Semen analysis in smokers and non-smokers
R
S A Kiran Singh,1Mahathi Thotakura1
1Dr.
R.S.A. Kiran Singh,Assistant Professor,2Dr. MahathiThotakura, Assistant
Professor, both authors areaffiliated with Department of Pathology, Katuri
Medical College, Guntur, Andhra Pradesh, India
Correspondence Author- Dr.MahathiThotakura, Assistant
Professor, Department of Pathology, Katuri Medical College, Guntur, Andhra
Pradesh.
Abstract
Background:
Semen analysis still remains as a
simple, cost effective screening test for evaluation of male in fertility
clinic, which provides information on quantitative and qualitative aspects of
testicular function. Except in cases of azoospermia, semen analysis does not
separate patients in to sterile and fertile group. Objective:The present study was undertaken to perform the
quantitative and qualitative Analysis of Semen and to compare the sperm
parameters in smokers and non-smokers. Materials
and methods: A total of 150 cases referred to Pathology department for
semen analysis in Katuri Medical College &Hospital, from September 2016 to
August 2018 were included in the study. The following criteria was used in the
selection of the participants.Results:
The overall quality of sperm was significantly decreased in smokers when
compared with non-smokers.Conclusion:Semen
parameters like volume, motility, count, morphologically normal spermatozoa
were reduced in cigarette smokers when compared to Non-smokers, but only sperm
count was found to have a high significant decrease in Smokers (P: <0.01 )
when compared to Non-smokers. In concordance with other researchers, results of
present study support that cigarette smoking have a relatively significant
effect on semen.
Key
words: Semen, Reproduction, Sperm,Males
Author Corrected: 10th September 2018 Accepted for Publication: 14th September 2018
Introduction
Reproductive medicine has undergone tremendous
advances. The concept of cloning humans from cells from a person’s nose
suggested in woody allensfilm ‘Bananas’ might not be as farfetched as it seemed
in 1971 when the film was released. The advances in current reproductive
technologies were made clear after cloning of sheep, with the birth of dolly.
Cloning of humans has not been accomplished and the concept remains highly
controversial. Steady advances in assisted reproductive techniques such as
blastocyst transfer, embryo biopsy and intra cytoplasmic sperm injection have
been made. With the success of these high technology and high cost procedures,
the complete evaluation of man can be bypassed. But basic semen analysis is
still essential for these techniques [1].Semen analysis still remains as a
simple, cost effective screening test for evaluation of male in fertility
clinic, which provides information on quantitative and qualitative aspects of
testicular function. Except in cases of azoospermia, semen analysis does not
separate patients in to sterile and fertile group [2]. In recent years,
infertility and sub fertility in men has increased which may be associated with
their advancing age, habits like tobacco use, alcoholism, working environment,
varicocele and other factors. Semen parameters might be sensitive markers for
these influencing factors [3,4], hence our study focuses on effects of factors
like cigarette smoking on semen parameters.The present study was undertaken to
perform the quantitative and qualitative Analysis of Semen and to Compare the
sperm parameters in smokers and non-smokers.
Materials and Methods
Study
design: Observational study
Study
setting: This study was conducted in Pathology
department in Katuri Medical College &Hospital, from September 2016 to
August 2018.
Study
Participants: A total of 150 cases referred to
Pathology department for semen analysis in Katuri Medical College
&Hospital, from September 2016 to August 2018 were included in the study.
The following criteria was used in the selection of the participants.
Inclusion
criteria: All patients referred from Obstetrics
and Urology and other departments were included.
Exclusion
criteria:Those patients who had cryptorchidism,
parotitis, testicular atrophy Proved by biopsy, history of systemic illness,
tuberculosis, diabetes mellitus, testicular injury were excluded from the
study.
Methods:
Detailed history of age, marital status,
and cigarette smoking was taken as per the proforma by questionnaire and
detailed physical examination including genital examination was done.
Collection
of semen samples:Semen samples were
collected from all patients by masturbation after 2-5 days of sexual abstinence
in wide mouthed polypropylene bottle. And these semen samples were processed
and analyzed by single qualified person.
