the state scale of the Spielberger State-Trait Anxiety Inventory (STAI). Br J Clin Psychol 31: 301-306.
Lerman C, Gold K, Boyd NR, Orleans CT, Wilfond B, Louben G, Caporaso N. 1997. Incorporating biomarkers of exposure and genetic susceptibility into smoking cessation treatment: Effects of smoking-related cognitions, emotions, and behavior. Health Psychol 16: 87-99.
Malinowski B. 1955. Magic, science, and religion. New York: Anchor Books.
Broadstock M, Michie S, Marteau T. 2000a. The psychological consequences of predictive genetic testing: A systematic review. Eur J Hum Genet 8: 731-738.
Roe L, Strong C, Whiteside C, Neil A, Mant D. 1994. Dietary intervention in primary care: Validity of the DINE method for dietary assessment. Fam Pract 11: 375-381.
DeCharms R. 1968. Personal causation. New York: Academic Press.
Broadstock M, Michie S, Gray J, Mackay J, Marteau TM. 2000b. The psychological consequences of offering mutation searching in the family for those at risk of hereditary breast and ovarian cancer-A pilot study. Psycho-Oncology 9: 537-548.
Wiggins S, Whyte P, Huggins M, Adam S, Theilmann J, Bloch M, Sheps SB, Schechter MT, Hayden MR. 1992. The psychological consequences of predictive testing for Huntington's disease. N Engl J Med 327: 1401-1405.
Koivisto PVI, Koivisto U-M, Miettinen TA, Kontula K. 1992. Diagnosis of heterozygous familial hypercholesterolaemia. DNA analysis complements clinical examination and analysis of serum lipid levels. Arterioscler Thromb 12: 584-592.
Rothbaum F, Weisz JR, Snyder SS. 1982. Changing the world and changing the self: A two-process model of perceived control. J Pers Soc Psychol 42: 5-37.
McClure JB. 2002. Are biomarkers useful treatment aids for promoting health behavior change? An empirical review. Am J Prev Med 22: 200-207.
Moss Morris R, Weinman J, Petrie KJ, Horne R, Cameron LD, Buick D. 2002. The Revised Illness Perception Questionnaire (IPQ-R). Psychol Health 17: 1-16.
Simon Broome Steering Committee. 1991. Risk of fatal coronary heart disease in familial hypercholesterolaemia. Scientific Steering Committee on behalf of the Simon Broome Register Group. Br Med J 303: 893-896.
Horne R, Weinman J. 1999. Patients' beliefs about prescribed medicines and their role in adherence to treatment in chronic physical illness. J Psychosom Res 47: 555-567.
Heath KE, Humphries SE, Middleton-Price H, Boxer M. 2001. A molecular genetic service for diagnosing individuals with familial hypercholesterolaemia (FH). Eur J Hum Genet 9: 244-252.
Imperial Cancer Research Fund OXCHECK Study Group. 1991. Prevalence of risk factors for heart disease in OXCHECK trial: Implications for screening in primary care. Br Med J 302: 1057-1060.
Brown T, Roberts S, LaRusse S, Barber M, Relkin N, Whitehouse P, Post S, Sadovnick AD, Quaid K, Ravdin L, Green R. 2002. Impact of genetic risk assessment for Alzheimer's disease. J Genet Counsel 11: 446-447.
Harvey-Berino JE, Casey Gold E, Smith West D, Shuldiner AR, Walston J, Starling RD, Nolan A, Silver K, Poehlman ET. 2001. Does genetic testing for obesity influence confidence in the ability to lose weight: A pilot investigation. J Am Diet Assoc 101: 1351-1353.
Schwartz D, Lellouch J. 1967. Explanatory and pragmatic attitudes in therapeutic trials. J Chronic Dis 20: 127-134.
Shiloh S, Rashuk-Rosenthal D, Benyamini Y. 2002. Illness causal attributions: An exploratory study of their structure and associations with other illness cognitions and perceptions of control. J Behav Med 25: 373-394.
