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Testosterone and gonadotropins but not SHBG vary with CKD stages in young and middle aged men



The aim of this study was to assess the effects chronic kidney disease (CKD) had on sex hormones and lipids in a subgroup of men between 18 and 50 years old with CKD 1–5 stage without diabetes and not treated with hemodialysis.


Data were collected from 101 men with different CKD stages.


Higher CKD stage (lower function) had a significant negative linear trend on total testosterone level (p < 0.01) and free testosterone level (p < 0.01), with a significant increase of luteinizing hormone (LH) (p < 0.01), and prolactin (p < 0.01), while SHBG remained unchanged between the CKD stages. Triglycerides but not total cholesterol, HDL –cholesterol or LDL-cholesterol increased with higher CKD stage. A negative correlation was observed between BMI, SHBG and free testosterone (p < 0.01 for both) but not with other sex hormones. Age per se was related to a significant decrease of total and free testosterone level (p < 0.01 for both) even after correction for BMI.

Decreased levels of total testosterone and estimated free testosterone levels had a significant correlation with an increased level of triglyceride levels (p <0.01).


Our results indicate that CKD stage per se is a factor affecting testosterone levels in combination with age in men between 18 and 50 years old with CKD 1–5 stage, not treated with hemodialysis.

With increased CKD stage there was a significant increase in LH level and a pattern of hypergonadotropic hypogonadism. SHBG remained unchanged between the CKD stages.



Le but de cette étude était d’évaluer les effets d’une maladie rénale chronique (MRC) sur les hormones sexuelles et les lipides dans une sous-population d’hommes âgés de 18 à 50 ans porteurs d’une MRC de stade 1-5, non diabétiques et non traités par hémodialyse.


Les données ont été obtenues chez 101 hommes qui présentaient différents stades de MRC.


Un stade plus élevé de MRC (fonction plus réduite) a une tendance linéaire négative sur les taux de testostérone totale (p<0,01) et de testostérone libre (p<0,01), avec une augmentation significative de la LH (p<0,01) et de la prolactine (p<0,01), alors que les taux de SHBG ne diffèrent pas entre les stades. Les triglycérides augmentent avec les stades plus élevés de MRC, ce qui n’est pas le cas du cholestérol total, du cholestérol HDL, ou du cholestérol LDL. L’IMC est négativement corrélé à la SHBG (p<0,01) et à la testostérone libre (p<0,01), mais n’est pas corrélé aux autres hormones sexuelles. L’âge per se est lié à une diminution significative des taux de testostérone totale (p<0,01) et de testostérone libre (p<0,01), corrélation qui persiste après ajustement sur l’IMC. Des taux diminués de testostérone totale et de testostérone libre estimée sont significativement corrélés à un niveau augmenté des taux de triglycérides (p<0,01).


Nos résultats indiquent que le stade de la MRC per se est un facteur qui affecte les taux de testostérone en combinaison avec l’âge chez les hommes de 18 à 50 ans porteurs d’une MRC de stade 1-5 et non traités par hémodialyse.

L’élévation du stade de MRC est associée à une augmentation significative du taux de LH et à un profil d’hypogonadisme hypergonadotrophique. La SHBG n’est pas modifiée par le stade de MRC.


Chronic kidney disease (CKD) is found in more than 10 % of the general population [1, 2]. It is well recognized that cardiovascular diseases (CVD) are linked to CKD [3], and that chronic kidney disease is recognized as an independent risk factor for premature CVD [3]. The exact role of androgens in the development of cardiovascular and CKD is still unclear.

In men with type 2 diabetes mellitus suboptimal testosterone concentration is a common finding in one-third of the men along with a normal LH [4]. And presence of type 2 diabetes and CKD increase the prevalence of hypogonadism from 5 % to 26 % [4]. Data from meta-analysis have also shown that men with non-diabetic CKD have a faster progression to end stage renal disease (ESRD) compared to female, although other studies did not identify gender as a risk factor for CKD or for CKD progression [5, 6]. In men with CKD gonadal dysfunction with elevation of serum gonadotropin concentration is a frequent finding, affecting 26–66 % of men with different stages of CKD [7].

