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Assisted reproductive techniques with congenital hypogonadotropic hypogonadism patients: a systematic review and meta-analysis

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Abstract

Background

After hormonal replacement therapy (HRT) including androgen replacement or sequential therapy of estrogen and progesterone, The combination of human chorionic gonadotropin (hCG) and human menopausal gonadotropin (hMG) and pulsatile GnRH, is not sufficient to produce sufficient gametes in some patients with Congenital hypogonadotropic hypogonadism (CHH). A Systematic review and meta-analysis was performed to determine that assisted reproductive techniques (ART) can effectively treat different causes of infertility.

Methods

To determine the effect of ART on fertility of CHH patients and investigate whether outcomes are similar to infertility due to other causes, we conducted a systematic review and meta-analysis of retrospective trials.

Clinical trials were systematically searched in Medline, Embase, and the Cochrane central register of controlled trials databases. The keywords and major terms covered “hypogonadotropic hypogonadism”, “kallmann syndrome”, “assisted reproductive techniques”, “intrauterine insemination”, “intracytoplasmic sperm injection”, “testicular sperm extraction”, “in vitro fertilization”, “embryo transplantation” and “intra-Fallopian transfer”.

Results

A total of 388 pregnancies occurred among 709 CHH patients who received ART (effectiveness 46, 95% confidence interval 0.39 to 0.53) in the 20 studies we included. The I2 in trials assessing overall pregnancy rate (PR) per embryo transfer (ET) cycle was 73.06%. Similar results were observed in subgroup analysis by different gender. Regression indicates pregnancy rate decreases with increasing age. Fertilization, implantation and live birth rates (72, 36 and 40%) showed no significant differences as compared to infertility due to other causes.

Conclusions

Despite CHH patients usually being difficult to generate gametes, their actual chances of fertility are similar to subjects with other non-obstructive infertility. ART is a suitable option for CHH patients who do not conceive after long-term gonadotropin treatment.

Background

Congenital hypogonadotropic hypogonadism (CHH) is a disorder characterized by lacking of puberty and infertility, with low levels of circulating gonadotropins and sex steroids. Two pathogenesis mechanisms exist for CHH. One is the reduced secretion of gonadotropin releasing hormone (GnRH) from the hypothalamus, and the other is the GnRH receptor defect in the pituitary. The incidence of CHH is approximately 1/10000–1/86000 [1], and the ratio of male versus female is about 3.6–1 which varies from race to race [2]. About 50% cases who show anosmia/hyponosmia simultaneously called Kallmann syndrome [3]. The Genetic defects are the main underlying mechanism. More than 30 pathogenic genes of CHH have been identified [4].

Therapy for CHH depends on the patients’ desire for fertility at the time of treatment. Androgen replacement or sequential therapy of estrogen and progesterone can be used for patients who do not wish to have children. The combination of human chorionic gonadotropin (hCG) and human menopausal gonadotropin (hMG) is used to induce fertility. Pulsatile GnRH is another option for CHH patients who desire a pregnancy.

Nevertheless, the treatment for inducing fertility may not be effective for all CHH patients. Alternate fertility inducing methods have been described for patients who do not respond to hormone replacement therapy (HRT) as HRT replaces lacking hormones rather than inducing ovulation or spermatogenesis. Different assisted reproductive techniques (ART) can improve conception rate. Intrauterine insemination (IUI) is suitable for patients with sexual dysfunction and obstructive fertility. In vitro fertilization-embryo transplantation (IVF-ET) is appropriate for infertility due to many causes, especially the disorder of sperm-egg binding. Intracytoplasmic sperm injection (ICSI) and testicular sperm extraction (TESE) are used for infertility due to decreased quality and quantity of sperms. ART might be an efficient approach to treat infertility in CHH patients due to various causes. The aim of this review was to meta-analyze the pregnancy outcomes in order to reveal the effect of ART on CHH patients, and whether it is distinct from infertility due to other causes.

