You all probably saw the sexy articles that were presented at the European Society for Human Reproduction and Embrylogy meeting in Prague last week. You know, the ones about the clowns during embryo transfer, and the one about how 20 anovulatory women who got therapy started ovulating, thus proving that we all have to just relax. Well, I was curious enough to go read all the available abstracts. Below is my summary. Because I used to be a scientist I've probably used more scientific language than is helpful, although I've tried to be clear. I hope it's helpful.
There was a lot going on at this meeting. Which puts the lie to H's rather cynical comment when I told him where Dr Candour was last week: "Good to know he's off drinking vodka and visiting titty bars." Then we both cracked up at the thought of Dr Candour in a titty bar. Sadly H's comment probably says more about H's experiences with sales conferences than about how our esteemed doctors spend their time.
I should point out that lots of studies contradict each other. I focused on the talks rather than the posters (at scientific meetings the sexy stuff gets presented in person, and the less sexy or less prestigious stuff is just stuck on a wall for people to look at if they have time). I lost the will to live part way through reading the abstracts for the 1000 or so posters. I also focused on the stuff that's relevant for me, so I'm sorry, I didn't read the stuff on PCOS or anything much on male infertility. I'm fairly sure you will forgive me.
Protocols, response rates and egg quality
- Antagonist (short) protocol gives lower pregnancy rate (Al-Inany, Egypt)
- Antagonist protocol doesn't give lower egg quality in a subsequent FET - pregnancy rates with blastocyst transfer in FET cycles are the same whether blastocysts came from antagonist or agonist cycles (Lee et al, Korea)
- The flare protocol is better than both long protocol and antagonist in poor responders (meta analysis of other studies by Franco et al, Brazil)
- In most cycles these days, the stimulation drug is recombinant FSH - rFSH (e.g., Follistim/Puregon). Making recombinant FSH involves isolating the gene and inserting it into a production cell culture like chinese hamster cells (lots of cells grown together in a nutrient broth). The hormone is purified out of the broth. Only the pure hormone is produced. This means that unlike un-medicated cycles, there is no involvement of LH in priming the follicles for release. This was not an issue with earlier protocols because earlier stimulation drugs (e.g., Menopur) were produced by purifying the urine of menopausal women, so there was a low level of LH present. This has been an area of investigation - to see if adding low levels of LH will improve the egg quality.
Adding rLH to stimulation protocols which use pure rFSH in agonist (long) cycles reduces the rate of miscarriage (pregnancy rates are the same). You might therefore expect that protocols using puregon/follistim which are pure recombinant (r)FSH, would give a slightly higher miscarriage rate than Menopur which contains LH as well in small quantities because it's produced by purification from human urine. This was not tested - the study just looked at adding rLH (e.g., Luveris) to the rFSH. Abdelmassih et al, Brazil. - BUT adding rLH to rFSH in a long agonist protocol did not result in higher ongoing pregnancy rate. Andersen et al, Copenhagen, Denmark. My thought is that perhaps women's metabolism is so finely tuned that it's hard to see population effects here, it's about the individual woman and her response. But then I'm not an endocrinologist.
- AND Pre-treating with rLH prior to starting rFSH stimulation in a long agonist cycle (treating with the rLH for a week after down-regging) resulted in a higher percentage of embryos fertilised (number of embryos was the same). No difference in pregnancy rate. Fleming et al, Glasgow, UK and lots of other places,
- Women with an abnormal response to FSH stimulation given their age and in vivo FSH level may have FSH-receptor mutations. Lalioti et al, Yale, USA.
- Taking longer to reach the blastocyst stage leads to poorer pregnancy rates in fresh cycles, but not in frozen ones. The hypothesis is that ovarian hyperstimulation may advance the day of receptivity of the uterus, so that putting back blastocysts a day later than the usual day 5 results in lower implantation - the window of implantation has already passed. The same would not be true in a frozen cycle. Mitwally et al, Detroit and Michigan, USA.
- Prolonged treatment with DHEA does improve ovarian function in women with decreased ovarian reserve. Although a small sample size, there were significant improvements in oocytes retrieved, fertilised oocytes, and normal day 3 embryos. Gleicher and Barad, New York, USA.
