Objective: Systemic sclerosis (SSc) is characterized by microvascular and macrovascular alterations. The D allele of the ACE I/D polymorphism is known to be associated with an increased incidence of atherosclerosis and has been recently proposed as associated with increased risk of SSc. This study evaluates the relationship between intima-media thickness (IMT), ankle-brachial pressure measurements (ABPI) and ACE I/D polymorphism in SSc patients. Methods: According to the presence of ACED allele (analysed by PCR), 53 SSc patients (47 females and 6 males; median age was 60.4±10.68 yrs; range 40-75 yrs) were divided in carriers of the D allele (DD+ID) (n=46) and carriers of the I allele (II) (n=7). In these patients, IMT and ABPI [calculated as the posterior tibial artery pressure (mmHg) divided by the brachial pressure] were obtained. Forty-three healthy controls (40 women and 13 men; median age 56.3±10.23; range 40-70 yrs) of the same ethnicity were recruited. Results: SSc patients had IMT significantly higher than controls (0.85±0.03 vs 0. 68±0.01; P<0.03). No significant differences (P>0.3) in ABPI values between patients (1.018±0.10) and controls (1.091±0.11) were found. SSc patients with ACE DD and ID genotype showed an IMT significantly greater (0.89±0.03) than those carrying the II genotype (0.61±0.01) (P>0.04). ABPI was not different among ACE gene genotypes. Conclusion: Our findings confirm an increased prevalence of macrovascular disease in SSc patients and show that IMT is greater in patients carrying the ACE DD and ID genotype in comparison with II homozygotes. This suggests that, in SSc, the presence of ACE D allele may predispose to an involvement of the macrovascular system. © The Author 2007. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved.
Angiotensin-converting enzyme I/D polymorphism and macrovascular disease in systemic sclerosis / Bartoli F.; Angotti C.; Fatini C.; Conforti M.L.; Guiducci S.; Blagojevic J.; Melchiorre D.; Fiori G.; Generini S.; Damjanov N.; Rednic S.; Pignone A.; Castellani S.; Abbate R.; Cerinic M.M.. - In: RHEUMATOLOGY. - ISSN 1462-0324. - ELETTRONICO. - 46:(2007), pp. 772-775. [10.1093/rheumatology/kel433]
Angiotensin-converting enzyme I/D polymorphism and macrovascular disease in systemic sclerosis
Angotti C.;Fatini C.;Guiducci S.;Blagojevic J.;Melchiorre D.;Generini S.;Pignone A.
;Abbate R.;Cerinic M. M.
2007
Abstract
Objective: Systemic sclerosis (SSc) is characterized by microvascular and macrovascular alterations. The D allele of the ACE I/D polymorphism is known to be associated with an increased incidence of atherosclerosis and has been recently proposed as associated with increased risk of SSc. This study evaluates the relationship between intima-media thickness (IMT), ankle-brachial pressure measurements (ABPI) and ACE I/D polymorphism in SSc patients. Methods: According to the presence of ACED allele (analysed by PCR), 53 SSc patients (47 females and 6 males; median age was 60.4±10.68 yrs; range 40-75 yrs) were divided in carriers of the D allele (DD+ID) (n=46) and carriers of the I allele (II) (n=7). In these patients, IMT and ABPI [calculated as the posterior tibial artery pressure (mmHg) divided by the brachial pressure] were obtained. Forty-three healthy controls (40 women and 13 men; median age 56.3±10.23; range 40-70 yrs) of the same ethnicity were recruited. Results: SSc patients had IMT significantly higher than controls (0.85±0.03 vs 0. 68±0.01; P<0.03). No significant differences (P>0.3) in ABPI values between patients (1.018±0.10) and controls (1.091±0.11) were found. SSc patients with ACE DD and ID genotype showed an IMT significantly greater (0.89±0.03) than those carrying the II genotype (0.61±0.01) (P>0.04). ABPI was not different among ACE gene genotypes. Conclusion: Our findings confirm an increased prevalence of macrovascular disease in SSc patients and show that IMT is greater in patients carrying the ACE DD and ID genotype in comparison with II homozygotes. This suggests that, in SSc, the presence of ACE D allele may predispose to an involvement of the macrovascular system. © The Author 2007. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved.I documenti in FLORE sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.