Follow-up of plasma semicarbazide-sensitive amine oxidase activity and retinopathy in Type 2 diabetes mellitus

被引:41
作者
Grönvall-Nordquist, JLE
Bäcklund, LB
Garpenstrand, L
Ekblom, J
Landin, B
Yu, PH
Oreland, L
Rosenqvist, U
机构
[1] Uppsala Univ, Dept Neurosci, Pharmacol Sect, Biomedicum, SE-75124 Uppsala, Sweden
[2] Karolinska Inst, St Eriks Eye Hosp, Dept Ophthalmol, Stockholm, Sweden
[3] Karolinska Inst, Huddinge Univ Hosp, Dept Clin Chem, Huddinge, Sweden
[4] Univ Saskatchewan, Dept Psychiat, Neuropsychiat Res Unit, Saskatoon, SK S7N 0W0, Canada
[5] Uppsala Univ, Dept Publ Hlth & Caring Sci, Uppsala, Sweden
关键词
benzylamine; hemoglobin A glycosylated; methylamine; vascular adhesion protein-1;
D O I
10.1016/S1056-8727(01)00151-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Plasma activity of the enzyme semicarbazide-sensitive amine oxidase (SSAO) is high in diabetes. Production of angiotoxic substances (an aldehyde, hydrogen peroxide, and ammonia) in vessel walls is catalysed by SSAO, suggesting a role for SSAO in the development of complications of diabetes. The objective of the present study was to follow up plasma SSAO activity (measured radiometrically), HbA(1c) (using ion exchange chromatography), and retinopathy (by fundus photography) after 2.8 years, in 34 patients with Type 2 diabetes. We also measured urinary levels of an SSAO substrate, methylamine, by fluorometric high-performance liquid chromatography (HPLC). As at baseline, plasma SSAO activity was now higher in subjects with retinopathy (mean 19.5) than in subjects without retinopathy (mean 16.0), 95% confidence interval (CI) for difference 0.6-6.3 nmol benzylamine ml(-1) plasma h(-1). SSAO activity had not changed significantly since baseline, mean difference -1.65 and 95% CI for difference -3.76 to 0.46 nmol benzylamine ml(-1) plasma h(-1). Mean HbA(1c) level remained higher for patients with retinopathy (now 7.9%) compared to those without retinopathy (6.1%), 95% CI for difference 0.6-3.0%. Comparing baseline and the present study, retinopathy was nonproliferative; level had worsened for five and improved for two patients. Urinary methylamine/creatinine ratio was lower in the group of patients with retinopathy (mean 0.99) than in those without retinopathy (mean 1.78), 95% CI for difference 0.1-1.5 mug mg(-1). The results of the present study are compatible with a role for SSAO in the development of diabetic retinopathy. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:250 / 256
页数:7
相关论文
共 33 条
[1]  
ALDINGTON SJ, 1995, DIABETOLOGIA, V38, P437, DOI 10.1007/BF00410281
[2]  
[Anonymous], 1991, Ophthalmology, V98, P786
[3]  
Backlund LB, 1998, DIABETIC MED, V15, pS32, DOI 10.1002/(SICI)1096-9136(1998110)15:3+<S32::AID-DIA728>3.3.CO
[4]  
2-4
[5]   Plasma semicarbazide-sensitive amine oxidase is elevated in patients with congestive heart failure [J].
Boomsma, F ;
vanVeldhuisen, DJ ;
deKam, PJ ;
ManintVeld, AJ ;
Mosterd, A ;
Lie, KI ;
Schalekamp, MADH .
CARDIOVASCULAR RESEARCH, 1997, 33 (02) :387-391
[6]   PLASMA SEMICARBAZIDE-SENSITIVE AMINE OXIDASE ACTIVITY IS ELEVATED IN DIABETES-MELLITUS AND CORRELATES WITH GLYCOSYLATED HEMOGLOBIN [J].
BOOMSMA, F ;
DERKX, FHM ;
VANDENMEIRACKER, AH ;
MANINTVELD, AJ ;
SCHALEKAMP, MADH .
CLINICAL SCIENCE, 1995, 88 (06) :675-679
[7]   Circulating semicarbazide-sensitive amine oxidase is raised both in Type I (insulin-dependent), in Type II (non-insulin-dependent) diabetes mellitus and even in childhood Type I diabetes at first clinical diagnosis [J].
Boomsma, F ;
van den Meiracker, AH ;
Winkel, S ;
Aanstoot, HJ ;
Batstra, MR ;
in't Veld, AJM ;
Bruining, GJ .
DIABETOLOGIA, 1999, 42 (02) :233-237
[8]  
BUFFONI F, 1977, MED BIOL, V55, P109
[9]   Therapeutic value of drugs inhibiting semicarbazide-sensitive amine oxidase: Vascular cytoprotection in diabetes mellitus [J].
Ekblom, J .
PHARMACOLOGICAL RESEARCH, 1998, 37 (02) :87-92
[10]   Elevated plasma semicarbazide-sensitive amine oxidase (SSAO) activity in Type 2 diabetes mellitus complicated by retinopathy [J].
Garpenstrand, H ;
Ekblom, J ;
Bäcklund, LB ;
Oreland, L ;
Rosenqvist, U .
DIABETIC MEDICINE, 1999, 16 (06) :514-521