Journal List > Korean J Urol > v.49(6) > 1005133

Lee and Kim: Correlation of the Serum Testosterone Level with Insulin Resistance and Metabolic Syndrome in Patients of Erectile Dysfunction and Benign Prostatic Hyperplasia

Abstract

Purpose

Testosterone deficiency has recently captured attention as a possible risk factor for metabolic syndrome. This study was conducted to investigate a correlation of the serum testosterone level with insulin resistance (IR) and metabolic syndrome (MS).

Materials and Methods

The metabolic risk factors, the blood pressure, the waist circumference and the fasting serum levels of glucose, triglyceride and high density lipoprotein cholesterol were measured for a total of 215 patients (mean age; 61.04±0.54 years) with erectile dysfunction (ED) or/and symptomatic benign prostatic hyperplasia (BPH). The serum total testosterone and insulin were measured at the same time, and the free testosterone, bioavailable testosterone and IR were calculated.

Results

The prevalence of MS and the number of associated MS risk factors were significantly higher in the insulin resistance group (IRG) than in the insulin sensitive group (ISG). The serum testosterone level significantly decreased with more risk factors. The IRG showed a significantly lower level of serum testosterone than the patients with ED and the total patients.

Conclusions

The negative correlation of a decrease in the serum testosterone level with IR and MS suggests that late onset hypogonadism might be a risk factor of MS.

REFERENCES

1. Cause of Death in Korea, The Department of Statistics. 2003. 5.
2. Ferrannini E, Haffner SM, Mitchell BD, Stern MP. Hyperinsulinemia: the key feature of a cardiovascular and metabolic syndrome. Diabetologia. 1991; 34:416–22.
3. Gray RS, Fabsitz RR, Cowan LD, Lee ET, Howard BV, Savage PJ. Risk factor clustering in the insulin resistance syndrome. The Strong Heart Study. Am J Epidemiol. 1998; 148:869–78.
crossref
4. Carantoni M, Zuliani G, Volpato S, Palmieri E, Mezzetti A, Vergnani L, et al. Relationships between fasting plasma insulin, anthropometrics, and metabolic parameters in a very old healthy population. Associazione Medica Sabin. Metabolism. 1998; 47:535–40.
5. Kalyani RR, Dobs AS. Androgen deficiency, diabetes, and the metabolic syndrome in men. Curr Opin Endocrinol Diabetes Obes. 2007; 14:226–34.
crossref
6. Stellato RK, Feldman HA, Hamdy O, Horton ES, McKinlay JB. Testosterone, sex hormone-binding globulin, and the development of type 2 diabetes in middle-aged men: prospective results from the Massachusetts male aging study. Diabetes Care. 2000; 23:490–4.
crossref
7. Oh J, Barrett-Connor E, Wedick NM, Wingard DL. Endogenous sex hormones and the development of type 2 diabetes in older men and women: the Rancho Bernardo study. Diabetes Care. 2002; 25:55–60.
crossref
8. Zitzmann M, Faber S, Nieschlag E. Association of specific symptoms and metabolic risks with serum testosterone in older men. J Clin Endocrinol Metab. 2006; 9:4335–43.
crossref
9. Kapoor D, Malkin CJ, Channer KS, Jones TH. Androgens, insulin resistance and vascular disease in men. Clin Endocrinol. 2005; 63:239–50.
crossref
10. Tan RS, Pu SJ. Impact of obesity on hypogonadism in the andropause. Int J Androl. 2002; 25:195–201.
crossref
11. Barrett-Connor E, Khaw KT, Yen SS. Endogenous sex hormone levels in older adult men with diabetes mellitus. Am J Epidemiol. 1990; 132:895–901.
crossref
12. Lunenfeld B. Testosterone deficiency and the metabolic syndrome. Aging Male. 2007; 10:53–6.
crossref
13. Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults. Executive summary of the third report of the national cholesterol education program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (adult treatment panel III). JAMA. 2001; 285:2486–97.
14. WHO Regional Office for the Western Pacific/International Association for the Study of Obesity/International Obesity Task Force. The Asia-Pacific perspective: redefining obesity and its treatment. Sydney, Health Communications Australia. 2000.
15. 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; 84:3666–72.
crossref
16. Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, Turner RC. Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia. 1985; 28:412–9.
17. DeFronzo RA, Ferrannini E. Insulin resistance. A multifaceted syndrome responsible for NIDDM, obesity, hypertension, dyslipidemia, and atherosclerotic cardiovascular disease. Diabetes Care. 1991; 14:173–94.
crossref
18. Kim SC. Insulin resistance and erectile dysfunction. Korean J Urol. 2006; 47:917–27.
crossref
19. Bojesen A, Kristensen K, Birkebaek NH, Fedder J, Mosekilde L, Bennett P, et al. The metabolic syndrome is frequent in Klinefelter's syndrome and is associated with abdominal obesity and hypogonadism. Diabetes Care. 2006; 29:1591–8.
crossref
20. Gustafson DR, Wen MJ, Koppanati BM. Androgen receptor gene repeats and indices of obesity in older adults. Int J Obes Relat Metab Disord. 2003; 27:75–81.
crossref
21. Lacko L, Wittke B, Geck P. Interaction of steroids with the transport system of glucose in human erythrocytes. J Cell Physiol. 1975; 86(Suppl 2):673–80.
crossref
22. Morimoto S, Mendoza-Rodriguez CA, Hiriat M, Larrieta ME, Vital P, Cerbon MA. Protective effect of testosterone on early apoptotic damange induced by streptozotocin in rat pancreas. J Endocrinol. 2005; 187:217–24.
23. Hellmich M, Evers T, Kubin M, Merchant S, Lehmacher W, Engelmann U, et al. Development and validation of a risk score for somatic erectile dysfunction: combined results from three cross-sectional surveys. Eur Urol. 2005; 48:495–502.
crossref
24. Kim JH, Shim BS, Hong YS. The relating factors of metabolic syndrome to benign prostatic hyperplasia. Korean J Urol. 2005; 46:1046–50.
25. Hammarsten J, Hogstedt B, Holthuis N, Mellstrom D. Components of the metabolic syndrome-risk factors for the development of benign prostatic hyperplasia. Prostate Cancer Prostatic Dis. 1998; 1:157–62.
crossref
26. Hammarsten J, Hogstedt B. Clinical, anthropometric, metabolic and insulin profile of men with fast annual growth rates of benign prostatic hyperplasia. Blood Press. 1999; 8:29–36.
27. Braga-Basaria M, Dobs AS, Muller DC, Carducci MA, John M, Egan J, et al. The metabolic syndrome in men with prostate cancer undergoing longterm androgen-deprivation therapy. J Clin Oncol. 2006; 24:3979–83.
28. Keating NL, O'Malley AJ, Smith MR. Diabetes and cardiovascular disease during androgen deprivation therapy for prostate cancer. J Clin Oncol. 2006; 24:448–56.
crossref
29. Nuver J, Smit AJ, Wolffenbuttel BH, Sluiter WJ, Hoekstra HJ, Sleijfer DT, et al. The metabolic syndrome and disturbances in hormone levels in longterm survivors of disseminated testicular cancer. J Clin Oncol. 2005; 23:3718–25.
crossref
30. Sampson N, Unterggasser G, Plas E, Berger P. The aging male reproductive tract. J Pathol. 2007; 211:206–18.