Mamotte CDS, van Bockxmeer FM. 1993. A robust strategy for screening and confirmation of familial defective apolipoprotein B100. Clin Chem 39: 118-121.
Senior V, Smith JA, Michie S, Marteau TM. 2002. Making sense of risk: An interpretative phenomenological analysis of vulnerability to heart disease. J Health Psychol 7: 157-168.
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References_xml – reference: Schwartz D, Lellouch J. 1967. Explanatory and pragmatic attitudes in therapeutic trials. J Chronic Dis 20: 127-134.
– reference: Ward AJ, O'Kane M, Nicholls DP, Young IS, Nevin N, Graham CA. 1996. A novel single base deletion in the LDLR gene (211 del G). Effect on serum lipid profiles and the influence of other genetic polymorphisms in the ACE, APOE and APOB genes. Atherosclerosis 120: 83-91.
– reference: Senior V, Smith JA, Michie S, Marteau TM. 2002. Making sense of risk: An interpretative phenomenological analysis of vulnerability to heart disease. J Health Psychol 7: 157-168.
– reference: Zigmond AS, Snaith RP. 1983. The Hospital Anxiety and Depression Scale. Acta Psychiatr Scand 67: 361-370.
– reference: Imperial Cancer Research Fund OXCHECK Study Group. 1991. Prevalence of risk factors for heart disease in OXCHECK trial: Implications for screening in primary care. Br Med J 302: 1057-1060.
– reference: Mamotte CDS, van Bockxmeer FM. 1993. A robust strategy for screening and confirmation of familial defective apolipoprotein B100. Clin Chem 39: 118-121.
– reference: Marteau TM, Bekker H. 1992. The development of a six-item short-form of the state scale of the Spielberger State-Trait Anxiety Inventory (STAI). Br J Clin Psychol 31: 301-306.
– reference: Godin G, Shephard RJ. 1985. A simple method to assess exercise behavior in the community. Can J Appl Sport Sci 10: 141-146.
– reference: McClure JB. 2002. Are biomarkers useful treatment aids for promoting health behavior change? An empirical review. Am J Prev Med 22: 200-207.
– reference: Rothbaum F, Weisz JR, Snyder SS. 1982. Changing the world and changing the self: A two-process model of perceived control. J Pers Soc Psychol 42: 5-37.
– reference: Simon Broome Steering Committee. 1991. Risk of fatal coronary heart disease in familial hypercholesterolaemia. Scientific Steering Committee on behalf of the Simon Broome Register Group. Br Med J 303: 893-896.
– reference: Blaxter M, Paterson E. 1982. Mothers and daughters: A three generational study of health attitudes and behaviour. London: Heinemann Education Books.
– reference: DeCharms R. 1968. Personal causation. New York: Academic Press.
– reference: Horne R, Weinman J. 1999. Patients' beliefs about prescribed medicines and their role in adherence to treatment in chronic physical illness. J Psychosom Res 47: 555-567.
– reference: Malinowski B. 1955. Magic, science, and religion. New York: Anchor Books.
– reference: Milne S, Sheeran P, Orbell S. 2000. Prediction and intervention in health related behavior: A meta-analytic review of protection motivation theory. J Appl Soc Psychol 30: 106-143.
– reference: Durrington PN. 2001. Rigorous detection and vigorous treatment of familial hypercholesterolaemia. Lancet 357(9256): 574-575.
– reference: Harvey-Berino JE, Casey Gold E, Smith West D, Shuldiner AR, Walston J, Starling RD, Nolan A, Silver K, Poehlman ET. 2001. Does genetic testing for obesity influence confidence in the ability to lose weight: A pilot investigation. J Am Diet Assoc 101: 1351-1353.
– reference: Broadstock M, Michie S, Marteau T. 2000a. The psychological consequences of predictive genetic testing: A systematic review. Eur J Hum Genet 8: 731-738.
