Home         Forums  

Go Back   Marrowforums > Bone Marrow Failure Diseases > AA
Register FAQ Search Today's Posts Mark Forums Read

AA Aplastic anemia

Reply
 
Thread Tools Search this Thread
  #1  
Old Sun Sep 28, 2014, 01:18 AM
curlygirl curlygirl is offline
Member
 
Join Date: Jun 2013
Posts: 151
Gene Identified for Short Telomeres in association with Aplastic Anemia

http://www.eurekalert.org/pub_releas...-gmd092314.php

Gene mutation discovered in blood disorder
CHOP expert, collaborators identify mutation in aplastic anemia that shortens telomeres on ends of chromosomes
Reply With Quote
  #2  
Old Sun Sep 28, 2014, 01:54 PM
KMac KMac is offline
Member
 
Join Date: Oct 2012
Location: Golden, Colorado
Posts: 103
Thanks for posting that Curlygirl, it sure is interesting.

I wonder if they think this telomere-related mutation is the cause only in cases of aplastic anemia that are diagnosed as genetic/inherited (as opposed to acquired). Or if alternately, with this discovery, they now think that many cases previously diagnosed as idiopathic/acquired actually have this telomere-related mutation as the root cause?
__________________
Kevin, male age 45; dx SAA 02/2012 - Hgb 5.8, platelets 14, ANC 200, 1% cellularity. Received ATG 03/2012. As of 03/2015, significant improvement - Hgb 15, platelets 158, ANC fluctuates around 1000, Lymphocytes 620. Tapering cyclosporine. BMB 20-30% cellularity.
Reply With Quote
  #3  
Old Sun Sep 28, 2014, 02:15 PM
triumphe64 triumphe64 is offline
Member
 
Join Date: Feb 2008
Location: Dallas, Texas
Posts: 455
Dr. Maciejewski told me last week that all of his bone marrow failure patients will be checked against all genetic defects known to cause these illnesses.
__________________
Dallas, Texas - Age 81 - Pure Red Cell Aplasia began March 2005 - Tried IVIG - Then cyclosporine and prednisone. Then Danazol, was added. Then only Danazol . HG reached 16.3 March 2015. Taken off all meds. Facebook PRCA group https://www.facebook.com/groups/PureRedCellAplasia/
Reply With Quote
  #4  
Old Mon Sep 29, 2014, 09:20 AM
Marlene Marlene is offline
Member
 
Join Date: Oct 2006
Location: Springfield, VA
Posts: 1,412
Very interesting. I don't think they went back to check John's telomere lengths once they understood the role they play in this disease. Finding the gene could be very helpful in determining the course of treatment I would imagine.

There have been a few with VSAA and SAA who failed AGT and were later found to have shortened telomeres.

I'm sure there are many unanswered questions surrounding this. Do those with the gene mutation all end up with blood disorders or does it need to be activated by some environmental trigger before it causes disease.

It would be good if they could go back and check everyone who has been diagnosed prior to this discovery.
__________________
Marlene, wife to John DX w/SAA April 2002, Stable partial remission; Treated with High Dose Cytoxan, Johns Hopkins, June 2002. Final phlebotomy 11/2016. As of July 2021 HGB 12.0, WBC 4.70/ANC 3.85, Plts 110K.
Reply With Quote
  #5  
Old Wed Oct 1, 2014, 07:02 AM
edithr edithr is offline
Member
 
Join Date: Feb 2011
Location: 30 mi West of Cleveland
Posts: 86
Oh, I thought telomere testing was standard, is that not the case? They tested my sons in 2011. At that time a lab Canada was the only place that tested them, I had to pay out of pocket for the test and then get reimbursed (out of network) from my insurance.

I have a Google alert set for any news on telomeres, I haven't seen this article yet so thanks for the heads up. I have my alert set for weekly notices though, so hopefully the alert works in the next few days.
__________________
Edith, mom to Eric, dx 2/11 at age 15 with SAA, began ATG/CsA 3/11, switched to Tacrolimis 8/11, off all meds 9/11 and is now considered to have bone marrow failure not otherwise specified.
Reply With Quote
  #6  
Old Wed Oct 1, 2014, 09:18 AM
Marlene Marlene is offline
Member
 
Join Date: Oct 2006
Location: Springfield, VA
Posts: 1,412
At the time John was diagnosed, they did not have the test. A few year later, they could test for shortened telomeres. I don't know if it's standard procedure to test everyone's telomeres now but sounds like it should be.