Table 1.
Patient characteristics
  ED (n=41) BPH+ED (n=72) BPH (n=102) Total (n=215)
Age (years) 59.22±1.26 63.71±0.77 61.50±0.76 61.80±0.54
Testosterone
 Total (ng/ml) 4.93±0.21 4.30±0.16 4.95±0.15 4.73±0.10
 Free (ng/dl) 7.66±0.32 6.40±0.26 6.86±0.26 6.86±0.16
 Bioavailable (ng/ml) 1.79±0.07 1.48±0.06 1.59±0.06 1.59±0.38
Metabolic syndrome risk factor
 TG (mg/dl) 146.79±0.21 112.97±7.05 102.76±6.10 114.28±4.53
 HDL (mg/dl) 47.41±1.28 47.37±1.39 51.48±1.11 49.33±0.75
 FBS (mg/dl) 113.17±6.28 114.28±3.45 100.63±1.00 107.63±1.78
 sBP (mmHg) 121.95±1.30 125.80±1.47 124.19±1.26 124.30±0.81
 dBP (mmHg) 81.58±1.16 83.62±1.15 82.51±0.82 82.70±0.59
 Waist (cm) 90.92±1.29 89.46±0.71 88.23±0.72 89.18±0.49
 TC (mg/dl) 193.20±5.21 180.36±4.12 192.45±3.32 188.54±2.34
 LDL (mg/dl) 115.02±4.84 108.07±3.11 114.58±2.72 112.48±1.90

ED: erectile dysfunction, BPH: benign prostatic hyperplasia, TG: triglyceride, HDL: high desity lipoprotein, FBS: fasting blood sugar, sBP: systolic blood pressure, dBP: diastolic blood pressure, Waist: waist circumference, TC: total cholesterol, LDL: low density lipoprotein

Table 2.
The relationship between insulin resistance and metabolic syndrome
    Metabolic syndrome Total
Yes No
Insulin resistance Yes 27 21 48
  No 38 122 160
Total   65 143 208∗

p<0.01, ∗: seven cases were excluded because homeostasis model assessment-insulin resistances (HOMA-IRs) were not available.

