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
Female |
Ulug 2005 | 58 | 32.2/5.2 | 21.09/1.3 | HCG, HMG, | TI | IUI, IVF (ICSI)-ET, 53 cycles | n/a | n/a | PR 56.6%, | abortion, |
14 days | n = 16 | FR 73.9%, | multiple pregnancy |
IR 32.4% | |
Kumbak 2006 | 27 | 32.8/4.9 | 25.7/4.5 | gonadotrophins, | UI | IVF (ICSI)-ET, | n/a | n/a | PR 59.3%, | multiple pregnancy |
14 days | n = 39 | 27 cycles | FR 89%, |
IR 36.5% |
Yildirim 2010 | 13 | 31.3/5.6 | 25.3/3.1 | gonadotrophins, | TI | IVF (ICSI)-ET, | n/a | n/a | PR 80%, | abortion |
13 days | n = 20 | 13 cycles | FR 81.9%, |
IR 38.3%, |
LBR 50% |
Dokuzeylul 2010 | 57 | ≤37 | n/a | gonadotrophins, | normal control | IVF (ICSI)-ET, | n/a | n/a | PR 56.14%, | n/a |
14 days | n = 95 | 57 cycles | IR 36.7% |
Caragia 2012 | 17 | 32.96/3.976 | n/a | FSH, LH, | TI/MI/UI | IVF (ICSI)-ET, | n/a | n/a | PR 55.6%, | no adverse events |
16 days | N = 56/56/56 | 28 cycles | FR 55.4%, |
LBR 54% |
Ghaffari 2013 | 81 | 33.5/5.3 | 26.1/4.0 | HMG, HCG, P, E2, | TI | IVF (ICSI)-ET, | n/a | n/a | PR 19.4%, | abortion, |
14 days | n = 89 | 72 cycles | FR 61.2%, | multiple pregnancy |
IR 40%, | |
LBR 15.2% | |
Pandurangi 2015 | 7 | 27 | 25.29/3.77 | HMG, uFSH, | n/a | IUI, IVF (ICSI)-ET, 19 cycles | n/a | n/a | PR 31.6%, | abortion, |
29 days | FR 85%, | multiple pregnancy |
LBR 85.7% |
Yilmaz 2015 | 33 | 32.5/4.73 | 26/ 3.81 | HMG, HCG, recFSH, P,12 days | MI | IVF (ICSI)-ET, | n/a | n/a | PR 30% | n/a |
n = 47 | 33 cycles |
Jiang 2017 | 46 | 30.9/3.9 | 21.26/1.89 | HCG, HMG, | TI | IUI, IVF (ICSI)-ET, 42 cycles | n/a | n/a | PR 59.52%, | abortion, |
13 days | n = 71 | FR 82.13%, | multiple pregnancy |
IR 41.46% | |
Mumusoglu 2017 | 57 | 30.6/5.1 | 25.6/4.5 | FSH, | TI | IVF (ICSI)-ET, | n/a | n/a | PR 36.8%, | abortion |
11 days | n = 114 | 57 cycles | IR 34.4%, |
LBR 36.8% |
Kuroda 2018 | 79 | 32.6/0.5 | 18/0.3 | HCG, HMG, | n/a | IVF (ICSI)-ET, | n/a | n/a | PR 59.3%, | abortion |
12.2 days | 117 cycles | LBR 45.9% |
Male |
Fahmy 2004 | 15 | 38.71/6.2 | n/a | HCG, HMG, | n/a | TESE+IVF (ICSI)-ET, | n/a | n/a | PR 16.7%, | multiple pregnancy |
6 months | 17 cycles | FR 41.7% |
Zorn 2005 | 4 | 37.75 | n/a | HCG, HMG, | n/a | IVF (ICSI)-ET, | fresh/ | 31.5 | PR 33.3%, | no adverse events |
13.25 months | 9 cycles | frozen sperm | IR 21% |
Bakircioglu 2007 | 25 | 34.5/5.2 | n/a | HCG, | n/a | TESE+IVF (ICSI)-ET, | fresh/ | n/a | PR 54.5% | abortion |
9.96 months | 22 cycles | frozen sperm |
Akarsu 2009 | 4 | 36.25 | n/a | HCG, HMG, | n/a | TESE+IVF (ICSI)-ET, | fresh/ | 29.5 | PR 16.7%, | abortion, |
