This web only provides the extract of this article. If you want to read the figures and tables, please reference the PDF full text on Blackwell Synergy. Thank you.
- Original Article -
Cross-sectional and longitudinal studies on interaction between bladder compliance and outflow obstruction in men
with benign prostatic hyperplasia
Li-Min Liao1, Werner Schaefer2
1Department of Urology, China Rehabilitation Research Center, Rehabilitation College of Capital Medical University,
Beijing 100068, China
2Continence Research Unit, Division of Geriatric Medicine, University of Pittsburgh, PA 15213, USA
Abstract
Aim: To explore the interaction between bladder compliance (BC) and bladder outflow obstruction (BOO) in men
with benign prostatic hyperplasia (BPH) using cross-sectional and longitudinal
studies. Methods: A total of 181 men with BPH were recruited, and 100 of them were followed for one year. Cystometry was performed in a standing or
a sitting position with 30 mL/min infusion. BC was manually corrected and defined. Obstruction coefficient (OCO),
linear passive urethral resistance relation and international continence society (ICS) nomogram were used to diagnose
BOO. The obstructed parameters were compared between the reduced BC group and the non-reduced group. BC
was compared between the first investigation at the beginning of study and the second investigation at the end of
study during the one-year follow-up
period. Results: The group with reduced BC had increased OCO and linear
passive urethral resistance relation. BC was significantly lower in the obstructed group (55.7 mL/cm water) than
that in unobstructed and equivocal one (74.9 mL/cm water,
P < 0.01). BC gradually reduced with the increased
obstructed grade. There was a significantly weak negative correlation between BC and OCO
(r = _ 0.132,
P < 0.01). Over the one-year follow-up period in the longitudinal study, BC for all men changed from 54.4 to 48.8 mL/cm water
(P > 0.05), and BC for the group with BOO fell from 58.4
± 70.1 to 46.5 ± 38.7 mL/cm water
(P > 0.05). Conclusion:
In men with BPH, a significant systematic decrease occurred in BC in the obstructed group and a significant
systematic increase with urethral resistance occurred in the low BC group. A longitudinal study of the tendency of BC reduction
in a group with BOO is necessary in the future.
(Asian J Androl 2007 Jan; 1: 51_56)
Keywords: benign prostatic hyperplasia; bladder compliance; bladder outflow obstruction
Correspondence to: Dr Li-Min Liao, Department of Urology, China Rehabilitation Research Center, Beijing 100068, China.
Tel: +86-10-8756-9346 Fax: +86-10-6757-0492
E-mail: lmliao@263.net
Received 2005-12-01 Accepted 2006-06-05
DOI: 10.1111/j.1745-7262.2007.00221.x
1 Introduction
According to the new definition from the International Continence Society (ICS), lower urinary tract symptoms
(LUTS) are divided into three groups: storage, voiding and post-micturition symptoms. Storage symptoms include
daytime frequency, nocturia, urgency and urinary incontinence. Voiding symptoms include slow stream, splitting or
spraying of the urine stream, intermittent stream, hesitancy and
straining [1]. Benign prostatic hyperplasia (BPH) is a
disease that has its etiology in the abnormal growth of the adult human prostate gland that accompanies the aging
process in men [2]. The presentation of LUTS suggestive of BPH, however, is related largely to degenerative changes
in the bladder that occur as a result of the increasing
urethral resistance and bladder outlet obstruction (BOO)
caused by the growing prostate gland. Bladder
dysfunction includes instability, impaired contractility and low
bladder compliance (BC). These pathophysiologic elements are
all common in elderly men, might be present alone or in all
possible combinations, each giving rise to specific
complaints [3_5]. Previous studies analyzed the roles of BOO,
detrusor instability (DI) and impaired detrusor
contractility (IDC) in LUTS. However, the change of BC in
men with LUTS suggestive of BPH has not received much
attention, especially the longitudinal change of BC in these
patients [4_9]. Therefore, the present study aims to
investigate the interaction of BC with urethral resistance
and BOO in elderly men with LUTS using a cross-sectional study and longitudinal observation.
2 Materials and methods
A cross-sectional study including 181 men aged
43_86 years (mean: 65.3 years) with BPH was performed.