Methods

This systematic review and meta-analysis was conducted following the Preferred Reporting Items for Systematic Review and Meta-Analyses (PRISMA) statement [5] (Additional file 1: Table S1). Moreover, the analyses were based on previous published studies, thus no ethical approval and patient consent are required according to the regulation of Peking Union Medical College Hospital ethic committee. All previous published studies were approved by ethics committee respectively.

Data sources and searches.

An electronic search of Medline, Embase, and the Cochrane central register of controlled trials was performed. We used keywords and major terms including “hypogonadotropic hypogonadism”, “kallmann syndrome”, “assisted reproductive techniques”, “intrauterine insemination”, “intracytoplasmic sperm injection”, “testicular sperm extraction”, “in vitro fertilization”, “embryo transplantation” and “intra-Fallopian transfer”.

There were no language restrictions, and the retrieval was till March 2018. The detailed search strategies are shown in Additional file 2: Table S2.

Study selection

The included studies were retrospective and researched the positive effect of ART treatment on CHH patients who did not achieve pregnancy after HRT. The inclusion criteria were trials that evaluated at least one of the primary or secondary outcomes mentioned below. The primary outcomes included several pregnancy-related indicators, including fertilization rate, implantation rate, clinical pregnancy per cycle or embryo transfer (ET), and live birth rate. Secondary outcomes included the comparison of pregnancy rates according to different genders, some adverse events arising from ART, such as abortion, multiple gestation and ovarian hyperstimulation syndrome (OHSS). In addition, all the 20 studies we included have clear patient inclusion criteria. The hypophyseal axis was checked by measuring TSH, cortisol, and prolactin, which showed no other combined pituitary hormone deficiency.

Exclusion criteria were [1]: klinefelter syndrome [2]; adult-onset (secondary) HH [3]; reviews and case reports [4]; no available end-points; and [5] duplications or sub-studies of the included trials.

Data extraction and quality assessment

All studies included in the meta-analysis were reviewed and data on author, year of publication, study design, time, location, number, age and gender of subjects, the duration and methods of HRT, type of surgery and number of cycles were extracted. In addition, fresh/frozen sperm and spouse’s age in males, and body mass index (BMI) in females were observed. The end-points after ART were also extracted for analysis, including fertilization rate, implantation rate, clinical pregnancies, clinical pregnancy per cycle or ET, live birth children, live birth rate and total number of adverse events reported (Table 1).

Table 1 Information of selected studies

Study quality was examined using inclusion and exclusion criteria, definition of end-points, adequacy of follow-up, data analysis and presentation. In addition, studies were scored for quality by Methodological Index for Non-randomized Studies (MINORS). The scores of quality assessment are listed in Table 2. There are eight methodological items for non-randomized studies and four additional criteria for comparative studies. The items are scored 0 (not reported), 1 (reported but inadequate) or 2 (reported and adequate). The global ideal scores are 16 for non-comparative studies and 24 for comparative studies [6].

Table 2 Assessment of risk of bias by Methodological Index for Non-randomized Studies (MINORS)

Data synthesis and statistical analysis

Data were pooled using a random effects model to obtain a more conservative estimate of ART on CHH patients who were unresponsive or not pregnant after long-term treatment with gonadotropins, allowing for any heterogeneity between studies.

Heterogeneity between studies was assessed using the I2 statistic with a cut-off of ≥50%, and the X2 test with a p < 0.10 to define a significant degree of heterogeneity. Where the degree of statistical heterogeneity was greater than this between trial results, possible explanations were investigated using subgroup analysis according to the gender. It can tell the possible reason of heterogeneity. These were exploratory analyses only and may explain some of the observed variability, but the results should be interpreted with caution. The 95% confidence intervals were used to generate Forest plots of pooled relative risks for primary and secondary outcomes. The sample size and risk of bias of included trials is crucial for the weighted differences, which means the more representative study is, the greater the weight is. We also performed a meta-regression analysis by age to show its influence on the pregnancy outcome.

