青春期多囊卵巢综合征患者临床、内分泌代谢特征的研究及二甲双胍治疗效果分析
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摘要
第一部分
     目的了解青春期女孩的月经状况,循环中促性腺激素、硫酸脱氢表雄酮(DHEA-S)和皮质醇(C)的水平;并计算青春期女性循环中黄体生成素(LH)、黄体生成素/卵泡刺激素比值(LH/FSH)和硫酸脱氢表雄酮(DHEA-S)的生理界定值。方法对象为月经正常的女中学生325例,问卷调查月经史,测定血清C、LH、FSH和DHEA-S,并计算LH/FSH比值,取研究人群第95百分位数得出LH、LH/FSH和DHEA-S的生理高限值。结果正常青春期女性近95%在初潮2年内建立规律月经,初潮后5年内100%建立规律月经。青春中晚期(15~18岁)C、LH、FSH、LH/FSH、DHEA-S不随年龄变化,LH的生理界定值为16.11U/L,LH/FSH比值的生理界定值为1.54,DHEA-S的生理界定值为407μg/dl。
     结论以初潮后2年内能否建立规律月经作为初步筛查青春期月经状况是否正常的年限指标是合适的。LH、LH/FSH比值、DHEA-S的生理界定值是判断青春期女性生殖内分泌紊乱的依据。
     第二部分
     目的分析青春期多囊卵巢综合征患者的临床、内分泌代谢特征。方法对象为青春期PCOS患者167例,其中肥胖型(0BPCOS组)90例、非肥胖型(NOBPCOS组)77例。以年龄匹配、月经规则的女中学生325例作为对照,其中肥胖(0BCON组)18例,非肥胖(NOBCON组)307例。对上述对象进行临床体征评分,内分泌、代谢指标测定。采用循环中睾酮水平(T)、游离雄激素指数(FAI)及硫酸脱氢表雄酮(DHEA-S)评估高雄激素血症,用空腹胰岛素(FINS)、稳态模型指数(HOMA-IR)评估胰岛素敏感性。结果①青春期PCOS患者的月经初潮年龄(12.74±1.31岁)较对照组(13.10±0.99岁)提前(P<0.05),84.85%的患者未能在初潮后2年内建立规律月经。青春期PCOS患者肥胖的发生率(53.89%)、其中腹部型肥胖的发生率(31.14%)均显著高于对照人群(分别为5.54%及0.62%,P均<0.001)。②青春期PCOS患者的血浆睾酮水平(0.83±0.32ng/ml)、FAI(6.87±7.42)、DHEA-S(747±714μg/d1)均显著高于对照人群(分别为0.48±0.19ng/ml、1.77±1.74,227±98μg/dl,P均<0.0001)。其中OBPCOS组的FAI(8.20±8.24)显著高于NOBPCOS组(5.27±5.96,P<0.05)。病例组黄体生成素(LH)水平(12.23±6.92IU/L)、LH/FSH比值(1.89±0.99)均显著高于对照组(分别为7.42±11.09IU/L及0.70±0.64,P均<0.01)。其中NOBPCOS组的LH(14.07±7.52IU/L)、LH/FSH比值(2.11±1.09)显著高于OBPCOS组(分别为10.64±5.961U/L及1.69±0.85,P均<0.01)。③青春期PCOS患者HOMA-IR值(取自然对数0.96±0.69)、空腹胰岛素(17.40±15.67mIU/L)均显著高于对照人群(分别为0.77±0.52及10.83±5.27mIU/L,P均<0.01);病理性胰岛素抵抗的发生率(29.94%)也显著高于对照人群(6.77%)。OBPCOS组黑棘皮症发生率(44.44%)、空腹胰岛素(21.73±17.21mlU/L)、HOMA-IR(1.27±0.62)及甘油三酯(TG)水平(1.40±0.63mmol/L)均显著高于NOBPCOS组(分别为6.49%、12.34±11.9lmIU/L、0.61±0.60、0.91±0.44mmol/L,P均<0.01)。④肥胖、脂溢性脱发、糖尿病、高血压的家族史与青春期PCOS的发病相关(P均≤0.001),其中肥胖和脂溢性脱发为独立的风险因素。BMI是雄激素增高和胰岛素抵抗共同的独立风险因素。结论青春期PCOS的基本特征是:①月经初潮提前,初潮2年后仍存在持续的月经紊乱;②肥胖发生率增高;③循环中雄激素水平异常增高;④促性腺激素分泌失调;⑤存在病理性胰岛素抵抗。其中肥胖型患者的雄激素生物学活性更强,胰岛素抵抗程度更严重。
     第三部分
     目的回顾性研究二甲双胍治疗青春期多囊卵巢综合征的效果。方法对象为接受二甲双胍治疗满一年的青春期PCOS患者42例,以治疗前是否存在病理性胰岛素抵抗分为1R组(29例)和NIR组(13例),评估治疗前后的排卵状况、肥胖程度、胰岛素敏感性和血清生殖内分泌参数。结果治疗前所有患者均为无排卵,二甲双胍治疗后76.19%(32/42)的患者恢复排卵,与用药前相比有显著改善(P<0.001);IR组和NIR组之间排卵恢复率未显示统计学差异(P>0.05)。IR组和NIR组均出现体重、BMI、FINS、HOMA-IR、胰岛素曲线下面积、总睾酮及LH的下降(P均<0.05);IR组还伴有FAI、LH/FSH比值的下降(P均<0.05)。排卵的恢复与空腹胰岛素(偏回归系数-0.234,95%CI:-0.449~-0.018)、HOMA-IR(偏回归系数-1.266,95%Ci:-2.495~-0.037)均呈负相关(P<0.05)。FAI与FINS呈正相关(r=0.3335,P=0.0309)。结论二甲双胍能成功改善青春期PCOS患者的排卵功能、生殖内分泌及代谢紊乱;排卵的恢复与胰岛素水平的下降相关。
Section 1
     Objective To investigate the menstruation state,the level of follicle stimulating hormone(FSH),luteininzinghormone(LH),chotisol(C) and dehydro-epiandrosterone sulfate(DHEA-S) in the adolescent girls,and determine the physiological ceiling value of LH,LH/FSH ratio and DHEA-S. Methods We performed a study of 325 adolescent middle school girls with normal menstruation.We knew the menstruation state according to a questionnaire.Then tested the measurement of serum levels of C,FSH,LH, DHEA-S and calculated LH/FSH ratio.We analyzed how the parameters changed along with the age and conputed the physiological ceiling value of LH,LH/FSH ratio and DHEA-S as the 95th percentile of the normal adolescent girls. Results It would take 2 years for almost 95%of the normal adolescent girls to establish a regular menstruation after menarche,while 100%of the normal girls have their regular menstruation within 5 years after menarche.The physiological ceiling value of the main parameters(aged 15-18 years):LH is 16.1IU/L;LH/FSH ratio is 1.54;DHEA-S is 407μg/dl.Conclusion It is suitable for adolescent girls using the limit of 2 years to screen the menstruation states.The diagnosis for disturbance of reproductive endocrinology should be according to the physiological ceiling values of the main parameters.
     Section 2
     Objective To investigate and analyze the clinical presentation,hormonal profile,and metabolic abnormalities of adolescent girls with polycystic ovary syndrome(PCOS).Methods The data of the anthropometric measurements,clinical manifestations of hyperandrogenism,serum levels of luteininzing hormone(LH),follicle stimulating hormone(FSH), testosterone(T),prolactin(PRL),dehydro-epiandrosterone sulfate (DHEA-S),sex-hormone-binding globulin(SHBG),17-oxyhydroprogesterone (17-OHP),fasting plasma glucose(FPG) and fasting insulin(FINS) detected after oral glucose tolerance test(OGTT),serum lipid levels, including total cholesterol(Chol),triglycerides(TG),high-density lipoprotein(HDL),and low-density lipoprotein(LDL),fasting plasma insulin(FINS) and homeostasis model assessment(HOMA) so as to assess the insulin resistance(IR),serum testosterone(T) and