THE IMMUNOCYTOCHEMICAL DEMONSTRATION OF A RELATIVE LACK OF NERVE-FIBERS IN THE ATRIOVENTRICULAR NODE AND BUNDLE OF HIS IN THE SUDDEN-INFANT-DEATH-SYNDROME (SIDS)
C. Fu et al., THE IMMUNOCYTOCHEMICAL DEMONSTRATION OF A RELATIVE LACK OF NERVE-FIBERS IN THE ATRIOVENTRICULAR NODE AND BUNDLE OF HIS IN THE SUDDEN-INFANT-DEATH-SYNDROME (SIDS), Forensic science international, 66(3), 1994, pp. 175-185
Whilst examining the variation with age of the nerve fibre content of
the cardiac conduction system (CCS), using an immunocytochemical appro
ach, it became evident that in two sudden infant death syndrome (SIDS)
cases there was a selective lack of S100 positive nerve fibres in the
atrioventricular (AV) node and His bundle. In the present study there
fore, the examination of CCS with S100 was extended to a further five
SIDS cases and three cases of sudden explained death. Also, in additio
n to S100 - which selectively marks Schwann cells associated with both
myelinated and non-myelinated nerves - PGP 9.5 (protein gene product)
was used to reveal the presence of nerve axonal elements associated w
ith the CCS. The results showed a uniform presence of S100 and PGP 9.5
positive nerve fibres in the sinoatrial (SA) node, the AV node and Hi
s bundle tissue of all three control cases. In contrast, five out of s
even SIDS cases showed a uniform lack of staining with these markers i
n the AV node and His bundle tissue, whilst in the two remaining cases
it was present in greatly diminished amounts. Staining in the SA node
, although present in all seven cases, was reduced when compared with
the control cases. This is the first time the CCS of SIDS cases has be
en studied with immunocytochemical markers of nerve elements. The over
all results taken in conjunction with the epidemiology of SIDS suggest
that the lack of AV node and His bundle innervation most probably ref
lects a delay in the development or maturation of the nerve elements o
f the CCS, similar to that noted for other parts of the central and pe
ripheral nervous systems in SIDS.