Skip to main content
Clinical and Experimental Reproductive Medicine logoLink to Clinical and Experimental Reproductive Medicine
. 2016 Jun 23;43(2):97–101. doi: 10.5653/cerm.2016.43.2.97

Serum and seminal plasma insulin-like growth factor-1 in male infertility

Hyo Serk Lee 1, Yong-Seog Park 2, Joong Shik Lee 1, Ju Tae Seo 1,
PMCID: PMC4925873  PMID: 27358827

Abstract

Objective

Growth hormone and its mediator, insulin-like growth factor-1 (IGF-1), have been suggested to exert gonadotropic actions in both humans and animals. The present study was conducted to assess the relationship between serum IGF-1 concentration, seminal plasma concentration, and sperm parameter abnormalities.

Methods

A total of 79 men were enrolled in this study from December 2011 to July 2012 and were prospectively analyzed. Patient parameters analyzed included age, body mass index, smoking status, urological history, and fertility history. Patients were divided into four groups based on their semen parameters: normal (A, n=31), abnormal sperm motility (B, n=12), abnormal sperm morphology (C, n=20), and two or more abnormal parameters (D, n=16). Patient seminal plasma and serum IGF-1 concentrations were determined.

Results

Patient baseline characteristics were not significantly different between any of the groups. The serum IGF-1 levels in groups B, C, and D were significantly lower than the levels in group A; however, the seminal plasma IGF-1 levels were not significantly different between any of the groups.

Conclusion

Men with abnormal sperm parameters had significantly lower levels of serum IGF-1 compared with men with normal sperm parameters. Seminal plasma IGF-1 levels, however, did not differ significantly between the groups investigated here. Further investigations will be required to determine the exact mechanisms by which growth hormone and IGF-1 affect sperm quality.

Keywords: Infertility, Insulin-like growth factor-1, Male, Semen, Serum

Introduction

Infertility is defined as the inability to conceive after 1 year of unprotected intercourse. Approximately 15% of all human couples are recognized as infertile, and about 50% of these cases are associated with male fertility factors. Although overall human fertility does not appear to have declined in recent years, some evidence indicates that sperm quality has declined [1]. To date, multiple factors have been implicated in reduced sperm count and motility. These factors include genito-urinary infections, environmental exposure to hazardous chemicals that are detrimental to spermatogenesis, anatomic and physical obstructions, hormonal imbalances, immunologic deficiencies, and abnormal morphology.

Spermatogenesis is a complex developmental process that requires pituitary gonadotrophins and testosterone, which indirectly regulate spermatogenic cells and testicular functions in autocrine, paracrine, and juxtacrine manners. One of the molecules thought to be involved in the development of germ cells is insulin-like growth factor-1 (IGF-1), a 7.6-kDa polypeptide of 70 amino acids that mediates the cell-proliferating actions of growth hormone (GH). IGF-1 is found in plasma and tissue fluid, and influences steroidogenesis, metabolism, cell proliferation, and differentiation [2,3]. IGF-1 also affects various reproductive processes and plays an essential role in the onset, progress, and regulation of spermatogenesis [4]. IGFs are produced mainly in the liver, and are released in response to pulsatile secretions of GH from the anterior pituitary [5]. In the male reproductive tract, IGF-1 has been found in the testis [6], where it is secreted by Leydig cells and Sertoli cells [7,8,9]. Receptors for IGF-1 have been identified on Sertoli cells [10], Leydig cells [8], secondary spermatocytes, spermatids [9,11], and spermatozoa [12,13]. Furthermore, IGF-1 is thought to be involved in spermatogenesis [14,15,16,17] and steroidogenesis [18]. IGF-1 also appears in the peripheral circulation, where it exists primarily in a heavy tertiary complex with IGF-binding protein-3 and acid-labile subunit [19,20].

However, only a few studies have investigated the semen and serum levels of IGF-1. One study investigated these levels in normal fertile and vasectomized men, whereas the other identified variable levels of IGF-1 in infertile men [3,21]. To obtain a better understanding of the role of IGF-l in fertility, the present study aimed to determine the relationship between serum IGF-1 concentration, seminal plasma IGF-1 concentration, and sperm parameter abnormalities.

