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不孕不育新进展(英文)

李蓉深圳试管婴儿

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6/22/2009

The relationship between anti-Mu¨ llerian hormone, androgen

The relationship between anti-Mu¨ llerian hormone, androgen
and insulin resistance on the number of antral follicles
in women with polycystic ovary syndrome
Mei-Jou Chen1,2, Wei-Shiung Yang2,3, Chi-Ling Chen2, Ming-Yih Wu1, Yu-Shih Yang1
and Hong-Nerng Ho1,4
1Department of Obstetrics and Gynecology, National Taiwan University Hospital, No. 7 Chung-Shan South Road, Taipei 100, Taiwan;
2Graduate Institute of Clinical Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan; 3Department of Internal
Medicine, National Taiwan University Hospital, Taipei, Taiwan
4Correspondence address. Tel: þ886-2-2356-2175; Fax: þ886-2-2341-8557; E-mail: hnho@ntu.edu.tw
BACKGROUND: Anti-Mu¨ llerian hormone (AMH) is a biomarker that predicts the number of antral follicles and is
involved in follicle arrest for women with polycystic ovary syndrome (PCOS). We investigated the association between
the characteristic hyperandrogenemia, insulin resistance (IR), AMH, and the morphology and size of ovaries for
women with PCOS. METHODS: A total of 99 Taiwanese women with PCOS who were willing to undergo vaginal
ultrasonography were enrolled in this cross-sectional study. RESULTS: The number of antral follicles and the
ovarian volume showed a significant correlation with AMH, total testosterone and the free androgen index, but not
with age, body mass index (BMI) or the homeostasis model assessment of insulin resistance (HOMA-IR). AMH
had a significant negative association with both BMI and HOMA-IR. Multiple stepwise regression analysis demonstrated
that AMH, BMI and total testosterone were independently related to the number of antral follicles.
AMH and total testosterone were the main determinants for ovarian volume in a stepwise regression model.
CONCLUSIONS: Our results suggest that not only the AMH level, but also obesity, IR and elevated androgen
levels may relate to the development of the large size of antral follicle pool and ovarian volume in women with
PCOS. Obesity and IR may enhance the follicular excess through the dysregulation of AMH or through the
pathway of hyperandrogenemia. These findings might partly explain why adequate body weight management and
improvement in IR can improve the ovulatory function for women with PCOS.
Keywords: polycystic ovary syndrome; anti-Mu¨llerian hormone; obesity; insulin resistance; antral follicle count

Impaired insulin-dependent glucose metabolism in granulosa-lutein cells from anovulatory women with polycystic ovaries

Impaired insulin-dependent glucose metabolism in granulosa-lutein cells from anovulatory women with polycystic ovaries

S. Rice1,4, N. Christoforidis2, C. Gadd2, D. Nikolaou2, L. Seyani3, A. Donaldson3, R. Margara2, K. Hardy1 and S. Franks1,5

1 Institute of Reproductive and Developmental Biology, 2 Department of Obstetrics and Gynaecology, Imperial College London, London and 3 Clinical Chemistry Laboratory, Hammersmith Hospital, Du Cane Road, London W12 0NN, UK

