Its summer
time! If you live in the UK that means you’re enjoying a hosepipe ban at the
same time your caravan is floating down what used to be the high street.
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| Does using the hosepipe to lash yourself to a lamp-post violate the terms of the ban? |
Anyway,
enough of my stereotypical British weather bashing; we’ve got endometriosis
news to go through.
If you read
last month’s post you may recall I reported on a case of male endometriosis; “It’s another report of endometriosis occurring in a man” I
said, “I say ‘another’ as if it happens
all the time, but this is only the fifth or so record of endo in a man, ever”
I said, flippantly rebuked myself. Haha, yeh endometriosis in a man, it’s not
like it happens every week is it? Well fate sure likes to make me feel like an
idiot because, not more than a week after I joked about the infrequency of male
endometriosis, there was another case report in the
literature.
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| A highly realistic portrait of my reaction |
Unlike last
month’s report though, where the man in question had mysteriously developed
endometriosis after taking anti-estrogen therapy for infertility, this latest
case is more what you would call a ‘typical’ case of male endometriosis and it
just goes to show how strange the world is when the phrase ‘typical male
endometriosis’ exists. This reason I call this case typical is because the man
in this latest case was an elderly gentleman undergoing long-term estrogen
therapy for prostate cancer. Out of the 6 cases of male endometriosis I know
of, 4 have been in men undergoing estrogen therapy for prostate cancer. This
could be further evidence of endometriosis arising from metaplasia, where some cells in the human body have the ability to
transform in endometrial cells given the correct stimulus (which in this case,
would be estrogen). Of course it could also be that endometriosis arose in this
man due to embryonic rests, where
tiny fragments of the primitive female reproductive system are found in men and
can become active given the correct stimulus (estrogen, again). Either way,
understanding the origin of endometriosis in males, may uncover some of the key
mysteries of how endometriosis develops in women, so I’ll be keeping an eye on
this.
Seeing as
we’re on the subject of strange cases of endometriosis, I nearly fell off my
chair when I found an article
making reference to endometriosis in horses. I’ve only ever seen reported cases of naturally
occuring endometriosis in primates, so to suddenly see reports in horses threw
me somewhat; especially as there were cases of this so-called horse endometriosis
going back decades! Has this strange phenomena been under my nose all these
years, an important piece of the endometriosis puzzle left ignored?
No, no it
has’t. It turns out that when the term endometriosis is applied to horses, it
doesn’t mean endometriosis. Allow me to clarify; horse ‘endometriosis’ refers
to a progressive degeneration of the endometrium inside the uterus, leading to
problems conceiving and retaining foetuses. That’s bad for the horses, but
that’s not what endometriosis is. Endometriosis is correctly defined as the
presence of endometrial glands and stroma in locations outside the uterus. So, veterinarians have dropped a massive ball
on this one and need to come up with a different name for the endometrial
degeneration seen in horses, sorry guys, ‘endometriosis’ is taken.
Moving on
now to something we’d all like to see, and that’s better diagnostic methods for
endometriosis. It seems that research into new diagnostics for endometriosis is
really taking off at the moment as I’m seeing more and more papers on the
subject being published, which can only be a good thing.
The first of
the studies published
this month is from Oxford, UK, which looked at whether it was possible to
predict the outcome of a woman’s laparoscopy by asking her to fill in a
questionnaire regarding her symptoms and other characteristics (such as overall
health and previous diagnoses of other conditions). This was a fairly large
study including 1,396 women that hadn’t yet been diagnosed with endometriosis from
nineteen hospitals across 13 countries. What the researchers found was that by
asking the right questions it was possible to identify women most likely to be
diagnosed with stage III and IV endometriosis with a good degree of accuracy.
This is important for several reasons; firstly it will allow women with a high
risk of stage III and IV endometriosis to be identified earlier, thus
decreasing diagnosis times. Secondly, if the surgeon knows what to expect
before doing a laparoscopy it will make it easier for them to plan ahead with
regard to what they are likely to encounter and how to treat it.
Next up is a
study from Poland
looking at markers to help diagnosis of endometriosis in girls aged between 13
and 19. Specifically these researchers were looking for markers in the blood or
peritoneal fluid that may identify young girls as having endometriosis. This
study took 50 girls who underwent laparoscopies for chronic pelvic pain and
then, depending on the results of their surgery, divided them into two groups.
Group 1 consisted of 33 girls who were diagnosed with endometriosis and Group 2
was the remaining 17 girls who had no evidence of endometriosis. The
researchers then analysed the blood and peritoneal fluid of the girls from each
of these groups for levels of proteins called interleukin-4 (IL-4) and
interleukin-2 (IL-2). These proteins are involved in regulating the immune
system and are also know to be involved in the process of inflammation. They
found that, in the girls with endometriosis, levels of IL-4 were significantly
higher in both the blood and peritoneal fluid and levels of IL-2 were lower.
This is excellent news as it could be a way of developing a blood test for
endometriosis in young girls with chronic pelvic pain, which would decrease
diagnosis times and hopefully mean they get treatment sooner. That said,
laparoscopy would still be a necessity to confirm the diagnosis because, although
an accurate blood test would tell you if endo was present, it wouldn’t be able
to tell you where the disease was, how severe it was or if any adhesions are
present. It’s still a massive step in the right direction though.