Macroscopic Examination
Liquefaction:
Normal semen sample liquefies within 60 minutes at room temperature. Occasionally,
samples may not liquefy, in which case additional treatment like, mechanical
mixing or enzyme digestion (e.g.bromolain) may be necessary.
Color:
Semen sample is examined
immediatelyafter liquefaction or within one hour of ejaculation. Normally, semen
is homogenous grey opalescent and may appear less opaque if sperm concentration
is low. Red brown when mixed with blood or yellow in patients with jaundice or
taking vitamins
Volume:
of ejaculate is measured using graduated cylinder.
Viscosity:
It is measured by gentle aspiration into wide bore 5 ml pipette and then,
allowing the semen to drop by gravity and observing the length of the thread. A
normal sample leaves the pipette as small discrete drops. In cases of abnormal
viscosity, the drop will form thread more than 2 cm long. Alternatively, the
viscosity may be evaluated by introducing a glass rod into sample and observing
the length of the thread that forms on withdrawal of the rod, which should not
exceed 2 cm.
PH:
PH of the semen is measured
using pH paper (pH: 6-10) by evenly spreading one drop of semen onto the pH
paper and after 30 seconds, the color change is compared with the calibration
strip to read the pH
Microscopic examination
Fixed volume 10µl semen is taken on to a clean glass
slide with micropipette and covered with a 22mmX 22mm cover slip. After
stabilizing for 1 minute, wet preparation is examined under light microscopy
(400X).
Motility:Select
the fields at least 5mm from the edges of the cover slip. At least 5
microscopic fields are assessed to classify 200 spermatozoa.Motility is graded
asThe motility of spermatozoa is graded as per WHO laboratory manual for the
examination and processing of human semen, 5th edition 2010.
Assessment
of sperm concentration: The concentration of
spermatozoa should be determined using hemocytometer method on two separate
preparations of semen sample, one on each side of counting chamber. The
dilution is determined from preliminary estimation of sperm concentration.
Assessment
of sperm morphology: Preparation of smears
of by feathering technique same as peripheral blood smear preparation. Air dry
the smear. Later fix in equal parts of 95% ethanol and ether for 5-15 minutes.
Oligozoospermia is defined as low concentration of
sperm [22] and Oligoasthenozoospermia is defined as reduced sperm motility and
count [23] and Oligoasthenoteratozoospermia is defined as decrease in the sperm
count, poor movement and abnormal shape of sperms [24].
Biochemical tests
Fructose
test: Use Resorcinol reagent (50 mg powdered
resorcinol plus 33ml of concentrated hydrochloric acid. Later, mixture is
diluted to 100ml with distilled water). Keep Resorcinol solution in dark-amber
bottle and refrigerate when not in use.
Ethical
considerations: The present study was approved by
Institutional human ethical committee. Informed consent was obtained from all
the participants. Confidentiality of the data was maintained.
Results
A total number of 150 cases were studied in the 2
year span. These cases were classified in to smokers and non-smokers. Smokers
(person who smoked more than 1 cigarette/day for more than 6 months) and
control group were non-smokers. Table 1 presents the distribution of semen
quality among age groups. Tableno 2 presents the distribution of semen quality
of Non- smokers (controls) among age groups. Table no 3 presents the mean
values of semen parameters in Non-smokers (controlsTable no-4 presents the mean
values of semen parameters in Smokers. Table no 5 presents the mean values of
semen parameters in Smoker. Table no 6 presents Mean comparison of parameters
between Smokers and Non-smokers. Table no 7 presents distribution of semen
quality among different types of Cigarette Smokers. Figure no1 presents the
microphotograph of spermatozoa.