9.96 months | 18 cycles | frozen sperm | FR 41.8%, | multiple pregnancy |
LBR 75% | |
Resorlu 2009 | 17 | 30.1 | n/a | HCG, FSH, | n/a | IVF (ICSI)-ET, | fresh | n/a | PR 54.5% | n/a |
24 months | 11 cycles | sperm |
Dokuzeylul 2010 | 31 | 34.82 | n/a | HCG, HMG, | n/a | TESE+IVF (ICSI)-ET, | n/a | n/a | PR 51.7%, | abortion, |
6 months | 29 cycles | FR 83%, | multiple pregnancy |
LBR 41.3% | |
Bakircioglu 2012 | 12 | 40.2 | n/a | HCG, FSH, | n/a | TESE+IVF (ICSI)-ET, | n/a | n/a | PR 66.7%, | multiple pregnancy |
15.3 months | 9 cycles | LBR 77.8% |
Sahin 2012 | 65 | n/a | n/a | gonadotrophins, | n/a | IVF (ICSI)-ET, | n/a | n/a | PR 43.9%, | n/a |
10.2 months | 57 cycles | LBR 60% |
Basar 2017 | 61 | 35.8/5.64 | n/a | HCG, HMG, | n/a | TESE+IVF (ICSI)-ET, | fresh/ | n/a | PR 47.1%, | n/a |
n/a | 119 cycles | frozen sperm | LBR 62.3% |
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)
Female |
Ulug (2005) | 2 | 2 | 2 | 2 | 2 | 0 | 0 | 2 | 2 | 2 | 2 | 2 | 20 |
Kumbak (2006) | 2 | 2 | 2 | 2 | 2 | 1 | 0 | 2 | 2 | 2 | 2 | 2 | 21 |
Yildirim (2010) | 2 | 0 | 2 | 2 | 2 | 0 | 0 | 2 | 2 | 2 | 2 | 2 | 18 |
Dokuzeylul (2010) | 2 | 0 | 2 | 2 | 2 | 0 | 0 | 2 | 2 | 2 | 2 | 2 | 18 |
Caragia (2012) | 2 | 0 | 1 | 2 | 2 | 0 | 0 | 2 | 2 | 2 | 2 | 2 | 17 |
Ghaffari (2013) | 2 | 2 | 2 | 2 | 2 | 0 | 0 | 2 | 2 | 2 | 2 | 2 | 20 |
Yilmaz (2015) | 2 | 2 | 2 | 2 | 2 | 0 | 0 | 2 | 2 | 2 | 2 | 2 | 20 |
Pandurangi (2015) | 2 | 2 | 2 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 10 |
Jiang (2017) | 2 | 2 | 2 | 2 | 2 | 0 | 0 | 2 | 2 | 2 | 2 | 2 | 20 |
Mumusoglu (2017) | 2 | 2 | 2 | 2 | 2 | 0 | 0 | 2 | 2 | 2 | 2 | 2 | 20 |
Kuroda (2018) | 2 | 2 | 2 | 2 | 2 | 1 | 0 | 2 | 0 | 0 | 0 | 0 | 13 |
Male |
Fahmy (2004) | 2 | 2 | 1 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 9 |
Zorn (2005) | 2 | 1 | 2 | 2 | 2 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 10 |
Bakircioglu (2007) | 2 | 1 | 2 | 2 | 2 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 10 |
Akarsu (2009) | 2 | 2 | 2 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 10 |
Resorlu (2009) | 2 | 1 | 2 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 9 |
Dokuzeylul (2010) | 2 | 0 | 1 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 7 |
Bakircioglu (2012) | 2 | 1 | 1 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 8 |
Sahin (2012) | 2 | 1 | 1 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 8 |
Basar (2017) | 2 | 0 | 1 | 2 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | 0 | 9 |
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.
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.