Hypercholesterolaemia is not associated with early atherosclerotic lesions in primary biliary cirrhosis

Background: Hypercholesterolaemia often occurs in primary biliary cirrhosis (PBC) as a result of chronic cholestasis, but whether these patients are exposed to greater cardiovascular risk is unknown. Aim: To establish whether hypercholesterolaemia is associated with subclinical atherosclerosis in PB...

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Published inGut Vol. 55; no. 12; pp. 1795 - 1800
Main Authors Allocca, M, Crosignani, A, Gritti, A, Ghilardi, G, Gobatti, D, Caruso, D, Zuin, M, Podda, M, Battezzati, P M
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Published London BMJ Publishing Group Ltd and British Society of Gastroenterology 01.12.2006
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Abstract Background: Hypercholesterolaemia often occurs in primary biliary cirrhosis (PBC) as a result of chronic cholestasis, but whether these patients are exposed to greater cardiovascular risk is unknown. Aim: To establish whether hypercholesterolaemia is associated with subclinical atherosclerosis in PBC. Patients: 103 consecutive patients with PBC (37 with total cholesterol ⩾6.21 mmol/l) and 37 controls with hypercholesterolaemia, and 141 matched controls with normocholesterolaemia. Methods: Ultrasound imaging of carotid artery to determine intima–media thickness (IMT) and stenosis. Results: Controls with hypercholesterolaemia had higher IMT and prevalence of carotid stenosis compared with patients with hypercholesterolaemic PBC (mean (SD) 0.850 (0.292) mm v 0.616 (0.137) mm, pc<0.001; 43% v 19%, pc = 0.129) who, in turn, were similar to the 66 patients with normocholesterolaemic PBC (0.600 (0.136) mm; 5%). Compared with subjects with normocholesterolaemia, controls with hypercholesterolaemia, but not patients with hypercholesterolaemic PBC, had an increased risk of raised IMT (odds ratio (OR) 5.4, 95% confidence interval (CI) 2.5 to 11.9, p<0.001; and 0.7, 0.3 to 2.0, p = 0.543) or carotid stenosis (8.2, 3.4 to 20, p<0.001; and 2.5, 0.9 to 6.9, p = 0.075). In PBC, compared with younger patients without hypertension, the risk of increased IMT was OR (CI) 3.1 (0.6 to 17; p = 0.192) in patients with hypertension or old age, but not hypercholesterolaemia, and 4.6 (0.8 to 27; p = 0.096) in patients who also had hypercholesterolaemia. The corresponding figures for risk of stenosis were 3.6 (0.4 to 36; p = 0.277) and 15.8 (1.8 to 141; p = 0.014). Conclusions: Hypercholesterolaemia is not consistently associated with subclinical atherosclerosis in PBC, but should be treated if other risk factors for cardiovascular disease are also present. The search for factors that may protect patients with hypercholesterolaemic PBC against atherosclerosis should be encouraged.
AbstractList Background: Hypercholesterolaemia often occurs in primary biliary cirrhosis (PBC) as a result of chronic cholestasis, but whether these patients are exposed to greater cardiovascular risk is unknown. Aim: To establish whether hypercholesterolaemia is associated with subclinical atherosclerosis in PBC. Patients: 103 consecutive patients with PBC (37 with total cholesterol [= or >, slanted]6.21 mmol/l) and 37 controls with hypercholesterolaemia, and 141 matched controls with normocholesterolaemia. Methods: Ultrasound imaging of carotid artery to determine intima-media thickness (IMT) and stenosis. Results: Controls with hypercholesterolaemia had higher IMT and prevalence of carotid stenosis compared with patients with hypercholesterolaemic PBC (mean (SD) 0.850 (0.292) mm v 0.616 (0.137) mm, pc <0.001; 43% v 19%, pc = 0.129) who, in turn, were similar to the 66 patients with normocholesterolaemic PBC (0.600 (0.136) mm; 5%). Compared with subjects with normocholesterolaemia, controls with hypercholesterolaemia, but not patients with hypercholesterolaemic PBC, had an increased risk of raised IMT (odds ratio (OR) 5.4, 95% confidence interval (CI) 2.5 to 11.9, p<0.001; and 0.7, 0.3 to 2.0, p = 0.543) or carotid stenosis (8.2, 3.4 to 20, p<0.001; and 2.5, 0.9 to 6.9, p = 0.075). In PBC, compared with younger patients without hypertension, the risk of increased IMT was OR (CI) 3.1 (0.6 to 17; p = 0.192) in patients with hypertension or old age, but not hypercholesterolaemia, and 4.6 (0.8 to 27; p = 0.096) in patients who also had hypercholesterolaemia. The corresponding figures for risk of stenosis were 3.6 (0.4 to 36; p = 0.277) and 15.8 (1.8 to 141; p = 0.014). Conclusions: Hypercholesterolaemia is not consistently associated with subclinical atherosclerosis in PBC, but should be treated if other risk factors for cardiovascular disease are also present. The search for factors that may protect patients with hypercholesterolaemic PBC against atherosclerosis should be encouraged.
