Genetic susceptibility of benign prostatic hyperplasia

M. G. Sanda, Terri L Beaty, Ray Stutzman, B. Childs, Patrick Walsh

Research output: Contribution to journalArticle

Abstract

In an effort to provide new insight into the etiology of benign prostatic hyperplasia (BPH), an evaluation of genetic factors was performed. Recognizing that early age of onset is a marker for hereditary disease, we performed a case-control study of men with early onset of significant BPH. Men in the youngest quartile (less than 64 years old) with a large prostate (greater than 37 gm. resected tissue) who underwent surgery for BPH were identified as case probands from 909 consecutive prostatectomies for BPH. Control probands, selected because of the ability to distinguish treatment for benign prostate disease from treatment for malignant prostate disease, were women whose spouses underwent radical prostatectomy during the same interval. Male relatives of men with early onset of BPH had a 66% cumulative lifetime risk of prostatectomy for BPH, compared to a 17% cumulative risk among control relatives (p = 0.001). A 4-fold increase in age-specific risk of prostatectomy for BPH was present among relatives of young men who had undergone prostatectomy for BPH (p = 0.0003), while brothers of these affected cases had a 6-fold increase in risk (p = 0.0089) compared to controls. To determine the likelihood that genetic factors account for this familial aggregation of BPH, segregation analysis was done. Although the small sample size prevented rigorous exclusion of nongenetic models, direct comparison of mendelian and nongenetic models showed that mendelian transmission provided the best overall explanation of the observed familial aggregation. The optimal model suggested mendelian dominant inheritance of a gene associated with early age at onset of BPH. These findings identify family history of BPH as a risk factor for clinical BPH and suggest the presence of a predisposing gene in patients with early onset BPH. Evidence of dominant mendelian transmission of this allele provides a framework for genetic studies to characterize this gene and elucidate the development of BPH in general.

Original languageEnglish (US)
Pages (from-to)115-119
Number of pages5
JournalJournal of Urology
Volume152
Issue number1
StatePublished - 1994

Fingerprint

Prostatic Hyperplasia
Genetic Predisposition to Disease
Prostatectomy
Prostate
Age of Onset
Genes
Inborn Genetic Diseases
Aptitude
Spouses
Sample Size
Case-Control Studies
Siblings

Keywords

  • genes
  • genetics
  • prostatic diseases
  • prostatic hypertrophy

ASJC Scopus subject areas

  • Urology

Cite this

Genetic susceptibility of benign prostatic hyperplasia. / Sanda, M. G.; Beaty, Terri L; Stutzman, Ray; Childs, B.; Walsh, Patrick.

In: Journal of Urology, Vol. 152, No. 1, 1994, p. 115-119.

Research output: Contribution to journalArticle

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