Additionally, 100 of 181 men were followed up for 1 year.
For each patient, cystometry was carried out in a
standing or a sitting position with a 30-mL/min infusion rate
using the Dantec Menuet urodynamic system (Dantec Company, Copenhagen, Denmark). Methods, definitions
and units comforted to the standards proposed by the
ICS, except where specifically noted. A total of 582
cystometric traces were reviewed and underwent
quality control. The exclusive criteria for the traces included
in the studies were that: (i) initial detrusor pressure
(Pdet) was negative; and (ii) the difference between initial
Pdet and Pdet at filling end was zero. According to the criteria,
a total of 571 traces entered into a cross-sectional study,
and 170 traces from 85 men with nature history of LUTS
participated in a longitudinal observation.
For each trace, BC was manually corrected and defined (Figure 1). BC
was calculated using the following method. The cystometric curve during
filling consisted of two components of different steepness, and the flat part was
considered to correspond to BC. Bladder capacity was
defined as the volume at which the slope of the flat part of
the cystometric curve (the tonus limb) crossed the slope
of the ascending part of the curve (the terminal limb).
The calculation of BC was made by dividing the bladder
capacity by the change of pressure corresponding to this
capacity (Figure 1). During filling, DI was recognized.
In the presence of involuntary detrusor contractions, the
point on the baseline of Pdet tracing before contraction
was used to calculate BC. Therefore, interferences of
bladder overdistention and DI with compliance
calculation were ruled out; and influence of bladder volume on
compliance calculation was reduced.
Three methods were used to assess for BOO. The
obstruction coefficient (OCO), developed by Schaefer
et al. [11], was used to quantitatively evaluate urethral
resistance, following the formula:
OCO = Pdet.Qmax/(40 + 2Q
max). Linear passive urethral resistance relation
(L-PURR) according to Schaefer nomogram was used to grade BOO; and ICS nomogram was used to classify
and diagnose BOO [11, 12].
In the cross-sectional study, the interaction between
BC and BOO was explored in two ways. First,
40 mL/cm water was considered the normal value for BC [7], and
the obstructed parameters in the reduced BC group were
compared with those in the non-reduced group. Second,
OCO = 1 was considered a cut-off value for
distinguishing BOO, and BC of the low urethral resistance group
was compared with that of the high resistance group.
BC was compared in the classifications for BOO in the
ICS nomogram and among the grades for BOO in the Schaefer nomogram. A correlation analysis between BC
and OCO was performed.
In the one-year follow-up study, the natural history
of BOO and BC was described, and the longitudinal change of BC was observed in the obstructed and the
unobstructed groups as well as among the groups with
the different L-PURR grades after one year. The changes
of OCO and BC were assessed at intervals over the
one-year follow-up period.
Statistical analyses were performed with the Wilcoxon
rank sum test for the measurement data and the ranked
data, and with the c2 test for the frequencies. Data was
assessed by nonlinear regression with the Newton_Raphson test. The level of significance (two-tailed) was
set at P < 0.05.
3 Results
According to our definition, the BC of 274 of 571
measurements (48%) fell, and the BC of 297 (52%) did
not fall. The reduced BC group underwent increased OCO
and L-PURR as well as more frequent obstruction in the
ICS nomogram (Table 1). Of the 571 measurements,
426 (74.6%) were classified into the obstructed group, and
145 (25.4%) were classified into equivocal and
unobstructed group. BC was significantly lower in the
obstructed group (55.7 mL/cm water) than that in the
others (74.9 mL/cm water,
P < 0.01, Table 2). According
to the Schaefer nomogram, the percentages of unobstructed (0_I), mild obstructed (II_III) and obstructed
(IV_VI) were 5.4, 45.4 and 49.2%, respectively; the values of
BC in these groups were 76.7, 70.7 and 51.7 mL/cm water,
respectively. This suggests that BC gradually reduced
with the increased obstructed grade (Table 2). The
correlation analyses showed that there was a statistically
significant weak negative correction between BC and OCO
(r = _ 0.132,
P < 0.01) or between BC and L-PURR
(r = _0.135,
P < 0.01).