Hypercholesterolaemia often occurs in primary biliary cirrhosis (PBC) as a result of chronic cholestasis, but whether these patients are exposed to greater cardiovascular risk is unknown. To establish whether hypercholesterolaemia is associated with subclinical atherosclerosis in PBC. 103 consecutive patients with PBC (37 with total cholesterol > or =6.21 mmol/l) and 37 controls with hypercholesterolaemia, and 141 matched controls with normocholesterolaemia. Ultrasound imaging of carotid artery to determine intima-media thickness (IMT) and stenosis. Controls with hypercholesterolaemia had higher IMT and prevalence of carotid stenosis compared with patients with hypercholesterolaemic PBC (mean (SD) 0.850 (0.292) mm v 0.616 (0.137) mm, p(c)<0.001; 43% v 19%, p(c) = 0.129) who, in turn, were similar to the 66 patients with normocholesterolaemic PBC (0.600 (0.136) mm; 5%). Compared with subjects with normocholesterolaemia, controls with hypercholesterolaemia, but not patients with hypercholesterolaemic PBC, had an increased risk of raised IMT (odds ratio (OR) 5.4, 95% confidence interval (CI) 2.5 to 11.9, p<0.001; and 0.7, 0.3 to 2.0, p = 0.543) or carotid stenosis (8.2, 3.4 to 20, p<0.001; and 2.5, 0.9 to 6.9, p = 0.075). In PBC, compared with younger patients without hypertension, the risk of increased IMT was OR (CI) 3.1 (0.6 to 17; p = 0.192) in patients with hypertension or old age, but not hypercholesterolaemia, and 4.6 (0.8 to 27; p = 0.096) in patients who also had hypercholesterolaemia. The corresponding figures for risk of stenosis were 3.6 (0.4 to 36; p = 0.277) and 15.8 (1.8 to 141; p = 0.014). Hypercholesterolaemia is not consistently associated with subclinical atherosclerosis in PBC, but should be treated if other risk factors for cardiovascular disease are also present. The search for factors that may protect patients with hypercholesterolaemic PBC against atherosclerosis should be encouraged.
Background: Hypercholesterolaemia often occurs in primary biliary cirrhosis (PBC) as a result of chronic cholestasis, but whether these patients are exposed to greater cardiovascular risk is unknown. Aim: To establish whether hypercholesterolaemia is associated with subclinical atherosclerosis in PBC. Patients: 103 consecutive patients with PBC (37 with total cholesterol ⩾6.21 mmol/l) and 37 controls with hypercholesterolaemia, and 141 matched controls with normocholesterolaemia. Methods: Ultrasound imaging of carotid artery to determine intima–media thickness (IMT) and stenosis. Results: Controls with hypercholesterolaemia had higher IMT and prevalence of carotid stenosis compared with patients with hypercholesterolaemic PBC (mean (SD) 0.850 (0.292) mm v 0.616 (0.137) mm, pc<0.001; 43% v 19%, pc = 0.129) who, in turn, were similar to the 66 patients with normocholesterolaemic PBC (0.600 (0.136) mm; 5%). Compared with subjects with normocholesterolaemia, controls with hypercholesterolaemia, but not patients with hypercholesterolaemic PBC, had an increased risk of raised IMT (odds ratio (OR) 5.4, 95% confidence interval (CI) 2.5 to 11.9, p<0.001; and 0.7, 0.3 to 2.0, p = 0.543) or carotid stenosis (8.2, 3.4 to 20, p<0.001; and 2.5, 0.9 to 6.9, p = 0.075). In PBC, compared with younger patients without hypertension, the risk of increased IMT was OR (CI) 3.1 (0.6 to 17; p = 0.192) in patients with hypertension or old age, but not hypercholesterolaemia, and 4.6 (0.8 to 27; p = 0.096) in patients who also had hypercholesterolaemia. The corresponding figures for risk of stenosis were 3.6 (0.4 to 36; p = 0.277) and 15.8 (1.8 to 141; p = 0.014). Conclusions: Hypercholesterolaemia is not consistently associated with subclinical atherosclerosis in PBC, but should be treated if other risk factors for cardiovascular disease are also present. The search for factors that may protect patients with hypercholesterolaemic PBC against atherosclerosis should be encouraged.
