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Pathology of benign prostatic hyperplasia

Abstract

The epidemiology of benign prostatic hyperplasia (BPH) is complex and not fully understood. The androgenic hormones testosterones and dihydrotestosterone play at least a permissive and important role. Growth factors and other hormones including estrogens may also play a role. BPH is a truely hyperplastic process resulting in growth of glandular-epithelial and stromal/muscle tissue in the prostate, leading to often measurable growth taking on different shapes and configurations which may impact symptoms and secondary outcomes. It is important to recognize that BPH is a histological conditions, which is one but not the only cause of lower urinary tract symptoms, and may or may not be associated with prostate enlargement and bladder outlet obstruction. Recognizing the different entities and determining their presence in individual patients may help with therapeutic decision making.

Introduction

Benign prostatic hyperplasia (BPH) is a pathologic process that contributes to, but is not the sole cause of, lower urinary tract symptoms (LUTS) in aging men.1 Despite intense research efforts in the past five decades to elucidate the underlying etiology of prostatic growth in older men, cause-and-effect relationships have not been established. For example, androgens are a necessary but not a clearly causative aspect of BPH. Notions held earlier that the clinical symptoms of BPH (prostatism) are simply because of a mass-related increase in urethral resistance are too simplistic. It is now clear that a significant portion of LUTS is because of age-related detrusor dysfunction. Bladder outlet obstruction itself may induce a variety of neural alterations in the bladder, which contribute to symptomatology. Moreover, bothersome LUTS may be seen in men with polyuria, sleep disorders and a variety of systemic medical conditions unrelated to the prostate bladder unit.

Etiology of BPH

Histopathologically, BPH is characterized by an increased number of epithelial and stromal cells in the periurethral area of the prostate. The observation of a new epithelial gland formation is normally seen only in fetal development and gives rise to the concept of embryonic reawakening of the stroma cell's inductive potential.2 The precise molecular etiology of this hyperplastic process is uncertain. The observed increase in cell number may be because of epithelial and stromal proliferation or to impaired programmed cell death or apoptosis leading to cellular accumulation. Androgens, estrogens, stromal–epithelial interactions, growth factors and neurotransmitters may play a role, either singly or in combination, in the etiology of the hyperplastic process.

The role of androgens

Although androgens do not cause BPH, the development of BPH requires the presence of testicular androgens during prostate development, puberty and aging.3 Patients castrated before puberty or who are affected by a variety of genetic diseases that impair androgen action or production do not develop BPH. Examples for such are the eunuchs having served at the imperial court in the Forbidden City in Peking and the Skoptzy.4 It is also known that prostatic levels of dihydrotestosterone (DHT) as well as the androgen receptor remain high with aging, despite the fact that peripheral levels of testosterone are decreasing with age. Moreover, androgen withdrawal leads to partial involution of established BPH.5 Assuming normal ranges, there is no clear relationship between the concentration of circulating androgens and prostate size in aging men or more specifically in men with BPH enrolled in clinical trials6 (Table 1).

Table 1 Absence of significant relationship between serum testosterone and serum PSA and prostate volume

In the brain, skeletal muscle and seminiferous epithelium, testosterone directly stimulates androgen-dependent processes. In the prostate, however, the nuclear membrane-bound enzyme steroid 5α-reductase converts the hormone testosterone into DHT, the principal androgen in this tissue (Figure 1).3 Overall, 90% of total prostatic androgen is in the form of DHT, principally derived from testicular androgens. Adrenal androgens may constitute 10% of total prostatic androgen, although the importance of this stored hormone source in the etiology of BPH is negligible. Inside the cell, both testosterone and DHT bind to the same high-affinity androgen receptor protein. DHT is a more potent androgen than testosterone because of its higher affinity for the androgen receptor.7 The hormone receptor then binds to specific DNA-binding sites in the nucleus, which results in increased transcription of androgen-dependent genes and ultimately stimulation of the protein synthesis. In contrast, androgen withdrawal from androgen-sensitive tissue results in a decrease in protein synthesis and tissue involution. Besides inactivation of key androgen-dependent genes (for example, prostate-specific antigen), androgen withdrawal leads to the activation of specific genes involved in programmed cell death.8, 9 In addition to these direct effects many growth factors and their receptors are regulated by androgens. Thus, the action of testosterone and DHT in the prostate is mediated indirectly through autocrine and paracrine pathways. The prostate, unlike other androgen-dependent organs, maintains its ability to respond to androgens throughout life, and levels of androgen receptors10, 11 as well as DHT12 in the prostate remain high throughout aging.