free androgen index(FAI) to estimate the extent of hyperandrogenism,were collected from 167 adolescent women with PCOS,aged 17±2,that were divided into 2 groups according to the body mass index(BMI) and waist-to-hip ratio(WHR):Group OBPCOS(n=90) with the BMI≥25 kg·m~(-2) or the WHR≥0.85 and Group NOBPCOS (n=77) with the BMI<25 kg·m~(-2) and the WHR<0.85,and 395 age-matched women with regular menstruation served as controls that were divided into 2 groups as well:Group OBCON(n=18) with the BMI≥25 kg·m~(-2) or the WHR≥0.85;and Group NOBCON(n=307) with the BMI<25 kg·m~(-2) and the WHR<0.85,and underwent a cross-sectional study.Results(1) Clinical phenotype:Adolescent girls with PCOS had precocious menarche compaired with the controls.84.85%of them could not establish a regular menstruation within 2 years after menarche.The presence of obesity was 53.89%(90/167) of which 57.78%(52/90) was central obesity,showed increased frequency of obesity compared with the controls(5.54%,18/325).The incidence of acanthosis nigricans was 26.95%(45/167),44.44%in Group OBPCOS and 6.49% in Group NOBPCOS(P<0.001).Group OBPCOS showed increased frequency of acanthosis nigricans compared with Group NOBPCOS.(2) Hormonal profile:The LH/FSHratio of the patients was 1.89±0.99,significantly higher than that of the controls(0.70±0.64)(P<0.01).The LH/FSH ratio of Group NOBPCOS (2.11±1.09) was significantly higher than that of Group OBPCOS(1.69±0.85)(P<0.01).T and DHEA-S level were higher in Group OBPCOS and Group NOBPCOS than in Group OBCON and Group NOBCON(both P<0.01).SHBG was lower in Group A and Group C compared with Group B and Group D(both P<0.01). FAI level was 8.20±8.24 in Group OBPCOS,significantly higher than those of Groups NOBPCOS(5.27±5.96),OBCON(4.02±4.63),and NOBCON(1.63±1.31)(all P<0.05).(3) Metabolic profile:The prevalence of pathological IR was 29.94%(50/167),significantly higher than that of the controls(6.77%,22/325,P<0.001),with a higher prevalence rate in Group OBPCOS(45.56%,41/90) compared with Group NOBPCOS(11.69%,9/77)(P<0.001).The FINS and HOMA-IR of the patients were significantly higher than those of the controls,and those of Groups OBPCOS and OBCON were both significantly higher than those of Groups NOBPCOS and NOBCON(all P<0.01). The TG of Group OBPCOS was significantly higher than that of Group NOBPCOS (P<0.01).(4) The family histories of obesity,a]opecia seborrheica, diabetes mellitus and hypertension were associated with adolescent PCOS(all P≤0.001).BMI was an independent risk factor of both hyperandrogenism and insulin resistance.Conclusion Adolescent PCOS is featured by premature menophania,failure to establish regular menstruation with 2 years after menarche,increased prevalence of obesity,hyperandrogenism,pathological insulin resistence.Obese girls with PCOS have more severe hyperandrogenism and IR than normal-weight PCOS girls,which may have some health implications later in life.
     Section 3
     Objective To evaluate the effects of metformin treatment in the adolescent girls with PCOS,and the role of insulin on metformin's efficacy.Methods This was a retrospective study.The patient population was 42 adolesecnt girls with PCOS undertaking metformin for 1 year.They were divide into Group IR(n=29) and Group NIR(n=13) according to pathological IR. Menstrual disturbance,insulin metabolism,and reproductive endocrinic parameters were assessed before and at the end of a treatment period of 1 year.Results All the patients were suffering from anovulation before treatment.The ovulation failure was successfully improved in 76.19% (32/42) of the patients after 1 year's metformin,significantly higher than that before treatment,and there were no difference of ovulation rate between Group IR and Group NIR(P>0.05).The body weight,body mass index, fasting insulin,HOMA-IR,area under the insulin-time curve,total testosterone,LH in both groups and free androgen index,LH/FSH ratio in Group IR were also improved(all P<0.001).The retrieve of ovulation was negative correlated with fasting insulin and HOMA-IR(both P<0.05).The free androgen index was negative correlated with fasting insulin(P<0.05). Conclusion Metformin treatment improves ovulatory function,reproductive endocrinology and metabolic disorder in adolescent girls with PCOS.The recovery of ovulating is associated with the role of decreasing serum level of insulin.
引文
[1] Revi P. Mathew, et al. Premature pubarche in girls is associated with functional adrenal but not ovarian hyperandrogenism[J]. The Journal of Pediatrics, july 2002, 141 (1) : 91-98.
    