Results

Literature search

The search strategy identified 1030 citations. After eliminating duplicates, 921 studies were subsequently reviewed. The titles and abstracts were screened, and 90 articles were potentially eligible for inclusion. Only 20 of these were retrieved after reading the full-texts. The data in these studies could be consolidated and analyzed (Fig. 1).

Fig. 1
figure1

Flow diagram of studies identified in the systematic review

Clinical characteristics of patients in the included studies

In the 20 studies included, a total of 475 female CHH patients were included in eleven studies and 234 male CHH patients in the other nine studies. The range of average ages of female CHH patients was 27 to 33.5 years old, and 30.1 to 40.2 years old for male CHH patients. Average BMI of female patients was between 18 to 27 kg/m2, and no BMI values were described in studies in male patients. Nine out of eleven studies on female CHH patients contained control groups which comprised a total of 659 infertile cases caused by other reasons including tubal factor, male factor or other unexplained factors.

Pregnancy outcomes

The majority treatment regimens used was hCG combined with hMG, duration was around two weeks in females and 6–12 months in males. The type of ART was in vitro fertilization (IVF)/intracytoplasmic sperm injection (ICSI), 3/11 female trials used extra IUI, and 6/9 male trials used TESE. The characteristics of the retrieved trials, including parameters on trial quality, are reported in Tables 1 and 2. A total of 388 pregnancies occurred among 709 individuals who received ART (effectiveness 46, 95% confidence interval 0.39 to 0.53) (Fig. 2). The I2 in trials assessing overall pregnancy rate (PR) per ET cycle was 73.06%. Similar results were observed in subgroup analysis by sex (Fig. 3). Pregnancy rate was 48% in the female group and 46% in the male group. Meta-regression analysis showed that PR per ET cycle decreased with increasing age (Fig. 4). Sufficient data was not available to evaluate the influence of infertility duration, basal BMI, testis volume or sperm counts and the levels of follicle-stimulating hormone (FSH), leuteinizing hormone (LH) and testosterone (T) on treatment effect of ART.

Fig. 2
figure2

Forest plot for the pregnancy rate. ES = effect size; CI = confidence interval

Fig. 3
figure3

Forest plot for subgroup analysis by different gender

Fig. 4
figure4

Influence of age at pregnancy rate Influence of age (X-axis) on pregnancy rate (Y-axis). The size of the circles indicates sample dimension.

The forest plots of fertilization rate, implantation rate and live birth rate are shown in Fig. 5. They showed no significant differences as compared to other cohorts.

Fig. 5
figure5

Forest plots for the fertilization rate a, implantation rate b and live birth rate (c)

Adverse events

Individual adverse events were reported in many of the included studies. Fourteen out of 20 trials included abortion rate and 11/20 included the outcomes of multiple pregnancies. Six trials mentioned ovarian hyperstimulation syndrome (OHSS) but there was no OHSS occurrence in the included studies. Only two trials reported ectopic pregnancies. The frequencies of abortion and multiple pregnancies are shown in Fig. 6. There was no statistically significant difference in the incidence of adverse events for CHH patients undergoing ART as compared to infertile cohorts with other causes. Therefore, ART appears to be a safe and effective method to induce fertility in CHH patients.

Fig. 6
figure6

Frequencies of abortion and multiple pregnancies. (a)Different colors represent four adverse events, including abortion(blue),multiple pregnancy(red),OHSS(green) and ectopic pregnancy(purple);(b)8.20% patients of all suffered abortion(red);(c)12.8% patients of all had multiple pregnancy. Y=Yes; N=No