5 To whom correspondence should be addressed. Email: s.franks@imperial.ac.uk

BACKGROUND: Insulin resistance and hyperinsulinaemia are well-recognized characteristics of anovulatory women with polycystic ovary syndrome (PCOS) but, paradoxically, steroidogenesis by PCOS granulosa cells remains responsive to insulin. The hypothesis to be tested in this study is that insulin resistance in the ovary is confined to the metabolic effects of insulin (i.e. glucose uptake and metabolism), whereas the steroidogenic action of insulin remains intact. METHODS: Granulosa-lutein cells were obtained during IVF cycles from seven women with normal ovaries, six ovulatory women with PCO (ovPCO) and seven anovulatory women with PCO (anovPCO). Mean body mass index was in the normal range in all three groups. Granulosa-lutein cells were cultured with insulin (1, 10, 100 and 1000 ng/ml) and LH (1, 2.5 and 5 ng/ml). Media were sampled at 24 and 48 h and analysed for glucose uptake, lactate production and (48 h only) progesterone production. RESULTS: Insulin-stimulated glucose uptake by cells from anovPCO was attenuated at higher doses of insulin (100 and 1000 ng/ml) compared with that by cells from either ovPCO (P=0.02) or controls (P=0.02). Insulin and LH stimulated lactate production in a dose-dependent manner, but insulin-dependent lactate production was markedly impaired in granulosa-lutein cells from anovPCO compared with either normal (P=0.002) or ovPCO (P<0.0001). By contrast, there was no difference in insulin-stimulated progesterone production between granulosa-lutein cells from the three ovarian types. CONCLUSIONS: Granulosa-lutein cells from women with anovPCOS are relatively resistant to the effects of insulin-stimulated glucose uptake and utilization compared with those from normal and ovPCO, whilst maintaining normal steroidogenic output in response to physiological doses of insulin. These studies support the probability of a post-receptor, signalling pathway-specific impairment of insulin action in PCOS.

Key words: granulosa cells/insulin resistance/LH/polycystic ovaries/progesterone

4 Present address: Department of Basic Medical Sciences, St George's Hospital Medical School, Cranmer Terrace, Tooting, London SW17 0RE, UK

The role of metformin in polycystic ovary syndrome: a systematic review

The role of metformin in polycystic ovary syndrome: a systematic review

Etelka Moll1, Fulco van der Veen and Madelon van Wely

Centre for Reproductive Medicine, Department of Obstetrics and Gynaecology, Academic Medical Centre, PO Box 22700, 1100 DE, Amsterdam, The Netherlands

1 Correspondence address. Tel: +31-20-5663557; Fax: +31-20-6963489; E-mail: e.moll@amc.uva.nl

This meta-analysis evaluated the effectiveness of metformin in subfertile women with polycystic ovary syndrome (PCOS). Only randomized trials investigating the effectiveness of metformin and PCOS definition consistent with the Rotterdam consensus criteria, were eligible. Primary outcome was live birth rate. A literature search identified 27 trials. In therapy naïve women, we found no evidence of a difference in live birth rate when comparing metformin with clomifene citrate (CC) [relative risks (RR) 0.73; 95% confidence interval (CI) 0.51–1.1] or comparing metformin plus CC with CC (RR 1.0; 95% CI 0.82–1.3). In CC-resistant women, metformin plus CC led to higher live birth rates than CC alone (RR 6.4; 95% CI 1.2–35); metformin also led to higher live birth rates than laparoscopic ovarian drilling (LOD) (RR 1.6; 95% CI 1.1–2.5). We found no evidence for a positive effect of metformin on live birth when added to LOD (RR 1.3; 95% CI 0.39–4.0) or FSH (RR 1.6; 95% CI 0.95–2.9), or when co-administered in IVF (RR 1.5; 95% CI 0.92–2.5). In IVF, metformin led to fewer cases of ovarian hyperstimulation syndrome (OHSS) (RR 0.33; 95% CI 0.13–0.80). This meta-analysis demonstrates that CC is still first choice therapy for women with therapy naïve PCOS. In CC-resistant women, the combination of CC plus metformin is the preferred treatment option before starting with LOD or FSH. At present, there is no evidence of an improvement in live birth when adding metformin to LOD or FSH. In IVF, metformin leads to a reduced risk of OHSS.