Table-1:Distribution of
semen quality among age groups
Semen quality |
Age groups( in years) |
||||
21-25 |
26-30 |
31-35 |
36-40 |
41-45 |
|
NZ |
21 |
43 |
22 |
09 |
02 |
OZ |
6 |
13 |
2 |
0 |
1 |
AZ |
2 |
5 |
1 |
0 |
0 |
OAZ |
5 |
8 |
3 |
1 |
0 |
OATZ |
0 |
2 |
1 |
0 |
0 |
AZOO |
2 |
0 |
1 |
0 |
0 |
Total |
36 |
71 |
30 |
10 |
03 |
Table-2: The
distribution of semen quality of Non- smokers (controls) among age groups
Semen quality |
Age groups( in years) |
||||
21-25 |
26-30 |
31-35 |
36-40 |
41-45 |
|
NZ |
17 |
31 |
15 |
5 |
1 |
OZ |
5 |
4 |
1 |
0 |
0 |
AZ |
0 |
5 |
1 |
0 |
0 |
OAZ |
2 |
5 |
3 |
1 |
0 |
OATZ |
0 |
0 |
1 |
0 |
0 |
AZOO |
1 |
0 |
1 |
0 |
0 |
Total |
25 |
45 |
22 |
6 |
1 |
Table-3: Mean values of semen parameters in
Smokers
Parameters |
Values |
N |
51 |
Age in years |
29.13 |
Volume in ml |
2.86 |
Liquefaction time |
21.86 |
Sperm count |
24.96 |
Total motility |
59.80 |
Progressive motile |
43.96 |
Morphologically normal sperms |
84.49 |
Morphologically abnormal sperms |
13.45 |
WBC(10ˆ6/ml) |
0.27 |
Table-4:
Mean values of smokers are stratified according to age groups
Parameters |
21-25 |
26-30 |
31-35 |
36-40 |
41-45 |
N |
12 |
25 |
8 |
4 |
2 |
Volume in ml |
2.58 |
2.8 |
3.18 |
3.3 |
3 |
Liquefaction time |
23.7 |
21.4 |
18.1 |
26.2 |
22.5 |
Sperm count |
22.7 |
21.3 |
36.5 |
30 |
27.5 |
Total motility |
47.5 |
59.2 |
68.7 |
70 |
85 |
Progressive motile |
32.5 |
41.8 |
55 |
56.2 |
70 |
Morphologically normal sperms |
76.6 |
85.8 |
85.6 |
96 |
87.5 |
Morphologically abnormal sperms |
15 |
14.2 |
13.7 |
4 |
12.5 |
WBC(10ˆ6/ml) |
0.41 |
0.36 |
0 |
0 |
0 |
Table-5: Mean values of
semen parameters in non-smokers and smokers
Parameters |
Values |
|
Non-smokers |
smokers |
|
n |
99 |
51 |
Age in years |
28.8 |
29.13 |
Volume in ml |
2.92 |
2.86 |
Liquefaction time |
20.91 |
21.86 |
Sperm count |
41.76 |
24.96 |
Total motility |
65.85 |
59.80 |
Progressive motile |
46.86 |
43.96 |
Morphologically normal sperms |
86.26 |
84.49 |
Morphologically abnormal sperms |
11.71 |
13.45 |
WBC(10ˆ6/ml) |
0.27 |
0.27 |
Table 6: Mean comparison of
parameters between Smokers and Non-smokers
Parameter |
Mean |
SD |
P-Value |
Inference |
Volume |
2.93 |
0.769 |
0.605 |
NS |
2.86 |
0.693 |
|||
liquefaction time |
20.92 |
7.744 |
0.52 |
NS |
21.86 |
9.745 |
|||
Sperm count |
41.77 |
28.269 |
<0.01 |
*HS |
24.96 |
20.59 |
|||
Total motility |
65.86 |
30.373 |
0.245 |
NS |
59.8 |
29.55 |
|||
Progressive motility |
46.87 |
29.913 |
0.563 |
NS |
43.96 |
27.507 |
|||
Normal |
86.26 |
20.79 |
0.638 |
NS |
84.49 |
23.741 |
|||
Abnormal |
11.72 |
16.736 |
0.58 |
NS |
13.45 |
20.566 |
Table-7:
Distribution of semen quality among different types of Cigarette Smokers
Type ofcigarette
smoker |
Semen quality |
|||||
NZ |
OZ |
AZ |
OAZ |
OATZ |
AZOO |
|
Less than 5/day |
8 |
1 |
0 |
0 |
0 |
1 |
Less than 10/day |
17 |
8 |
2 |
3 |
1 |
0 |
More than 10/day |
3 |
3 |
0 |
3 |
1 |
0 |
Discussion
The present study was aimed to perform the
quantitative and qualitative Analysis of Semen and to Compare the sperm
parameters in smokers and non-smokers.Among 51 cases of smokers, maximum cases
(31) 60.78%.belong to smokers who smoke less than 10 cigarettes/ day. Of which
17 cases showed Normozoospermia and 14 cases showed abnormal semen quality
among them 8 cases showed Oligozoospermia, 3 showed Oligoasthenozoospermia, 2
showed Asthenozoospermia and 1oligosthenoteratozoospermia. Smokers who smoked
more than 10 cigarettes/ day were 10/51, of which majority 7% showed abnormal
semen quality reported as Oligozoospermia and Oligoasthenozoospermia and
Oligoasthenoteratozoospermia.Maximum number of cases belong to age group