Hypercholesterolaemia often occurs in primary biliary cirrhosis (PBC) as a result of chronic cholestasis, but whether these patients are exposed to greater cardiovascular risk is unknown.BACKGROUNDHypercholesterolaemia often occurs in primary biliary cirrhosis (PBC) as a result of chronic cholestasis, but whether these patients are exposed to greater cardiovascular risk is unknown.To establish whether hypercholesterolaemia is associated with subclinical atherosclerosis in PBC.AIMTo establish whether hypercholesterolaemia is associated with subclinical atherosclerosis in PBC.103 consecutive patients with PBC (37 with total cholesterol > or =6.21 mmol/l) and 37 controls with hypercholesterolaemia, and 141 matched controls with normocholesterolaemia.PATIENTS103 consecutive patients with PBC (37 with total cholesterol > or =6.21 mmol/l) and 37 controls with hypercholesterolaemia, and 141 matched controls with normocholesterolaemia.Ultrasound imaging of carotid artery to determine intima-media thickness (IMT) and stenosis.METHODSUltrasound imaging of carotid artery to determine intima-media thickness (IMT) and stenosis.Controls with hypercholesterolaemia had higher IMT and prevalence of carotid stenosis compared with patients with hypercholesterolaemic PBC (mean (SD) 0.850 (0.292) mm v 0.616 (0.137) mm, p(c)<0.001; 43% v 19%, p(c) = 0.129) who, in turn, were similar to the 66 patients with normocholesterolaemic PBC (0.600 (0.136) mm; 5%). Compared with subjects with normocholesterolaemia, controls with hypercholesterolaemia, but not patients with hypercholesterolaemic PBC, had an increased risk of raised IMT (odds ratio (OR) 5.4, 95% confidence interval (CI) 2.5 to 11.9, p<0.001; and 0.7, 0.3 to 2.0, p = 0.543) or carotid stenosis (8.2, 3.4 to 20, p<0.001; and 2.5, 0.9 to 6.9, p = 0.075). In PBC, compared with younger patients without hypertension, the risk of increased IMT was OR (CI) 3.1 (0.6 to 17; p = 0.192) in patients with hypertension or old age, but not hypercholesterolaemia, and 4.6 (0.8 to 27; p = 0.096) in patients who also had hypercholesterolaemia. The corresponding figures for risk of stenosis were 3.6 (0.4 to 36; p = 0.277) and 15.8 (1.8 to 141; p = 0.014).RESULTSControls with hypercholesterolaemia had higher IMT and prevalence of carotid stenosis compared with patients with hypercholesterolaemic PBC (mean (SD) 0.850 (0.292) mm v 0.616 (0.137) mm, p(c)<0.001; 43% v 19%, p(c) = 0.129) who, in turn, were similar to the 66 patients with normocholesterolaemic PBC (0.600 (0.136) mm; 5%). Compared with subjects with normocholesterolaemia, controls with hypercholesterolaemia, but not patients with hypercholesterolaemic PBC, had an increased risk of raised IMT (odds ratio (OR) 5.4, 95% confidence interval (CI) 2.5 to 11.9, p<0.001; and 0.7, 0.3 to 2.0, p = 0.543) or carotid stenosis (8.2, 3.4 to 20, p<0.001; and 2.5, 0.9 to 6.9, p = 0.075). In PBC, compared with younger patients without hypertension, the risk of increased IMT was OR (CI) 3.1 (0.6 to 17; p = 0.192) in patients with hypertension or old age, but not hypercholesterolaemia, and 4.6 (0.8 to 27; p = 0.096) in patients who also had hypercholesterolaemia. The corresponding figures for risk of stenosis were 3.6 (0.4 to 36; p = 0.277) and 15.8 (1.8 to 141; p = 0.014).Hypercholesterolaemia is not consistently associated with subclinical atherosclerosis in PBC, but should be treated if other risk factors for cardiovascular disease are also present. The search for factors that may protect patients with hypercholesterolaemic PBC against atherosclerosis should be encouraged.CONCLUSIONSHypercholesterolaemia is not consistently associated with subclinical atherosclerosis in PBC, but should be treated if other risk factors for cardiovascular disease are also present. The search for factors that may protect patients with hypercholesterolaemic PBC against atherosclerosis should be encouraged.