Key words: infertility / metformin / PCOS / pregnancy / review

Received on April 12, 2007; revised June 7, 2007; accepted on June 29, 2007

Metformin reduces serum müllerian-inhibiting


Richard Fleming, Ph.D.,a Lyndal Harborne, B.Med.,a David T. MacLaughlin, Ph.D.,b
Daniel Ling,b Jane Norman, M.D.,a Naveed Sattar, M.R.C.Path.,a and David B. Seifer, M.D.c
a University Department of Obstetrics and Gynaecology, Royal Infirmary, Glasgow, United Kingdom; b Paediatric Research
Laboratory, Massachusetts General Hospital for Children and Harvard Medical School, Boston, Massachusetts; and c Department
of Obstetrics, Gynecology and Reproductive Sciences, Division of Reproductive Endocrinology and Infertility, University
of Medicine and Dentistry of New Jersey—Robert Wood Johnson Medical School, New Brunswick, New Jersey
Objective: Assessment of ovarian responses to metformin treatment in obese women with polycystic ovary
syndrome (PCOS).
Design: Prospective treatment with randomization to two doses of metformin.
Setting: University teaching hospital.
Patient(s): Obese women (n  82) with PCOS.
Intervention(s): Markers of ovarian function were assessed after 4 and 8 months.
Main Outcome Measure(s): Hormone (androgens and müllerian-inhibiting substance [MIS]) changes over time.
Result(s): There was no difference in the reproductive hormone changes between the doses of metformin, and
data were combined for further analyses. Significant responses to treatment were recorded for menstrual
frequency and androstenedione (A) (reduction) within the first 4 months of treatment. However, suppression of
the elevated circulating MIS concentrations required protracted treatment, because no change was observed in the
first 4 months—only in the second 4-month assessment period.
Conclusion(s): Metformin treatment of PCOS leads to rapid suppression of A and improved menstrual frequency.
Suppression of MIS is a delayed response that may be secondary to the development of a cohort of follicles that
underwent initial recruitment in an environment of reduced insulin stimulation. (Fertil Steril 2005;83:130–6. ©
2005 by American Society for Reproductive Medicine.)
Key Words: Müllerian-inhibiting substance, PCOS, metformin, ovarian follicles

Metformin effects on ovarian ultrasound appearance and steroidogenic function in normal-weight normoinsulinemic women with polycystic ovary syndrome: a randomized double-blind placebo-controlled clinical trial

Metformin effects on ovarian ultrasound appearance and steroidogenic function in normal-weight normoinsulinemic women with polycystic ovary syndrome: a randomized double-blind placebo-controlled clinical trial

Daniela Romualdi, M.D.a, Maddalena Giuliani, M.D.a, Francesca Cristello, M.D.a, Anna Maria Fulghesu, M.D.c, Luigi Selvaggi, M.D.a, Antonio Lanzone, M.D.ab, Maurizio Guido, M.D., Ph.D.aCorresponding Author Informationemail address

Received 1 October 2008; received in revised form 14 January 2009; accepted 19 January 2009. published online 06 March 2009.
Corrected Proof

Objective

To investigate metformin effects on the endocrine-metabolic parameters and ovarian morphology in normoinsulinemic women with polycystic ovary syndrome (PCOS).

Design

Randomized double-blind study.

Setting

Operative Division of Endocrinological Gynecology, Università Cattolica del Sacro Cuore.

Patient(s)

Twenty-eight normal-weight normoinsulinemic PCOS women.

Intervention(s)

Patients were randomized to receive metformin 500 mg twice a day (group A, 15 subjects) or placebo (group B, 13 subjects) for 6 months. Ultrasonographic pelvic exams, hormonal and lipid features, and oral glucose tolerance test were performed at baseline and after 3 and 6 months of treatment.

Main Outcome Measure(s)

Hormonal and glycoinsulinemic assessment, ovarian ultrasound appearance.

Result(s)

Glycoinsulinemic assessment remained unvaried in both groups. About 70% of patients in group A experienced a restoration of menstrual cyclicity. Metformin significantly decreased testosterone levels at 3 and 6 months) and 17-hydroxyprogesterone levels at 6 months, and improved hirsutism score at 6 months. No clinical or hormonal modifications occurred in group B. Metformin, but not placebo, reduced ovarian volume and stromal/total area ratio at 3 and 6 months.

Conclusion(s)

Metformin seems to improve the menstrual pattern and ultrasonographic ovarian features in normoinsulinemic PCOS women. These effects seem to be, at least in part, independent of the insulin-lowering properties of the drug.

Metformin has direct effects on human ovarian steroidogenesis.

Metformin has direct effects on human ovarian steroidogenesis.

 

Mansfield R, Galea R, Brincat M, Hole D, Mason H
Fertil Steril 2003; 79:956-62.