Subfertility is also a common problem in men with CKD and we have previously shown that CKD stage per se is a factor determining the number of spermatozoa available in epididymis for ejaculation. This was in part independent of age-related decrease of testosterone level and BMI in a subgroup of men between 18 and 50 years old with CKD 1–5 stage, not treated with hemodialysis [8].

Hypergonadotropic hypogonadism is a well established hormonal derangement associated with CKD [9]. In a population free from renal disease, testosterone deficiency is suggested to take part in the atherosclerotic process. Emerging evidence indicates that androgens may provide a protective effect against the development and/or progression of atherosclerosis in men [10]. Hypogonadism in men with CKD not yet on dialysis, has been associated with arterial stiffness and endothelial dysfunction [11] supporting the theory that hypogonadism could be a key link with CVD in this group of men [12]. However it cannot be excluded that the atherosclerotic process significantly increases as a consequence of progression of the kidney disease (e.g. low testosterone levels in CKD may therefore be an adaptive mechanism during progression) rather than as a consequence of low testosterone level per se [13].

It is also possible that prescribed medications to patients with CKD could interfere directly with synthesis of sex hormones e.g. statins, angiotensin-converting enzyme (ACE) inhibitors and angiotensin II receptor blockers (ARBs) [7, 14, 15]. Several expert groups have presented guidelines for the diagnosis of testosterone deficiency [16, 17]. Those guidelines recommend that the diagnosis of hypogonadism should only be made in men with characteristic symptoms or signs of testosterone deficiency in combination with a documented low serum testosterone level.

The most widely accepted parameters to establish the presence of hypogonadism is the measurement of total serum testosterone. There are no generally accepted lower limits of normal total testosterone levels. There is, however, general agreement that patients with a total serum testosterone level above 12 nmol/L generally do not benefit from treatment [17].

Most studies of sex hormones in men with CKD have been focused on patients with end stage renal disease (CKD 5 without dialysis) and on patients on hemodialysis, and there is little information about sex hormone level development and serum lipid profiles throughout the different CKD stages. This study analyzes aspects of sex hormone levels and lipids, among a subgroup of Swedish men between 18–50 years old in CKD 1–5 stage, without diabetes mellitus and not treated with hemodialysis.



Patients with different CKD stages aged 18–50 years from the Department of Nephrology, Karolinska University Hospital, Stockholm, Sweden were recruited from December 2012 to December 2013 and divided into five groups according to their stage of renal impairment (CKD 1-CKD 5). Staging of CKD was defined according to the presence or absence of kidney damage and level of kidney function, irrespective of type of kidney diagnosis [18], according to Table 1. The CKD stage was based on Creatinine–Cystatin C Equation) for Estimating Glomerular Filtration Rate (eGFR) [19].

Table 1 Stages of chronic kidney disease (CKD) was defined according to the presence or absence of kidney damage and level of kidney function, irrespective of the type of kidney disease (diagnos) [43]

Of the 145 men invited 101 fulfilled inclusion criteria and volunteered to provide fasting blood samples. In Tables 2 and 3 characteristics of the participants are included. Participants were not included if they were smokers or former smokers (>3 months), had type 1 or type 2 diabetes mellitus, had a previous renal transplantation, or were treated with testosterone replacement therapy. Patients with diabetes mellitus were excluded because both forms of diabetes may be associated with hypercholesterolemia and hypertriglyceridemia at hyperglycemia [20].

Table 2 Baseline clinical characteristics of participants in stage CKD 1–5
Table 3 Diagnosis of participants in stage CKD 1–5

All participants gave written and oral informed consent to participate, and the study was approved by the Ethics Committee of Karolinska Institute.


All samples were taken in morning (07.00-09.00 a.m.) after an overnight fast (12 hrs).

Total testosterone level was measured with a chemiluminescent immunoassay for quantitative determination of total testosterone level in human serum and plasma using the Access Imunoassay System (Beckman Coulter). The intra-assay and inter-assay coefficients of variation for testosterone were less than 5.0 %. Free serum testosterone was calculated by the method of Vermeulen [21].