    [2] Littlejohn EE. Intractable early childhood obesity as the initial sign of insulin resistant hyperinsulinism and precursor of polycystic ovary syndrome. Journal of Pediatric Endocrinology 20(1):41—51, 2007 Jan.
    
    [3] The Rotterdam ESHRE/ASRM-sponsored PCOS Consensus Workshop Group.Revised 2003 consensus on diagnostic criteria and longterm health risks related to polycystic ovary syndrome (PCOS). Hum Rep rod, 2004, 19: 41-47.
    
    [4] Tang TT, Lin JF. Investigation of menstrual cyclicity and determination of upper limits of serum androgen and insulin resistance in adolenscent girls.13~(th) World Congress of Gynecology Endocrinology, 2008.
    
    [5] Christopher R. McCartney, et al. The Association of Obesity and Hyperandrogenemia during the Pubertal Transition in Girls: Obesity as a Potential Factor in the Genesis of Postpubertal Hyperandrogenism [J]. The Journal of Clinical Endocrinology & Metabolism 91(5):1714 - 1722.
    
    [6] Silva A. Arslanian, et al. Polycystic ovary syndrome in adolescents: is there an epidemic [J] Current Opinion in Endocrinology & Diabetes. 9(1): 32-42,February 2002.
    
    [7] Dunaif A. Insulin resistance and the polycystic ovary syndrome: mechanism and implications for pathogenesis. Endocr Rev 1997; 18:774 - 800.
    
    [8] Richardson MR. Current perspectives in polycystic ovary syndrome. Am Fam Physician 2003;68:697 - 704.
    
    [9] Baillargeon JP, Iuorno MJ, Nestler JE. Comparison of metformin and thiazolidinediones in the management of polycystic ovary syndrome. Curr Opin Endocrinol Diabetes 2002:9:303-311.
    