Methods

1. Study design

Data from 79 men who were enrolled in this study from December 2011 to July 2012 were prospectively analyzed. Written informed consent was obtained from each subject before entering the study. This study was performed in accordance with the principles of the Declaration of Helsinki and with the approval of the Cheil General Hospital Institutional Review Board (CGH-IRB-2011-76). All patients received medical care from the same doctor at a single hospital. Patient parameters analyzed included age, height, weight, body mass index (BMI), smoking status, urological history, and fertility history. Exclusion criteria included diabetes mellitus; liver, renal, or thyroid disease; past or current cancer; a history of genito-urinary tract infections; azoospermia; and any surgical history or medications that could have affected semen parameters. According to the fifth edition of the World Health Organization guidelines, the patients were divided into the following four groups based on their semen parameters: normal (A, n=31), abnormal sperm motility (B, n=12), abnormal sperm morphology (C, n=20), and two or more abnormal parameters (D, n=16). Seminal plasma and serum concentrations of IGF-1 were determined for each subject.

2. Hormonal assay

Serum and seminal IGF-1 levels were assessed via radioimmunoassay. Briefly, samples and standards were incubated in tubes that had previously been coated with the first monoclonal antibody in the presence of a second monoclonal antibody, which was labeled with iodine-125. After incubation, the tube contents were removed and the amounts of bound radioactive iodine-125 were measured. Unknown values were determined by interpolation from a standard curve; standard curve measurements were taken at the same time as those of the samples. The amount of bound radioactivity was directly proportional to the IGF-1 concentration in each sample. All reagents in the kit used were stable until the expiry date, per the kit label, if stored at 2℃ to 8℃. Storage conditions for reagents after reconstitution or dilution are included in the detailed description of the assay procedures.

3. Statistical analysis

The PRISM software package ver. 4.10 (GraphPad, La Jolla, CA, USA) was used for statistical analysis. Significance was set at p<0.05 with a confidence interval of 95%. Spearman's rank correlation analysis was used to assess the relationships between serum IGF-1 levels, semen IGF-1 levels, and other semen variables. Quantitative parametric data are represented as means and standard deviations. Student's t-test was used to compare means between groups, whereas one-way analysis of variance was used to compare more than two groups. Intra-group differences were assessed using a post hoc test and by calculating the least significant difference.

Results

The principal characteristics of patients with normal and abnormal semen parameters are listed in Table 1. Body weight is heavier in group C; however, BMI did not significantly differ between groups. The serum IGF-1 levels of the abnormal sperm motility group (B), the abnormal sperm morphology group (C), and the group with two or more abnormal parameters (D) were significantly lower than those of the normal group (A). However, no significant between-group differences were observed regarding the IGF-1 levels of seminal plasma (Table 2). Next, the IGF-1 levels of the normal (A) and abnormal (B, C, and D) groups were compared. This analysis revealed that the abnormal group showed significantly lower serum levels of IGF-1 compared with the normal group. However, the seminal plasma IGF-1 levels were not significantly different between the normal (A) and abnormal (B, C, and D) groups (Table 3). In a Spearman's correlation test, the serum IGF-1 level is correlated with semen volume, sperm motility, and sperm viability (Table 4).

Table 1. Baseline characteristics of each group.

graphic file with name cerm-43-97-i001.jpg

Values are presented as mean±standard deviation.

Group A, normal semen parameters; Group B, abnormal sperm motility; Group C, abnormal sperm morphology; Group D, more than two abnormal semen parameters.

Table 2. Semen parameters, serum IGF-1 level, and seminal plasma IGF-1 level of each group.

graphic file with name cerm-43-97-i002.jpg

Values are presented as mean±standard deviation.

Group A, normal semen parameters; Group B, abnormal sperm motility; Group C, abnormal sperm morphology; Group D, more than two abnormal semen parameters; IGF-1, insulin-like growth factor-1.

a)p<0.001; b)p<0.05; c)p<0.01; multiple comparison test.