- Antagonist protocol for priming egg donor recipients has a higher pregnancy rate than the traditional agonist treatment. Casan et al, Valencia, Spain.
Implantation and embryo quality
- Endometrial receptivity is governed by the upregulation and down-regulation of 100s of genes. This gene expression is different between un-treated cycles at day 7 after the LH surge when compared to ovarian hyperstimulation cycles at day 7 after hcg. At days 1, 3, 5, and 9 the gene expression pattern was the same between the two sets. This indicates that at the day of maximum receptivity the endometrium differs in a stimulated cycle, possibly leading to lower receptivity - although we don't know that. Horcajadas et al, Valencia, Spain.
- Embryo scoring parameters that affect implantation significantly are: Nuclear alignment; nucleolar (the nucleolus is one part of the cell nucleus) number, size and alignment; day 2 cell number, symmetry and nucleation. Everything else did not significantly affect implantation rate (ie many of the characteristics our clinics use including day 3 cell number and alignment etc, and the morphology at day 5). L. Scott, address not given.
- Many embryos are mosaic - i.e., some cells are chromosomally normal, while others are abnormal. Oocytes are much less frequently abnormal than the resulting embryos (7-10% versus 70% in young women), indicating that errors come during embryonic cell division, rather than arising in the egg itself. The only way currently to screen for mosaically abnormal embryos is PGS, which is controversial and has yet to be proven in a large scale study to result in higher levels of implantation. Lundin, no address given.
- Cigarette smokers have less receptive uteruses (uteri?). Statement of the bleeding obvious by Soares et al, Valencia, Spain.
Other factors affecting cycle outcome
- With a yah, boo, and sucks to the article which got all the publicity, which showed that some women with no ovulation who received therapy started ovulating, this study shows that levels of stress had no effect on IVF cycle outcome. Lintsen et al, Nijmegen, Netherlands.
Miscarriage
- Women with premature ovarian aging have a lower pregnancy rate and higher miscarriage rate, need higher doses of stimms yada yada yada, but interestingly their embryos do NOT show a higher rate of aneuploidy. I.e. something else is causing the higher miscarriage rate , not a simple eggs are crap --> embryos have the wrong chromosomes problem. Weghofer et al, USA
- Women with recurrent fetal loss (pregnancy loss after seeing cardiac activity) had increased expression of inhibins a1β1and a4β1 compared to women with recurrent loss of empty gestational sacs. They can't figure out the mechanism. Anim-Somuah et al, Liverpool, UK
- The strongest predictive factor for secondary recurrent miscarriage (after number of previous miscarriages) is the gender of the first child - having a boy is hypothesised to activate the mother's immune system. How that fits with all the controversy around the immunology stuff I don't know. Nielsen et al, Copenhagen, Denmark
Immunology
- Peripheral blood concentration of natural killer cells (PBNK) bears no relationship to uterine concentrations of natural killer (uNK) cells. PBNK levels don't vary during the menstrual cycle. Levels of PBNK were similar between recurrent miscarriers who carried their pregnancy to term versus those who had another miscarriage. Rai et al, London UK (From Lesley Regan's lab)
- Uterine NK cells have a strong role to play in implantation, providing the mechanism guiding maternal epithelial cells towards the embryonic trophoblas cells via oxygen sensing and synthesis of a compound called VEGF. Higher concentration of uNKs leads to higher pregnancy survival rate in pigs - concentration goes up three-fold at critical points in healthy embryonic development. Croy et al, Ontario, Canada.
Genetics
- The egg's polar body can be used to do genetic testing even before selecting which eggs to use for insemination (very creative technique developed by an Italian group in response to the law in Italy which says that only 3 embryos can be created and all must be transferred). More than 50% of eggs in women over 35 had aneuploidy. Ferraretti et al, Bologna, Italy.
- BUT this misses post-fertilisation genetic problems. Evidence from Delhanty (not sure of address) says that more than 50% of genetic abnormalities in the embryo are post-meiosis and would therefore not be picked up in polar body testing. They found a similar ratio of abnormal embryos in those with recurrent miscarriage and those with recurrent IVF failure.