    [10] Nestler JE, Jakubowicz DJ, de Vargas AF, Brik C, Quintero N, Medina F.Insulin stimulates testosterone biosynthesis by human thecal cells from women with polycystic ovary syndrome by activating its own receptor and using inositolglycan mediators as the signal transduction system. J Clin Endocrinol Metab 1998;83:2001 -2005.
    [11]Azziz R.Androgen excess is the key element in polycystic ovary syndrome.Fertil Steril 2003;80:252-254.
    [12]Pasquali R,Casimirri F.The impact of obesity on hyperandrogenism and polycystic ovary syndrome in premenopausal women.Clin Endocrinol,1993,39:1-16.
    [13]Treloar AE,Boynton RE,Behn BG,Brown BW.Variation of the human menstrual cycle through reproductive life.Int J Fertil 1967;12:77-126.
    [14]Hatch R,Rosenfield RL,Kim MH,Tredway D.Hirsutism:Implications,etiology and management.AM J Obstet Gynecol,1981:140:815-30.
    [15]糖尿病诊断标准与分型[J].中国糖尿病杂志,2000,8(1):5-6.
    [16]Wheeler MJ.The determination of bio-available testosterone.Ann Clin Biochem,1995,32:345-357.
    [17]Mather KJ,Hunt AJ,Steinberg HO,et al.Repeatability characteristics of simple indices of insulin resistance:implications for research applications.J Clin Endocrinol Metab,2001,86:5457-5464.
    [18]中华医学会糖尿病学分会代谢综合征研究协作组.中华医学会糖尿病学分会关于代谢综合征的建议.中华糖尿病杂志2004年第12卷第3期 Chin J Diabetes,June 2004,Vol 12,No 3.
    [19]Zukauskaite S,Seibokaite A,Lasas L,Lasiene D,Urbonaite B,Kiesylyte J.Serum hormone levels and anthropometric characteristics in girls with hyperandrogenism.Medicina(Kaunas).2005;41(4):305-12.
    [20]Dunger DB,Ahmed ML,Onq KK.Effects of obesity on growth and puberty [J].Best Pract Res Clin Endocrinol Metab,2005,19(3):375-390.
    [21]No authors listed.ACOG Committee Opinion No.349,November 2006:Menstruation in girls and adolescents:using the menstrual cycle as a vital sign[J].Obstetrics and gynecology,2006,108(5):1323-8.
    [22]Glueck CJ,Morrison JA,Friedman LA,Goldenberg N,Stroop DM,Wang P.Obesity,free testosterone,and cardiovascular risk factors in adolescents with polycystic ovary syndrome and regularly cycling adolescents.Metabolism.2006 Apt;55(4):508-14.
    [23]Vryonidou A,Papatheodorou A,Tavridou A,Terzi T,Loi V,Vatalas IA, Batakis N,Phenekos C,Dionyssiou-Asteriou A.Association of hyperandrogenemic and metabolic phenotype with carotid intima-media thickness in young women with polycystic ovary syndrome.J Clin Endocrinol Metab.2005 May;90(5):2740-6.
    [24]Avvad C1,Holeuwerger R,Silva VC,Bordallo MA,Breitenbach MM.Menstrual irregularity in the first postmenarchal years:an early clinical sign of polycystic ovary syndrome in adolescence.Gynecol Endocrinol.2001Jun;15(3):170-7.
    [25]Fernandes AR,de Sa Rosa e Silva AC,Romao GS,Pata MC,dos Reis RM.insulin resistance in adolescents with menstrual irregularities.J Pediatr Adolesc Gynecol.2005 Aug;18(4):269-74.
    [26]Silfen ME,Denburg MR,Manibo AM,Lobo RA,Jaffe R,Ferin M,Levine LS,Oberfield SE.Early endocrine,metabolic,and sonographic characteristics of polycystic ovary syndrome(PCOS):comparison between non-obese and obese adolescents.J Clin Endocrinol Metab.2003 0ct;88(10):4682-8.
    [27]Moran C,Reyna R,Boots LS,et al.Adrenocortical hyperresponsiveness to corticotropin in polycystic ovary syndrome patients with adrenal androgen excess.Fertil Steril,2004,81:126-311.
    [28]LIKITMASKUL S,COWELL CT,DONAGHUE K,et al."Exaggerated adrenarche" in children presenting with premature adrenarche[J].Clin Endocrinol,1995,42:265.
    [29]TAO Hong,MI Shu-hua,LU Zhao-lin.Insulin resistance and adrenal androgen excess in adolescents with polycystic ovary syndrome.Chin J Diabetes,June 2006,Vol 14,No 3.
    陶红,米树华,陆召麟。青春期多囊卵巢综合征肾上腺雄激素合成与胰岛素抵抗的关系。中国糖尿病杂志2006年第14卷第3期。
    [30]Gambineril A,Pelusil C,Vicennatil V,et al.besity and the polycystic ovary syndrome.Int J Obesity,2002,26:883-896.
    [31]FulghesuAM,Angioni S,Portoghese E,Milano F,Batetta B,Paoletti AM,Melis GB.Failure of the homeostatic model assessment calculation score for detecting metabolic deterioration in young patients with polycystic ovary syndrome.Fertil Steril.2006 Aug;86(2):398-404.
    [32]Svetlana Ten,Noel Maclaren.Insulin Resistance Syndrome in Children.The Journal of Clinical Endocrinology & Metabolism 89(6):2526-2539.
    [33]Coviello AD,Legro RS,DunaifA.Adolescent girls with polycystic ovary syndrome have an increased risk of the metabolic syndrome associated with increasing androgen levels independent of obesity and insulin resistance.J Clin Endocrinol Metab.2006 Feb;91(2):492-7.
    [34]毛文伟,李美芝,赵一鸣等。多囊卵巢综合征患者父母亲遗传表型的探讨[J]。中华妇产科杂志,2000;35(10):583-585。
    [35]侯灵彤,等。糖尿病家族青春期多囊卵巢综合征胰岛素抵抗的临床特征和治疗[J]。现代妇产科进展,2006,15(2):110-113。
    [36]张碧云,范保维,毛玲芝。多囊卵巢综合征危险因素的Logistic回归分析。海峡预防医学杂志2006年第12卷第4期。Strait J Prey Med 2006 VF1.12 No.4.
    [37]Ricardo Azziz,Enrico Carmina,Didier Dewailly,Evanthia Diamanti-Kandarakis,Hector F.Escobar-Morreale,Walter Futterweit,Onno E.Janssen,Richard S.Legro,Robert J.Norman,Ann K Taylor and Selma F.Witchel.Position statement:criteria for defining polycystic ovary syndrome as a predominantly hyperandrogenic syndrome:An androgen excess society guideline.The Journal of Clinical Endocrinology & Metabolism 2006;Vol.91,No.11 4237-4245.
    [38]林金芳,李昕,朱铭伟.多囊卵巢综合征的分形探讨[J].中华妇产科杂志,2006,41(10):684-88.
    [39]Franks,S.Polycystic ovary syndrome:a changing perspective[J].Clinical Endocrinology,1989,31(1):87-120.
    [40]Charles Sultan,Francoise Paris.Clinical expression of polycystic ovary syndrome in adolescent girls.Fertility and Sterility,Vol 86,Suppl1,6,July 2006.
    [41]De Leo V,Musacchio MC,Morgante G,Piomboni P,Petraglia F.Metformin treatment is effective in obese teenage girls with PCOS.Hum Reprod.2006Sep;21(9):2252-6.
    [42]Glueck CJ,Aregawi D,Winiarska M,Agloria M,Luo G,Sieve L,Wang P.Metformin-diet ameliorates coronary heart disease risk factors and facilitates resumption of regular menses in adolescents with polycystic ovary syndrome. J Pediatr Endocrinol Metab. 2006 Jun;19(6):831-42.
    