Discussion

In this study, we systematically reviewed and meta-analyzed pregnancy outcomes in CHH patients undergoing ART. For this specific population, the overall pregnancy rate per ET cycle was about 46% (95% confidence interval 0.39 to 0.53), which was comparable to the patients with other etiological infertility including tubal factor infertility (TI), male factor infertility (MI) and unexplained infertility (UI). The fertilization rate (72%), implantation rate(36%) and live birth rate(51%) were not significantly different from other cohorts. Hence, ART is a viable option for CHH patients with unsuccessful long-term HRT. However, this review had a high risk of potential bias and clinical heterogeneity caused by the study design and the inconsistency in results across the included studies. Factors such as age, BMI, sex hormone levels, pathogenesis of CHH and function of ovary in women, testis volume in men and HRT before ART may have different effects on fertility outcomes in CHH patients treated by ART, and not all these factors were analyzed in the included studies.

Two methods, including hCG combined with hMG and pulsatile GnRH, are common fertility promoting treatments for CHH patients. However, the effectiveness is around 70% [7]. About 30% male CHH patients had no or few sperm with conventional therapy (i.e. azoospermia, oligospermia). ICSI combined with TESE may improve their fertility and the pregnancy rates could be similar to those observed in other forms of infertility.

Intra-Fallopian transfer was initially applied for the spouse of a male patient with Kallmann’s syndrome [8]. Impaired semen quality prevented his spouse from conceiving and IVF helped the couple in having a healthy baby. Thereafter, some studies presented pregnancies achieved through IVF/ICSI in CHH patients not responding to hormonal treatment [9, 10], and pregnancy rates from the large studies were 50–60% [11, 12]. Gonadotropin replacement combined with TESE-ICSI cycles improved pregnancy rate of CHH patients [13], the clinical pregnancy rate was 17.6%. With the advancement of technology, various ART treatments were applied on CHH patients in different situations such as age, sex, region, duration and extent of illness. The success rate increased to 55% [14, 15]. Furthermore, a study in 1997 first emphasized that initiation of ICSI treatment after testicular maturity induced by hormonal treatment contributed to the success of ART [16].

Waiting may be advisable as maximal sperm counts are not attained until 12–18 months of treatment, and even longer in cases of cryptorchidism. However, like the general population, chances of fertility in CHH patients after ART reduced with increasing age. Quality and quantity of follicles both decreased. Older women require higher doses of gonadotropins to achieve the desired outcome due to diminished ovarian function with aging [12, 17]. Therefore, early ART for unresponsive CHH patients who received HRT for some time may be beneficial.

Multiple pregnancy, abortion, ectopic pregnancy [18] and OHSS [19] are common adverse events of ART. The multiple pregnancy and abortion rates were around 30% [20] and 14.7% [21], respectively. These rates did not increase in CHH patients who received ART therapy. Severe OHSS was not observed during ovulation induction in CHH patients [11, 22, 23]. The ovaries were dormant and needed to be stimulated with higher doses of gonadotropins, which might theoretically increase the risk of OHSS in the CHH group [24], but the frequency of OHSS was not increased in our review.

Several limitations of this meta-analysis should be emphasized. First, the number of included studies was small, which may create selective bias. Second, all included studies were retrospective. Hence, the significant statistical heterogeneities (I2 = 73.06% in pregnancy rate) may have influenced our findings. Third, the baseline characteristics were not described in detail, which could influence the outcomes by the confounding variables. For example, testis volume and cryptorchidism (maldescended testes) is an important indicator for sperm production, but adequate data was not available for analysis. Great progress in ART treatment also made sense to patients in different decades. Last, it seems that not all studies reported adverse events, and some like OHSS is not considered to be an adverse event, so more studies should be included to avoid the reporting bias.

Conclusions

In summary, the present study showed that despite CHH patients usually being azoospermic, their actual chances of fertility are similar to subjects with other types of obstructive infertility. If CHH patients do not conceive after long-term gonadotropin treatment, ART should be initiated.