In the group with BC < 40 mL/cm water, the
percentages of DI were higher than that in group with BC
³ 40 mL/cm water (Table 1). BC in the group with DI
(40.1 ± 35.9 mL/cm water) was lower than that in the
group with stable detrusor (71.3 ± 62.7 mL/cm water).
This suggests that DI interfered with the assessment for
BC. Furthermore, the association between BC and BOO
in the group with stable detrusor was assessed. In 376
measurements with stable detrusor, 36.7% of traces showed
BC < 40 mL/cm water, and 63.3% of traces showed BC
³ 40 mL/cm water. The results also indicated that OCO,
L-PURR and percentage of obstruction in the group with BC
< 40 mL/cm water were significantly higher than those in
the group with BC ³ 40 mL/cm water (Table 3).
In the longitudinal study, a change of BC from
54.4 mL/cm water to 48.8 mL/cm water
(P > 0.05, Table 4) was observed in 85 pairs of traces at the
one-year follow-up. These pairs of traces were divided into an
obstructed group and an unobstructed group: the BC of the
obstructed group changed from 58.4 to 46.5 mL/cm water
(P > 0.05, Table 4) whereas a significant increase in BC
was observed in the unobstructed group
(P < 0.05, Table 4). After one year, the patients with BOO
underwent a slight change in urethral resistance
(DOCO = 0.01 ± 0.34), and a change of BC
(DBC = _11.9 ± 76.5 mL/cm water). These results suggest that BC showed a
possible tendency of reduction with the aggravation of
BOO during the longitudinal one-year observation period.
4 Discussion
In the past, most urodynamic studies in men with
LUTS as a result of BPH focused on identifying lower
urinary tract dysfunction (LUTD), including BOO, DI,
IDC and abnormal BC. BC is an important and
sophisticated biomechanical parameter of the bladder during the
filling phase. Although several studies on BC have been
carried out in animal models of BOO [3, 13], the
research in human is limited. BC is a parameter worthy of
much attention in men with LUTS resulting from BPH.
A few published papers have contributed to the
discussion of the abnormality of BC to LUTS suggestive of
BPH. Madersbacher et al. [8] presented a direct
investigation into the interaction of BC with BOO in men with
BPH. However, their study was cross-sectional without
a longitudinal observation, and the interferences of DI
and bladder overdistention as a result of a problematic
BC calculation were not ruled out. Moreover, different
filling rates from 30 to 50 mL/min were used in the study
by Madersbacher et al. [8]. These factors can influence
the accuracy of BC measurements. Both the 2001
publication [14] and the 2002 [15] publication from Boon's
group only mentioned that a significantly low BC is an
exceptional finding and, therefore, was not suited for a
further analysis. Rule et al. [9] discussed a longitudinal
decrease of BC after observing longitudinal changes of
post-void residual and voided volume in men.
The purpose of the present study was to explore the
interaction between BC and BOO in men with LUTS resulting from BPH by studying cross-sectional and
longitudinal samples. To investigate the association between
BC and BOO under clinical conditions, an exact
calculation for BC and a precise assessment for urethral
resistance were a prerequisite. BC was defined using the ICS
as the change of volume per unit change of pressure
during filling [1]. According to this definition, several
factors, such as bladder volume or size, bladder shape,
detrusor instability, bladder distention and bladder filling
rate, could influence the determination of BC [14, 16].
In particular, different bladder sizes and shapes
introduced considerable problems into the calculation of BC
and the comparison in clinical research. In the present
study, we could not normalize the bladder volume, and
could not get rid of the impact of the bladder volume and
shape on BC calculation under clinical conditions; but we
could rule out some artifacts caused by DI, bladder
overdistention and fast bladder filling using the
appropriate definition for the filling-end point and a fixed low filling
rate. In the present study, continuous quantitative and
semi-quantitative indexes as well as a nomogram were
used to assess urethral resistance and BOO, respectively.
The cross-sectional study demonstrated that there
was a statistically significant weak negative correlation
between urethral resistance (OCO) and BC. There was
a high urethral resistance or more obstruction in the group
with low BC, and there was a low BC in the group with
high urethral resistance. This suggests that BC showed
a systematic reduction with the increase of urethral
resistance or obstruction.