LH and FSH were determined with an AutoDELFIA hLH assay (PerkinElmer Life and Analytical Sciences, Turku, Finland) two-site immunoradiometric assay. The intra-assay and inter-assay coefficients of variation were 1.9 and 2.2 % respectively for LH and 2.2 and 3.5 % for FSH. SHBG and prolactin were measured with a paramagnetic particle chemiluminescent immunoassay (Access SHBG assay UniCel DxI 800, Beckman Coulter, Inc, USA). The intra-assay and inter-assay coefficients of variation for SHBG were 4.0 and 5. 5 % respectively, and for prolactin 3.5 and 5.0 %. Plasma glucose concentration was measured by a glucose oxydase method (Glukos HK, Modular P, Roche Diagnostics, Indianapolis, IN). The intra-assay and inter-assay coefficients of variation for glucose were 1.2 and 1.9 % respectively.

Total cholesterol, High-density lipoprotein (HDL)-cholesterol, Low-density lipoprotein (LDL) – cholesterol, creatinine and cystatin C were measured by the routine chemistry accredited laboratory at the Karolinska University Hospital (Modular P, Roche Diagnostics, Mannheim). LDL-cholesterol was calculated according to the Friedewald formula [22]. All participants had plasma triglycerides < 4.5 mmol /L (the upper limit for estimates with the formula). Reference range for healthy men between 18–50 years of age is included in the Additional file 1: Table S1.

Statistical analysis

All data shown are expressed as means ± SD. The normality was tested with a probability plot and the Kolmogorov-Smirnov one-sample test. Log transformed values were used for prolactin, SHBG and triglycerides levels in the analysis and then back transformed for data presentation. One way Analysis of Variance (ANOVA) was used to test the differences between CKD stages for age, BMI, Hemoglobin, creatinine, eGFR, sex hormones and lipids. A Spearman´s rank test was used to determine univariate correlations between variables. Multiple linear regression analyses were performed with BMI and age as covariates. Data were considered statistically significant at p < 0. 05.

Statistical analyses were performed using Statistica, Statsoft version 10.0 (Tulsa, OK, USA).


Clinical characteristics

The clinical characteristics of the 101 men who were included and had accepted to participate in the study are shown in Tables 2 and 3. The group of men enrolled in this study did not differ significantly in age or BMI between the different five CKD stages.

Sex hormone level in serum

There was a significant decrease in total testosterone level and estimated free testosterone with CKD stages, p <0.01 for trend for both. LH and prolactin levels increased significantly, p <0.01. FSH showed a tendency to increase, although not significantly. No significant differences were observed for SHBG levels among the different CKD stages, Table 4.

Table 4 Comparison of the levels of sex hormones and lipid levels in serum in participants in stage CKD 1–5

Serum lipid profile

In men with CKD stage 1–5 a significant increase in triglycerides levels was seen with increased CKD stage, p < 0.01. No significant differences were observed for total cholesterol, HDL-cholesterol or LDL-cholesterol levels among the different CKD stages, Table 4.

Relationships between testosterone and lipids

The effect of decreased total testosterone levels on lipid parameters had a significant correlation with level of triglycerides (r = − 0. 42, p <0.001) and HDL –cholesterol (r =0.25, p = 0.01), Table 5. A decrease although not significant was also seen for total cholesterol level but not for LDL-cholesterol, Table 5. Free testosterone correlated with level of triglycerides but not with HDL-cholesterol. A borderline significant decrease was seen for total cholesterol, Table 5.

Table 5 Multiple linear regression analyses were performed with BMI and age as covariates

Effect of BMI and age on sex hormones

In this study BMI had no significant correlation with total testosterone, LH, FSH or prolactin. A significant correlation with free testosterone was observed, Table 5. There was a negative significant correlation with SHBG (p < 0.01), Table 5. This significant correlation persisted after correction for age. Age was correlated to a decrease in total testosterone level and free testosterone level (p < 0.01) even after correction for BMI.