Table 3. Semen parameters, serum IGF-1 levels, and seminal plasma IGF-1 levels of the normal and abnormal semen parameter groups.

graphic file with name cerm-43-97-i003.jpg

Values are presented as mean±standard deviation.

IGF-1, insulin-like growth factor-1; Group A, normal semen parameters; Group B, abnormal sperm motility; Group C, abnormal sperm morphology; Group D, more than two abnormal semen parameters.

a)p<0.001, two-sided t-test.

Table 4. Correlation analysis between serum IGF-1 and clinical parameters.

graphic file with name cerm-43-97-i004.jpg

IGF-1, insulin-like growth factor-1; BMI, body mass index; NS, not significant; TMSC, total motile sperm count.

Discussion

Studies of children and adolescents have indicated an age-related increase in serum IGF-1 levels during the prepubertal and early pubertal stages, followed by a decrease in late puberty [22,23,24,25]. Other studies have also shown that serum IGF-1 levels change with age; for instance, Korean men aged 30 to 49 years old were shown to have serum IGF-1 levels that exceeded 180 ng/mL [24]. The mean subject age in our study was 35.2 years, with a range of 30 to 49 years.

Overall, the serum IGF-1 levels measured in our study were relatively low. This finding might be due to the size of our target group, which could have affected the results due to bias in the measuring tools. We found that the serum IGF-1 levels of the abnormal motility group (B, mean=137.3±7.3 ng/mL), the abnormal morphology group (C, mean=144.4±25.8 ng/mL), and the group with two or more abnormal parameters (D, mean=130.6±28.2 ng/mL) were significantly lower than the levels in the normal group (A, mean=175.4±42.7 ng/mL).

Only a few studies have assessed the relationship between serum/seminal IGF-1 and semen quality. In these studies, males with infertility due to oligospermia had the lowest mean and median levels of seminal IGF-1. These levels were significantly different from the levels in the fertile and immuno-infertile groups, as well as from the other male-factor infertile subgroups. These findings suggest that lower seminal IGF-1 levels are associated with oligospermia [2]. However, we did not observe a significant relationship between semen parameters and seminal IGF-1 in this study, although we did identify a significant relationship between semen parameters and the serum level of IGF-1.

Both morphologically normal sperm and the seminal levels of IGF-1 have been reported to be decreased in males who smoke. Specifically, infertile smokers had the lowest seminal IGF-1 values, followed by infertile nonsmokers, fertile smokers, and control subjects [26]. These findings indicate that reduced IGF-1 is associated with both smoking and infertility.

Seminal IGF-1 has also been shown to have a significant positive correlation with the number of motile and rapid linear progressive spermatozoa [24]. IGF-1 production stimulates spermatozoa maturation in a paracrine/autocrine manner, thereby increasing sperm motility [3]. Thus, IGF-1 might function as a differentiation marker in male germ cells. Colombo and Naz [2] also showed that the seminal IGF-1 level exhibited a significant linear correlation with the total sperm count. Although sperm count was not directly investigated in the present study, it is taken indirectly into account for group D. Consistent with other studies, we observed decreased seminal IGF-1 levels in this group; however, this decrease was not significant. A limitation of this study is that subjects in the normal semen parameter group are also infertile male patients; thus, improved fertile male subjects will be needed for comparison of IGF-1 levels.

We found that the groups with abnormal sperm parameters exhibited significantly lower levels of serum IGF-1 compared with the normal group. Seminal plasma IGF-1 levels, however, did not differ significantly between the groups investigated here. Further investigations will be required to determine the exact mechanisms by which GH and IGF-1 affect fertility.

Footnotes

This study received financial support from LG Life Sciences (IIT-2011-04).

Conflict of interest: No potential conflict of interest relevant to this article was reported.