Author Allocca, M
Gobatti, D
Ghilardi, G
Caruso, D
Podda, M
Crosignani, A
Battezzati, P M
Gritti, A
Zuin, M
AuthorAffiliation M Allocca , A Crosignani , A Gritti , M Zuin , M Podda , P M Battezzati , Clinica Medica, Dipartimento di Medicina, Chirurgia e Odontoiatria, School of Medicine Ospedale San Paolo, University of Milan, Milan, Italy
G Ghilardi , D Gobatti , Division of General and Vascular Surgery, Dipartimento di Medicina Chirurgia e Odontoiatria, School of Medicine Ospedale San Paolo, University of Milan, Milan, Italy
D Caruso , Laboratory of Biochemistry and Molecular Biology of Lipids–Mass Spectrometry, Dipartimento di Scienze Farmacologiche, University of Milan, Milan, Italy
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– name: M Allocca , A Crosignani , A Gritti , M Zuin , M Podda , P M Battezzati , Clinica Medica, Dipartimento di Medicina, Chirurgia e Odontoiatria, School of Medicine Ospedale San Paolo, University of Milan, Milan, Italy
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https://www.ncbi.nlm.nih.gov/pubmed/16632556$$D View this record in MEDLINE/PubMed
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Issue 12
Keywords Primary biliary cirrhosis
Cardiovascular disease
Hepatic disease
Metabolic diseases
Lipids
Hyperlipoproteinemia
Lipoprotein
Cholesterol
Vascular disease
Hypercholesterolemia
Atherosclerosis
Digestive diseases
Lesion
Dyslipemia
Language English
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Correspondence to:
 P M Battezzati
 Dipartimento di Medicina, Chirurgia e Odontoiatria, Polo Universitario Ospedale San Paolo, Via Di Rudinì, 8, 20143 Milano, Italy; piermaria.battezzati@unimi.it
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PublicationTitle Gut
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References 12117892 - Gut. 2002 Aug;51(2):265-9
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15138215 - Gut. 2004 Jun;53(6):865-70
9794902 - Hepatology. 1998 Nov;28(5):1199-205
9878640 - N Engl J Med. 1999 Jan 7;340(1):14-22
8978479 - J Lipid Res. 1996 Nov;37(11):2280-7
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11254756 - J Lipid Res. 2001 Mar;42(3):437-41
11368702 - JAMA. 2001 May 16;285(19):2486-97
10374976 - Ultrasound Med Biol. 1999 Mar;25(3):323-30
7886711 - Stroke. 1995 Mar;26(3):386-91
8900092 - N Engl J Med. 1996 Nov 21;335(21):1570-80
8477962 - Hepatology. 1993 Apr;17(4):577-82
9018771 - Scand J Gastroenterol. 1997 Jan;32(1):77-83
16054067 - Cell Metab. 2005 Apr;1(4):223-30
7737632 - Hepatology. 1995 May;21(5):1261-8
7934188 - Mayo Clin Proc. 1994 Oct;69(10):923-9
4118161 - Gut. 1972 Sep;13(9):682-9
1568727 - Hepatology. 1992 May;15(5):858-62
9056605 - Stroke. 1997 Mar;28(3):518-25
2719423 - Ann Intern Med. 1989 Jun 1;110(11):916-21
15128074 - J Clin Gastroenterol. 2004 Mar;38(3):264-71
205385 - Clin Sci Mol Med. 1978 Apr;54(4):369-79
8614933 - Stroke. 1996 Apr;27(4):695-9
8614934 - Stroke. 1996 Apr;27(4):700-5
References_xml – reference: 9056605 - Stroke. 1997 Mar;28(3):518-25
– reference: 7886711 - Stroke. 1995 Mar;26(3):386-91
– reference: 8614933 - Stroke. 1996 Apr;27(4):695-9