Figure 1
figure1

Testosterone (T) diffuses into the prostate epithelial and stromal cell. T can interact directly with the androgen (steroid) receptors bound to the promoter region of androgen-regulated genes. In the stromal cell, a majority of T is converted into dihydrotestosterone (DHT)—a much more potent androgen, which can act in an autocrine manner in the stromal cell or in a paracrine manner by diffusing into epithelial cells in close proximity. DHT produced peripherally, primarily in the skin and liver, can diffuse into the prostate from the circulation and act in a true endocrine manner. In some cases, the basal cell in the prostate may serve as a DHT production site, similar to the stromal cell.1

Two steroid 5α-reductase enzymes have been discovered, each encoded by a separate gene.13 Type I 5α-reductase, the predominant enzyme in extraprostatic tissues, such as skin and liver, is normally expressed in the 5α-reductase deficiency syndrome and is inhibited by the dual inhibitor dutasteride but not substantially by finasteride. Type II 5α-reductase is the predominant prostatic 5α-reductase, although it is also expressed in extraprostatic tissues. Mutations in the type II enzyme are responsible for the clinical phenotype observed in the 5α-reductase deficiency syndrome.14 The type II is sensitive to inhibition by both five alpha reductase inhibitors.15

These data demonstrate that the stromal cell plays a central role in androgen-dependent prostatic growth and that the type II 5α-reductase enzyme within the stromal cell is the key androgenic amplification step. Thus, a paracrine model for androgen action in the gland (Figure 1) is evident.

The role of growth factors

Growth factors are small peptide molecules that stimulate, or in some cases inhibit, the cell division and differentiation processes.16 Cells that respond to the growth factors have on their surface receptors specific for that growth factor that in turn are linked to a variety of transmembrane and intracellular signaling mechanisms. Interactions between growth factors and steroid hormones may alter the balance of cell proliferation versus cell death to produce BPH (Figure 2) Subsequent to the first description of the basic fibroblast growth factor in BPH by Story,18 a variety of growth factors have been characterized in normal, hyperplastic and neoplastic prostatic tissue.19 In addition to bFGF (FGF-2), acidic FGF (FGF-1), Int-2 (FGF-3), keratinocyte growth factor (FGF-7), transforming growth factors (TGF-β) and epidermal growth factor have been implicated in prostate growth. TGF-β is a potent inhibitor of proliferation in normal epithelial cells in a variety of tissues. In models of prostatic cancer, there is evidence that malignant cells have escaped the growth inhibitory effect of TGF-β. There is mounting evidence of interdependence between growth factors, growth factor receptors and the steroid hormone milieu of the prostate.16 Although data on the absolute level of growth factor and growth factor receptors in hyperplastic as opposed to normal tissue are conflicting, it is likely that growth factors play some role in the pathogenesis of BPH.

Figure 2
figure2

Balance between growth stimulatory and inhibitory factors involved in cellular homeostasis in the prostate gland. The respective roles of androgens (testosterone and dihydrotestosterone (DHT)) are shown. The right hand panel illustrates the imbalance and abnormal growth in benign prostatic hyperplasia (BPH).17

Pathology

McNeal20 first showed that BPH first develops (Figures 3, 4 and 5) in the periurethral ‘transition zone’ of the prostate (Figure 4). The transition zone consists of two separate glands immediately external to the preprostatic sphincter. The main ducts of the transition zone arise on the lateral aspects of the urethral wall at the point of urethral angulation near the verumontanum. Proximal to the origin of the transition zone ducts are the glands of the ‘periurethral zone’ that are confined within the preprostatic sphincter and course parallel to the axis of the urethra. All BPH nodules develop either in the transition zone or in the periurethral region. The transition zone also enlarges with age, unrelated to the development of nodules21 (Figure 4).