The association of different stages of CKD with sex hormones has been examined in several previous studies [11, 23]. As far as we know most studies in men with CKD have been performed in older patients or patients with end stage renal disease. It has been shown previously that there is a negative correlation between endogenous testosterone and CKD stage 1–5 [7, 11]. The mechanism for this is likely to involve, at least in some part some alteration or derangement of the male reproductive hormone profile [9]. This supports our findings of a significant decrease in testosterone level with increased CKD stages even in younger men and middle-aged men.

Whether decreased testosterone level is a result of degradation of uremic metabolites accumulated mainly in testes and affecting the Leydig cells as a result of progressive kidney disease or an inhibition of cAMP production associated with inhibition of 125I-human chorionic gonadotropin binding of the luteinizing hormone receptor in Leydig cells [23] is still unknown. A previous study has supported the theory that chronic kidney disease mainly affect testes by a defect in 17 ~ −hydroxysteroid dehydrogenase evidenced by a decrease in testosterone/androstenedione ratio at progressive CKD and a lack of correction by hCG administration [24]. With higher CKD stages there was a significant increase in the LH level and the development of a pattern of hypergonadotropic hypogonadism, which indicates that uremic metabolites secondary to the increased CKD stage affect testes more than the hypothalamic or pituitary function. Alternatively the degradation of uremic metabolites in the hypothalamic or pituitary region is faster and more pronounced than in testes. Previous studies have shown that hemodialysis does not improve the function of the HPT axis [25] but that renal transplantation may reverse the uremic damage to testicular function, suggesting that clearance of uremic metabolites is insufficient on hemodialysis treatment.

A novel finding was that SHBG level was unchanged between CKD stages, supporting the theory that also bioavailable testosterone decreases with CKD staging. The unchanged SHBG level does not support previous finding that estradiol level increases in men with CKD [26]. A high concomitant estradiol level is a common finding in men with CKD and gives a concomitant increase of SHBG level [26, 27]. However we cannot exclude that estradiol levels increase with CKD stages and then compensate the effect of decreasing testosterone on SHBG levels. The discrepancy between our results and previous studies could in part be explained by exclusion of patients with diabetes mellitus included in this study, and also that there were no patients with high BMI included, thus the metabolic impact could be minor in our study.

Of additional interest is insulin even among CKD patients without manifest or overt diabetes mellitus. Clearance of insulin is reduced with progressive CKD stage [28] and insulin resistance appears at an earlier stage of CKD [28] . Induction of insulin resistance in podocytes leads to glomerulosclerosis in animal models and development of CKD in observational human studies [29]. Elevated insulin level also produces a decrease in the hepatic production of SHBG [30] which in part can explain our results.

SHBG is also down regulated by proinflammatory cytokines that are associated with the prevalence and severity of CKD [31]. And SHBG levels can therefore represent a sensitive indicator of low-grade inflammation.

Hyperprolactinemia has been shown to affect at least 30 % of patients with CKD [32] and is the consequence of both reduced renal clearance [33] and increased production [34]. Prolactin might influence the metabolism of SHBG [35] by its inhibiting hormonal influences and decrease of SHBG in hyperprolactinemia [35]. In our study and a previous study of men without renal diseases [36] there was no correlation between SHBG and prolactin, but that does not exclude a correlation at a higher threshold level.

Hyperprolactinemia in CKD may be a contributing factor in the atherosclerotic process [37]. Increased expression of prolactin receptors has been found in human atherosclerotic plaques [38] and may be contributing factor to vascular derangements per se [37]. The lack of significant changes in SHBG levels among the participants in our study could be multifactorial due to medications, lifestyle comorbidity and dietary factors [16, 39]. With nephrotic syndrome as a condition associated with alternations in SHBG concentration [16].

In the present study there was a significant negative correlation with triglyceride levels and CKD stages. Furthermore decreased testosterone levels were seen in more severe CKD stages with more than 58 percent increase of triglycerides in CKD stage 5 compared with CKD 1 stage. It has previously been shown that a higher triglyceride level contributes to a more rapid decline in renal function in a non-diabetic patient cohort with CKD [40].