The present study was descriptive and observational
in nature. The longitudinal study indicated that BC had a
possible tendency of reduction with the aggravation of
BOO and the development of LUTS resulting from BPH
in the one-year follow-up. This suggested that BOO
contributed to the development of decreased BC. Slight
changes of urethral resistance and BC suggest that the
development of BOO and the alterations of BC in human
beings is a slow and long progressive process. The
longitudinal changes of obstruction and BC in the one-year
follow-up period were not tatistically significant;
therefore, a longer follow-up period is encouraged in
further studies. There were major differences [3, 13]
between the clinical studies in human beings and those in
animal experiments. A longer longitudinal observation
on the interaction between BC and BOO is necessary in
the future [17].
Obstructed bladder dysfunction secondary to BPH
is a slow, progressive disease that is strongly associated
with human aging. However, there are some
age-dependent alterations in detrusor function. The
pathophysiologic changes in aging detrusor include DI, IDC,
detrusor hyperactivity with impaired contractility in older men
and women [18, 19], and reduced BC in rats [20]. In
the present study, after 1 year BC in the non-obstructed
group increased and was higher than that in the obstructed
group. A possible explanation could be that the aging
detrusor underwent an aging-related change including
increased BC or IDC in human beings, but not in rats.
Therefore, the complications of interactions among aging
detrusor, BOO and BC made it difficult to assess the change
of BC in men with LUTS resulting from BPH. In future
longitudinal research, multivariate analysis should be
performed for the assessment of the impact of age to clarify
the contribution of each factor to BC in patients with LUTS.
Although some studies suggest that low BC after
obstruction is the result of the change in the passive
properties of the bladder wall rather than the active ones [4],
several clinical and animal studies show that the active
properties of the bladder wall related to the
neuromuscular aspect are involved in the change of BC after
obstruction [16]. Animal and clinical studies demonstrate
that overdistention and increased wall tension of the
bladder caused by BOO could result in nerve degeneration
with the supersensitivity of the detrusor to acetylcholine.
This denervation supersensitivity could cause DI. Our
results are in accord with those of published papers,
suggesting that BC was lower in the group with an unstable
detrusor than in the group with a stable detrusor.
However, Yokoyama et al. [16] found that BC increased after prostatic urethral anesthesia. This finding suggests
that easy irritability of the anatomically altered prostatic
urethra is considered an important factor affecting BC
through the spinal reflex arc. The above-mentioned
evidence suggests that neuromuscular aspects play an
important role in the development of low BC after
obstruction.
Even through a systematic reduction of BC in the
obstructed group and a possible tendency of BC
reduction with the aggravation of obstruction, the reverse
change in individuals was possible as a result of the
complex alterations of detrusor in structure and function
after obstruction. In particular, a patient with LUTS
resulting from BPH could undergo a long interval from
occurrence of obstruction to the development of LUTS.
During this one-year interval, there were many factors
that could affect the changes of BC. Some of them had
been studied, but others had not been researched well,
for example, aging-related alterations in detrusor and the
compensation of detrusor function. At present, the
studies focused on interactions among BOO, BC and aging
detrusor and on the changes of BC and the mechanism of
changes after obstruction in elderly men with LUTS
resulting BPH are still lacking. A clinical longitudinal
long-term study on the age-dependent changes of BC is
necessary.
In conclusion, in a cross-sectional study, a
statistically significant weak negative correction between BC
and urethral resistance was demonstrated. A statistically
significant systematic reduction of BC in the obstructed
group, a statistically significant systematic increase of
urethral resistance in the low BC group, and a
statistically significant weak negative correction between BC
and urethral resistance were observed. In a longitudinal
study, a possible tendency of BC reduction with the
aggravation of BOO was observed in one-year follow-up
period. A statistically significant increase of BC in the
non-obstructed group was shown one-year follow-up period. We conclude that BOO contributes to the
development of decreased BC but aging can impact on
detrusor function, and there are complex interactions among
BC, BOO and aging detrusor in elderly men with LUTS
resulting from BPH.
References
1 Abram P, Cardozo L, Fall M, Griffiths D, Rosier P, Ulmsten
U, et al. The standardisation of terminology of lower urinary
tract function: report from the standardisation sub-committee
of the international continence society. Neurourol Urodyn
2002; 21: 167_78.