Figure 3
figure3

Different gross appearances of hyperplastic prostatic tissue obstructing the prostatic urethra forming ‘lobes.’ (a) Isolated middle lobe enlargement. (b) Isolated lateral lobe enlargement. (c) Lateral and middle lobe enlargement. (d) Posterior commissural hyperplasia (median bar).

Figure 4
figure4

(a) Sagittal (top panel) and (b) coronal (bottom panel) section of the prostate showing peripheral zone (PZ), transition zone (TZ), central zone (CZ), the verumontanum (V), the proximal urethral segment (UP), as well as preprostatic sphincter (s), bladder neck (bn) and ejaculatory duct (E). OC, oblique plane (bottom view) and C, coronal plane.

Figure 5
figure5

Panel shows glandular tissue to the left and stromal tissue to the right.

One of the unique features of the human prostate is the presence of the prostatic capsule, which plays an important role in the development of LUTS.22 In the dog, the only other species known to develop naturally occurring BPH, symptoms of bladder outlet obstruction (BOO) and urinary symptoms rarely develop because the canine prostate lacks a capsule. Presumably, the capsule transmits the ‘pressure’ of tissue expansion to the urethra and leads to an increase in urethral resistance. Thus, the clinical symptoms of BPH in men may be not only because of age-related increases in prostatic size but also to the unique anatomic structure of the human gland. Clinical evidence of the importance of the capsule can be found in series that clearly document that incision of the prostatic capsule (transurethral incision of the prostate) results in a significant improvement in outflow obstruction, despite the fact that the volume of the prostate remains the same.

The size of the prostate does not correlate with the severity of symptoms or the degree of obstruction. Thus, other factors such as dynamic urethral resistance, the prostatic capsule, and anatomic pleomorphism are more important in the production of clinical symptoms than the absolute size of the gland.

Histological features

BPH is a true hyperplastic process (Figure 5). Histologic studies document an increase in the cell number.21 McNeal's studies show that the majority of early periurethral nodules are purely stromal in character. In contrast, the earliest transition zone nodules represent the proliferation of glandular tissue that may be associated with an actual reduction in the relative amount of stroma. During the first 20 years of BPH development, the disease may be predominantly characterized by an increased number of nodules, and the subsequent growth of each new nodule is generally slow. Then a second phase of evolution occurs in which there is a significant increase in large nodules. In the first phase, the glandular nodules tend to be larger than the stromal nodules. In the second phase, when the size of individual nodules is increasing, the size of glandular nodules clearly predominates.

There is a significant pleomorphism in stromal–epithelial ratios in resected tissue specimens. Studies from primarily small-resected glands show a predominance of fibromuscular stroma.23 Larger glands, predominantly those removed by enucleation, show primarily epithelial nodules. However, an increase in stromal–epithelial ratios does not necessarily indicate that this is a ‘stromal disease’; stromal proliferation may well be because of ‘epithelial disease.’

Importance of smooth muscle

Regardless of the exact proportion of epithelial to stromal cells in the hyperplastic prostate, there is no question that prostatic smooth muscle represents a significant volume of the gland.24 Although the smooth muscle cells in the prostate have not been extensively characterized, presumably their contractile properties are similar to those seen in other smooth muscle organs. The spatial arrangement of smooth muscle cells in the prostate is not optimal for force generation; however, there is no question that both passive and active forces in prostatic tissue play a major role in the pathophysiology of BPH. Stimulation of the adrenergic nervous system clearly results in a dynamic increase in prostatic urethral resistance. Blockade of this stimulation by α-receptor blockers clearly diminishes this response.