Abbreviations

ART:

Assisted reproductive techniques

CHH:

Congenital hypogonadotropic hypogonadism

ET:

Embryo transfer

GnRH:

Gonadotropin releasing hormone

hCG:

Human chorionic gonadotropin

hMG:

Human menopausal gonadotropin

HRT:

Hormonal replacement therapy

ICSI:

Intracytoplasmic sperm injection

IUI:

Intrauterine insemination

IVF-ET:

In vitro fertilization-embryo transplantation

OHSS:

Ovarian hyperstimulation syndrome

PR:

Pregnancy rate

TEST:

Testicular sperm extraction

References

  1. 1.

    Fraietta R, Zylberstejn DS, Esteves SC. Hypogonadotropic hypogonadism revisited. Clinics (Sao Paulo). 2013;68(Suppl 1):81–8.

  2. 2.

    Dzemaili S, Tiemensma J, Quinton R, Pitteloud N, Morin D, Dwyer AA. Beyond hormone replacement: quality of life in women with congenital hypogonadotropic hypogonadism. Endocr Connect. 2017;6(6):404–12.

  3. 3.

    Kim SH. Congenital Hypogonadotropic Hypogonadism and Kallmann syndrome: past, present, and Future. Endocrinol Metab (Seoul). 2015;30(4):456–66.

  4. 4.

    Stamou MI, Georgopoulos NA. Kallmann syndrome: phenotype and genotype of hypogonadotropic hypogonadism. Metab Clin Exp. 2017;86:124–34.

  5. 5.

    Moher D, Liberati A, Tetzlaff J, Altman DG. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann Intern Med. 2009;151(4):264–9 w264.

  6. 6.

    Slim K, Nini E, Forestier D, Kwiatkowski F, Panis Y, Chipponi J. Methodological index for non-randomized studies (minors): development and validation of a new instrument. ANZ J Surg. 2003;73(9):712–6.

  7. 7.

    Rastrelli G, Corona G, Mannucci E, Maggi M. Factors affecting spermatogenesis upon gonadotropin-replacement therapy: a meta-analytic study. Andrology. 2014;2(6):794–808.

  8. 8.

    Tournaye H, Van Steirteghem A, Devroey P. Pregnancy after zygote intra-fallopian transfer using spermatozoa from a patient with Kallmann's syndrome. Hum Reprod. 1992;7(9):1268–70.

  9. 9.

    Smith YR, Ansbacher R, Christman GM, Hurd WW, Randolph JF Jr. Kallmann's syndrome: pregnancy achieved through gamete intrafallopian transfer. Fertil Steril. 1993;60(4):737–9.

  10. 10.

    Szilagyi A, Manfai Z, Kiesel L, Szabo I. Kallmann's syndrome: pregnancy through intracytoplasmic sperm injection and complicated by gestational diabetes. Gynecol Endocrinol. 2001;15(5):325–7.

  11. 11.

    Ulug U, Ben-Shlomo I, Tosun S, Erden HF, Akman MA, Bahceci M. The reproductive performance of women with hypogonadotropic hypogonadism in an in vitro fertilization and embryo transfer program. J Assist Reprod Genet. 2005;22(4):167–71.

  12. 12.

    Kumbak B, Kahraman S. Women with hypogonadotropic hypogonadism: cycle characteristics and results of assisted reproductive techniques. Acta Obstet Gynecol Scand. 2006;85(12):1453–7.

  13. 13.

    Fahmy I, Kamal A, Shamloul R, Mansour R, Serour G, Aboulghar M. ICSI using testicular sperm in male hypogonadotrophic hypogonadism unresponsive to gonadotrophin therapy. Hum Reprod. 2004;19(7):1558–61.

  14. 14.

    Bakircioglu E, Ulug U, Tosun S, et al. MicroTESE and ICSI outcomes of azoospermic men with hypogonadotropic hypogonadism after one year combined HCG and FSH treatment. Hum Reprod. https://doi.org/10.1093/humrep/27.S2.73.

  15. 15.

