MALE HYPOGONADISM AT A TERTIARY CARE HOSPITAL IN KARACHI, PAKISTAN

Authors

  • Nanik Ram
  • Ali Asghar
  • Fauzan Hashmi
  • Najmul Islam

Abstract

Background: Male hypogonadism is defined as '˜inadequate gonadal function, manifested by
deficiency in gametogenesis and/or secretion of gonadal hormones'. Signs and symptoms of
hypogonadism depend primarily on the age of onset. It can be classified according to the site
primarily involved: the gonads, the hypothalamus, or the pituitary gland. The objective this study
was to determine the presentation and aetiology of male hypogonadism seen in a tertiary care
hospital. Methods: This cross-sectional study was conducted at Endocrine Clinics, Aga Khan
University Hospital Karachi. Data of male patients with hypogonadism who attended clinics
during January 2009 to August 2011 were reviewed. All male patients with clinical and
biochemical evidence of hypogonadism were included in the study. Patients with Diabetes
Mellitus, Metabolic Syndrome, Andropause, AIDS, Chronic Renal Failure, and Cirrhosis were
excluded. Mean±SD were computed for quantitative variables. Frequency and percentages were
computed for qualitative variables. Aetiology of male hypogonadism was categorised as primary
and secondary hypogonadism. Results: A total of 85 patients with male hypogonadism attended
the endocrine clinic. Mean age of patients was 25±10 years. Clinical presentations were small
genitalia (65%), absent secondary sexual characteristics (53%), not attained puberty (47%),
infertility (53%), erectile dysfunction (41%) and loss of libido (29%). Seventy-three (86%)
patients had hypogonadotrophic hypogonadism (secondary hypogonadism) and 12 (14%) patients
had hypergonadotrophic hypogonadism (primary hypogonadism). Among the patients with
hypogonadotrophic hypogonadism 38 had idiopathic hypogonadotrophic hypogonadsim, 7 had
pituitary adenoma, 6 had empty sella syndrome, 3 had Kallman's syndrome, and 1 patient had
haemosiderosis due to thalassaemia major; 18 patients did not undergo brain imaging.
Conclusion: Small genitalia, absent secondary sexual characteristics and infertility were the main
presenting features of hypogonad men. Majority of patients had hypogonadotrophic
hypogonadsim.
Keywords: Male Hypogonadism, Erectile dysfunction, Libido, Infertility

References

Petak SM, Nankin HR, Spark RF, Swerdloff RS, RodriguezRigau LJ; American Association of Clinical

Endocrinologists. American Association of Clinical

Endocrinologists Medical guidelines for clinical practice for

the evaluation and treatment of hypogonadism in adult male

patients-2002 update. Endocr Pract 2002;8:440-56.

Andrea M, Elisa G, Andrea L. Male hypogonadism. Pituitary

;11:171-80.

Rosenfield RL Clinical review 6: diagnosis and management of

delayed puberty. J Clin Endocrinol Metab 1990;70:559-62.

Weiss J, Crowley WF Jr, Jameson JL Normal structure of the

gonadotropin-releasing hormone (GnRH) gene in patients with

GnRH deficiency and idiopathic hypogonadotropic

hypogonadism. J Clin Endocrinol Metab 1989;69:299-303.

Green JS, Parfrey PS, Harnett JD, Farid NR, Cramer

BC, Johnson G, et al. The cardinal manifestations of BardetBiedl syndrome, a form of Laurence-Moon-Biedl syndrome. N

Engl J Med 1989;321:1002-9.

Habiby RL, Boepple P, Nachtigall L, Sluss PM, Crowley WF

Jr, Jameson JL. Adrenal hypoplasia congenita with

hypogonadotropic hypogonadism: evidence that DAX-1

mutations lead to combined hypothalmic and pituitary defects

in gonadotropin production. J Clin Invest 1996;98:1055-62.

Sykiotis GP, Hoang XH, Avbelj M, Hayes FJ, Thambundit A,

Dwyer A, et al. Congenital idiopathic hypogonadotropic

hypogonadism: evidence of defects in the hypothalamus,

pituitary, and testes. J Clin Endocrinol Metab 2010;95:3019-27.

Bianco SD, Kaiser UB. The genetic and molecular basis of

idiopathic hypogonadotropic hypogonadism. Nat Rev

Endocrinol 2009;5:569-76.

Whitcomb RW, Crowley WF Jr. Clinical review 4: Diagnosis

and treatment of isolated gonadotropin-releasing hormone

deficiency in men. J Clin Endocrinol Metab 1990;70(1):3-7.

Citron JT, Ettinger B, Rubinoff H, Ettinger VM, Minkoff J,

Hom F, et al. Prevalence of hypothalamic-pituitary imaging

abnormalities in impotent men with secondary hypogonadism.

J Urol 1996;155(2):529-33.

Johnson AR Jr, Jarow JP. Is routine endocrine testing of

impotent men necessary? J Urol 1992;147:1542-3.

Nickel JC, Morales A, Condra M, Fenemore J, Sumdge DH.

Endocrine dysfunction in impotence: incidence, significance

and cost-effective screening. J Urol 1984;132:40-3.

Slag MF, Morley JE, Elson MK, Trence DL, Nelson

CJ, Nelson AE, et al. Impotence in medical clinic outpatients.

JAMA 1983;249:1736-40.

Rhoden EL, Estrada C, Levine L, Morgentaler A. The value of

pituitary magnetic resonance imaging in men with

hypogonadism. J Urol 2003;170(3):795-8.

Lubs HA Jr. Testicular size in Klinefelter's syndrome in men

over fifty-Report of a Case with XXY/XY Mosaicism. N

Engl J Med 1962;267:326-31.

Boisen E. Testicular size and shape of 47, XYY and 47, XXY

men in a double-blind, double-matched population survey. Am

J Hum Genet 1979;31:697-70.

Downloads

Published

2012-06-01

How to Cite

Ram, N., Asghar, A., Hashmi, F., & Islam, N. (2012). MALE HYPOGONADISM AT A TERTIARY CARE HOSPITAL IN KARACHI, PAKISTAN. Journal of Ayub Medical College Abbottabad, 24(2), 65–67. Retrieved from https://jamc.ayubmed.edu.pk/index.php/jamc/article/view/2194