– reference: Simon Broome Steering Committee. 1999. Steering committee on behalf of the Simon Broome Register Group. Mortality in treated heterozygous familial hypercholesterolaemia: Implications for clinical management. Atherosclerosis 142: 105-112.
– reference: Wiggins S, Whyte P, Huggins M, Adam S, Theilmann J, Bloch M, Sheps SB, Schechter MT, Hayden MR. 1992. The psychological consequences of predictive testing for Huntington's disease. N Engl J Med 327: 1401-1405.
– reference: Brown T, Roberts S, LaRusse S, Barber M, Relkin N, Whitehouse P, Post S, Sadovnick AD, Quaid K, Ravdin L, Green R. 2002. Impact of genetic risk assessment for Alzheimer's disease. J Genet Counsel 11: 446-447.
– reference: Stata Corporation. 2001. Stata release 7. Vol. 4. Su-Z. College Station, Texas: Stata Press. p 434-455.
– reference: Wright AJ, Weinman J, Marteau TM. 2003. The impact of learning of a genetic vulnerability to nicotine addiction: An analogue study. Tob Control 12: 227-230.
– reference: Myant NB. 1993. Familial defective apolipoprotein B-100: A review, including some comparisons with familial hypercholesterolaemia. Atherosclerosis 104: 1-18.
– reference: Senior V, Marteau TM, Peters TJ. 1999. 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 48: 1857-1860.
– reference: Broadstock M, Michie S, Gray J, Mackay J, Marteau TM. 2000b. The psychological consequences of offering mutation searching in the family for those at risk of hereditary breast and ovarian cancer-A pilot study. Psycho-Oncology 9: 537-548.
– reference: Hicken B, Tucker D. 2002. Impact of genetic risk feedback: Perceived risk and motivation for health protective behaviours. Psychol Health Med 7: 725-736.
– reference: Koivisto PVI, Koivisto U-M, Miettinen TA, Kontula K. 1992. Diagnosis of heterozygous familial hypercholesterolaemia. DNA analysis complements clinical examination and analysis of serum lipid levels. Arterioscler Thromb 12: 584-592.
– reference: Lerman C, Gold K, Boyd NR, Orleans CT, Wilfond B, Louben G, Caporaso N. 1997. Incorporating biomarkers of exposure and genetic susceptibility into smoking cessation treatment: Effects of smoking-related cognitions, emotions, and behavior. Health Psychol 16: 87-99.
– reference: Nelkin D, Lindee MS. 1995. The DNA mystique. New York: WH Freeman & Company.
– reference: Moss Morris R, Weinman J, Petrie KJ, Horne R, Cameron LD, Buick D. 2002. The Revised Illness Perception Questionnaire (IPQ-R). Psychol Health 17: 1-16.
– reference: Heath KE, Humphries SE, Middleton-Price H, Boxer M. 2001. A molecular genetic service for diagnosing individuals with familial hypercholesterolaemia (FH). Eur J Hum Genet 9: 244-252.
– reference: Roe L, Strong C, Whiteside C, Neil A, Mant D. 1994. Dietary intervention in primary care: Validity of the DINE method for dietary assessment. Fam Pract 11: 375-381.
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Snippet This trial tests the hypothesis that confirming a clinical diagnosis of familial hypercholesterolemia (FH) by finding a genetic mutation reduces patients'...
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SubjectTerms Adult
Aged
Awareness
Emotions
familial hypercholesterolemia
Female
genetic testing
Genetic Testing - psychology
health behavior
Humans
Hyperlipoproteinemia Type II - diagnosis
Hyperlipoproteinemia Type II - psychology
illness perceptions
Male
Middle Aged
Mutation - genetics
perceived control
psychological consequences
Title Psychological impact of genetic testing for familial hypercholesterolemia within a previously aware population: A randomized controlled trial
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https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fajmg.a.30102
https://www.ncbi.nlm.nih.gov/pubmed/15216550
https://www.proquest.com/docview/66645005
Volume 128A
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