- Women with recurrent miscarriage or multiple IVF failures produce very few viable embryos. Only 7.5% of embryos surveyed were normal with PGS, only 1.5% implanted and only 1% produced ongoing pregnancies. Bianchi et al, Yale, USA.
- Severe male factor infertility contributes to a high rate of chromosomally abnormal embryos (95% in non-obstructive azoospermia). Magli et al, Bologna, Italy.
Endo
- Endometriosis may be present in everyone, and only become a pathology when a certain stage is crossed. Not clear what that stage is
- Women with mild or moderate endometrisis have a decreased ovarian reserve as measured by anti-mullerian hormone (AMH) which is produced by small antral follicles. Antral follicles are also more diverse in size in women with endometriosis compared to those without endo. Cunha-Filho et al, Porto Allegre, Brasil.
- Surgery of even mild endo has a positive effect on pregnancy and live birth rates. Mohammed Saleh et al, Saudi Arabia
Long term effects of IVF/ICSI
- ICSI children at 8 years old had no substantial differences in development to children who were not the result of ICSI. There was a higher incidence of congenital malformations (10% vs 3.3%) but these were all correctable by minor surgery.
Pregnancy
- Vanishing twins lead to a higher incidence of intrauterine growth restriction later in pregnancy for the surviving singleton. The later the twin vanishes, the more likely there is to be an issue. Pinborg et al, Denmark
Hi Thalia
You make me feel thick!
Can you give me a link to the stuff about miscarriage, as it affects women losing the 'empty gestational sac' (doesn't that sound soulless?) I think that's me, and if there is any more I can understand about it, I would be grateful. This is the first time I have ever heard a distinction made between the two.
Thanks for all this, but I fear you have made a rod for your back!
Posted by: Vivien Jane | Tuesday, 27 June 2006 at 17:17
#2 & #3 under miscarriage are most relevant to me- particularly the bit about having a boy first may activate the immune system. Interesting...
Posted by: Leggy | Tuesday, 27 June 2006 at 17:26
Wow . . . Doctor Thalia, impressive and informative summary. Thanks for taking the time to share it with us all!
Posted by: beagle | Tuesday, 27 June 2006 at 17:38
You have missed your calling. Excellent summary. I had no idea that endo affected egg numbers. I wonder why.
Posted by: Cricket | Tuesday, 27 June 2006 at 17:40
Wonderful summary!!! I didn't even feel stupid when I read that...Yay!
Posted by: Gravida Zero | Tuesday, 27 June 2006 at 17:46
Thalia, thanks so much for this. Now I can go to the titty bar without sifting through all this on my own!
Posted by: Julie | Tuesday, 27 June 2006 at 17:51
My brain hurts.
Posted by: PBfish | Tuesday, 27 June 2006 at 17:58
Good info! Thanks for netting it out for us like that.
My brain hurts, too :-) I'll come back to read a second time. Haaa.
Posted by: Louise | Tuesday, 27 June 2006 at 18:02
Thalia, you are full of useful information.
Posted by: Molly | Tuesday, 27 June 2006 at 18:11
Wow... very impressive and interesting. Thanks for sharing with all of us! Would you post a link to the PCOS info... I'd like to have that information since I still battle PCOS after my successful IVF.... having a baby doesn't cure us infertiles and our issues! Have been reading your blog for a few weeks, as well as your archives... thank you for blogging and sharing your life and experience with us. Hoping that you will have success soon so that we can celebrate with you when the time comes. In the mean time, I hope that the knowledge that others are thinking about you will help you find peace and give you strength in the days ahead as you take your next steps! Kristin
Posted by: Kristin | Tuesday, 27 June 2006 at 18:33
DUH! You did link to it... I'm such a block head! Thanks so much... I'm off to read about PCOS ... let the fun begin! Kristin
Posted by: kristin - again | Tuesday, 27 June 2006 at 18:57
Thanks for posting this. Very informative. #4 under Genetics has been my theory about why my husband and I have had so many failed cycles.
Posted by: amanda | Tuesday, 27 June 2006 at 19:09
Wow, that's a lot to take in. Some of the stuff is stuff I've read and some is new. All helpful. For the most part, the numbers make me lose the will to live too...
