Ethinylestradiol-drospirenone, flutamide-metformin, or both for adolescents and women with hyperinsulinemic hyperandrogenism:: Opposite effects on adipocytokines and body adiposity

被引:122
作者
Ibáñez, L
de Zegher, F
机构
[1] Univ Barcelona, Endocrinol Unit, Hosp St Joan Deu, Barcelona 08950, Spain
[2] Univ Leuven, Dept Pediat, B-3000 Louvain, Belgium
关键词
D O I
10.1210/jc.2003-031281
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hyperinsulinemic hyperandrogenism with anovulation, the so-called polycystic ovary syndrome (PCOS), is the most frequent endocrine disorder of young women. One of the stigmata of PCOS is a deficit of lean mass and an excess of fat, in particular, abdominal fat, even in the absence of obesity. Adiponectin and IL-6 are among the adipocytokines that have recently been related to abdominal fat excess, insulin resistance states, and cardiovascular disease risk. We studied the effects of two new treatment options, ethinylestradioldrospirenone and flutamide-metformin, and of their combination on adipocytokinemia and body adiposity in adolescents and women with PCOS. Adolescents with PCOS (n=32; age, similar to15 yr; body mass index, similar to22 kg/m(2)) were randomly assigned to receive the oral contraceptive (OC) ethinylestradiol-drospirenone, or the low-dose generic duo of flutamide (62.5 mg/d) plus metformin (850 mg/d). Young women with PCOS (n=22; age, similar to19 yr; body mass index, similar to22 kg/m(2)) were randomized to receive the same OC, either alone or with flutamide-metformin. Fasting blood glucose, serum insulin, lipids, androgens, IL-6, adiponectin, and body composition (by absorptiometry) were assessed at the start, and after 3 and/or 9 months. At the start, serum concentrations of the proinflammatory IL- 6 were high, and those of the antiinflammatory adiponectin were low; body composition was adipose in each subpopulation. Abnormal adipocytokine levels, hypertriglyceridemia, and body adiposity diverged further from the norm in adolescents on OC; in contrast, girls on flutamide-metformin reverted all study indices toward normal, lost part of their fat excess, and reduced their lean mass deficit. In comparison to the girls on OC, those on flutamide-metformin lost a mean of approximately 4 kg of fat and gained approximately 4 kg of lean mass. Similarly, abnormal adipocytokine levels and adiposity were aggravated in women on OC alone and improved in women on OC plus flutamide-metformin; within 9 months, the latter subgroup lost a mean of approximately 3 kg of fat and gained approximately 3 kg of lean mass, in comparison to women on OC alone. In conclusion, young and nonobese PCOS patients were found to be in a low-grade, chronic inflammation state, and to have a body adiposity that evolves according to the balance of circulating adipocytokines and lipids, rather than to androgen excess or fasting hyperinsulinemia. Monotherapy with ethinylestradiol-drospirenone may not be a prime choice for PCOS, given its inefficacy to attenuate abnormal adipocytokine levels and body adiposity; ethinylestradiol-drospirenone plus flutamide-metformin, however, is a first OC combination that was found capable of reverting both the adipocytokine balance and the body composition toward normal, and that may therefore improve the long-term cardiovascular perspectives of women with PCOS.
引用
收藏
页码:1592 / 1597
页数:6
相关论文
共 50 条
[1]   Serum and follicular fluid cytokines in polycystic ovary syndrome during stimulated cycles [J].
Amato, G ;
Conte, M ;
Mazziotti, G ;
Lalli, E ;
Vitolo, G ;
Tucker, AT ;
Bellastella, A ;
Carella, C ;
Izzo, A .
OBSTETRICS AND GYNECOLOGY, 2003, 101 (06) :1177-1182
[2]   Polycystic ovary syndrome in adolescence [J].
Baumann, EE ;
Rosenfield, RL .
ENDOCRINOLOGIST, 2002, 12 (04) :333-348
[3]   Inflammatory markers and onset of cardiovascular events - Results from the Health ABC study [J].
Cesari, M ;
Penninx, BWJH ;
Newman, AB ;
Kritchevsky, SB ;
Nicklas, BJ ;
Sutton-Tyrrell, K ;
Rubin, SM ;
Ding, JZ ;
Simonsick, EM ;
Harris, TB ;
Pahor, M .
CIRCULATION, 2003, 108 (19) :2317-2322
[4]  
DE L, 1998, J CLIN ENDOCR METAB, V83, P99
[5]   A modern medical quandary: Polycystic ovary syndrome, insulin resistance, and oral contraceptive pills [J].
Diamanti-Kandarakis, E ;
Baillargeon, JP ;
Iuorno, MJ ;
Jakubowicz, DJ ;
Nestler, JE .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (05) :1927-1932
[6]   The effect of a pure antiandrogen receptor blocker, flutamide, on the lipid profile in the polycystic ovary syndrome [J].
Diamanti-Kandarakis, E ;
Mitrakou, A ;
Raptis, S ;
Tolis, G ;
Duleba, AJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (08) :2699-2705
[7]   Glucose-to-insulin ratio rather than sex hormone-binding globulin and adiponectin levels is the best predictor of insulin resistance in Nonobese women with polycystic ovary syndrome [J].
Ducluzeau, PH ;
Cousin, P ;
Malvoisin, E ;
Bornet, H ;
Vidal, H ;
Laville, M ;
Pugeat, M .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (08) :3626-3631
[8]   The insulin-sensitizing agent troglitazone improves metabolic and reproductive abnormalities in the polycystic ovary syndrome [J].
Dunaif, A ;
Scott, D ;
Finegood, D ;
Quintana, B ;
Whitcomb, R .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (09) :3299-3306
[9]   Current concepts in the polycystic ovary syndrome [J].
Dunaif, A ;
Thomas, A .
ANNUAL REVIEW OF MEDICINE, 2001, 52 :401-419
[10]   Clinical, endocrine and metabolic effects of metformin added to ethinyl estradiol-cyproterone acetate in non-obese women with polycystic ovarian syndrome: a randomized controlled study [J].
Elter, K ;
Imir, G ;
Durmusoglu, F .
HUMAN REPRODUCTION, 2002, 17 (07) :1729-1737