In a previous study by Gungor et al. [41] a negative correlation was seen between total cholesterol, triglyceride and testosterone levels in the cases on the chronic hemodialysis schedule. It is likely that we could not find a significant correlation between CKD staging and total cholesterol due to the small number of participants and high number of patients using antihyperlipidemic agents.

Our study has several limitations. Firstly, this was a cross-section observational study performed in a small cohort of patients with different diagnoses and CKD stages, and different medical treatment including statins, Table 2. Although the most prominent effects attributable to statin therapy are the potent LDL-cholesterol lowering properties, it is also well established that statins significantly reduce triglycerides [42]. It can therefore not be excluded that some of the difference observed could be related to statin treatment. However statin treatment among patients was more common with increased CKD staging, Table 2.

There was a negative correlation between age and decreased testosterone level and also between triglycerides and the testosterone level. No correlation was seen with BMI and sex hormones, except a negative correlation with SHBG. This might be explained by the limited number of participants and lack of overweight and obese participants included.


CKD stage per se is a factor determining testosterone level together with age. A decreased testosterone level is also correlated with an increased level of triglycerides but not with cholesterol SHBG remained unchanged between the CKD stages.. With an increased CKD stage there was a significant increase in LH level, which indicates that uremic metabolites secondary to increased CKD stage in men between 18 and 50 years old with CKD 1–5 stage, not treated with hemodialysis affect testes more than the hypothalamic or pituitary function.



Chronic kidney disease


Cardiovascular disease


End stage renal disease


Analysis of variance


luteinizing hormone


Sex hormone-binding globulin


Follicle stimulating hormone




estimated Glomerular Filtration Rate

ACE inhibitors:

Angiotensin-converting enzyme inhibitor


Angiotensin II receptor blockers


  1. 1.

    Hallan SI, Coresh J, Astor BC, Asberg A, Powe NR, Romundstad S, et al. International comparison of the relationship of chronic kidney disease prevalence and ESRD risk. J Am Soc Nephrol. 2006;17(8):2275–84. doi:10.1681/ASN.2005121273.

    Article  PubMed  Google Scholar 

  2. 2.

    Jha V, Garcia-Garcia G, Iseki K, Li Z, Naicker S, Plattner B, et al. Chronic kidney disease: global dimension and perspectives. Lancet. 2013;382(9888):260–72. doi:10.1016/S0140-6736(13)60687-X.

    Article  PubMed  Google Scholar 

  3. 3.

    Afsar B, Turkmen K, Covic A, Kanbay M. An update on coronary artery disease and chronic kidney disease. Int J Nephrol. 2014;2014:767424. doi:10.1155/2014/767424.

    PubMed Central  PubMed  Google Scholar 

  4. 4.

    Dhindsa S, Reddy A, Sukhmoy Karam J, Bilkis S, Chaurasia A, Mehta A, et al. Prevalence of subnormal testosterone concentrations in men with type 2 diabetes and chronic kidney disease. Eur J Endocrinol. 2015;173(3):359–66. doi:10.1530/EJE-15-0359.

    CAS  Article  PubMed  Google Scholar 

  5. 5.

    Jafar TH, Schmid CH, Stark PC, Toto R, Remuzzi G, Ruggenenti P, et al. The rate of progression of renal disease may not be slower in women compared with men: a patient-level meta-analysis. Nephrol Dial Transplant. 2003;18(10):2047–53. doi:10.1093/ndt/gfg317.

    Article  PubMed  Google Scholar 

  6. 6.

    Neugarten J, Acharya A, Silbiger SR. Effect of gender on the progression of nondiabetic renal disease: a meta-analysis. J Am Soc Nephrol. 2000;11(2):319–29.

    CAS  PubMed  Google Scholar 

  7. 7.

    Iglesias P, Carrero JJ, Diez JJ. Gonadal dysfunction in men with chronic kidney disease: clinical features, prognostic implications and therapeutic options. J Nephrol. 2012;25(1):31–42. doi:10.5301/JN.2011.8481.

    CAS  Article  PubMed  Google Scholar 

  8. 8.

    Lehtihet M, Hylander B. Semen quality in men with chronic kidney disease and its correlation with chronic kidney disease stages. Andrologia. 2014. doi:10.1111/and.12388.

