Antiphospholipid antibodies as a risk factor for atherosclerotic events in renal transplant recipients

被引:25
作者
Ducloux, D
Bourrinet, E
Motte, G
Chalopin, JM
机构
[1] Univ Hosp, Dept Nephrol Dialysis & Renal Transplantat, Besancon, France
[2] Univ Hosp, Dept Endocrinol, Besancon, France
关键词
antiphospholipid antibodies; renal transplantion; atherosclerosis;
D O I
10.1046/j.1523-1755.2003.00155.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background. Epidemiologic studies reported that antiphospholipid antibodies (APAs) were independent predictors of atherosclerotic events. We recently reported a high prevalence of APAs in renal transplant recipients. Nevertheless, the role of APAs on atherosclerotic events has not been prospectively studied in this high-risk population. Methods. Participants in the study were 324 consecutive renal transplant recipients. Patients were enrolled between January 1996 and May 1998 and followed up until June 2002. Results. The patients were followed for a mean duration of 62 +/- 26 months. Eighty seven (26.8%) patients exhibited APAs. We found a slight, but significant, correlation between total plasma homocysteine (tHcy) concentration and anticardiolipin (ACA) titers (r = 0.26; P = 0.036). Fifty six athersclerotic events (17.2%) occurred in 54 patients. Atherosclerotic events occurred more frequently in patients with APAs (33% vs. 9%; P = 0.0003) and ACAs levels were higher in patients who experienced atherosclerotic events (23.7 +/- 13.1 IU vs. 13.9 +/- 9.4 IU; P = 0.003). APAs were associated with an increased risk of atherosclerotic events (RR, 2.82; 95% CI, 1.17 to 5.31). Cox regression analysis also revealed that age above the median (RR, 5.21; 95% CI, 1.67 to 17.13), a previous history of cardiovascular disease (RR, 3.54; 95% CI, 1.57 to 10.43), hyperhomocysteinemia (RR, 4.01; 95% CI, 1.22 to 14.61), and current smoking (RR, 2.17; 95% CI, 1.01 to 6.72) were risk factors for atherosclerotic events. Conclusion. The presence of APAs is an independent cardiovascular risk factor in renal transplant recipients. Prevention trials are necessary to assess the efficacy and safety of anticoagulation therapy in transplant patients with APAs.
引用
收藏
页码:1065 / 1070
页数:6
相关论文
共 29 条
[1]   Hyperhomocysteinemia is common in patients with antiphospholipid syndrome and may contribute to expression of major thrombotic events [J].
Avivi, I ;
Lanir, N ;
Hoffman, R ;
Brenner, B .
BLOOD COAGULATION & FIBRINOLYSIS, 2002, 13 (02) :169-172
[2]   Anticardiolipin antibodies and recurrent coronary events - A prospective study of 1150 patients [J].
Bili, A ;
Moss, AJ ;
Francis, CW ;
Zareba, W ;
Watelet, LFM ;
Sanz, I .
CIRCULATION, 2000, 102 (11) :1258-1263
[3]   β2-glycoprotein 1-dependent anticardiolipin antibodies and risk of ischemic stroke and myocardial infarction -: The Honolulu Heart Program [J].
Brey, RL ;
Abbott, RD ;
Curb, JD ;
Sharp, DS ;
Ross, GW ;
Stallworth, CL ;
Kittner, SJ .
STROKE, 2001, 32 (08) :1701-1706
[4]   Prevalence and clinical significance of antiphospholipid antibodies in renal transplant recipients [J].
Ducloux, D ;
Pellet, E ;
Fournier, V ;
Rebibou, JM ;
Bresson-Vautrin, C ;
Racadot, E ;
Fellmann, D ;
Chalopin, JM .
TRANSPLANTATION, 1999, 67 (01) :90-93
[5]  
Ducloux D, 2000, J AM SOC NEPHROL, V11, P134, DOI 10.1681/ASN.V111134
[6]   Antiphospholipid antibodies and thrombosis [J].
Greaves, M .
LANCET, 1999, 353 (9161) :1348-1353
[7]   The pathophysiology of alveolar osteonecrosis of the jaw: Anticardiolipin antibodies, thrombophilia, and hypofibrinolysis [J].
Gruppo, R ;
Glueck, CJ ;
McMahon, RE ;
Bouquot, J ;
Rabinovich, BA ;
Becker, A ;
Tracy, T ;
Wang, P .
JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 1996, 127 (05) :481-488
[8]   Immune mechanisms in atherosclerosis [J].
Hansson, GK .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2001, 21 (12) :1876-1890
[9]   Involvement of beta(2)-glycoprotein I and anticardiolipin antibodies in oxidatively modified low-density lipoprotein uptake by macrophages [J].
Hasunuma, Y ;
Matsuura, E ;
Makita, Z ;
Katahira, T ;
Nishi, S ;
Koike, T .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 1997, 107 (03) :569-573
[10]   Immunological responses to oxidized LDL [J].
Hörkkö, S ;
Binder, CJ ;
Shaw, PX ;
Chang, MK ;
Silverman, G ;
Palinski, W ;
Witztum, JL .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 28 (12) :1771-1779