    [43] Diamanti-Kandarakis E, Kouli C, Tsianateli T, et al. Therapeutic effects of metformin on insulin resistance and hyperandrogenism in polycystic ovary syndrome. Eur J Endocrinol, 1998;138:269-274.
    
    [44] Allen HF, Mazzoni C, Heptulla RA, Murray MA, Miller N, Koenigs L, Reiter E0. Randomized controlled trial evaluating response to metformin versus standard therapy in the treatment of adolescents with polycystic ovary syndrome. J Pediatr Endocrinol Metab. 2005 Aug;18(8):761-8.
    
    [45] Sahin I, Serter R, Karakurt F, Demirbas B, Culha C, Taskapan C, Kosar F, Aral Y. Metformin versus flutamide in the treatment of metabolic consequences of non-obese young women with polycystic ovary syndrome: a randomized prospective study. Gynecol Endocrinol. 2004 Sep;19(3) :115-24.
    
    [46] Bridger T, MacDonald S, Baltzer F, Rodd C. Randomized placebo controlled trial of metformin for adolescents with polycystic ovary syndrome.Arch Pediatr Adolesc Med. 2006 Mar;160(3):241-6.
    
    [47] Nestler JE, Jakubowicz DJ, Evans WS, Pasquali R. Effects of metformin on spontaneous and clomiphene-induced ovulation in the polycystic ovary syndrome. N Engl J Med 1998;338:1876 - 1880.
    
    [48] Moghetti P, Castello R, Negri C, Tosi F, Perrone F, Caputo M, Zanolin E, Muggeo M. Metformin effects on clinical features, endocrine and metabolic profiles, and insulin sensitivity in polycystic ovary syndrome: a randomized,double-blind, placebo-controlled 6-month trial, followed by open, long-term clinical evaluation. J Clin Endocrinol Metab 2000;85:139 - 146.
    
    [49] Pirwany IR, Yates RWS, Cameron IT, Fleming R. Effects of the insulin sensitizing drug metformin on ovarian function, follicular growth and ovulation rate in obese women with oligomenorrhoea. Hum Reprod 1999;14:2963-2968.
    
    [50] Harborne L, Fleming R, Lyall H, Sattar N, Norman J. Metformin or antiandrogen in the treatment of hirsutism in polycystic ovary syndrome. J Clin Endocrinol Metab 2003;88:4116 - 4123.
    