Abstract
OBJECTIVE: To investigate the possibility of direct effects of metformin on ovarian steroidogenesis. DESIGN: Cultured ovarian cells. SETTING: Academic research environment. PATIENT(S): Women undergoing bilateral salpingoophorectomy for benign gynecological disease. MAIN OUTCOME MEASURE(S): Estradiol and P were measured in granulosa cell (GC) conditioned medium and androstenedione (A) and P in theca conditioned medium. RESULT(S): The effect of addition of metformin alone to GCs was variable, but significant inhibition of both P and E2 was seen (range 0%-30%). Metformin dose-dependently inhibited gonadotrophin and insulin-stimulated P and E2 production (range 25%-50%). In theca, metformin inhibited A production (0%-40%) with no effect on P. In the presence of insulin, A was inhibited dose-dependently and P increased by a similar magnitude. CONCLUSION(S): These results demonstrate a direct effect of metformin on ovarian steroidogenesis. The inhibitory effects on androgen production in particular would be beneficial in polycystic ovary syndrome (PCOS).

MeSH
Adult; Androstenedione; Estradiol; Female; Granulosa Cells; Humans; Hypoglycemic Agents; Metformin; Middle Aged; Ovarian Follicle; Progesterone; Theca Cells

Metformin alters insulin signaling and viability of

Metformin alters insulin signaling and viability of
human granulosa cells
Barbara Sonntag, M.D., Martin Götte, Ph.D., Pia Wülfing, M.D., Andreas N. Schüring, M.D.,
Ludwig Kiesel, M.D., and Robert R. Greb, M.D.
Department of Obstetrics and Gynecology, University Hospital of Münster, Münster, Germany
Objective: To study whether insulin signaling pathways in the ovary are altered by metformin.
Design: In vitro human granulosa cell culture system.
Setting: Academic research environment.
Patient(s): Infertility patients undergoing oocyte retrieval for IVF/ICSI.
Main Outcome Measure(s): Cell viability and phosphorylated protein kinase B (PKB/AKT) and p44/42 mitogenactivated
protein kinase (MAPK) expression of human primary and HGL5 granulosa cells.
Result(s): Basal cell viability of primary granulosa cells was significantly increased relative to control by metformin
preincubation, without an additional stimulatory effect of insulin or IGF. Phosphorylated AKT expression in lysates of
the human granulosa cell line HGL5 was significantly increased in contrast to decreased phosphorylated MAPK
expression by metformin preincubation.
Conclusion(s): Besides systemic effects, the ovulation inducing action of metformin may at least partially be due
to direct effects on insulin signaling intermediates and follicular growth patterns in the ovary. (Fertil Steril 2005;
84(Suppl 2):1173–9. ©2005 by American Society for Reproductive Medicine.)
Key Words: AKT, granulosa, insulin signaling, MAPK, metformin, polycystic ovary syndrome