    PubMed  Google Scholar 

  9. 9.

    Holley JL. The hypothalamic-pituitary axis in men and women with chronic kidney disease. Adv Chronic Kidney Dis. 2004;11(4):337–41.

    Article  PubMed  Google Scholar 

  10. 10.

    Traish AM, Kypreos KE. Testosterone and cardiovascular disease: an old idea with modern clinical implications. Atherosclerosis. 2011;214(2):244–8. doi:10.1016/j.atherosclerosis.2010.08.078.

    CAS  Article  PubMed  Google Scholar 

  11. 11.

    Yilmaz MI, Sonmez A, Qureshi AR, Saglam M, Stenvinkel P, Yaman H, et al. Endogenous testosterone, endothelial dysfunction, and cardiovascular events in men with nondialysis chronic kidney disease. Clin J Am Soc Nephrol. 2011;6(7):1617–25. doi:10.2215/CJN.10681210.

    CAS  Article  PubMed  Google Scholar 

  12. 12.

    Meuwese CL, Carrero JJ. Chronic kidney disease and hypothalamic-pituitary axis dysfunction: the chicken or the egg? Arch Med Res. 2013;44(8):591–600. doi:10.1016/j.arcmed.2013.10.009.

    Article  PubMed  Google Scholar 

  13. 13.

    Dousdampanis P, Trigka K, Fourtounas C, Bargman JM. Role of testosterone in the pathogenesis, progression, prognosis and comorbidity of men with chronic kidney disease. Ther Apher Dial. 2014;18(3):220–30. doi:10.1111/1744-9987.12101.

    CAS  PubMed  Google Scholar 

  14. 14.

    Carrero JJ, Stenvinkel P. The vulnerable man: impact of testosterone deficiency on the uraemic phenotype. Nephrol Dial Transplant. 2012;27(11):4030–41. doi:10.1093/ndt/gfs383.

    CAS  Article  PubMed  Google Scholar 

  15. 15.

    Isidori AM, Lenzi A. Risk factors for androgen decline in older males: lifestyle, chronic diseases and drugs. J Endocrinol Invest. 2005;28(3 Suppl):14–22.

    CAS  PubMed  Google Scholar 

  16. 16.

    Bhasin S, Cunningham GR, Hayes FJ, Matsumoto AM, Snyder PJ, Swerdloff RS, et al. Testosterone therapy in men with androgen deficiency syndromes: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2010;95(6):2536–59. doi:10.1210/jc.2009-2354.

    CAS  Article  PubMed  Google Scholar 

  17. 17.

    Wang C, Nieschlag E, Swerdloff R, Behre HM, Hellstrom WJ, Gooren LJ, et al. Investigation, treatment, and monitoring of late-onset hypogonadism in males: ISA, ISSAM, EAU, EAA, and ASA recommendations. Eur Urol. 2009;55(1):121–30. doi:10.1016/j.eururo.2008.08.033.

    Article  PubMed  Google Scholar 

  18. 18.

    Tsai CW, Grams ME, Inker LA, Coresh J, Selvin E. Cystatin C- and creatinine-based estimated glomerular filtration rate, vascular disease, and mortality in persons with diabetes in the U.S. Diabetes Care. 2014;37(4):1002–8. doi:10.2337/dc13-1910.

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  19. 19.

    Inker LA, Schmid CH, Tighiouart H, Eckfeldt JH, Feldman HI, Greene T, et al. Estimating glomerular filtration rate from serum creatinine and cystatin C. N Engl J Med. 2012;367(1):20–9. doi:10.1056/NEJMoa1114248.

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  20. 20.

    Robinson DS, Speake BK. Role of insulin and other hormones in the control of lipoprotein lipase activity. Biochem Soc Trans. 1989;17(1):40–2.

    CAS  Article  PubMed  Google Scholar 

  21. 21.

    Vermeulen A, Verdonck L, Kaufman JM. A critical evaluation of simple methods for the estimation of free testosterone in serum. J Clin Endocrinol Metab. 1999;84(10):3666–72. doi:10.1210/jcem.84.10.6079.

