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AORTIC STENOSIS IN THE BOXER
By Bruce Cattanach
Boxer '92
(pages 10-16)
BASIC INFORMATION ON
AORTIC STENOSIS IN BOXERS AND PROPOSED INTERIM MEASURES FOR ITS CONTROL.
1. BACKGROUND
1.1 A number of heart
conditions are known in the dog. These include aortic stenosis, pulmonic
stenosis, cardiomyopathy, mitral valve degeneration and myocarditis.
Mitral valve degeneration commonly occurs in Cavalier King Charles
Spaniels but has not been reported in Boxers; myocarditis is caused by
infections, such as parvo-virus, and therefore can occur in all breeds,
but is known to be a cause of puppy deaths in Boxers. The remaining
three conditions, notably aortic stenosis, have been found in Boxers and
are the major cause of fainting and collapse, as well as sudden death
generally ascribed to heart disease in the breed.
1.2 Aortic stenosis
has been reported to occur with high frequencies in a number of breeds.
Notably Newfoundlands and Golden Retrievers in North America. High
incidences have also been observed in Boxers, however. At a recent (Oct.
1991) cardiovascular conference in Vienna, vets from various parts of
the world were in agreement that exceptionally high incidences of aortic
stenosis generally occur in the breed.
2. THE SITUATION
IN THE U.K.
2.1 U.K. Boxers have
also been recognised by the veterinary profession to be particularly
subject to aortic stenosis. Moreover, there is some indication that the
frequency of clinical cases (showing symptoms or dying) is rising. At
Edinburgh Veterinary School, Boxers referred to the cardiology group
have represented almost 40% of cases of aortic stenosis found across all
breeds in recent years. Cambridge Veterinary School has also reported
aortic stenosis (and cardiomyopathy) as a major problem in present-day
Boxers. Furthermore, even Boxer breeders have become aware of unusually
high incidences of heart-associated sudden deaths among Boxers over the
last 5 or more years. Data has been collated on such deaths and reported
to Breed Council at their meetings since 1987.
3. VETERINARY ASPECTS
3.1 Aortic stenosis
is a heart abnormality in which fibrous tissue develops in or close to
the aortic valve narrowing the aperture. Because of this narrowing (stenosis),
the blood is forced through the valve faster and this results in a
turbulence that can be heard on stethoscopic examination. Generally,
there is a good correlation between degree of stenosis and volume of
sound. The range of stenosis is wide; minor stenosis does not result in
clinical effects; more major stenosis results in collapsing, especially
with sudden exercise or even death.
3.2 Aortic stenosis
may occur in very young (4 months) puppies when it may be so severe as
to cause sudden death. More typically, it develops rapidly in dogs
between 6 and 12 months of age after which progression may decline so
that the condition probably does not worsen greatly with increasing age.
The most severe cases therefore tend to develop clinical signs or die as
young adults.
3.3 Pulmonic stenosis
represents a narrowing of the pulmonic valve. The sound so caused cannot
be clearly distinguished from that due to aortic stenosis by
stethoscopic examination but can be distinguished by more sophisticated
methods such as Doppler echocardiography (see 4.3). The clinical signs
may be similar.
3.4 Cardiomyopathy is
an entirely different form of heart disease. It is usually distinguished
by irregular heart beats on stethoscopic examination and causes other
clinical signs such as fluid on the lungs and abdomen, coughing and
general lethargy. Port-mortem examination can confirm the cause of
deaths due to aortic stenosis pulmonic stenosis, or cardiomyopathy, as
well as myocarditis.
4. DIAGNOSIS OF AORTIC
STENOSIS
4.1 STETHOSCOPIC
EXAMINATION
4.1.1 Stethoscopic
examination can be used as a method of screening for aortic stenosis.
Specialist cardiologists are able to grade the sounds (heart murmurs)
and this is now standardly done on a scale of I (minor) to VI (major).
General veterinary practitioners may only detect louder murmurs.
4.1.2 As already
indicated (3.3), murmurs attributable to stenosis of the pulmonic valve
cannot be usually distinguished from those due to aortic stenosis;
further testing is necessary to identify which valve is affected.
4.1.3 More
importantly, purportedly innocent 'flow' murmurs can be confused with
established stenosis murmurs. 'Flow' murmurs are commonly found in young
puppies (-3 months) but usually disappear by 6 months of age. Their
relationship, if any, to stenosis in adults is not known. However,
'flow' murmurs may also be heard in adult dogs when they are usually of
mild degree (grade I). Typically, they are variable such that they may
be heard on some occasions but not on others. While the significance of
these adult 'flow' murmurs is not yet understood, 'flow' murmurs in
Newfoundlands are associated with mild degree of fibrous tissue in the
aorta, and it has been observed that 'flow' murmurs are rarely found in
breeds that have low incidences of aortic stenosis.