Sticking
with novel diagnostics and a study from Atlanta
examining the differences in the endometrium between women with and without
endometriosis. There have been several studies over the years that have shown
that the normal endometrium in women with endometriosis is different in certain
ways to the endometrium in women without endometriosis. Most notably the recent finding that
women with endometriosis are much more likely to have nerve fibres in their
endometrium. This latest study is a logical extension of this as they were
looking at the levels of proteins that cause nerves to grow (called neurotrophins) in the endometrium. What
they found was that there was a far higher level of proteins called BDNF and
NT-4/5 in the endometrium of women with endometriosis. What this means is that
there are now ways to identify women with endometriosis purely from an
endometrial biopsy. Although this still wouldn’t be able to replace a
laparoscopy, it all goes towards reducing diagnosis times and may even be able
to predict a woman’s fertility status, giving her the best options for
treatment.
Speaking of
fertility, you may recall last
month I talked about the outcome of IVF in women with endometriosis and how
women with endometriosis were more at risk of preterm birth (though the child’s
overall health wasn’t affected). Well this month a study may go some way to
explain why this might be the case. This latest investigation suggests that it
is inflammation that plays a role in preterm birth in women with endo. It has
been known for a long time that endometriosis is a disease of chronic
inflammation and it’s not surprising when you look a little deeper at how the
disease works. We’ve probably all seem pictures of what an endometriotic
implant looks like, usually a red or bluey-black spot that grows and bleeds.
Your body reacts to this in much the same way it would to any other injury,
i.e. it initiates an inflammatory reaction. If you cut your hand this
inflammatory reaction speeds up the healing process and helps prevent
infection; but inside your body this inflammatory reaction to the endometriosis
is persistent and is thought by some to contribute to the pain generated by
endometriotic implants. Your body controls the inflammatory reaction by
secreting proteins which tell the immune system when and where to initiate it
and we find a very high level of these inflammatory proteins in the peritoneal fluid and blood
of women with endometriosis. All these inflammatory proteins floating around in
your body may have an effect on your ability to conceive and subsequently may
also put you at an increased risk of preterm birth. It will probably come as
little surprise then that another study, published very
recently, found that pregnancy rates were significantly improved after
endometriotic implants had been surgically removed.
A quick
rundown of a couple more stories before we end for this month. Starting with a review from authors in
Oxford, UK looking at the evidence concerning the age at which a girl starts
her periods (menarche) and how this relates to her subsequent risk of
developing endometriosis. The authors examined 45 papers published between 1980
and 2011 and found that, once they had narrowed the studies down to those with
the best methodology, that a woman with endometriosis is 55% more likely to
have started her periods earlier than a woman without endo. Of course that’s not a massive majority
because it means if you picked two women at random, one with endo and one without,
only around half the time the woman with endo would have started her periods
earlier. It’s still significant though and it raises the question of whether an
early menarche is cause or effect, i.e. do you have endometriosis because you
started your periods early, or did you start your periods early because you
have endo? These questions still remain unanswered.
Finally is a
piece of research
about vitamin supplementation for the treatment of endo pain symptoms. In the
past I’ve read plenty of supposed ‘research’ about vitamin supplements as a
panacea for everything from cancer to AIDS and invariably they turn out to be
a complete load of bullcrap by some quack doctor trying to exploitatively sell
their worthless snake oil to desperate and
vulnerable people.
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| Your typical cure-all vitamin supplement doctor |
However, I
am glad to say this latest research is nothing like that and is infact a
serious scientific investigation into the effect of taking supplements of
vitamins E and C on the painful symptoms of endometriosis. In order to test this
the researchers took 59 women with endo and randomly assigned them to one of
two groups; one group got the vitamin supplements (1200 IU of vitamin E and
1000mg of vitamin C) and the other group got a placebo (a fake pill that has no
active ingredient). What they found was
that the women who received the vitamins had a 43% improvement in everyday
pain; dysmenorrhoea (excessive period pain) was decreased 37% and dyspareunia
(painful sex) was decreased 24%. Inflammatory markers, like the one I was
taking about above, were also decreased in the group who took the vitamins. The
one criticism I have of this study though is that it wasn’t double blind, and
by that I don’t mean everyone having tape put over their eyes. Double-blinding
means that neither the patient getting the treatment nor the doctor
administering it knows whether they are having the real treatment or the fake
placebo. The reason this is done is because in some people, if they don’t know
they’re taking the fake pill, their body will react to the fake pill in the
same way it would to the genuine treatment (this is called the placebo effect and we still don’t
understand why it happens). But if a patient knows they are getting the fake pill this placebo effect disappears
so we can’t accurately compare patient’s reaction to the genuine and fake
pills.
It is
confusing and no-one truly understands the placebo effect, but it has a real
effect on drug trials so it must be taken into account. Nevertheless it is nice
to see some proper science going into vitamin research, however I hope this doesn’t
become a green light for charlatans to charge £50 for a bottle of vitamin
tablets. If you want to try vitamin supplements for yourself I recommend your
local pharmacy (I get a month’s worth of vitamin pills from mine for 99p which
is roughly $1.50). If it works for you, that’d be fantastic, if not then you
never know, next month they might find a cure (hey it has to happen sometime).