References

  • 1.Auger J, Kunstmann JM, Czyglik F, Jouannet P. Decline in semen quality among fertile men in Paris during the past 20 years. N Engl J Med. 1995;332:281–285. doi: 10.1056/NEJM199502023320501. [DOI] [PubMed] [Google Scholar]
  • 2.Colombo JB, Naz RK. Modulation of insulin-like growth factor-1 in the seminal plasma of infertile men. J Androl. 1999;20:118–125. [PubMed] [Google Scholar]
  • 3.Glander HJ, Kratzsch J, Weisbrich C, Birkenmeier G. Insulin-like growth factor-I and alpha 2-macroglobulin in seminal plasma correlate with semen quality. Hum Reprod. 1996;11:2454–2460. doi: 10.1093/oxfordjournals.humrep.a019136. [DOI] [PubMed] [Google Scholar]
  • 4.Dyck MK, Ouellet M, Gagn M, Petitclerc D, Sirard MA, Pothier F. Testes-specific transgene expression in insulin-like growth factor-I transgenic mice. Mol Reprod Dev. 1999;54:32–42. doi: 10.1002/(SICI)1098-2795(199909)54:1<32::AID-MRD5>3.0.CO;2-U. [DOI] [PubMed] [Google Scholar]
  • 5.Bartke A. Effects of growth hormone on male reproductive functions. J Androl. 2000;21:181–188. [PubMed] [Google Scholar]
  • 6.Hess MF, Roser JF. The effects of age, season and fertility status on plasma and intratesticular insulin-like growth factor I concentration in stallions. Theriogenology. 2001;56:723–733. doi: 10.1016/s0093-691x(01)00602-1. [DOI] [PubMed] [Google Scholar]
  • 7.Handelsman DJ, Spaliviero JA, Scott CD, Baxter RC. Identification of insulin-like growth factor-I and its receptors in the rat testis. Acta Endocrinol (Copenh) 1985;109:543–549. doi: 10.1530/acta.0.1090543. [DOI] [PubMed] [Google Scholar]
  • 8.Smith EP, Svoboda ME, Van Wyk JJ, Kierszenbaum AL, Tres LL. Partial characterization of a somatomedin-like peptide from the medium of cultured rat Sertoli cells. Endocrinology. 1987;120:186–193. doi: 10.1210/endo-120-1-186. [DOI] [PubMed] [Google Scholar]
  • 9.Vannelli BG, Barni T, Orlando C, Natali A, Serio M, Balboni GC. Insulin-like growth factor-I (IGF-I) and IGF-I receptor in human testis: an immunohistochemical study. Fertil Steril. 1988;49:666–669. doi: 10.1016/s0015-0282(16)59837-9. [DOI] [PubMed] [Google Scholar]
  • 10.Borland K, Mita M, Oppenheimer CL, Blinderman LA, Massague J, Hall PF, et al. The actions of insulin-like growth factors I and II on cultured Sertoli cells. Endocrinology. 1984;114:240–246. doi: 10.1210/endo-114-1-240. [DOI] [PubMed] [Google Scholar]
  • 11.Tres LL, Smith EP, Van Wyk JJ, Kierszenbaum AL. Immunoreactive sites and accumulation of somatomedin-C in rat Sertoli-spermatogenic cell co-cultures. Exp Cell Res. 1986;162:33–50. doi: 10.1016/0014-4827(86)90424-6. [DOI] [PubMed] [Google Scholar]
  • 12.Henricks DM, Kouba AJ, Lackey BR, Boone WR, Gray SL. Identification of insulin-like growth factor I in bovine seminal plasma and its receptor on spermatozoa: influence on sperm motility. Biol Reprod. 1998;59:330–337. doi: 10.1095/biolreprod59.2.330. [DOI] [PubMed] [Google Scholar]
  • 13.Naz RK, Padman P. Identification of insulin-like growth factor (IGF)-1 receptor in human sperm cell. Arch Androl. 1999;43:153–159. doi: 10.1080/014850199262661. [DOI] [PubMed] [Google Scholar]
  • 14.Skinner MK. Cell-cell interactions in the testis. Endocr Rev. 1991;12:45–77. doi: 10.1210/edrv-12-1-45. [DOI] [PubMed] [Google Scholar]