4.1.4 The general
conclusions are therefore that dogs which are free of heart murmurs
(HM-free) are unlikely to have aortic (or pulmonic) stenosis; and those
with minor murmurs which cannot be consistently heard ('flow' murmurs)
are also unlikely to have any physical form of valvular stenosis.
4.1.5 Stethoscopic
examination can also detect cardiomyopathy and myocarditis. Other
systems, together with post-mortem examination findings can confirm
diagnosis of these conditions.
4.2 ULTRASOUND
SCANNING
4.2.1 This painless
procedure, carried out without anaesthesia, enables the internal anatomy
of the heart to be seen. A thickening of the heart walls or abnormality
of the valves may be distinguished. Fibrous tissue in or close to the
valves may be seen.
4.2.2 Both aortic and
pulmonic stenosis may be distinguished in this test but minor degrees of
affect may not be detectable.
4.3 DOPPLER
ECHOCARDIOGRAPHY
4.3.1 This procedure
is usually carried out concurrently with ultrasound scanning when
equipment is available and is the most effective method of detecting and
quantitating aortic (and pulmonic) stenosis. It does this by directly
measuring the velocity of blood flow through the valves.
4.3.2 The accepted
upper limit of normal blood velocity through the aortic valve is 1.5
metre/second; velocities ranging up to 2.0 metre/second are taken to
correspond with 'flow' murmurs; but yet higher velocities are attributed
to aortic stenosis. Maximal velocities are 6-7 metres/ second. With the
highest velocities, life expectancy is usually short; with intermediate
velocities, clinical signs may be seen in some dogs but not others.
Doppler echocardiography serves as the key test for functional aortic
stenosis.
4.4 POST-MORTEM
EXAMINATION
4.4.1 Post-mortem
examination remains the ultimate method of ascertaining the
presence/absence of aortic stenosis (and other heart conditions). Even
minor amounts of fibrous tissue can be detected.
5. RESULTS OF RECENT
HEART SCREENING IN UK BOXERS
5.1 The screening
clinics held at six shows over the period August 1990- August 1991 have
revealed that, overall, 54% of Boxers tested were HM-free, 24% had Grade
I murmurs, 16% had Grade II murmurs, and 5% and 1 % had Grade III and IV
murmurs, respectively.
5.2 Very few of these
dogs have yet been taken for follow-up ultrasound scanning and Doppler
echocardiography. However, so far, all dogs with Grade I murmurs have
been shown to have blood velocities within the normal to 'flow' ranges
(up to 2.0 metres/sec). Evidence of aortic stenosis has been found in a
major proportion of dogs with Grade II murmurs, and all but two dogs
with Grade III murmurs have been shown to have abnormally high blood
velocities consistent with aortic stenosis.
5.3 The observed high
incidence of heart murmurs together with the direct evidence of aortic
stenosis in the various veterinary schools confirms that aortic stenosis
is a problem in UK Boxers, as elsewhere.
6. GENETIC ASPECTS
6.1 The inheritance
of aortic stenosis has been investigated in Newfoundlands. In this breed
the mode of inheritance appears as that of a dominant gene with variable
expression, i.e. other genetic factors may be involved. If verified, the
inheritance could be modelled on that of the dominance of the gene for
brindle over its recessive form, red; although dominant to red, brindle
shows a range of expression from minor degree, golden brindle to major
degree, 'black' brindle. The variation in degree of aortic stenosis may
be so understood.
6.2 On the basis of
such a dominant inheritance, any dog carrying the gene for aortic
stenosis (As) would be expected to transmit this gene to approximately
half its progeny, irrespective of its own grade of murmur or level of
stenosis. About half their progeny from crosses with HM- free dogs would
therefore have some level of stenosis, whereas about 75% of the progeny
from crosses between two As carriers (affected) would have some degree
of affect. Both crosses could produce normal progeny, these occurring
with frequencies of approximately 50% and 25%, respectively. Crosses
between two carriers would also be expected to produce progeny carrying
two doses of the As gene. Such dogs have not yet been identified; they
might be so severely affected that the onset occurs very early -
possibly even within a few days of birth.
6.3 A further
important expectation for the dominant form of inheritance is that
normal, HM-free dogs when mated together would produce only normal
progeny. How true this will prove will depend upon the certainty with
which normal dogs can be distinguished from those with the mildest
degrees of stenosis. To date, amongst the very limited amount of Boxer
breeding data available, affected dogs have always proven to have at
least one affected, or potentially (heart murmur) affected parent.