    CAS  Article  PubMed  Google Scholar 

  22. 22.

    Knopfholz J, Disserol CC, Pierin AJ, Schirr FL, Streisky L, Takito LL, et al. Validation of the friedewald formula in patients with metabolic syndrome. Cholesterol. 2014;2014:261878. doi:10.1155/2014/261878.

    PubMed Central  Article  PubMed  Google Scholar 

  23. 23.

    Dunkel L, Raivio T, Laine J, Holmberg C. Circulating luteinizing hormone receptor inhibitor(s) in boys with chronic renal failure. Kidney Int. 1997;51(3):777–84.

    CAS  Article  PubMed  Google Scholar 

  24. 24.

    Blacker C, Provost M, Kerdelhue B, Scholler R. Testicular function in uremic rats: in vivo assessment of testosterone biogenesis. J Steroid Biochem Mol Biol. 1991;39(3):395–403.

    CAS  Article  PubMed  Google Scholar 

  25. 25.

    Hamdi SM, Walschaerts M, Bujan L, Rostaing L, Kamar N. A prospective study in male recipients of kidney transplantation reveals divergent patterns for inhibin B and testosterone secretions. Basic Clin Androl. 2014;24:11. doi:10.1186/2051-4190-24-11.

    PubMed Central  Article  PubMed  Google Scholar 

  26. 26.

    Yi S, Selvin E, Rohrmann S, Basaria S, Menke A, Rifai N, et al. Endogenous sex steroid hormones and measures of chronic kidney disease (CKD) in a nationally representative sample of men. Clin Endocrinol. 2009;71(2):246–52. doi:10.1111/j.1365-2265.2008.03455.x.

    CAS  Article  Google Scholar 

  27. 27.

    Eckersten D, Giwercman A, Christensson A. Male patients with terminal renal failure exhibit low serum levels of antimullerian hormone. Asian J Androl. 2014. doi:10.4103/1008-682X.135124.

    PubMed Central  Google Scholar 

  28. 28.

    Kobayashi S, Maesato K, Moriya H, Ohtake T, Ikeda T. Insulin resistance in patients with chronic kidney disease. Am J Kidney Dis. 2005;45(2):275–80.

    CAS  Article  PubMed  Google Scholar 

  29. 29.

    De Cosmo S, Menzaghi C, Prudente S, Trischitta V. Role of insulin resistance in kidney dysfunction: insights into the mechanism and epidemiological evidence. Nephrol Dial Transplant. 2013;28(1):29–36. doi:10.1093/ndt/gfs290.

    Article  PubMed  Google Scholar 

  30. 30.

    Veldhuis JD, Bondar OP, Dyer RB, Trushin SA, Klee EW, Singh RJ, et al. Immunological and mass spectrometric assays of SHBG: consistent and inconsistent metabolic associations in healthy men. J Clin Endocrinol Metab. 2014;99(1):184–93. doi:10.1210/jc.2013-2642.

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  31. 31.

    Lee BT, Ahmed FA, Hamm LL, Teran FJ, Chen CS, Liu Y, et al. Association of C-reactive protein, tumor necrosis factor-alpha, and interleukin-6 with chronic kidney disease. BMC Nephrol. 2015;16:77. doi:10.1186/s12882-015-0068-7.

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  32. 32.

    Hou SH, Grossman S, Molitch ME. Hyperprolactinemia in patients with renal insufficiency and chronic renal failure requiring hemodialysis or chronic ambulatory peritoneal dialysis. Am J Kidney Dis. 1985;6(4):245–9.

    CAS  Article  PubMed  Google Scholar 

  33. 33.

    Yavuz D, Topcu G, Ozener C, Akalin S, Sirikci O. Macroprolactin does not contribute to elevated levels of prolactin in patients on renal replacement therapy. Clin Endocrinol. 2005;63(5):520–4. doi:10.1111/j.1365-2265.2005.02375.x.

    CAS  Article  Google Scholar 

  34. 34.

