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 in | American journal of medical genetics. Part A Vol. 128A; no. 3; pp. 285 - 293 |
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Main Authors | , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
30.07.2004
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Subjects | |
Online Access | Get full text |
ISSN | 1552-4825 1552-4833 |
DOI | 10.1002/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. |
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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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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/15216550$$D View this record in MEDLINE/PubMed |
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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. 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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. 2002; 17 2001; 101 1967; 20 2002; 7 1999; 48 2000a; 8 2002; 11 1999; 47 2000b; 9 1999; 142 1992; 327 1995 1996; 120 1992; 31 1992; 12 1993; 104 1955 2003; 12 2002; 25 1993; 39 2001 2000 1982; 42 2001; 9 2000; 30 2002; 22 1994; 11 1997; 16 1982 1991; 303 1985; 10 1991; 302 2001; 357 1968 1983; 67 e_1_2_6_32_1 e_1_2_6_10_1 e_1_2_6_31_1 e_1_2_6_30_1 Godin G (e_1_2_6_8_1) 1985; 10 Stata Corporation (e_1_2_6_34_1) 2001 DeCharms R (e_1_2_6_6_1) 1968 e_1_2_6_36_1 e_1_2_6_14_1 e_1_2_6_35_1 Brown T (e_1_2_6_5_1) 2002; 11 e_1_2_6_11_1 e_1_2_6_12_1 e_1_2_6_33_1 Hunt K (e_1_2_6_13_1) 2000 e_1_2_6_15_1 e_1_2_6_38_1 e_1_2_6_37_1 Lerman C (e_1_2_6_16_1) 1997; 16 e_1_2_6_21_1 Blaxter M (e_1_2_6_2_1) 1982 Malinowski B (e_1_2_6_17_1) 1955 e_1_2_6_20_1 Nelkin D (e_1_2_6_25_1) 1995 Mamotte CDS (e_1_2_6_18_1) 1993; 39 e_1_2_6_9_1 e_1_2_6_4_1 e_1_2_6_7_1 e_1_2_6_24_1 e_1_2_6_3_1 e_1_2_6_23_1 e_1_2_6_22_1 e_1_2_6_29_1 Marteau TM (e_1_2_6_19_1) 1995 e_1_2_6_28_1 e_1_2_6_27_1 e_1_2_6_26_1 |
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. – reference: 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. – volume: 303 start-page: 893 year: 1991 end-page: 896 article-title: Risk of fatal coronary heart disease in familial hypercholesterolaemia. Scientific Steering Committee on behalf of the Simon Broome Register Group publication-title: Br Med J – volume: 120 start-page: 83 year: 1996 end-page: 91 article-title: 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 publication-title: Atherosclerosis – volume: 104 start-page: 1 year: 1993 end-page: 18 article-title: Familial defective apolipoprotein B‐100: A review, including some comparisons with familial hypercholesterolaemia publication-title: Atherosclerosis – volume: 142 start-page: 105 year: 1999 end-page: 112 article-title: Steering committee on behalf of the Simon Broome Register Group. Mortality in treated heterozygous familial hypercholesterolaemia: Implications for clinical management publication-title: Atherosclerosis – start-page: 434 year: 2001 end-page: 455 – year: 1968 – volume: 67 start-page: 361 year: 1983 end-page: 370 article-title: The Hospital Anxiety and Depression Scale publication-title: Acta Psychiatr Scand – volume: 9 start-page: 537 year: 2000b end-page: 548 article-title: The psychological consequences of offering mutation searching in the family for those at risk of hereditary breast and ovarian cancer—A pilot study publication-title: Psycho‐Oncology – volume: 12 start-page: 584 year: 1992 end-page: 592 article-title: Diagnosis of heterozygous familial hypercholesterolaemia. DNA analysis complements clinical examination and analysis of serum lipid levels publication-title: Arterioscler Thromb – year: 2000 – volume: 22 start-page: 200 year: 2002 end-page: 207 article-title: Are biomarkers useful treatment aids for promoting health behavior change? An empirical review publication-title: Am J Prev Med – volume: 39 start-page: 118 year: 1993 end-page: 121 article-title: A robust strategy for screening and confirmation of familial defective apolipoprotein B100 publication-title: Clin Chem – volume: 42 start-page: 5 year: 1982 end-page: 37 article-title: Changing the world and changing the self: A two‐process model of perceived control publication-title: J Pers Soc Psychol – volume: 48 start-page: 