GENE EXPRESSION OF IGF-1 RECEPTOR IN HUMAN LUTEINIZED

GENE EXPRESSION OF IGF-1 RECEPTOR IN HUMAN LUTEINIZED
GRANULOSA CUMULUS CELLS FROM NON OBESE
AND NON INSULIN RESISTANT WOMEN WITH POLYCYSTIC
OVARY SYNDROME (PCOS) WITH AND WITHOUT METFORMIN
TREATMENT. L. F. Santana, J. M. Ferna´ndez-Santoss, M. J. Herna´ez,
C. Caligara, R. M. Reis, M. Ferna´ndez-Sa´nchez. Department of Obstetrics
& Gynaecology, Faculty of Medicine of Ribeira˜o Preto, University of Sa˜o
Paulo, Ribeira˜o Preto, Sa˜o Paulo, Brazil; Department of Normal and Pathologic
Cytology and Histology, The University of Seville School of Medicine,
Sevilla, Spain; IVF Laboratory, IVI Sevilla, Sevilla, Spain; Reproductive
Medicine, IVI Sevilla, Sevilla, Spain.
OBJECTIVE: The aim of this study was to evaluate gene expression of
IGF-1 receptor in human luteinized granulosa cumulus cells from non obese
and non insulin resistant (IR) women with PCOS with and without metformin
treatment.
DESIGN: Randomized controlled clinical trial.
MATERIALS AND METHODS: We evaluated twelve women with ovulatory
cycles; 9 women with PCOS and 8 women with PCOS treated with
metformin for at least 8 weeks at a dose of 1700 mg/day. All groups were similar
regarding weight, body mass index and waist circumference. None of
them had IR. All women underwent controlled ovarian hyperstimulation using
a GnRH analogue long protocol and a personalized dose of FSHrþhMG.
Granulosa cells were obtained from the cumulus oocytes complex by microdissection
from the five largest pre-ovulatory follicles. IGF-1 receptor gene
expression was determined by semi-quantitative RT-PCR. Serum and follicular
fluid levels of E2, progesterone, testosterone, FSH, LH, insulin, SHBG
and IGF-1 were determined in each patient. For statistical analysis, ANOVA,
Newman-Keuls and Pearson’s correlation tests were used.
RESULTS: A tendency to higher expression of IGF-1 receptor gene was
observed in PCOS women without metformin treatment (33.88) . A similar
expression was detected in PCOS women who received metformin treatment
(27.5) as in the control group (24.0). The number of oocytes (20.4 vs. 13.1 vs.
11.5), the serum levels of E2 (1,896 pg/mL vs. 985.20 pg/mL vs. 908.1 pg/
mL) and testosterone (1.43 ng/mL vs. 0.89 ng/mL vs. 0.82 ng/mL) were
higher in PCOS women without metformin treatment in comparison to the
women with ovulatory cycles and PCOS women who received metformin
treatment, respectively.
CONCLUSIONS: The tendency to higher gene expression of IGF-1 receptor
observed in this study in women with PCOS without metformin treatment,
in association with higher serum levels of testosterone and E2, higher number
of oocytes retrieved, lead us to conclude that women with PCOS possibly
have higher stimulation of ovarian steroidogenesis compared to those without
this disease. The similarity of the results in this study between the
PCOS women treated with metformin and those with ovulatory cycles lead
us to hypothesize that one of the possible mechanisms of metformin action
in the IGF-1 system on the granulosa cumulus cells could be through postreceptor
mechanisms.
Supported by: This work was supported in part by a scholarship from Fundac
¸a˜o, Coordenac¸a˜o de Aperfeic¸oamento de Pessoal de Nı´vel Superior
(CAPES) - Brazil to Laura Ferreira Santana.
5/8/2009

Do stimulation characteristics of the first in vitro fertilization cycle predict pregnancy in women of 40 years old and over?

Roy Homburg, FRCOG., Simion Meltcer, M.D., Jacob Rabinson, M.D., Efraim Zohav, M.D., Eyal Y. Anteby, M.D., Raoul Orvieto, M.D., M.M.Sc.Corresponding Author Informationemail address

Received 7 January 2008; received in revised form 24 January 2008; accepted 24 January 2008. published online 01 April 2008.

The failure of tests of ovarian reserve to predict clinical pregnancy in women 40 years old and older prompted this study of the predictive value of information obtained during the first cycle of in vitro fertilization (IVF). Stimulation characteristics during the first IVF cycle attempt were unhelpful in predicting the possibility of clinical pregnancy within the first three consecutive IVF cycles.

Article Outline

Abstract

References

Copyright

Women in the age group ≥40 years now represent about 12.5% of women attending in vitro fertilization (IVF) clinics (1). For the older woman desiring pregnancy, chronologic age is the best single predictor for clinical pregnancy. However, within this age group, the selection of those with the best prognosis for pregnancy and live birth has proved difficult (2). Although ovarian reserve tests, both static and dynamic, may predict ovarian response to controlled ovarian hyperstimulation (COH) with varying degrees of success, they have been found to be of limited use for the prediction of pregnancy 3, 4, 5, 6.

