Erythrocyte hyperaggregation in obesity:: Determining factors and weight loss influence

被引:23
作者
Sola, Eva
Vaya, Amparo
Corella, Dolores
Santaolaria, Maria-Luisa
Espania, Francisco
Estelles, Amparo
Hernandez-Mijares, Antonio
机构
[1] Doctor Peset Univ Hosp, Dept Endocrinol, Serv Endocrinol, Valencia 46017, Spain
[2] La Fe Univ Hosp, Hermorheol & Thrombosis Unit, Dept Clin Pathol, Valencia, Spain
[3] La Fe Univ Hosp, Res Ctr, Valencia, Spain
[4] Univ Valencia, Sch Med, Dept Prevent Med, Valencia, Spain
[5] Univ Valencia, Sch Med, CIBER Fisiopatol Obesidad & Nutr, Valencia, Spain
关键词
insulin resistance; erythrocytes; thrombosis;
D O I
10.1038/oby.2007.253
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To compare erythrocyte aggregation (EA) in patients with severe obesity without other cardiovascular risk factors with a control group, using the Myrenne and the Sefam aggregometers, and to evaluate the effect of weight loss on this parameter. Research Methods and Procedures: This was a longitudinal, clinical intervention study of a very low-calorie diet for 4 weeks followed by a low-calorie diet for 2 months. In 67 severely obese patients, an anthropometric and analytical evaluation [plasmatic lipids, fibrinogen (Fbg), and EA] was performed at baseline and 3 months after diet. The same determinations were performed in 67 normal-weight volunteers. EA was measured with the Myrenne MA(1) which determines EA at stasis (EA(0)) and at a low shear of 3 seconds(-1) (EA,), and the Sefarn aggregometer, which determines aggregation index at 10 seconds(-1) (IA(10)), aggregation time (Ta), and disaggregation threshold (gamma D). Insulin resistance (IR) was calculated by homeostasis model assessment. Results: Obese patients showed higher Fbg levels, EA, EA, IA(10), and gamma D values, and lower Ta values. Differences between obese patients and control group for EA(0), EA I, Ta, IA(10), and gamma D disappeared after adjusting for BMI or for homeostasis model assessment but were maintained after adjusting for Fbg or low-density lipoprotein-cholesterol. Obese patients with IR showed higher EA(0) and EA, values. After weight loss, EA, showed a significant improvement. Discussion: Obese patients show increased EA. Erythrocyte hyperaggregation does not seem to be related to a high Fbg level or to an abnormal lipid profile but to IR. Hyperagreggation improves after weight loss.
引用
收藏
页码:2128 / 2134
页数:7
相关论文
共 28 条
[11]  
Le Dévéhat C, 2004, CLIN HEMORHEOL MICRO, V30, P297
[12]  
LEDEVEHAT C, 1992, DIABETES METAB, V18, P43
[13]   HOMEOSTASIS MODEL ASSESSMENT - INSULIN RESISTANCE AND BETA-CELL FUNCTION FROM FASTING PLASMA-GLUCOSE AND INSULIN CONCENTRATIONS IN MAN [J].
MATTHEWS, DR ;
HOSKER, JP ;
RUDENSKI, AS ;
NAYLOR, BA ;
TREACHER, DF ;
TURNER, RC .
DIABETOLOGIA, 1985, 28 (07) :412-419
[14]  
Mijares AH, 2003, MED CLIN-BARCELONA, V121, P204
[15]  
Pérez-Martin A, 2001, CLIN HEMORHEOL MICRO, V25, P91
[16]  
POGGI M, 1994, INT J OBESITY, V18, P490
[17]   INFLUENCE OF HDL SUBFRACTIONS ON ERYTHROCYTE AGGREGATION IN HYPERCHOLESTEROLEMIC MEN [J].
RAZAVIAN, SM ;
ATGER, V ;
GIRAL, P ;
CAMBILLAU, M ;
DELPINO, M ;
SIMON, AC ;
MOATTI, N ;
LEVENSON, J .
ARTERIOSCLEROSIS AND THROMBOSIS, 1994, 14 (03) :361-366
[18]   Flow-resistant red blood cell aggregation in morbid obesity [J].
Samocha-Bonet, D ;
Ben-Ami, R ;
Shapira, I ;
Shenkerman, G ;
Abu-Abeid, S ;
Stern, N ;
Mardi, T ;
Tulchinski, T ;
Deutsch, V ;
Yedgar, S ;
Barshtein, G ;
Berliner, S .
INTERNATIONAL JOURNAL OF OBESITY, 2004, 28 (12) :1528-1534
[19]   Enhanced erythrocyte adhesiveness/aggregation in obesity corresponds to low-grade inflammation [J].
Samocha-Bonet, D ;
Lichtenberg, D ;
Tomer, A ;
Deutsch, V ;
Mardi, T ;
Goldin, Y ;
Abu-Abeid, S ;
Shenkerman, G ;
Patshornik, H ;
Shapira, I ;
Berliner, S .
OBESITY RESEARCH, 2003, 11 (03) :403-407
[20]   Significant dominance of fibrinogen over immunoglobulins, C-reactive protein, cholesterol and triglycerides in maintaining increased red blood cell adhesiveness/aggregation in the peripheral venous blood: a model in hypercholesterolaemic patients [J].
Schechner, V ;
Shapira, I ;
Berliner, S ;
Comaneshter, D ;
Hershcovici, T ;
Orlin, J ;
Zeltser, D ;
Rozenblat, M ;
Lachmi, K ;
Hirsch, M ;
Beigel, Y .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2003, 33 (11) :955-961