Active smooth muscle tone in the human prostate is regulated by the adrenergic nervous system.25 The α1-adrenoreceptor nomenclature has been standardized to reconcile differences in nomenclature based on pharmacologic and molecular studies. Receptor-binding studies clearly show that the α1A is the most abundant adrenoreceptor subtype present in the human prostate.26, 27 Moreover, the α1A receptor clearly mediates active tension in human prostatic smooth muscle. It is still unclear whether other factors may regulate smooth muscle contraction. The presence of type IV and type V phosphodiesterase isoenzymes in the prostate implies that phosphodiesterase inhibitors may be appropriate candidate therapies for BPH-related LUTS.28, 29

Autonomic nervous system overactivity may contribute to LUTS in men with BPH.30, 31 The activity of the autonomic nervous system, as measured by a standard set of physiologic tests, plasma and urinary catecholamines correlates positively with symptom score and other BPH measures.

The bladder's response to obstruction

Current evidence suggests that the bladder's response to obstruction is largely an adaptive one. However, it is also clear that many lower tract symptoms in men with BPH or prostate enlargement are related to obstruction-induced changes in bladder function rather than to outflow obstruction directly. Approximately one third of men continue to have a significant irritative or storage symptoms after surgical relief of obstruction.32 Obstruction-induced changes in the bladder are of two basic types. First, the changes that lead to ‘detrusor instability’ or decreased ‘compliance’ are clinically associated with symptoms of frequency and urgency. Second, the changes associated with decreased ‘detrusor contractility’ are associated with further deterioration in the force of the urinary stream, hesitancy, intermittency, increased residual urine and (in a minority of cases) detrusor failure. Acute urinary retention should not be viewed as an inevitable result of this process. Many patients presenting with acute urinary retention have more than adequate detrusor function, with evidence of a precipitating event leading to the obstruction. Independent of obstruction, aging produces some of the same changes in bladder function, histology and cellular function. There is a suggestive evidence from animal models that atherosclerosis and the resultant chronic bladder ischemia or hypoxia induced by other mechanisms (for example, increased bladder wall tension) may contribute to bladder pathology.33, 34

The complex interrelationship between BPH, LUTS, prostatic enlargement and BOO

From the foregoing discussion it is clear that BPH itself is actually only a histological diagnosis, which in itself is without much clinical significance. However, it becomes a clinical entity when associated with bothersome LUTS, significant prostatic enlargement and/or BOO. Figure 6 illustrates this complex relationship. Among all men over the age of 40 years, in an age-dependent manner, approximately 50% will develop histological hyperplasia or BPH;1 of those, 30–50% will have bothersome LUTS, which may also be caused by other conditions;35, 36, 37, 38, 39 some will develop a significant enlargement of the prostate, which can only exist in men with histological BPH; some will develop BOO, which may also exist because of causes other than BPH and enlargement of the prostate. Treatment should take into consideration whether the patient has LUTS with or without enlargement of the prostate and with or without BOO.

Figure 6
figure6

Among all men over the age of 40 years, in an age-dependent manner approximately 50% will develop histological hyperplasia or benign prostatic hyperplasia (BPH); of those, 50% will have bothersome lower urinary tract symptoms (LUTS), which may also be caused by other conditions; some will develop a significant enlargement of the prostate (EP), which can only exist in men with histological BPH; some will develop bladder outlet obstruction (BOO), which may also exist owing to causes other than BPH and EP. Treatment should take into consideration whether the patient has LUTS with or without EP and with or without BOO.

Figure 7 shows that across a wide range of continents/countries and ethnic groups, the incidence of histological hyperplasia increases linearly with age, starting approximately at the age 40 years. Figure 8 illustrates that approximately 30–50% of men with BPH—depending on age—will develop bothersome LUTS indicated by a symptom score of >7 points on the international prostate symptom score instrument.

Figure 7
figure7

Prevalence of histological benign prostatic hyperplasia (BPH) by age group in nine autopsy series from around the world.1

Figure 8
figure8

Presence of bothersome lower urinary tract symptoms (LUTS) in seven series from different continents/countries and ethnic groups.35

It is interesting to note that prostate size does have an impact on various aspects of life, not only LUTS. In the Olmsted County Study increasing prostate size was associated with increasing symptom, bother, interference and even sexual dissatisfaction (Figure 9).39 In the Medical Therapy for Prostate Symptoms study, increasing transition zone of the prostate was significantly associated with a deterioration in five domains of sexual function (Figure 10).