Posted by: zarqa | Tuesday, 27 June 2006 at 19:31
Thanks so much for the summaries!
W/ regards to the behavioural therapy, this isn't the first study to find that in women with FHA, behavioural therapy can and does help. But that doesn't mean that every case of FHA is due to stress, nor does it have anything to do with any of the myriad of other infertility diagnoses out there. I really wish that the media would do a better job of distinguishing!
Posted by: Nico | Tuesday, 27 June 2006 at 19:49
Good stuff, Thalia! Many thanks for sifting through all that and putting it out there so succinctly.
There's a lot of stuff to think about there, but unfortunately my warped mind is focusing on the hilarious question of whether any gynos or REs go to titty bars, after a hard day of looking at cooters.
I hope you're doing OK.
Posted by: Kath | Tuesday, 27 June 2006 at 20:45
thanks, Thalia! I will print out your summary and put it in my ever growing folder.
Posted by: kati | Tuesday, 27 June 2006 at 20:57
Thalia--first of all thanks for sharing all this info and taking the time posting it. Second of all...I have to agree with the other women...my brain hurts, but in a good way!
Posted by: MoMo | Tuesday, 27 June 2006 at 21:06
Immpressive summary. You must have put a lot of time into this, and I hope it'll be helpful for you and others (even with all the contradictory stuff).
Posted by: EJW | Tuesday, 27 June 2006 at 22:24
Thanks for spending the time to write out summaries of these results.
Now, let's hope all our RE's are keeping up to date with this as well.
Posted by: Summer | Tuesday, 27 June 2006 at 23:14
Fantastic summary of such a wide range of topics! Thanks so much for putting this together!
Posted by: Kay | Tuesday, 27 June 2006 at 23:19
Impressive distillation of what must have been lots and lots of articles. Thanks!
Posted by: sube | Wednesday, 28 June 2006 at 01:31
Wow this post has a lot of wonderful and helpful information. Thanks so much for taking the time to summarize and share it with us!
Posted by: Mary Ellen | Wednesday, 28 June 2006 at 04:05
Wow, Thalia!
Thanks SO much for distilling all of this information for us!! It's fabulous, and very interesting.
How are you doing though??? I've been wondering how you are and what's going on.
I've been checking for "updates" daily, but I guess now I know what you've been "up to" these last few days -- sorting through reams and reams of abstracts!! ;)
I hope you are doing okay though, given everything you've been through lately.
wishing you the best,
'Nilla
Posted by: VanillaDreams | Wednesday, 28 June 2006 at 07:16
tremendous post - an excellent summary. i have been reading a lot this week but missed a lot of that. fascinating.
yes, i would like to know how you're doing as well. thinking about you. hugs
Posted by: Utrus | Wednesday, 28 June 2006 at 07:29
T, I hope you are doing OK.
Posted by: Pamplemousse | Wednesday, 28 June 2006 at 11:36
Wouldn't it have been interesting to be around for that conference (and not just for the purposes of punching the clown people)?
I was encouraged and discouraged at the same time about the research being done on implantation. It's such an important part of the process, and they seem so far behind. But wouldn't it be fascinating to learn more about cell division?
-The endometriosis stuff sounds right on target, as does the research on protocols.
-For the life of me, I cannot understand what "aneuplody" means, even when I looked it up. Said the never had anything to do with science or math woman.
-Is PGS the same as PGD in the US? A lot of this would suggest that screening embryos before transfer might be beneficial to more IVFers than previously thought.
I hope you are doing OK too. Given what little I know, I think throwing yourself into research has helped you in the past. I hope it has helped a little now.
Posted by: fisher queen | Wednesday, 28 June 2006 at 13:16
Thanks, Thalia! Great summaries. I'm off to look up the male factor stuff.
Posted by: Ellen K. | Wednesday, 28 June 2006 at 13:39
Impressive! I know I just wouldn't have the patience for something like this - thanks for sharing.
I hope you're travelling OK and the hormonal crash has been gentle on you.
