Editors note: On
October 28, 1999, Linda Holland posted ten questions about sub-aortic stenosis (SAS) to
the Showboxer-L. Dr. Bruce Cattanach, one of the authors of the UK Heart Control Scheme
for Aortic Stenosis (please see the October Boxer Underground), responded to
Lindas post. With the permission of both Linda and Bruce, we have reprinted their
questions and answers here in article form.
QUESTIONS (Ms. Linda Holland) &
ANSWERS (Dr. Bruce Cattanach)
LH: I would like to learn more about SAS. There is lots of information
on BCM, but I have not been able to find nearly as much on SAS. If someone could answers
some of my questions and/or point me in the right direction to find this information I
would appreciate it. Below are some of the questions that I am searching for answers to:
If sire and dam are clear, is it one parent or both that are carriers?
If one or both are carriers what does that mean in regard to their
parents and so forth?
Does SAS skip generations? In other words, could it be that the affected
dog got it from a great-grandfather?
Is there a test available to determine which one is a carrier? Is there
anything that can be done to determine the carrier?
Should both parents of affected pups be removed from breeding?
What does this mean in regard to the affected dog's littermates? Should
they all be removed from breeding whether or not they have it, because they could be
carriers?
Should any dog with SAS be bred?
Should a cardiologist treat affected dogs? Are there medications?
Does SAS worsen as the dog gets older?
.Do dogs with BCM typically have problems with SAS, too?
BC: Linda Holland has asked a number of questions about SAS and she
has asked me to answer on this list. The questions are difficult to answer, in part
because there are no certain answers, but more because they are not set against the real
situation.
The problem is that the mode of inheritance of Aortic Stenosis has not
been clearly established even in the researched breed, the Newfoundland. In this breed
some evidence was obtained that a single dominant gene was responsible but this became
confused upon crossing to another breed. From my background in genetics I would expect
that a single gene is primarily responsible for the condition but this is not to say that
any other genes, such as those playing a role in heart development, blood vessel walls,
elasticity of the wall, or the biochemical milieu behind the nodule and fibrous ring
formation that leads to AS, etc., do not play a part. I drop the first S of SAS for
reasons that will become clear later.
Add to this that the cardiologists choose to GRADE the murmurs and MEASURE
blood velocities and you have a situation in which a polygenic inheritance is almost
forced. Blood velocities vary even in dogs with normal hearts - i.e., dogs with no AS in
their breed - and I don't think any cardiologist would put hand on heart to say that such
normal dogs never have at least minor murmurs.
So a real question is what is normal and how in all the variability does
one distinguish AS? Well, I don't think the answer is clear but, nevertheless, if one
knows that some dogs in the breed are dying or are badly impaired, some action needs to be
taken.
The UK control scheme takes the simplest approach: we just say that we
will breed from the best and avoid the worst. This is familiar territory to dog breeders;
everyone can take part. All that is needed is an economical test such that everyone can
test all their dogs and that the essential results, meaning which dogs are the best, are
available for all to see. This enables those with bitches to choose a dog of the required
standard, and makes it possible for stud dog owners to be careful which bitches they
accept.
This is all fine if the opportunities for testing are widely available and
the test is reliable. Many readers will have read posts in which I have talked about the
difficulties on both points. We have had really bad problems over the near-10 year period
of testing. But, having been seriously depressed by these problems I now find that
cardiologist after cardiologist is now reporting that the numbers of referred cases of
Boxers across the whole country has dropped dramatically. At Edinburgh, the starting
figure position was that Boxers alone made up 45% of all referred cases of AS. That was in
1990. Now Boxers are not even among the top ten breeds. Despite all the problems with the
scheme and all the difficulties with distinguishing the minor grades of AS upon which the
scheme was built, the UK scheme has been remarkably successful.
So, now, how to answer the questions:
Q. Sire and dam are clear, is one or both responsible for a case of AS?
A. Depending upon the frequency of any single responsible gene, it
might be one, or the other; and we don't know what happens with any hypothetical
homozygote with two doses of the gene. (If you get a brindle, does this mean that one or
both parents are brindles? Same rationale!) In other words, an apparently clear dog may
produce AS for all sorts of reasons, but the principal reason is that he might not have
genetically been clear; he just tested clear and the testing is not that precise.
He is likely to be in the better range, however. The same for the bitch.
We have no idea on homozygotes. They may be the more affected and then
also ALL their pups would be potentially affected; or they might die in the nest or before
birth. Here I have long wanted to see if matings between "affecteds" give lower
litter sizes, or higher neonatal deaths, or just fading puppies. But I think I would have
a hard time trying to get such information. I am in trouble as it is.