Figure 9
figure9

With increasing prostate size, symptoms, bother, interference and sexual dissatisfaction increase.39

Figure 10
figure10

In the Medical Therapy for Prostate Symptoms study, five domains of sexual function showed a deterioration when stratified by increasing prostate size, here in quartiles of the transition zone of the prostate.40

Conclusions

When evaluating and treating men presenting with LUTS, health care providers must keep in mind the complexity of the potentially underlying condition. For one, these symptoms should not be universally attributed to the prostate, and the terms ‘prostatism’ is therefore to be avoided, drawing undue attention to the prostate as the sole cause. The presence of histological stromo-glandular hyperplasia alone is not a condition in need of treatment, except when associated with bothersome symptoms. The presence or absence of noticeable enlargement and/or obstruction, and the anatomy of the prostate (lateral versus middle lobes) all play an important role in deciding what the best strategy for treatment might be. Further and more detailed understanding of the etiology, the interrelationship between androgens and growth factors, the potential role of ischemia, the autonomic nervous system and the PDE5 receptor may all aid our ability to develop better and more targeted treatment for more patients presenting with bothersome LUTS in an ever-increasing number.

Disclosure

Claus G Roehrborn has received consulting fees and lecture fees from GSK, Eli Lilly, Spectrum Pharmaceuticals, Aeterna Zentaris, Pfizer and AMS.

References

  1. 1

    Roehrborn C, McConnell J . Etiology, pathophysiology, epidemiology and natural history of benign prostatic hyperplasia. In: Walsh P, Retik A, Vaughan E, Wein A (eds). Campbell's Urology, 8th edn. Saunders: Philadelphia, 2002, pp 1297–1336.

    Google Scholar 

  2. 2

    Cunha GR . Role of mesenchymal-epithelial interactions in normal and abnormal development of the mammary gland and prostate. [Review]. Cancer 1994; 74: 1030–1044.

    CAS  Article  Google Scholar 

  3. 3

    McConnell JD . Prostatic growth: new insights into hormonal regulation. [Review]. Br J Urol 1995; 76 (Suppl 1): 5–10.

    CAS  PubMed  PubMed Central  Google Scholar 

  4. 4

    Wilson JD, Roehrborn C . Long-term consequences of castration in men: lessons from the Skoptzy and the eunuchs of the Chinese and Ottoman courts. J Clin Endocrinol Metab 1999; 84: 4324–4331.

    CAS  Article  Google Scholar 

  5. 5

    Peters CA, Walsh PC . The effect of nafarelin acetate, a luteinizing-hormone-releasing hormone agonist, on benign prostatic hyperplasia [published erratum appears in N Engl J Med 1988; 318(9): 580]. N Engl J Med 1987; 317: 599–604.

    CAS  Article  Google Scholar 

  6. 6

    Marberger M, Roehrborn CG, Marks LS, Wilson T, Rittmaster RS . Relationship among serum testosterone, sexual function, and response to treatment in men receiving dutasteride for benign prostatic hyperplasia. J Clin Endocrinol Metab 2006; 91: 1323–1328.

    CAS  Article  Google Scholar 

  7. 7

    Andriole G, Bruchovsky N, Chung LW, Matsumoto AM, Rittmaster R, Roehrborn C et al. Dihydrotestosterone and the prostate: the scientific rationale for 5alpha-reductase inhibitors in the treatment of benign prostatic hyperplasia. J Urol 2004; 172 (4 Pt 1): 1399–1403.

    CAS  Article  Google Scholar 

  8. 8

    Martikainen P, Kyprianou N, Isaacs JT . Effect of transforming growth factor-beta on proliferation and death of rat prostatic cells. Endocrinology 1990; 127: 2963–2968.

    CAS  Article  Google Scholar 

  9. 9

    Kyprianou N, Isaacs JT . ‘Thymineless’ death in androgen-independent prostatic cancer cells. Biochem Biophys Res Commun 1989; 165: 73–81.