Table 3.
Comparison of the serum total, free, and bioavailable testosterone between the insulin resistant and sensitive groups
  Insulin resistance (+) Insulin resistance (−) p-value
Total patients group (n=48) (n=160)  
Total testosterone 4.31±0.18 4.86±0.12 0.022
Free testosterone 6.53±0.31 7.00±0.19 NS
Bioavailable testosterone 1.52±0.08 1.61±0.04 NS
ED patients group (n=14) (n=25)  
Total testosterone 4.43±0.32 5.24±0.27 NS
Free testosterone 6.50±0.56 8.34±1.71 0.005
Bioavailable testosterone 1.58±0.52 1.92±0.07 0.020
ED+BPH patient group (n=16) (n=55)  
Total testosterone 3.98±0.28 4.38±0.20 NS
Free testosterone 6.16±0.38 6.47±0.31 NS
Bioavailable testosterone 1.38±0.09 1.50±0.07 NS
BPH patient group (n=18) (n=80)  
Total testosterone 4.50±0.31 5.07±0.17 NS
Free testosterone 6.87±0.63 6.96±0.28 NS
Bioavailable testosterone 1.60±0.15 1.60±0.06 NS

seven cases (ED: 2 cases, ED+BPH: 1 case, BPH: 4 cases) were excluded because homeostasis model assessment-insulin resistances (HOMA-IRs) were not available. ED: erectile dysfunction, BPH: benign prostatic hyperplasia, NS: not significant

Table 4.
Correlation of the serum total, free and bioavailable testosterone with insulin resistance
HOMA-IR Total testosterone Free testosterone Bioavailable testosterone
Total
 r −0.21 −0.14 −0.13
 p-value 0.001 0.023 0.036
ED
 r −0.31 −0.62 −0.58
 p-value 0.030 <0.001 <0.001
ED+BPH
 r −0.18 −0.06 −0.07
 p-value NS NS NS
BPH
 r −0.23 −0.07 −0.06
 p-value 0.012 NS NS

NS: not significant, ED: erectile dysfunction, BPH: benign prostatic hyperplasia, HOMA-IR: homeostasis model assessment-insulin resistance, r: Pearson correlation coefficient

Table 5.
Correlation of the serum total, free and bioavailable testosterone with the number of metabolic syndrome risk factors
No. of risk factors of metabolic syndrome Total testosterone Free testosterone Bioavailable testosterone
Total patients group
 r −0.24 −0.02 0.01
 p-value 0.001 NS NS
ED patients group
 r −0.23 −0.46 −0.384
 p-value NS 0.017 NS
ED+BPH patient group
 r −0.026 −0.007 0.076
 p-value NS NS NS
BPH patient group
 r −0.143 −0.013 0.002
 p-value NS NS NS

NS: not significant, ED: erectile dysfunction, BPH: benign prostatic hyperplasia, r: Pearson correlation coefficient

Table 6.
Correlation of the serum total, free and bioavailable testosterone with each risk factor
  Total testosterone Free testosterone Bioavailable testosterone
Waist
 r −0.11 0.01 0.03
 p-value NS NS NS
sBP
 r −0.003 −0.01 0.03
 p-value NS NS NS
dBP
 r −0.15 −0.1 −0.11
 p-value NS NS NS
TG
 r 0.03 −0.02 −0.03
 p-value NS NS NS
HDL      
 r 0.1 −0.05 -0.03
 p-value NS NS NS
TC
 r −0.09 0.01 0.02
 p-value NS NS NS
LDL
 r 0.11 0.03 0.03
 p-value NS NS NS
FBS
 r −0.17 −0.23 −0.18
 p-value 0.026 0.004 0.020

ED: erectile dysfunction, BPH: benign prostatic hyperplasia, NS: not significant, Waist: waist circumference, sBP: systolic blood pressure, dBP: diastolic blood pressure, TG: triglyceride, HDL: high desity lipoprotein, TC: total cholesterol, LDL: low density lipoprotein, FBS: fasting blood sugar, r: Pearson correlation coefficient

TOOLS
Similar articles