Q. If the sire or dam are carriers, what does that mean in regard to
the grandparents, and beyond?
A. Same line of reasoning can be applied to this question regarding
grandparents and behind them.
Q. Does AS skip generations? In other words, could it be that the
affected dog got it from a great-grandfather?
A. Obviously, normal appearing dogs can produce affected dogs, so
there is at this level a skipping of generations. But are the parents really normal? Here
we get to the grading. This is supposed to distinguish dogs with the most minor levels of
AS, but the system is not that perfect. (To continue with the fawn/brindle analogy, most
brindles are distinct from reds, but under poor light conditions there would be a
possibility of missing the most lightly marked tiger brindles!!)
Q. Is there a test available to determine which one is a carrier? Is
there anything that can be done to determine the carrier?
A. I think it is obvious that the testing systems are not infallible
at the murmur or blood velocity levels, and there is no DNA or other such test.
Q. Should parents of affecteds be removed from breeding?
A. That depends on how affected the pups are, and how many affecteds
the parents produce. It may be possible that any extensively used dog may produce one or
more seriously affected pups, but if the mean score of his progeny (to bitches of known
scores) is low, then he is one of the best. However, the other side of the coin is where a
dog regularly produces more seriously affected pups, or even higher scoring pups, then he
would be one to avoid. Here a little bit of history might be justified: we had a dog that
graded as 0 on two occasions up to 18 months of age. At stud he was found to produce a
number of Grade 2 progeny, to Grade 0 bitches. On retest it was found that he had a Grade
3 murmur and an elevated blood velocity on Doppler. He was clearly not a dog to breed
from, but what had gone wrong? On ultrasound scanning it was found that the Stenosis
(narrowing) involved the valve itself and therefore was not, as commonly recorded, below
the valve (Sub-AS). Valvular As appears to progress and get worse whereas Sub-AS
appears to change little after adulthood. So there are two messages in this highly
informative case. At least one other such case has since been found. Add to this that the
"bad" days of AS in UK Boxers are said (I have no evidence) to be largely
attributable to some extensively used stud dogs which had louder murmurs. There certainly
was a family of seriously affected cases.
Q. What does this mean in regard to the affected dog's littermates?
Should they all be removed from breeding whether or not they have it, because they could
be carriers?
A. This is a difficult question. I think at this stage one should rely
more on the test results, preferably making the tests more extensive and more rigorous in
view of family background. This would certainly be the best course of action if the
condition is so frequent that clear lines cannot be found. And that is unfortunately the
situation today.
By the way, there does seem to be some link between AS and BCM; they have
often been found together. This may only mean that a heart impaired by one condition may
be more susceptible to another. Who knows!
Q. Should any dog with SAS be bred?
A. As must be evident, it is best to avoid the more seriously
affected. Where the line is drawn will vary with the magnitude of the problem within the
breed/country. If there are few affected with even minor murmurs then one can be hard; if
there are many, one must be less rigorous. In the UK we tried to knock off the worst 10 -
15% with Grade 2 as the starting cutoff point, but with tougher grading we find we have
30% Grade 2s and it is hard to take such a high proportion of dogs out of the breeding
population. However, this number can be cut by about 50% by re-testing (and Doppler at a
2.00 meters/second blood velocity limit, which everyone admits is too high).
Q. Should a cardiologist treat affected dog(s)? Are there medications?
A. So far as I am aware, there is no treatment other than perhaps
sedation for AS. For my part I would prefer to let dogs have some quality of life and risk
sudden death or fainting, but!!! In any case it is only the Grade 4s and above which are
at risk. Very few Grade 3s and no Grade 2s develop clinical symptoms. For BCM there are
surely some treatments possible, but I know little about this disease. Obviously, one
should not treat to allow breeding, only to alleviate pain, etc.
Q. Does AS worsen with age?
A. Supposedly not, but I have cited one case that did. It is
supposed to develop with age from puppyhood through to adulthood. Having said this, I have
no evidence from all my records to support this. Aside from the latter this is really a
veterinary question and should not be addressed to me.
Q. Do dogs with BCM typically have problems with SAS, too?
A. I have already commented above on the tendency for dogs to have
more than one heart condition.
I am afraid that this response is no more than an off the cuff answer to
Linda's questions. AS is a complex problem. I cannot have done it much justice, but this
is my immediate response to what I regard as a very delicate and perplexing situation.
I finish up by drawing attention once again to the finding that the
application of simple sound breeding principles can achieve much. Don't get bogged down
with the difficulties.
Bruce