    CAS  Article  Google Scholar 

  10. 10

    Barrack ER, Bujnovszky P, Walsh PC . Subcellular distribution of androgen receptors in human normal, benign hyperplastic, and malignant prostatic tissues: characterization of nuclear salt-resistant receptors. Cancer Res 1983; 43: 1107–1116.

    CAS  PubMed  PubMed Central  Google Scholar 

  11. 11

    Rennie PS, Bruchovsky N, Goldenberg SL . Relationship of androgen receptors to the growth and regression of the prostate. Am JClin Oncol 1988; 11 (Suppl 2): S13–S17.

    Article  Google Scholar 

  12. 12

    Walsh PC, GM H, LL E . Tissue content of dihydrotestosterone in human prostatic hyperplasia is not supernormal. J Clin Invest 1983; 72: 1772–1777.

    CAS  Article  Google Scholar 

  13. 13

    Russell DW, Wilson JD . Steroid 5alpha-reductase: two genes/two enzymes. Annu Rev Biochem 1994; 63: 25.

    CAS  Article  Google Scholar 

  14. 14

    Imperato-McGinley J, Guerrero L, Gautier T, Peterson RE . Steroid 5 alpha reductase deficiency in man: an inherited form of male pseudohermaphroditism. Science 1974; 186: 1213.

    CAS  Article  Google Scholar 

  15. 15

    Carson III C, Rittmaster R . The role of dihydrotestosterone in benign prostatic hyperplasia. Urology 2003; 61 (4 Suppl 1): 2–7.

    Article  Google Scholar 

  16. 16

    Lee KL, Peehl DM . Molecular and cellular pathogenesis of benign prostatic hyperplasia. J urol 2004; 172 (5 Pt 1): 1784–1791.

    CAS  Article  Google Scholar 

  17. 17

    Griffiths K . Molecular control of prostate growth. In: Kirby R, McConnell J, Fitzpatrick JM, Roehrborn CG, Boyle P (eds). Textbook of Benign Prostatic Hyperplasia. Isis Medical Media: Oxford, 1996, pp 23–56.

    Google Scholar 

  18. 18

    Story MT, Livingston B, Baeten L, Swartz SJ, Jacobs SC, Begun FP et al. Cultured human prostate-derived fibroblasts produce a factor that stimulates their growth with properties indistinguishable from basic fibroblast growth factor. Prostate 1989; 15: 355–365.

    CAS  Article  Google Scholar 

  19. 19

    Lawson RK . Role of growth factors in benign prostatic hyperplasia. Eur Urol 1997; 32 (Suppl 1): 22–27.

    CAS  PubMed  PubMed Central  Google Scholar 

  20. 20

    McNeal JE . Origin and evolution of benign prostatic enlargement. Invest Urol 1978; 15: 340.

    CAS  PubMed  PubMed Central  Google Scholar 

  21. 21

    McNeal J . Pathology of Benign Prostatic Hyperplasia. Insight into Etiology. In: Lepor H, Walsh PC (eds). The Urologic Clinics of North America, 17th edn. WB Saunders Company: Philadelphia, 1990, pp 477–486.

    Google Scholar 

  22. 22

    Caine MLS . The ‘capsule’ in benign prostatic hypertrophy. US Department of Health and Human Services 1987; No. 87-2881: 221.

    Google Scholar 

  23. 23

    Shapiro E, Becich MJ, Hartanto V, Lepor H . The relative proportion of stromal and epithelial hyperplasia is related to the development of symptomatic benign prostate hyperplasia. J Urol 1992; 147: 1293–1297.

    CAS  Article  Google Scholar 

  24. 24

    Shapiro E, Hartanto V, Lepor H . Quantifying the smooth muscle content of the prostate using double-immunoenzymatic staining and color assisted image analysis. J Urol 1992; 147: 1167–1170.

    CAS  Article  Google Scholar 

  25. 25

    Roehrborn CG, Schwinn DA . Alpha1-adrenergic receptors and their inhibitors in lower urinary tract symptoms and benign prostatic hyperplasia. J Urol 2004; 171: 1029–1035.