2 Xia SJ, Xu XX, Teng JB, Xu CX, Tang XD. Characteristic
pattern of human prostatic growth with age. Asian J Androl
2002; 4: 269_71.
3 Levin R, Chichester P, Levin S, Buttyan R. Role of
angiogenesis in bladder response to partial outlet obstruction. Scand J Urol
Nephrol 2004; 215 (Suppl): 37_47.
4 Liao LM, Shi BY, Liang CQ, Schafer W. Evaluation for
Madigan's prostatectomy in patients with benign prostatic
hyperplasia. Asian J Androl 2001; 3: 33_7.
5 Poulakis V, Ferakis N, Witzsch U, de Vries R, Becht E.
Erectile dysfunction after transurethral prostatectomy for lower
urinary tract symptoms: results from a center with over 500
patients. Asian J Androl 2006; 8: 69_74.
6 Blaivas J. Editorial comment: bladder compliance in patients with
benign prostatic hyperplasia. Neurourol Urodyn 1997; 16: 28.
7 Abrams P. Editorial comment: bladder compliance in patients with
benign prostatic hyperplasia. Neurourol Urodyn 1997; 16: 29.
8 Madersbacher S, Pycha A, Klingler CH, Christine M, Djavan B,
Stulnig T, et al. Interrelationships of bladder compliance with age,
detrusor instability, and obstruction in elderly men with lower
urinary tract symptoms. Neurourol Urodyn 1999; 18: 3_15.
9 Rule AD, Jacobson DJ, McGree ME, Girman CJ, Lieber MM,
Jacobsen SJ. Longitudinal changes in post-void residual and
voided volume among community dwelling men. J Urol 2005;
174: 1317_21.
10 Schaefer W, Sterling AM. Simple analysis of voiding function
by coefficients: obstruction coefficient, OCO, and detrusor
strength coefficient, DECO. In: Proceedings of the 25th
Annual Meeting of International Continence Society. 1995, Oct
17-20, Sydney, Australia. p. 338.
11 Schaefer W. Basic principles and clinical application of
advanced analysis of bladder voiding function. Urol Clin North
N Am 1990; 17: 553_66.
12 Griffiths D, Höfner K, van Mastrigt R, Rollema HJ, Rollema
HJ, Spangberg A, et al. Standardization of terminology of
lower urinary tract function: pressure-flow studies of voiding,
urethral resistance, and urethral obstruction. Neurourol Urodyn
1997; 16: 1_18.
13 Damaser MS, Arner A, Uvelius B. Partial outlet obstruction
induces chronic distension and increased stiffness of rat
urinary bladder. Neurourol Urodyn 1996; 15: 650_65.
14 Eckhardt MD, van Venrooij GE, Boon TA. Interactions
between prostate volume, filling cystometric estimated
parameters, and data from pressure-flow studies in 565 men
with lower urinary tract symptoms suggestive of benign
prostatic hyperplasia. Neurourol Urodyn 2001; 20: 579_90.
15 van Venrooij GE, Eckhardt MD, Gisolf KW, Boon TA. Data
from frequency-volume charts versus filling cystometric
estimated capacities and prevalence of instability in men with
lower urinary tract symptoms suggestive of benign prostatic
hyperplasia. Neurourol Urodyn 2002; 21: 106_11.
16 Yokoyama O, Mita E, Yoshiyuki I, Nakamura Y, Nagano KI,
Namiki M. Bladder compliance in patients with benign
prostatic hyperplasia. Neurourol Urodyn 1997; 17: 19_27.
17 McGuire E. Editorial comment: Interrelationships of bladder
compliance with age, detrusor instability, and obstruction in
elderly men with lower urinary tract symptoms. Neurourol
Urodyn 1999; 18: 13.
18 Elbadawi A, Diokno AC, Millard RJ. The aging bladder:
morphology and urodynamics. World J Urol 1998; 16: 10_34.
19 Pfisterer MH, Griffiths DJ, Schaefer W, Resnick NM. The
effect of age on lower urinary tract function: a study in women.
J Am Geriatr Soc 2006; 54: 405_12.
20 Kohan AD, Danziger M, Vaughan ED Jr, Felsen D. Effect of
aging on bladder function and the response to outlet
obstruction in female rats. Urol Res 2000; 28: 33_7.
|