26-30(n=25), In this study, the semen volume, sperm count, motility and
percentage of normal sperms of the smokers were decreased as compared to the
non-smokers.Examination of semen parameters amongall the 3 categories, persons
who smoked more than 10 cigarettes/day were showing decrease in semen volume,
High liquefaction time, Least sperm count, Least total and progressive
motility, high abnormal sperm percentage and Majority of morphological defects.It
was reported that, cigarette smoking was associated with a significant decrease
in sperm density, total sperm count and total number of motile sperms [5].
Earlier studies reported that there was decrease in the sperm count in chronic
smokers [6-9]. Further, the motility of the sperms also lower in smokers when
compared with non-smokers [10,11]. Abnormal morphology of sperms was reported
in the smokers when compared with non-smokers [12]. Smoking was considered as
one of the public health hazard according to the WHO. It was reported that
smokers are at risk of reproductive problems [13]. Tobacco consumption directly
damages the germ cells in both males and females through the chemical
constituents present in it [14]. Several studies reported that smoking has a
negative impact on the quality of sperm. The major changes in the sperms in
smokers are decrease in the motility, sperm concentration; total spermcount,
semen volume, and altered morphology [14-16].It was reported that overall
quality of sperm decreased in smokers [17]. Vine et al. reported negative
correlation between smoking and the quality of sperm [18]. The exact mechanism
of these deleterious effects of nicotine on reproductive system is not clear.
However, it was reported that the nicotine can pass through the blood testes
barrier and causes damage of the sperm morphology [19]. The nicotine was
reported to decrease the motility by damaging the flagella [20]. Interestingly,
it was observed that when the smokers sperm washed and placed in nonsmokers
seminal plasma, it regained normal motility [21-24].Moskova
et al reported that there was decrease in the motility but increase in the
morphology of sperms in the smokers when compared with non-smokers. However,
there was no [25]. Mutagenic and carcinogenic substances present in the smoke
was reported to cause these effects on the motility and morphological changes
in smokers [26]. The results of the present study was in accordance with
earlier studies.
Limitations:
The study was conducted at one center. Hence, the results cannot be
generalized.
Conclusion
Semen parameters like volume, motility, count,
morphologically normal spermatozoa were reduced in cigarette smokers when
compared to Non-smokers, but only sperm count was found to have a high
significant decrease in Smokers (P: <0.01 ) when compared to Non-smokers. In
concordance with other researchers, results of present study support that
cigarette smoking have a relatively significant effect on semen.
Addition
to existing knowledge: The study highlights
the hazardous effects of smoking on reproductive functions which increase the
awareness of general public about the smoking and its dangerous effects. It
also helps researchers to understand further the association of smoking and
reproductive functions which may help to develop effective management methods.
Conflicts
of interest: None declared
Source
of funding: Self-funding
Author
contributions: All the authors equally contributed
from planning, designing, collection of data, analysis and interpretation and
writingthe manuscript and editing the manuscript.
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