    CAS  Article  Google Scholar 

  26. 26

    Lepor H, Tang R, Shapiro E . The alpha-adrenoceptor subtype mediating the tension of human prostatic smooth muscle. Prostate 1993; 22: 301–307.

    CAS  Article  Google Scholar 

  27. 27

    Lepor H, Tang R, Meretyk S, Shapiro E . Alpha1 adrenoceptor subtypes in the human prostate. J Urol 1993; 149: 640–642.

    CAS  Article  Google Scholar 

  28. 28

    Uckert S, Kuthe A, Stief CG, Jonas U . Phosphodiesterase isoenzymes as pharmacological targets in the treatment of male erectile dysfunction. World J Urol 2001; 19: 14–22.

    CAS  Article  Google Scholar 

  29. 29

    McVary KT, Roehrborn CG, Kaminetsky JC, Auerbach SM, Wachs B, Young JM et al. Tadalafil relieves lower urinary tract symptoms secondary to benign prostatic hyperplasia. J Urol 2007; 177: 1401–1407.

    CAS  Article  Google Scholar 

  30. 30

    McVary KT . Erectile dysfunction and lower urinary tract symptoms secondary to BPH. Eur Urol 2005; 47: 838–845.

    Article  Google Scholar 

  31. 31

    McVary KT, Razzaq A, Lee C, Venegas MF, Rademaker A, McKenna KE . Growth of the prostate gland is facilitated by the autonomic system. Biol Reprod 1994; 51: 99–107.

    CAS  Article  Google Scholar 

  32. 32

    Abrams PH, Farrar DJ, Turner-Warwick RT, Whiteside CG, Feneley RC . The results of prostatectomy: a symptomatic and urodynamic analysis of 152 patients. J Urol 1979; 121: 640–642.

    CAS  Article  Google Scholar 

  33. 33

    Azadzoi KM, Radisavljevic ZM, Siroky MB . Effects of ischemia on tachykinin-containing nerves and neurokinin receptors in the rabbit bladder. Urology 2008; 71: 979–983.

    Article  Google Scholar 

  34. 34

    Azadzoi KM, Yalla SV, Siroky MB . Oxidative stress and neurodegeneration in the ischemic overactive bladder. J Urol 2007; 178: 710–715.

    CAS  Article  Google Scholar 

  35. 35

    Oishi K, Boyle P, Barry M, Farah R, Gu F-L, Jacobsen S et al. Epidemiology and natural history of benign prostatic hyperplasia. In: 4th International Consultation on Benign Prostatic Hyperplasia. Plymbridge Distributors Ltd: Plymouth, United Kingdom, 1998, pp 23–59.

    Google Scholar 

  36. 36

    Girman CJ . Natural history and epidemiology of benign prostatic hyperplasia: relationship among urologic measures. Urology 1998; 51 (4A Suppl): 8–12.

    CAS  Article  Google Scholar 

  37. 37

    Girman CJ, Epstein RS, Jacobsen SJ, Guess HA, Panser LA, Oesterling JE et al. Natural history of prostatism: impact of urinary symptoms on quality of life in 2115 randomly selected community men. Urology 1994; 44: 825–831.

    CAS  Article  Google Scholar 

  38. 38

    Girman CJ, Jacobsen SJ, Guess HA, Oesterling JE, Chute CG, Panser LA et al. Natural history of prostatism: relationship among symptoms, prostate volume and peak urinary flow rate. J Urol 1995; 153: 1510–1515.

    CAS  Article  Google Scholar 

  39. 39

    Girman CJ, Jacobsen SJ, Rhodes T, Guess HA, Roberts RO, Lieber MM . Association of health-related quality of life and benign prostatic enlargement. Eur Urol 1999; 35: 277–284.

    CAS  Article  Google Scholar 

  40. 40

    McConnell J, Committee TMS . The long term effects of medical therapy on the progression of BPH: results from the MTOPS trial. J urol 2002; 167 (4 Suppl): 265A.

    Google Scholar 

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Roehrborn, C. Pathology of benign prostatic hyperplasia. Int J Impot Res 20, S11–S18 (2008). https://doi.org/10.1038/ijir.2008.55

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