    [51] Homburg R. Polycystic ovary syndrome in adolescence: new insights in pathophysiology and treatment. Endocr Dev 2005; 8:137-149.
    [52] Mansfied R, Galea R, Brincat M, Hole D, Mason H. Metformin has direct effects on human ovarian steroidogenesis. Fertil Steril 2003; 79:956 - 962.
    [53] Attia GR, Rainey WE, Carr B. Metformin directly inhibits androgen production in human thecal cells. Fertil Steril 2001;76:517 - 524.
    [54] Jakubowicz DJ, Nestler JE. Lean women with polycystic ovary syndrome respond to insulin reduction with decrease in ovarian P450cl7 activity and serum androgens. J Clin Endocrinol Metab 1997;82:4075 - 4079.
    [55] Nestler JE. Role of hyperinsulinemia in the pathogenesis of the polycystic ovary syndrome, and its clinical implications. Semin Reprod Endocrinol, 1997, 15:111-122.
    [56] Chavez-Ross A, Franks S, Mason HD, et al. Modeling the control of ovulation and polycystic ovary syndrome. J Math Biol, 1997, 36:95-118.
    [57] Diamanti-Kandarakis E, Dunaif A. New perspectives in polycystic ovary syndrome. Trends Endocrinol Metab, 1996, 7:267-271.
    [58] ibanez L, Ferrer A, Ong K, Amin R, Dunger D, de Zegher F. Insulin sensitization early after menarche prevents progression from precocious pubarche to polycystic ovary syndrome. J Pediatr. 2004 Jan;144(1):23-9.
    [59] S. Eisenhardt, N. Schwarzmann, V. Henschel, A. Germeyer, M. von Wolff, A. Hamann, and T. Strowitzki. Early Effects of Metformin in Women with Polycystic Ovary Syndrome: A Prospective Randomized, Double-Blind, Placebo-Controlled Trial. The Journal of Clinical Endocrinology & Metabolism 2006, 91 (3):946 - 952.
    [1]Dunaif A.Hyperandrogenic anovulation(PCOS):a unique disorder of insulin action associated with an increased risk of non-insulin-dependent diabetes mellitus[J].Am J Med,1995,98(1):33239.
    [2]Van Hooff,et al.Polycystic ovaries in adolescents and the relationship with menstrual cycle patterns luteinizing hormone,androgens,and insulin.Fertil and Steril[J].2000,74(1):49-58.
    [3]Silfen ME,Denburg MR,Manibo AM,Lobo RA,Jaffe R,Ferin M,Levine LS,Oberfield SE.Early endocrine,metabolic,and sonographic characteristics of polycystic ovary syndrome(PCOS):comparison between nonobese and obese adolescents.J Clin Endocrinol Metab.2003 0ct;88(10):4682-8.
    [4]韩玉昆,等。青春期多囊卵巢综合征的临床研究[J]。天津医药,2002,30(2): 79-81。
    
    [5] Van Hooff, et al. Polycystic ovaries in adolescents and the relationship with menstrual cycle patterns luteinizing hormone, androgens, and insulin.Fertil and Steril[J]. 2000, 74(1): 49-58.
    
    [6] Revi P. Mathew, et al., Premature pubarche in girls is associated with functional adrenal but not ovarian hyperandrogenism[J] . The Journal of Pediatrics, july 2002, 141 (1): 91-98.
    
    [7] Zukauskaite S, Seibokaite A, Lasas L, Lasiene D, Urbonaite B, Kiesylyte J. Serum hormone levels and anthropometric characteristics in girls with hyperandrogenism. Medicina (Kaunas). 2005;41 (4):305-12.
    
    [8] Chhabra S, McCartney CR, Yoo RY, Eagleson CA, Chang RJ, Marshall JC.Progesterone inhibition of the hypothalamic gonadotropin-releasing hormone pulse generator: evidence for varied effects in hyperandrogenemic adolescent girls. J Clin Endocrinol Metab. 2005 May;90(5):2810-5.
    
    [9] S. K. Blank, et al. The origins and sequelae of abnormal neuroendocrine function in polycystic ovary syndrome[J]. Human Reproduction Update,2006,12(4): 351-361.
    
    [10] Siow Y, Kives S, Hertweck P, Perlman S, Fallat MB. Serum Mullerian-inhibiting substance levels in adolescent girls with normal menstrual cycles or with polycystic ovary syndrome. Fertil Steril. 2005 Oct;84(4):938-44.
    
    [11] Christopher R. McCartney, et al. The Association of Obesity and Hyperandrogenemia during the Pubertal Transition in Girls: Obesity as a Potential Factor in the Genesis of Postpubertal Hyperandrogenism[J]. The Journal of Clinical Endocrinology & Metabolism 91(5):1714 - 1722.
    
    [12] Silva A. Arslanian, et al. Polycystic ovary syndrome in adolescents:is there an epidemic[J]? Current Opinion in Endocrinology & Diabetes.9(1):32-42, February 2002.
    
    [13] Littlejohn EE. Intractable early childhood obesity as the initial sign of insulin resistant hyperinsulinism and precursor of polycystic ovary syndrome. Journal of Pediatric Endocrinology 20(1):41-51, 2007 Jan
    