Posted by: StellaNova | Wednesday, 28 June 2006 at 14:00
Damn, you're good! This is exactly why I read people's fertility blogs--hoping to learn something I don't already know. Many times this doesn't happen, but your post has given me at least two questions to ask my doctor. Thanks so much for being such a smart, pro-active person. I have a lot of respect for you.
Posted by: Lea | Wednesday, 28 June 2006 at 14:20
great stuff thalia. you rock!
Posted by: Sue/HoldingPattern | Wednesday, 28 June 2006 at 18:08
Thanks for all of the info!!
Posted by: Alli | Wednesday, 28 June 2006 at 19:14
So when are you opening your own clinic? Thanks for the informations!
Posted by: KIMMER | Wednesday, 28 June 2006 at 19:18
This is excellent! Thank you!
Posted by: Sarah | Wednesday, 28 June 2006 at 21:15
What a lot of good information! Nice summary!
Posted by: Angie | Wednesday, 28 June 2006 at 21:18
Thank you for the summary - very nicely done.
P.
Posted by: P. | Wednesday, 28 June 2006 at 21:43
Thank you for putting your time and effort into this post. This is going into my 'keep' folder.
Posted by: Lut C. | Wednesday, 28 June 2006 at 22:46
my gosh.useful clear wonderfully written. thanks.
Posted by: katty | Thursday, 29 June 2006 at 00:10
Thank you so much, Thalia. Really really interesting and informative. x
Posted by: Meg | Thursday, 29 June 2006 at 02:53
thalia - a huge thank you, I feel as tho I were a delegate at this conference,.....I'll digest it all & hopefully this new info will be helpful for all of us. Thank you. And also - it wasnt a stupid question -whether id read the coming to term book - believe it or not, despite my being thorough in researching RPL - id never seen this book. Most of my research was on the net. Nikole told me abt it only recently & ive ordered it thru amazon - thanks again x
Posted by: Womb in waiting | Thursday, 29 June 2006 at 13:02
Is it mean if I say that I wish you were male factor so I could benefit more from your super smarts? Wow, you probably could do your own cycles if only you had a didlo cam!
Posted by: Jenny | Thursday, 29 June 2006 at 14:06
My head is spinning. Very impressive summary. Thanks for this. Not sure what it all means but I also hope that our RE's are keeping up with all this new research. It's encouraging and discouraging at the same time.
My hubby always asks what golf course my RE is on when he's out of the office, but I like the idea of him being at a titty bar much better -- trading cooters for hooters!
Posted by: LisaGray | Thursday, 29 June 2006 at 21:52
Well, my brain has recovered enough to post but not enough to say more than thanks. Great information.
Posted by: zhl | Thursday, 29 June 2006 at 21:58
Wow. This is absolutely fantastic information. Thank you, thank you, thank you for putting this together. I had found some of these articles but not some of the most interesting ones. I am bookmarking this post.
--Bugs
Posted by: Dead Bug | Friday, 30 June 2006 at 02:32
Thanks for the interesting information!
I am just back from my vacation and am catching up. I am so very sorry about your loss.
Take care
Posted by: soralis | Friday, 30 June 2006 at 05:04
Any chance you're an RE and just haven't told us? You explain everything much better than the professionals!
Posted by: Jennifer | Saturday, 01 July 2006 at 04:14
Wow, Thalia, I'm impressed! As I was reading I had a flashback to the blogger's luncheon in D.C. where you told us that your degree helped you understand scientific studies to see whether the researchers were lying or not. You weren't kidding! You must have worked hard on this post...thank you.
It's all a bit much for me to take in at once but I think I'm going to make a permanent link to this post on my sidebar. This is a great reference site. Thanks again!
Posted by: Flicka | Saturday, 01 July 2006 at 23:40
Thanks so much for all of this information. You are amazing!
Posted by: Nikole | Sunday, 09 July 2006 at 19:12
Hi Dr Thalia,
could you please tell me if DHEA is still considered beneficial forn women with age relatied fertility issues about to undergoing IVF? I did an IVF cycle recently and no eggs were foudn in the two follicles that developed.
kind regards,
Suparna
Posted by: Suparna Tyers | Monday, 23 April 2007 at 23:23