  • 15.Söder O, Bang P, Wahab A, Parvinen M. Insulin-like growth factors selectively stimulate spermatogonial, but not meiotic, deoxyribonucleic acid synthesis during rat spermatogenesis. Endocrinology. 1992;131:2344–2350. doi: 10.1210/endo.131.5.1425434. [DOI] [PubMed] [Google Scholar]
  • 16.Spiteri-Grech J, Nieschlag E. Paracrine factors relevant to the regulation of spermatogenesis: a review. J Reprod Fertil. 1993;98:1–14. doi: 10.1530/jrf.0.0980001. [DOI] [PubMed] [Google Scholar]
  • 17.Tsuruta JK, O'Brien DA. Sertoli cell-spermatogenic cell interaction: the insulin-like growth factor-II/cation-independent mannose 6-phosphate receptor mediates changes in spermatogenic cell gene expression in mice. Biol Reprod. 1995;53:1454–1464. doi: 10.1095/biolreprod53.6.1454. [DOI] [PubMed] [Google Scholar]
  • 18.Saez JM. Leydig cells: endocrine, paracrine, and autocrine regulation. Endocr Rev. 1994;15:574–626. doi: 10.1210/edrv-15-5-574. [DOI] [PubMed] [Google Scholar]
  • 19.Baxter RC, Martin JL, Beniac VA. High molecular weight insulin-like growth factor binding protein complex: purification and properties of the acid-labile subunit from human serum. J Biol Chem. 1989;264:11843–11848. [PubMed] [Google Scholar]
  • 20.Rechler MM. Insulin-like growth factor binding proteins. Vitam Horm. 1993;47:1–114. doi: 10.1016/s0083-6729(08)60444-6. [DOI] [PubMed] [Google Scholar]
  • 21.Ovesen P, Flyvbjerg A, Orskov H. Insulin-like growth factor I (IGF-I) and IGF binding proteins in seminal plasma before and after vasectomy in normal men. Fertil Steril. 1995;63:913–918. doi: 10.1016/s0015-0282(16)57502-5. [DOI] [PubMed] [Google Scholar]
  • 22.Andrade Olivié MA, Garcia-Mayor RV, Gonzalez Leston D, Rodriguez Sousa T, Segura Dominguez A, Alvarez-Novoa R, et al. Serum insulin-like growth factor (IGF) binding protein-3 and IGF-I levels during childhood and adolescence: a cross-sectional study. Pediatr Res. 1995;38:149–155. doi: 10.1203/00006450-199508000-00003. [DOI] [PubMed] [Google Scholar]
  • 23.Juul A, Holm K, Kastrup KW, Pedersen SA, Michaelsen KF, Scheike T, et al. Free insulin-like growth factor I serum levels in 1430 healthy children and adults, and its diagnostic value in patients suspected of growth hormone deficiency. J Clin Endocrinol Metab. 1997;82:2497–2502. doi: 10.1210/jcem.82.8.4137. [DOI] [PubMed] [Google Scholar]
  • 24.Lee KO, Ng SC, Lee PS, Bongso AT, Taylor EA, Lin TK, et al. Effect of growth hormone therapy in men with severe idiopathic oligozoospermia. Eur J Endocrinol. 1995;132:159–162. doi: 10.1530/eje.0.1320159. [DOI] [PubMed] [Google Scholar]
  • 25.Löfqvist C, Andersson E, Gelander L, Rosberg S, Blum WF, Albertsson Wikland K. Reference values for IGF-I throughout childhood and adolescence: a model that accounts simultaneously for the effect of gender, age, and puberty. J Clin Endocrinol Metab. 2001;86:5870–5876. doi: 10.1210/jcem.86.12.8117. [DOI] [PubMed] [Google Scholar]
  • 26.Hassan A, Abo-Azma SM, Fayed SM, Mostafa T. Seminal plasma cotinine and insulin-like growth factor-I in idiopathic oligoasthenoteratozoospermic smokers. BJU Int. 2009;103:108–111. doi: 10.1111/j.1464-410X.2008.07929.x. [DOI] [PubMed] [Google Scholar]

Articles from Clinical and Experimental Reproductive Medicine are provided here courtesy of Korean Society for Reproductive Medicine

RESOURCES