    [14] Sawathiparnich P, Weerakulwattana L, Santiprabhob J, Likitmaskul S. Obese adolescent girls with polycystic ovary syndrome(PCOS) have more severe insulin resistance measured by HOMA-IR score than obese girls without PCOS.J Med Assoc Thai.2005 Nov;88 Suppl 8:S33-7.
    [15]Azziz R.Polycystic ovary syndrome,insulin resistance,and molecular defects of insulin signaling[J].J Clin EndocrinolMetab,2002,87:4085-4087.
    [16]DeUgarte C.M.,Bartolucci A.A.,Azziz R.Prevalence of insulin resistance in the polycystic ovary syndrome using the homeostasis model assessment[J].FERTIL.STERIL.2005,83(5):1454-1460.
    [17]陆湘,等.关于青春期多囊卵巢综合征胰岛素抵抗的探讨[J].中国实用妇科与产科杂志,2004,20(12):746-748。
    [18]Muller G,Ertl J,Gerl M,et al.Leptin impairs metabolic actions of insulin in isolated rat adipocytes[J].J Biol Chem,1997,272:105852-10593.
    [19]Mendonca HC,Montenegro RM Jr,Foss MC,Silva de Sa MF,Ferriani RA.Positive correlation of serum leptin with estradiol levels in patients with polycystic ovary syndrome.Braz J Med Biol Res.2004 May;37(5):729-36.
    [20]Fernandes AR,de Sa Rosa e Silva AC,Romao GS,Pata MC,dos Reis RM.Insulin resistance in adolescents with menstrual irregularities.JPediatr Adolesc Gynecol.2005 Aug;18(4):269-74.
    [21]Ibanez L,et al.Insulin sensitization early after menarche prevents progression from precocious pubarche to polycystic ovary syndrome[J].J Pediatr JT-The Journal of pediatrics,2004,144(1):23-9.
    [22]CovielloAD,hegroRS,DunaifA.Adolescent girls withpolycystic ovary syndrome have an increased risk of the metabolic syndrome associated with increasing androgen levels independent of obesity and insulin resistance.J Clin Endocrinol Metab.2006 Feb;91(2):492-7.
    [23]Leibel NI,Baumann EE,Kocherginsky M,Rosenfield RL.Relationship of adolescent polycystic ovary syndrome to parental metabolic syndrome.J Clin Endocrinol Metab.2006 Apr;91(4):1275-83.
    [24]侯灵彤,等.糖尿病家族青春期多囊卵巢综合征胰岛素抵抗的临床特征和治疗[J].现代妇产科进展,2006,15(2):110-113。
    [25]Vryonidou A,Papatheodorou A,Tavridou A,Terzi T,Loi V,Vatalas IA, Batakis N,Phenekos C,Dionyssiou-Asteriou A.Association of hyperandrogenemic and metabolic phenotype with carotid intima-media thickness in young women with polycystic ovary syndrome.J Clin Endocrinol Metab.2005 May;90(5):2740-6.
    [26]Trent M,Austin SB,Rich M,Gordon CM.Overweight status of adolescent girls with polycystic ovary syndrome:body mass index as mediator of quality of life.Ambul Pediatr.2005 Mar-Apr;5(2):107-11.
    [27]Trent ME,Rich M,Austin SB,Gordon CM.Fertility concerns and sexual behavior in adolescent girls with polycystic ovary syndrome:implications for quality of life.J Pediatr Adolesc Gynecol.2003 Feb;16(1):33-7.
    [28]The Rotterdam ESHRE/ASRM-sponsored PCOS consensus workshop group.Revised 2003 consensus on diagnostic criteria and longterm health risks related to polycystic ovary syndrome(PCOS),[J].Hum Reprod,2004,19(1):41-47.
    [29]Ankarberg,Carina,et al.Diurnal Rhythm of Testosterone Secretion before and throughout Puberty in Healthy Girls:orrelation with 17[beta]-Estradiol and Dehydroepiandrosterone Sulfate[J].Journal of Clinical Endocrinology & Metabolism.84(3):975-984,March 1999.
    [30]Type 2 diabetes in children and adolescents.American Diabetes Association.Diabetes Care,2000:23:3812389.
    [31]李颖,等.儿童和青少年胰岛素抵抗影响因素的研究[J].中华预防医学杂志,2004,38(4):234-236。
    [32]张锋,贾伟平,陆俊茜,等。上海社区自然人群基础胰岛素水平与年龄的关系[J]。上海医学,2005,28(1):10-12。
    [33]Gungor N,Saad R,Janosky J,et al.Validation of surrogate estimates of insulin sensitivity and insulin secretion in children and adolescents[J].J Pediatr JT - The Journal of pediatrics,2004,144(1):47-55.
    [34]Rosenfield,Robert L.Identifying Children at Risk forPolycystic Ovary Syndrome.J Clin Endocrinol Metab.Volume:92,Issue:3,Date:2006 3 7,Pages:787-796.
    [35]Yoo RY,Sirlin CB,Gottschalk M,Chang RJ.Ovarian imaging by magnetic resonance in obese adolescent girls with polycystic ovary syndrome:a pilot study. Fertil Steril. 2005 Oct;84(4):985-95.
    
    [36] Glueck CJ, Aregawi D, Winiarska M, Agloria M, Luo G, Sieve L, Wang P.Metformin-diet ameliorates coronary heart disease risk factors and facilitates resumption of regular menses in adolescents with polycystic ovary syndrome. J Pediatr Endocrinol Metab. 2006 Jun;19(6):831-42.
    
    [37] Taner C, Inal M, Basogul O, et al. Comparison of the clinical efficacy and safety of flutamide versus flutamide plus an oral contraceptive in the treatment of hirsutism[J]. Gynecol Obstet invest, 2002 ,54 (2) :105-108.
    
    [38] Ibanez L, Zegher F. Low-dose combination of flutamide, metformin and an oral contraceptive for non-obese, young women with polycystic ovary syndrome [J]. Hum Reprod, 2003,18(1): 57-60.
    
    [39] Moghetti P, Tosi F, Tosti A, et al. Comparison of spironolactone,flutamide, and finasteride efficacy in the treatment of hirsutism: a randomized double-blind, placebo-controlled trial [J]. J Clin Endocrinol Metab, 2000, 85: 89-94.
    
    [40] Mastorakos G, Koliopoulos C, Deligeoroglou E, Diamanti-Kandarakis E,Creatsas G. Effects of two forms of combined oral contraceptives on carbohydrate metabolism in adolescents with polycystic ovary syndrome.Fertil Steril. 2006 Feb;85(2):420-7.
    