    McKenna TM, Woolf PD. Prolactin metabolic clearance and resistance to dopaminergic suppression in acute uremia. Endocrinology. 1985;116(5):2003–7. doi:10.1210/endo-116-5-2003.

    CAS  Article  PubMed  Google Scholar 

  35. 35.

    Vermeulen A, Ando S, Verdonck L. Prolactinomas, testosterone-binding globulin, and androgen metabolism. J Clin Endocrinol Metab. 1982;54(2):409–12. doi:10.1210/jcem-54-2-409.

    CAS  Article  PubMed  Google Scholar 

  36. 36.

    Gann PH, Hennekens CH, Ma J, Longcope C, Stampfer MJ. Prospective study of sex hormone levels and risk of prostate cancer. J Nat Cancer Inst. 1996;88(16):1118–26.

    CAS  Article  PubMed  Google Scholar 

  37. 37.

    Carrero JJ, Kyriazis J, Sonmez A, Tzanakis I, Qureshi AR, Stenvinkel P, et al. Prolactin levels, endothelial dysfunction, and the risk of cardiovascular events and mortality in patients with CKD. Clin J Am Soc Nephrol. 2012;7(2):207–15. doi:10.2215/CJN.06840711.

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  38. 38.

    Reuwer AQ, Twickler MT, Hutten BA, Molema FW, Wareham NJ, Dallinga-Thie GM, et al. Prolactin levels and the risk of future coronary artery disease in apparently healthy men and women. Circ Cardiovasc Genet. 2009;2(4):389–95. doi:10.1161/CIRCGENETICS.109.853572.

    CAS  Article  PubMed  Google Scholar 

  39. 39.

    Allen NE, Appleby PN, Davey GK, Key TJ. Lifestyle and nutritional determinants of bioavailable androgens and related hormones in British men. Cancer Causes Control. 2002;13(4):353–63.

    Article  PubMed  Google Scholar 

  40. 40.

    Samuelsson O, Attman PO, Knight-Gibson C, Larsson R, Mulec H, Weiss L, et al. Complex apolipoprotein B-containing lipoprotein particles are associated with a higher rate of progression of human chronic renal insufficiency. J Am Soc Nephrol. 1998;9(8):1482–8.

    CAS  PubMed  Google Scholar 

  41. 41.

    Gungor O, Kircelli F, Carrero JJ, Asci G, Toz H, Tatar E, et al. Endogenous testosterone and mortality in male hemodialysis patients: is it the result of aging? Clin J Am Soc Nephrol. 2010;5(11):2018–23. doi:10.2215/CJN.03600410.

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  42. 42.

    Plosker GL, McTavish D. Simvastatin. A reappraisal of its pharmacology and therapeutic efficacy in hypercholesterolaemia. Drugs. 1995;50(2):334–63.

    CAS  Article  PubMed  Google Scholar 

  43. 43.

    National KF. K/DOQI clinical practice guidelines for chronic kidney disease: evaluation, classification, and stratification. Am J Kidney Dis. 2002;39(2 Suppl 1):S1–266.

    Google Scholar 

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We thank Pia Brushammar, research nurse at Department of Nephrology, Karolinska University Hospital Solna, Stockholm, Sweden for excellent logistic work.


The authors were financially supported by the kidney foundation, Sweden.


The authors state no conflicts of interest.

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Correspondence to Mikael Lehtihet.

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Authors’ contributions

ML and BH-R contributed to conception and design, acquisition, analysis and interpretation of data and were involved in drafting the manuscript. ML and BH-R both agree 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. All authors read approved the final manuscript.

Co-author Britta Hylander

Additional file

Additional file 1: Table S1.

A summary of the reference range for healthy men between 18–50 years of age. The conversion factor for prolactin from mass to units is 21.2. ((μg/L) x 21.2 = mIU/L). (DOC 33 kb)

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Hylander, B., Lehtihet, M. Testosterone and gonadotropins but not SHBG vary with CKD stages in young and middle aged men. Basic Clin. Androl. 25, 9 (2015).

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  • Chronic kidney disease
  • Hypogonadism
  • Testosterone level


  • maladie rénale chronique/hypogonadisme/taux de testostérone