1857 year: 1999 end-page: 1860 article-title: Will genetic testing for predisposition for disease result in fatalism? A qualitative study of parents responses to neonatal screening for familial hypercholesterolaemia publication-title: Soc Sci Med – volume: 11 start-page: 446 year: 2002 end-page: 447 article-title: Impact of genetic risk assessment for Alzheimer's disease publication-title: J Genet Counsel – volume: 10 start-page: 141 year: 1985 end-page: 146 article-title: A simple method to assess exercise behavior in the community publication-title: Can J Appl Sport Sci – volume: 101 start-page: 1351 year: 2001 end-page: 1353 article-title: Does genetic testing for obesity influence confidence in the ability to lose weight: A pilot investigation publication-title: J Am Diet Assoc – volume: 7 start-page: 725 year: 2002 end-page: 736 article-title: Impact of genetic risk feedback: Perceived risk and motivation for health protective behaviours publication-title: Psychol Health Med – volume: 16 start-page: 87 year: 1997 end-page: 99 article-title: Incorporating biomarkers of exposure and genetic susceptibility into smoking cessation treatment: Effects of smoking‐related cognitions, emotions, and behavior publication-title: Health Psychol – volume: 357 start-page: 574 issue: 9256 year: 2001 end-page: 575 article-title: Rigorous detection and vigorous treatment of familial hypercholesterolaemia publication-title: Lancet – year: 1982 – volume: 8 start-page: 731 year: 2000a end-page: 738 article-title: The psychological consequences of predictive genetic testing: A systematic review publication-title: Eur J Hum Genet – start-page: 185 year: 1995 end-page: 199 – volume: 30 start-page: 106 year: 2000 end-page: 143 article-title: Prediction and intervention in health related behavior: A meta‐analytic review of protection motivation theory publication-title: J Appl Soc Psychol – volume: 47 start-page: 555 year: 1999 end-page: 567 article-title: Patients' beliefs about prescribed medicines and their role in adherence to treatment in chronic physical illness publication-title: J Psychosom Res – volume: 17 start-page: 1 year: 2002 end-page: 16 article-title: The Revised Illness Perception Questionnaire (IPQ‐R) publication-title: Psychol Health – volume: 31 start-page: 301 year: 1992 end-page: 306 article-title: The development of a six‐item short‐form of the state scale of the Spielberger State‐Trait Anxiety Inventory (STAI) publication-title: Br J Clin Psychol – volume: 20 start-page: 127 year: 1967 end-page: 134 article-title: Explanatory and pragmatic attitudes in therapeutic trials publication-title: J Chronic Dis – volume: 25 start-page: 373 year: 2002 end-page: 394 article-title: Illness causal attributions: An exploratory study of their structure and associations with other illness cognitions and perceptions of control publication-title: J Behav Med – volume: 11 start-page: 375 year: 1994 end-page: 381 article-title: Dietary intervention in primary care: Validity of the DINE method for dietary assessment publication-title: Fam Pract – year: 1995 – volume: 7 start-page: 157 year: 2002 end-page: 168 article-title: Making sense of risk: An interpretative phenomenological analysis of vulnerability to heart disease publication-title: J Health Psychol – volume: 302 start-page: 1057 year: 1991 end-page: 1060 article-title: Prevalence of risk factors for heart disease in OXCHECK trial: Implications for screening in primary care publication-title: Br Med J – volume: 12 start-page: 227 year: 2003 end-page: 230 article-title: The impact of learning of a genetic vulnerability to nicotine addiction: An analogue study publication-title: Tob Control – year: 1955 – volume: 327 start-page: 1401 year: 1992 end-page: 1405 article-title: The psychological consequences of predictive testing for Huntington's disease publication-title: N Engl J Med – volume: 9 start-page: 244 year: 2001 end-page: 252 article-title: A molecular genetic service for diagnosing individuals with familial hypercholesterolaemia (FH) publication-title: Eur J Hum Genet – 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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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