In their systematic and meta-analytic reviews, Broekmans et al. (2) concluded that the ovarian reserve tests known to date have only very modest predictive properties for pregnancy and are therefore far from suitable for relevant clinical use. Moreover, Mol et al. (7), while evaluating whether the expected benefits based on probabilities and value judgments of outcomes would justify testing for ovarian reserve before a first-cycle IVF, found that, for realistic ranges of the success rate after IVF and for distress ranges as were measured, treatment of all couples without testing was found to generate less distress than testing for ovarian reserve. They therefore concluded that, where current test accuracy and preference inventory among patients and physicians were used, testing for ovarian reserve did not seem to be useful for current IVF programs.

Ovarian stimulation characteristics during an IVF cycle are considered the most reliable sign of decrease ovarian reserve (8). Moreover, in older patients undergoing IVF, high estradiol (E2) to follicle or E2 to oocyte ratios on day of human chorionic gonadotropin (hCG) administration were associated with poor IVF outcome (9).

Following the aforementioned thorough systematic review of tests predicting IVF outcome, Broekmans et al. (2) asked whether the a priori identification of actual poor responders in the first IVF cycle has any prognostic value for their chances of conception in the course of a series of IVF cycles. Thus, our preliminary study of women in the 40 to 45 years age group undergoing IVF for the first time examined whether information obtained from the first IVF cycle has any prognostic value for the achievement of pregnancy within the first three treatment cycles.

Basal and IVF parameters immediately before and during each woman's first ever IVF cycle were carefully recorded for 97 women aged 40 to 45 years. All but three reached the stage of ovum retrieval after ovarian stimulation with either a midluteal gonadotropin-releasing hormone (GnRH) long protocol or flexible multidose GnRH antagonist protocol. Gonadotropins were administered in doses adjusted according to follicular development and serum E2 concentrations performed every 2 to 3 days. Clinical pregnancy was defined as fetal heart activity and visualization of a gestational sac on transvaginal ultrasound.

Ovarian stimulation characteristics, number of oocytes retrieved, and number of embryos transferred in the first IVF cycle attempt as well as the outcome of up to three consecutive cycles were recorded for each woman. A comparison of the data from the first treatment cycle was made for those who achieved a clinical pregnancy within three treatment cycles as compared with those who did not.

Results are presented as mean ± standard deviation. Differences in variables between the patients who conceived (pregnant group) and those who did not (nonpregnant group) were statistically analyzed with nonparametric Wilcoxon signed rank test and Student's t-test, as appropriate. P<.05 was considered statistically significant.

Of the 97 patients aged 40 to 45 years who started treatment with IVF, 25 achieved a clinical pregnancy in one of their first three consecutive treatment cycles. Table 1 shows the clinical characteristics of the first IVF cycle in women who conceived in one of the three consecutive IVF cycle attempts compared with those who did not.

Table 1.

Comparison of basal and IVF stimulation characteristics in the first treatment cycle according to whether a clinical pregnancy was achieved in the first three consecutive cycle attempts.

Pregnant group (n = 25) Nonpregnant group (n = 72) P value
Age (years) 41.2 ± 1.3 42.2 ± 1.8 <.001
Gravidity 2.1 ± 2.3 1.4 ± 1.5 NS
Parity 0.7 ± 0.7 0.9 ± 1.0 NS
Day-3 FSH (IU/L) 6.0 ± 2.7 7.3 ± 3.3 NS
Days of stimulation 9.5 ± 2.2 10.1 ± 2.4 NS
Gonadotropins required (IU) 3300 ± 1275 4025 ± 1725 NS
Estradiol on day of hCG administration (pg/mL) 1628 ± 1213 1365 ± 1056 NS
Progesterone on day of hCG administration (ng/mL) 0.7 ± 4.8 0.8 ± 0.6 NS
Number of follicles of >14 mm on day of hCG administration 7.5 ± 4.8 6.7 ± 4.7 NS
Number of oocytes recovered 7.8 ± 5.5 5.3 ± 4.2 <.02
Number of embryos transferred 2.6 ± 0.9 2.2 ± 1.1 NS

Note: NS, not statistically significant.