– reference: 15138215 - Gut. 2004 Jun;53(6):865-70
– reference: 12853201 - Lancet. 2003 Jul 5;362(9377):53-61
– reference: 12117892 - Gut. 2002 Aug;51(2):265-9
– reference: 11368702 - JAMA. 2001 May 16;285(19):2486-97
– reference: 15128074 - J Clin Gastroenterol. 2004 Mar;38(3):264-71
– reference: 9794902 - Hepatology. 1998 Nov;28(5):1199-205
– reference: 7934188 - Mayo Clin Proc. 1994 Oct;69(10):923-9
– reference: 9471928 - Ann Intern Med. 1998 Feb 15;128(4):262-9
– reference: 4118161 - Gut. 1972 Sep;13(9):682-9
– reference: 8614934 - Stroke. 1996 Apr;27(4):700-5
– reference: 8900092 - N Engl J Med. 1996 Nov 21;335(21):1570-80
– reference: 11254756 - J Lipid Res. 2001 Mar;42(3):437-41
– reference: 9018771 - Scand J Gastroenterol. 1997 Jan;32(1):77-83
– reference: 2719423 - Ann Intern Med. 1989 Jun 1;110(11):916-21
– reference: 8477962 - Hepatology. 1993 Apr;17(4):577-82
– reference: 16054067 - Cell Metab. 2005 Apr;1(4):223-30
– reference: 1568727 - Hepatology. 1992 May;15(5):858-62
– reference: 9878640 - N Engl J Med. 1999 Jan 7;340(1):14-22
– reference: 8978479 - J Lipid Res. 1996 Nov;37(11):2280-7
– reference: 10374976 - Ultrasound Med Biol. 1999 Mar;25(3):323-30
– reference: 205385 - Clin Sci Mol Med. 1978 Apr;54(4):369-79
– reference: 7737632 - Hepatology. 1995 May;21(5):1261-8
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Snippet Background: Hypercholesterolaemia often occurs in primary biliary cirrhosis (PBC) as a result of chronic cholestasis, but whether these patients are exposed to...
Hypercholesterolaemia often occurs in primary biliary cirrhosis (PBC) as a result of chronic cholestasis, but whether these patients are exposed to greater...
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StartPage 1795
SubjectTerms Age
Age Factors
Alcohol
Apo
apolipoprotein
Atherosclerosis
Atherosclerosis (general aspects, experimental research)
Atherosclerosis - complications
Atherosclerosis - diagnostic imaging
Biological and medical sciences
Blood and lymphatic vessels
BMI
body mass index
Cardiology. Vascular system
Cardiovascular disease
Carotid arteries
Carotid Arteries - diagnostic imaging
Carotid Stenosis - diagnostic imaging
Cholesterol
Cholesterol - blood
Colleges & universities
Diabetes
Disorders of blood lipids. Hyperlipoproteinemia
Female
Gastroenterology. Liver. Pancreas. Abdomen
HDL
Hepatitis
high-density lipoprotein
Humans
Hypercholesterolemia - complications
Hypercholesterolemia - diagnostic imaging
Hypertension
Hypertension - complications
IMT
interquartile range
intima–media thickness
IQR
LDL
Lipids
Liver
Liver Cirrhosis, Biliary - complications
Liver Cirrhosis, Biliary - diagnostic imaging
Liver diseases
Liver. Biliary tract. Portal circulation. Exocrine pancreas
low-density lipoprotein
Male
Medical sciences
Medicine
Metabolic diseases
Middle Aged
Mortality
Other diseases. Semiology
Patients
PBC
primary biliary cirrhosis
Risk Factors
Tunica Intima - diagnostic imaging
Ultrasonic imaging
Ultrasonography
Title Hypercholesterolaemia is not associated with early atherosclerotic lesions in primary biliary cirrhosis
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