Edithr, what were your son's result?
__________________
Marlene, wife to John DX w/SAA April 2002, Stable partial remission; Treated with High Dose Cytoxan, Johns Hopkins, June 2002. Final phlebotomy 11/2016. As of July 2021 HGB 12.0, WBC 4.70/ANC 3.85, Plts 110K.
Reply With Quote
  #7  
Old Wed Oct 1, 2014, 11:08 AM
tom30 tom30 is offline
Member
 
Join Date: Sep 2010
Location: Brooklyn, New York
Posts: 108
Hi, I have not asked for this test and I'm hesitant to throw it into the mix of tests that little can be done about. My hematologist doctor is not a fan of some tests I asked about MTFR and he dismissed it out of hand saying it wouldn't mean anything and lots of people have that defect with no problems. But my GP will test me for anything I ask for. But I generally go with the advise of the hematologist. I think I would look at it differently if my numbers were heading the wrong way. Anyway Dean Ornish has done some work on Lifestyle changes that lengthen telomeres. The diet he recommended is pretty much vegan and when I tried it my overall blood counts dropped so I added in meat. I do not think his study isolated the low fat component of the diet as a reason for success, I seem to do better on a paleo/organic/minimal processed diet the organic and minimal processing is also part of the ornish diet.
http://ornishspectrum.com/proven-program/the-research/
__________________
Tom- 62 yrs old, dx-eosinophilic fasciitis 2004, 1 yr prednisone resolves EF- now low counts, HGB has been ok... EF has been associated with MDS along with AA.
Reply With Quote
  #8  
Old Wed Oct 1, 2014, 05:21 PM
Chirley Chirley is offline
Member
 
Join Date: Oct 2007
Location: Logan City Australia
Posts: 1,100
I'm positive for one of then MTHFR mutations (homozygous) it hasn't made any difference to me, as far as I know, as long as it's not connected to copper pathways as well somehow.
Reply With Quote
  #9  
Old Wed Oct 1, 2014, 09:25 PM
curlygirl curlygirl is offline
Member
 
Join Date: Jun 2013
Posts: 151
My son's telomeres were tested prior to treatment and they came out normal for his age group. Which is another reason why I think the cause of the Aplastic Anemia isn't the same for each case.

I actually asked at one of the AAMDS.org regional meetings if getting ATG would lengthen your telomeres if you had short ones and the Dr. from NIH that was briefing, Dr. Townsley, said that ATG is such a harsh treatment on your body that they would actually expect your telomeres to shorten as a result of it rather than lengthen. I don't know if that has been shown through tests or is an educated hypothesis that they need to test.
Reply With Quote
Reply


Thread Tools Search this Thread
Search this Thread:

Advanced Search

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

vB code is On
Smilies are On
[IMG] code is On
HTML code is Off
Forum Jump

Similar Threads
Thread Thread Starter Forum Replies Last Post
JUST diagnosed with Aplastic Anemia TASHMAC Questions and Answers 6 Tue Mar 27, 2018 10:09 AM
I am NOT aplastic anemia (new member) KristinR Tell Your Story 3 Wed Jul 16, 2014 12:51 PM
aplastic anemia and sudden severe hip pain Ellen McDonough AA 18 Fri Dec 6, 2013 09:10 AM
Free Aplastic Anemia Update in Houston, May 2010 Marrowforums News and Events 0 Fri Apr 16, 2010 03:43 AM
Aplastic Anemia and Myelodysplasia Association of Canada - Education Day smarchesin Canada 1 Sun Sep 23, 2007 11:48 PM


All times are GMT -4. The time now is 03:19 AM.


Powered by vBulletin® Version 3.6.7
Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.
Forum sites may contain non-authoritative and unverified information.
Medical decisions should be made in consultation with qualified medical professionals.
Site contents exclusive of member posts Copyright © 2006-2020 Marrowforums.org