TY - JOUR
T1 - Chronobiologically-interpreted ABPM reveals another vascular variability anomaly (VVA)
T2 - Excessive pulse pressure product (PPP) updated conference report
AU - Cornelissen-Guillaume, Germaine G
AU - Siegelova, Jarmila
AU - Watanabe, Yoshihiko
AU - Otsuka, Kuniaki
AU - Halberg, And Franz
PY - 2012
Y1 - 2012
N2 - To assess the risk associated with an Excessive Pulse Pressure Product (EPPP, where PPP = systolic blood pressure x heart rate / 100), PPP was determined from Chronobiologically and chronomically interpreted aroundthe- clock Ambulatory Blood Pressure Monitoring (CABPM) and related to outcomes in three different investigations, carried out in the Czech Republic, Japan, and Taiwan. In these three outcome studies, values of PPP above 100 were associated with a statistically significant increase in cardiovascular disease risk. As such, EPPP in a 7-day or longer around-the-clock record qualifies as a new Vascular Variability Anomaly (VVA), or, if it persists in a series of 7-day records, a Vascular Variability Disorder (VVD). Being the product of blood pressure and heart rate, EPPP is not independent from MESOR-hypertension. The extent to which EPPP may contribute additive cardiovascular disease risk to other VVDs will require larger outcome studies capable of separating the risk associated with each VVD. In any event, PPP offers itself as another harbinger of risk, as a gauge for the optimization of treatment by timing, and as a variable with a time structure of its own, differing in terms of components with long periods found in time series covering decades from concomitantly measured systolic and diastolic blood pressure and heart rate. Since cardiovascular disease risk is dramatically increased by the co-existence of several VVAs (up to 100% in a 6-year prospective outcome study), sole reliance on the mean without consideration of other VVAs can no longer be forgiven as ignorance and should rather be viewed as indolence, eventually even as criminal negligence.
AB - To assess the risk associated with an Excessive Pulse Pressure Product (EPPP, where PPP = systolic blood pressure x heart rate / 100), PPP was determined from Chronobiologically and chronomically interpreted aroundthe- clock Ambulatory Blood Pressure Monitoring (CABPM) and related to outcomes in three different investigations, carried out in the Czech Republic, Japan, and Taiwan. In these three outcome studies, values of PPP above 100 were associated with a statistically significant increase in cardiovascular disease risk. As such, EPPP in a 7-day or longer around-the-clock record qualifies as a new Vascular Variability Anomaly (VVA), or, if it persists in a series of 7-day records, a Vascular Variability Disorder (VVD). Being the product of blood pressure and heart rate, EPPP is not independent from MESOR-hypertension. The extent to which EPPP may contribute additive cardiovascular disease risk to other VVDs will require larger outcome studies capable of separating the risk associated with each VVD. In any event, PPP offers itself as another harbinger of risk, as a gauge for the optimization of treatment by timing, and as a variable with a time structure of its own, differing in terms of components with long periods found in time series covering decades from concomitantly measured systolic and diastolic blood pressure and heart rate. Since cardiovascular disease risk is dramatically increased by the co-existence of several VVAs (up to 100% in a 6-year prospective outcome study), sole reliance on the mean without consideration of other VVAs can no longer be forgiven as ignorance and should rather be viewed as indolence, eventually even as criminal negligence.
KW - Ambulatory blood pressure monitoring
KW - Cardiovascular disease risk
KW - Outcome
KW - Pulse pressure product (PPP)
KW - Vascular variability disorder (VVD)
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M3 - Article
AN - SCOPUS:84892428846
SN - 1556-4002
VL - 4
SP - 237
EP - 245
JO - World Heart Journal
JF - World Heart Journal
IS - 4
ER -