Dear Editor,
Anejaculation is a rare ejaculatory disorder in men (1%–4% of sexually active men)
that can cause male factor infertility.1 Although these patients are generally healthy
individuals that may have erections and nocturnal emissions, they cannot ejaculate.
As we all know, there is evidence that the etiology of ejaculatory dysfunction is
partially genetic, especially related to serotonergic genes.2 Here, we report two
polymorphic regions in serotonin transporter (5-HTT) gene for the first time in three
Chinese males with anejaculation.
Case 1 was a married male suffering lifelong anejaculation. He presented to the Andrology
Outpatient Clinic complaining of an inability to consciously ejaculate even after
>50 min of masturbation. His sexual potency was normal, but no nocturnal emission
was reported. Case 2 was a 32-year-old male referred from the reproductive medicine
unit, where he and his wife had presented for evaluation of infertility after 3 years
of marriage. He complained of an inability to ejaculate, despite no loss of libido
or erectile function. He did not experience ejaculation during either coitus or masturbation,
however, continued to experience erections and normal nocturnal emissions every few
months. Case 3 was a college student. He presented initially to the clinic complaining
of anejaculation, but otherwise normal sexual function, after the commencement of
a relationship 2 years ago. He had anejaculation specific to penetrative sex, but
could ejaculate normally during masturbation and had nocturnal emissions. Cases’ detailed
information and clinical characteristics are shown in
Table 1
.
Table 1
Information of cases and clinical characteristics
Three cases were from unrelated families and diagnosed as idiopathic anejaculation.
Their past medical history was not significant. Careful gynecologic evaluation of
female partners revealed no female factor contributing to anejaculation. Neurologic
examination revealed normal sensory and motor systems and intact reflexes. Serum concentrations
of follicle stimulating hormone (FSH), luteinizing hormone (LH), testosterone (T),
prolactin (PRL), and estradiol (E2) were in the normal range. In three cases, obstruction
of the ejaculatory duct and retrograde ejaculation were ruled out by transrectal ultrasound
and examination of urine after masturbation, respectively. Digital rectal examination
and transrectal ultrasound to define prostate and seminal vesicles were normal.
The 5-HTT linked polymorphic region (5-HTTLPR) is a 43 bp insertion/deletion (L/S)
polymorphism in the promoter region of SLC6A4, which encodes 5-HTT. Another polymorphism
is a variable number of tandem repeat in the second intron of SLC6A4, which is called
STin2 VNTR. The STin2 allelic variants were identified as 9-repeat, 10-repeat and
12-repeat alleles of a 16/17 bp element that have been identified. Informed consent
to carry out molecular genetic analysis was obtained. The study was approved by Ethics
Committee of the First Affiliated Hospital of Anhui Medical University (No. 20150047).
We designed PCR primers (
Table 2
) by Primer3 Software Online Program (http://frodo.wi.mit.edu/cgi-bin/primer3/primer3_www.cgi).
The 5-HTTLPR and STin2 VNTR polymorphisms were genotyped using a PCR-based technology
(
Supplemental Information
). The PCR products were analyzed on a 3730XL Genetic Analyzer (Applied Biosystems,
Carlsbad, California, USA). Genotypes were called by visual observation of peak sizes
using GeneMapper 4.0 (Applied Biosystems, Carlsbad, California, USA).
Table 2
Oligonucleotide primers used for genomic DNA amplification of human SLC6A4 gene 5-HTTLPR
and STin2 VNTR polymorphisms
SUPPLEMENTAL INFORMATION
Click here for additional data file.
At the beginning of the scientific research on the mechanism of ejaculation, the hypothesis
was formulated that this symptom could be considered a neurobiological disorder, with
a major role played by a hypothetical genetic diathesis in the central serotoninergic
pathway. Central 5-HT is the main drive controlling ejaculation.3 There is substantial
evidence showing that the use of selective serotonin reuptake inhibitors (SSRIs),
by increasing central serotoninergic tone, delays ejaculation.4 By determining magnitude
and duration of 5-HT synaptic signal, 5-HTT plays a key role in the regulation of
serotonergic neurotransmission,5 and is therefore considered to be an interesting
candidate in ejaculatory association studies.
In the controls, the allelic frequencies distribution of 5-HTTLPR were 0.54 for S
and 0.46 for L, and allelic distribution of STin2 VNTR were 0.75 for STin2.12, 0.23
for STin2.10 and 0.02 for STin2.9, respectively. However, the genotypes of three cases
were S/S + STin2.10/12, S/S + STin2.10/10 and S/L + STin2.10/12, respectively. Obviously,
S and STin2.10 alleles were more common in three patients with anejaculation. Replying
the study in a bigger cohort of anejaculation patients is needed in further study.
The previous study had shown that 5-HTTLPR polymorphism contributes to the regulation
of the expression of SLC6A4,6 and S allele could reduce the transcriptional activity
of SLC6A4, hence decreasing transporter expression.7 As well, STin2 VNTR polymorphism
acts as a transcriptional regulator, and the transcriptional regulatory activity is
determined by the number of the repeat, with the STin2.12 allele having a higher expression
than the STin2.10 allele.8 In this study, we found all the three cases carried lower
expressing alleles, such as S and STin2.10 alleles, which could have less functioning
5-HTT and therefore lead to a higher 5-HT availability. As a result, at least in some
degree, they experienced the trouble of anejaculation.
According to the theory of De Jong et al.9 it has been hypothesized that the ejaculatory
threshold for men with low 5-HT levels and/or 5-HT2C receptor hyposensitivity may
be genetically set at a lower point, resulting in a more rapid ejaculation. In contrast,
men with a very high set point may experience delayed or even absence of ejaculation
despite prolonged sexual stimulation and despite achieving a full erection. However,
nocturnal emission is a type of spontaneous orgasm, involving ejaculation during sleep.
This is an autonomous reflex mediated by the sympathetic nervous system, so it may
also occur in patients with anejaculation.
The etiologies of the anejaculation can be categorized into three major groups: organic,
idiopathic and drug related.10 The word “idiopathic” is used frequently when we cannot
determine the accurate physiologic cause of a problem, but it is also used frequently
when describing conditions that are functional. With the etiology of idiopathic anejaculation
remaining largely unknown, the former use of the word seems appropriate. Furthermore,
the current study showed evidence that there might be some genetic component of idiopathic
anejaculation. Although anejaculation is uncommon, further research in this interesting
field is needed to replicate our results in the adolescent population for a better
understanding of male ejaculatory disorders.
AUTHOR CONTRIBUTIONS
YYH carried out the molecular genetic studies, participated in the sequence alignment
and drafted the manuscript. XSZ and CZL participated in the design of the study and
performed the statistical analysis. JJG and PG conceived of the study, and participated
in its design and coordination and helped to draft the manuscript. All authors read
and approved the final manuscript.
COMPETING INTERESTS
All authors declare no competing interests.