The only statistically significant differences during the first treatment cycle between those who conceived and those who did not are in mean age (41.2 versus 42.2 years, respectively; P<.001) and mean number of oocytes recovered (7.8 versus 5.3, respectively; P<.02). Notably, there were no differences between the groups regarding day-3 follicle-stimulating hormone (FSH) concentrations, duration or amount of gonadotropin stimulation, serum E2 and progesterone levels on the day of hCG administration, or number of embryos transferred.

After the relative failure of a large battery of ovarian reserve tests to accurately predict clinical pregnancy resulting from IVF treatment (2), this study examined whether parameters obtained during the first IVF cycle of patients aged 40 to 45 years can improve the predictive value. The current data do not support this suggestion.

The well-documented prognosticators of age and number of oocytes recovered remained the only statistically significant differences between women who achieved a clinical pregnancy and those who did not. As age is obviously known and number of oocytes recovered is closely paralleled by the number of larger follicles obtained on ovarian stimulation, the stimulation characteristics and endocrinologic parameters obtained during the first cycle of IVF seem to offer little more in terms of prediction of clinical pregnancy than age, cycle day-3 FSH, inhibin B, or antimüllerian hormone serum levels, antral follicle count, or any combination of these.

Further research is thus needed to find reliable indicators for patients in the advanced maternal age group who can benefit from treatment with IVF and those who should be refused IVF. It has been suggested that, in view of the unreliability of tests that can predict pregnancy in this group, entering the first cycle of IVF without any prior testing is the preferable strategy today (2), but our current findings demonstrate that this strategy is also unhelpful as far as prediction of pregnancy is concerned and merely demonstrates our helplessness.

Influence of overweight and underweight in women with polycystic ovarian syndrome who undergo in vitro fertilization

OBJECTIVE: To determine whether underweight and overweight affect controlled ovarian hyperstimulation and IVF outcomes in PCOS women.

DESIGN: Retrospective cohort analysis.

MATERIALS AND METHODS: A retrospective analysis involving 57 patients with PCOS diagnosis according to 2003 Rotterdam criteria. Patients were divided in two groups: group “lean PCOS” with BMI < 18.5 (n = 16) and group “overweight PCOS” with BMI > 25, (n = 41). Maternal and controlled ovarian hyperstimulation variables and IVF outcomes were analyzed: FSH, LH and E2 on day 3, dose of r-FSH, E2 level the day of hCG, ovarian responsiveness to gonadotropins defined by r-FSH dose per retrieved oocyte, number of oocytes, number of embryos and clinical pregnancy rate.

RESULTS: No difference was observed concerning the age between the two groups (31.8 years in group “lean PCOS” and 31.7 years in group “overweight PCOS”, p = 0.98). No difference was seen in basal hormonal status on day 3 (FSH = 5.8 IU/L versus 6.1 IU/L, p = 0.67 and LH = 7.4 IU/L versus 7.3 IU/L, p = 0.88 in “lean PCOS” and “overweight PCOS” respectively). Higher doses of gonadotropins were used for overweight PCOS (1790 IU versus 1042 IU, p < 0.001). No significant difference was observed concerning the number of retrieved oocytes but a trend to a higher number of retrieved oocytes in the group “lean PCOS” was noticed (14.8 versus 10.8, p = 0.08). Ovarian responsiveness to gonadotrophins was significantly higher in lean PCOS (93.5 r-FSH IU per retrieved oocyte versus 208 r-FSH IU per retrieved oocyte, p = 0.016) with higher E2 peak the day of hCG (3312.3 pg/mL versus 2208.9 pg/mL, p = 0.02). A higher number of embryos was obtained in the group “lean PCOS” (8.1 versus 4.5, p < 0.001). No significant difference was found in term of implantation rate (50% in group “lean PCOS” and 34.7% in group “overweight PCOS”, p = 0.22). No significant difference was observed concerning the pregnancy rate even if a trend to a higher pregnancy rate was noticed in group “lean PCOS” (31.3% per cycle versus 12.1%, p > 0.05).

CONCLUSIONS: In PCOS women, weight is an important parameter of r-FSH dose requirement. Lean PCOS have a greater ovarian responsiveness to gonadotropins and a milder stimulation is recommended. Overweight PCOS require more r-FSH dose in relation to a lower ovarian sensitivity.