Coronary Artery Disease Clinical Trial
Official title:
Innate Human Collateral Supply to Different Vascular Regions
Both clinical and experimental studies demonstrate the importance of the pre-existing, ie
innate collateral supply in different vascular regions. Furthermore, pathophysiological
considerations and experimental data imply an important role for the association of
collateral function between different vascular regions.
STUDY HYPOTHESES 1. In the absence of atherosclerotic stenoses, there is a direct
association between the collateral function in the coronary, renal and peripheral
circulation. 2. The increase in plasma renin in response to a unilateral main renal artery
balloon occlusion is inversely related to its functional collateral supply. 3. The decrease
in renal vein oxygen saturation in response to a unilateral main renal artery occlusion is
inversely related to its functional collateral supply.
Background
PROTECTIVE EFFECT AND INTER-INDIVIDUAL DISTRIBUTION OF THE COLLATERAL CIRCULATION IN
DIFFERENT VASCULAR REGIONS
Of all vascular regions, the collateral circulation of the heart is probably the most
extensively studied since the initial studies by Fulton.1 The clinical importance of the
coronary collateral circulation2 has been established by numerous investigations
demonstrating a protective role of well vs. poorly grown coronary collateral arteries.
Whereas involvement of the peripheral arterial network by obstructive arterial disease is
frequently asymptomatic, it is, nevertheless, relevant through the association with
increased mortality and as a strong predictor of adverse cardiovascular outcomes. The
clinical relevance of the collateral circulation in the lower extremities can be epitomized
by the discrepancy of frequently encountered long segmental occlusions and the rare
occurrence of severe ischemia or amputation. With regard to a systematic evaluation of this
apparently well-collateralized region, it was, however, only very recently that assessment
using a direct and quantitative method was performed.
Regarding the kidney, the collateral circulation has hitherto been subject to systematic
research only in experimental studies,while data in humans are sparse and limited to
angiographic assessment. While the hypertensive effect of renal arterial constriction is
well-known since the seminal studies of Goldblatt in 1934, the effect of renal collaterals
in this context has been neglected despite the readily apparent effects therefrom in the
same experiment. The duration of the ensuing hypertension was only short in Goldblatt's
experiments with dogs, an observation explained by the abating effect of efficient
collaterals on renal artery constriction and consequently developing reduction of the renal
ischemia. In humans, only limited and indirect data on the compensatory effect of the renal
collateral circulation in the setting of renal arterial constriction exist.The ratio of
selective renin concentrations sampled from the renal vein of both kidneys
(affected/unaffected) is commonly used to assess the hemodynamic significance of a
unilateral renal artery stenosis. Ernst et al., in 37 patients with unilateral renal
stenosis, determined the (selective) renal vein renin ratio and additionally performed
angiography for presence of renal collaterals( documented in 68%). Renal collaterals tended
to normalize renin excretion in a kidney affected by renal artery stenosis. Indeed, 7
patients with a severe stenosis and visible renal collaterals had a normal renin ratio below
the cut-off of 1.4. The clinical relevance of renal artery stenosis is underscored by its
prevalence in a significant proportion of patients undergoing routine cardiac
angiography.22, 23 In the above context, it is noteworthy that hypertension is not present
in almost one half of patients with angiographically significant narrowing of a renal
artery.
PRE-EXISTING COLLATERAL CIRCULATION AND ITS INTRA-INDIVIDUAL DISTRIBUTION As alluded to
before, acute vascular occlusion in arteriosclerosis can ensue in the absence of relevant
narrowing. In this situation, solely the native, pre-existing collateral extent can lessen
the ischemic tissue injury. On the other hand, the gradual narrowing of a vessel allows
development of large arterial anastomoses from pre-existing smaller arterioles in the
process known as arteriogenesis. The notion that the pre-existing collateral extent
nevertheless remains the basis for the capacity of anastomoses to enlarge is supported by an
instructive experimental study by Zbinden et al.: Flow recovery after superficial femoral
artery ligation correlated strikingly with the pre-existing collateral extent. Thus, mice
with an already high level of pre-existing collaterals had concordantly high flow recovery,
while mice with low levels of pre-existing collaterals had low flow recovery.
Given the systemic process of atherosclerosis, the preformed or innate human collateral
function in the different vascular regions mentioned before is of interest. On a patient
level, this relates to the intra-, as opposed to the inter-individual distribution of the
collateral network. While the inter-individual distribution of collateral function in humans
has been shown to vary widely also in the absence of vascular narrowings, recent
experimental studies in mice have shown that innate collateral extent is shared
qualitatively in different tissues. However, in humans, the association between the
collateral function in different vascular regions in humans has so far not been
investigated.
In conclusion, both clinical and experimental studies demonstrate the importance of the
pre-existing, ie innate collateral supply in different vascular regions. Furthermore,
pathophysiological considerations and experimental data imply an important role for the
association of collateral function between different vascular regions.
Objective
To determine the in vivo prevalence and distribution of functional collateral supply in the
coronary, renal and peripheral circulation, and the intra-individual association of
collateral function between the different vascular territories. Additionally, the effect of
renal collaterals on the response of the kidney to a short bout of ischemia will be
investigated.
Methods
DESIGN Prospective, comparative observational study with collateral function measurements in
the coronary, renal and superficial femoral artery.
PRIMARY STUDY ENDPOINT Pressure-derived collateral flow index (CFI) SECONDARY STUDY
ENDPOINTS Intracoronary ECG ST segment shift during temporary coronary balloon occlusion;
plasma renin concentration before, immediately and 10 minutes after main renal artery
occlusion, sampled from the suprarenal inferior vena cava ; transcutaneous oxygen tension
(tcpO2) as obtained during left superficial femoral artery occlusion from the left
anteromedial lower leg.
;
Observational Model: Cohort, Time Perspective: Prospective
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