    [41] Fleming R, Hop kinson Z E, Wallace A M, et al. Ovarian function and metabolic factors in women with oligomenorrhea treated with metformin in randomized double blind placebo controlled trial [J]. J Clin Endocrinol Metab,2002, 87: 569-574.
    
    [42] De Leo V, Musacchio MC, Morgante G, Piomboni P, Petraglia F. Metformin treatment is effective in obese teenage girls with PCOS. Hum Reprod. 2006 Sep;21(9):2252-6.
    
    [43] Bridger T, MacDonald S, BaltzerF, Rodd C. Randomized placebo-controlled trial of metformin for adolescents with polycystic ovary syndrome. Arch Pediatr Adolesc Med. 2006 Mar;160(3):241-6.
    
    [44] Chou K H, Von Eye C H, Capp E, et al. Clinical, metabolic and endocrine parameters in response to metformin in obese women with polycystic ovary syndrome: a randomized, double-blind and placebo-controlled trial [J]. Horm Metab Res, 2003, 35(2): 86-91.
    
    [45] Kazerooni T, Dehghan K M. Effects of metformin therapy on hyperandrogenism in women with polycystic ovarian syndrome [J]. Gynecol Endocrinol, 2003, 17(1): 51-56.
    
    [46] Allen HF, Mazzoni C, Heptulla RA, Murray MA, Miller N, Koenigs L, Reiter E0. Randomized controlled trial evaluating response to metformin versus standard therapy in the treatment of adolescents with polycystic ovary syndrome. J Pediatr Endocrinol Metab. 2005 Aug;18(8):761-8.
    
    [47] Morin P L C, Vauhkonen I, Koivunen R M, R et al. Endocrine and metabolic effects of metformin versus ethinyl estradiol-cyproterone acetate in obese women with polycysticovary ovary syndrome: a randomized study [J]. J Clin Endocrinol Metab, 2000,85: 3161-3168.
    
    [48] Sahin I, Serter R, Karakurt F, Demirbas B, Culha C, Taskapan C, Kosar F, Aral Y. Metformin versus flutamide in the treatment of metabolic consequences of non-obese young women with polycystic ovary syndrome: a randomized prospective study. Gynecol Endocrinol. 2004 Sep;19(3) :115-24.
    
    [49] Ibanez L, de Zegher F. Flutamide-metformin plus ethinylestradiol-drospirenone for lipolysis and antiatherogenesis in young women with ovarian hyperandrogenism: the key role of metformin at the start and after more than one year of therapy. J Clin Endocrinol Metab. 2005 Jan; 90(1): 39-43.
    
    [50] Ibanez L, Valls C, Cabre S, De Zegher F. Flutamide-metformin plus ethinylestradiol-drospirenone for lipolysis and antiatherogenesis in young women with ovarian hyperandrogenism: the key role of early, low-dose flutamide. J Clin Endocrinol Metab. 2004 Sep;89(9):4716-20.
    
    [51] Ibanez L, de Zegher F. Ethinylestradiol-drospirenone,flutamide-metformin, or both for adolescents and women with hyperinsulinemic hyperandrogenism: opposite effects on adipocytokines and body adiposity. J Clin Endocrinol Metab. 2004 Apr;89(4):1592-7.
    
    [52] Ibanez L, Ong K, Ferrer A, Amin R, Dunger D, de Zegher F. Low-dose flutamide-metformin therapy reverses insulin resistance and reduces fat mass in nonobese adolescents with ovarian hyperandrogenism. J Clin Endocrinol Metab. 2003 Jun;88(6):2600-6.
    
    [53] Ibanez L, De Zegher F. Flutamide-metformin plus an oral contraceptive (OC) for young women with polycystic ovary syndrome: switch from third- to fourth-generation 0C reduces body adiposity. Hum Reprod. 2004 Aug;19(8):1725-7.
    
    [54] Garmes HM, Tambascia MA, Zantut-Wittmann DE. Endocrine-metabolic effects of the treatment with pioglitazone in obese patients with polycystic ovary syndrome. Gynecol Endocrinol. 2005 Dec;21(6):317-23.
    
    [55] Ortega-Gonzalez C, Luna S, Hernandez L, Crespo G, Aguayo P,Arteaga-Troncoso G, Parra A. Responses of serum androgen and insulin resistance to metformin and pioglitazone in obese, insulin-resistant women with polycystic ovary syndrome. J Clin Endocrinol Metab. 2005 Mar;90(3):1360-5.
    
    [56] Glueck CJ, Moreira A, Goldenberg N, Sieve L, Wang P. Pioglitazone and metformin in obese women with polycystic ovary syndrome not optimally responsive to metformin. Hum Reprod. 2003 Aug;18(8):1618-25.
    
    [57] Rautio, Katrina Morin-Papunen, Laure C Tapanainen, Juha S Ruokonen, Aimo.Rosiglitazone treatment alleviates inflammation and improves liver function in overweight women with polycystic ovary syndrome: a randomized placebo-controlled study. Fertil Steril. Volume: 87, Issue: 1, Date: 2007 01 01, Pages: 202-6.

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