6.4 It is still
possible that aortic stenosis will show a multifactorial inheritance in
Boxers, such as established for HD in a number of breeds. In this case,
a less clear pattern of inheritance would be evident and it would be
less unexpected for two unaffected (normal) parents to produce some
affected pups. Nevertheless, as with HD, the least affected parents
would, overall, be expected to produce fewer, less affected puppies.
6.5 Despite the
possibility of a multifactorial inheritance, it might be noted that
aortic stenosis in humans is generally regarded as showing something
closer to a single gene, rather than a multifactorial inheritance. It
has also been predicted that Golden Retrievers, which in North America
show a high incidence of heart murmurs and established cases of aortic
stenosis, will show the similar dominant-type of inheritance to that
indicated in Newfoundlands. On the same basis, aortic stenosis not only
may be expected to be inherited in Boxers, but a dominant-type mode of
inheritance would seem most probable.
7. FUTURE RESEARCH NEEDS
7.1 For the breed as
a whole, further heart screening at a series of shows throughout the
country over a number of years is needed in order to monitor the
situation and provide research information.
7.2 For individual
breeders, regular heart screening clinics are necessary to allow them to
conduct their own family studies and to identify HM- free dogs that can
be used to produce sound, aortic stenosis free stock.
7.3 As no studies
have yet been carried out upon 'normal' Boxer hearts, there is a clear
need to evaluate HM--free dogs by ultrasound scanning and Doppler
echocardiography. Edinburgh veterinary school (see list of diagnostic
centres) has offered to examine such normal dogs for research purposes
at no charge. Bristol (Langford) Veterinary School has also indicated a
willingness to test a few normal dogs by the above methods. Breeder’s
cooperation is required.
7.4 Much further
information is needed to establish firmly the correlation between grade
of murmur and velocity of blood flow and assess the meaning of those
exceptions to the correlation that are detected. In particular, the
significance of the lower grade murmurs and their distinction from
'flow' murmurs needs elucidation. It is therefore essential that
additional animals with different grades of murmur be investigated by
ultrasound scanning and Doppler echocardiography to provide substantive
information on the variable levels of aortic stenosis. Such testing
would also provide individual breeders with a quantitative
assessment of the severity of any effect in their own dogs or,
alternatively establish normality despite the existence of murmurs.
Costs at Edinburgh have been set at £25, and £30 at Bristol. Cambridge
and London (Dr Cobb) can undertake such testing as a service at a cost
of about £80 (see list of diagnostic centres). Breeder cooperation is
required.
7.5 Post-mortem
evidence on the hearts of Boxers that have died of aortic stenosis (or
other heart conditions) is as yet limited. There is therefore a need to
have hearts of dogs that have died of any suspected heart condition sent
to the veterinary schools for final diagnosis and direct evaluation of
the degree of any aortic stenosis found. It would be particularly useful
if the hearts of dogs which had screened for heart murmurs at any age
could be made available. There would be no charge for such investigation
at Edinburgh; costs elsewhere have yet to be determined. Breeder
cooperation would be appreciated.
7.6 Post-mortem
examination of the hearts of dogs that had previously been shown to the
HM-free could also help characterise the normal Boxer heart. Such hearts
are being sought by the veterinary schools, notably Edinburgh, for this
purpose. Breeder cooperation would be appreciated.
7.7 The possibility
exists that some early puppy deaths (within a few days of birth to a few
weeks) might in some case be due to heart abnormality (Para 6.2). London
Veterinary School (specifically Dr Brownlie) has expressed an interest
in investigating such early puppy deaths.
7.8 Research upon the
treatment of dogs suffering from aortic stenosis (and other heart
conditions) is in progress in several of the veterinary schools,
certainly in Edinburgh and in London (Dr Brownlie) where the work is
being conducted in collaboration with Guys' Hospital Medical School.
Owners of dogs with aortic stenosis therefore now have the opportunity
of alleviating the disabling effects of the condition while incidentally
contributing towards human medicine.
References
O'Grady, M.F. et a/. Canine congenital aortic stenosis: A
review of the literature and commentary. Can. Vet. J. 30:811-815
(1989).
Patterson, D.F. Congenital defects of the cardiovascular system of dogs:
Studies in comparative cardiology. Adv. Vet. Sci. Compo Med. 20:1-37
(1976).
Pyle, R.L. et a/. The genetics and pathology of discrete sub
aortic stenosis in the Newfoundland dog. Am. Heart Jour. 92:324-334
(1976).
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