    Resorlu B, Abdulmajed MI, Kara C, Unsal A, Aydos K. Is intracytoplasmic sperm injection essential for the treatment of hypogonadotrophic hypogonadism? A comparison between idiopathic and secondary hypogonadotrophic hypogonadism. Hum Fertil (Camb). 2009;12(4):204–8.

  16. 16.

    Yong EL, Lee KO, Ng SC, Ratnam SS. Induction of spermatogenesis in isolated hypogonadotrophic hypogonadism with gonadotrophins and early intervention with intracytoplasmic sperm injection. Hum Reprod. 1997;12(6):1230–2.

  17. 17.

    Yavangi M, Farahani L. Does ovarian response decrease by increasing age in hypogonadotropic hypogonadism women undergoing ovarian stimulation? Iranian Journal of Reproductive Medicine. 2012;10:18.

  18. 18.

    Clayton HB, Schieve LA, Peterson HB, Jamieson DJ, Reynolds MA, Wright VC. Ectopic pregnancy risk with assisted reproductive technology procedures. Obstet Gynecol. 2006;107(3):595–604.

  19. 19.

    Papanikolaou EG, Tournaye H, Verpoest W, et al. Early and late ovarian hyperstimulation syndrome: early pregnancy outcome and profile. Hum Reprod. 2005;20(3):636–41.

  20. 20.

    Fauser BC, Devroey P, Macklon NS. Multiple birth resulting from ovarian stimulation for subfertility treatment. Lancet. 2005;365(9473):1807–16.

  21. 21.

    Schieve LA, Tatham L, Peterson HB, Toner J, Jeng G. Spontaneous abortion among pregnancies conceived using assisted reproductive technology in the United States. Obstet Gynecol. 2003;101(5 Pt 1):959–67.

  22. 22.

    Yilmaz S, Ozgu-Erdinc AS, Yumusak O, Kahyaoglu S, Seckin B, Yilmaz N. The reproductive outcome of women with hypogonadotropic hypogonadism undergoing in vitro fertilization. Syst Biol Reprod Med. 2015;61(4):228–32.

  23. 23.

    Jiang ST, Kuang YP. Research progresses of the assisted reproductive techniques for hypogonadotropic hypogonadism patients. Journal of Shanghai Jiaotong University (Medical Science). 2017;37(1):128–33.

  24. 24.

    Ghaffari F, Arabipoor A, Lankarani NB, Etminan Z, Tehraninejad ES. Assisted reproductive technique outcomes in hypogonadotropic hypogonadism women. Annals of Saudi medicine. 2013;33(3):235–40.

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Acknowledgements

Not applicable.

Funding

This work was supported by the National Natural Science Foundation of China (Grant No. 81771576), National Natural Science Foundation of China (Grant No. 81270879), National Key Research and Development Program of China (2016YFC0905100) and CAMS Innovation Fund for Medical Sciences (2016-I2M-1-002).

Availability of data and materials

The available data and materials section refers to the raw data used in our study are included in manuscript with tables, figures and its supplementary information files. All the authors agreed that the data could be shared if researchers required.

Author information

MN and XYW made substantial contributions to conception and design of data; data statistics and analysis was completed by YJG, BQY and XW; manuscript was written by YJG and JFM, XYW and MN revised the manuscript critically for important intellectual content. All authors have given final approval of the version to be published and everyone agreed to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Correspondence to Min Nie or Xueyan Wu.

Ethics declarations

Ethics approval and consent to participate

All analyses were based on previous published studies, thus no ethical approval and patient consent are required according to the regulation of Peking Union Medical College Hospital ethic committee. All previous published studies were approved by ethics committee respectively.

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Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Additional files

Additional file 1: Table S2.

PRISMA 2009 checklist. (DOC 61 kb)

Additional file 2: Table S1.

Search strategy for PubMed. (DOCX 15 kb)

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Keywords

  • Congenital hypogonadotropic hypogonadism
  • Assisted reproductive techniques
  • Fertility
  • Hormonal replacement therapy