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Principal Investigator: MARK C CHAPPELL
Organization: WAKE FOREST UNIVERSITY HEALTH SCIENCES
Fiscal Year: 2022
Award: $774,719
Funding agency: National Heart Lung and Blood Institute
ABSTRACT
Hypertension is the leading risk factor for cardiovascular disease, is highly prevalent with high lifetime
cumulative incidence rates, and is the leading cause of death compared to any other risk factor. Premature
birth is an emerging and important risk factor for hypertension and cardiovascular disease, as both preterm
birth rates and infant survival increase worldwide. Hypertension and cardiovascular disease begin in early
adulthood in individuals born prematurely, but the reasons – especially in regard to the role of preterm birth –
are unknown. An improved understanding of why hypertension and cardiovascular disease occur in early
adulthood in individuals born preterm will enable the development of prevention and treatment strategies to
mitigate the burden of cardiovascular disease. Salt sensitivity of blood pressure (SSBP; the change in blood
pressure in response to a change in salt intake) is an emerging risk factor for hypertension and cardiovascular
disease. However, little is known about the pathophysiology of SSBP, which limits its treatment and prevention.
Individuals born preterm may be at higher risk for SSBP, but this too is unknown. Uric acid, which is higher in
those born preterm due to altered uric acid metabolism, has been linked to development of SSBP in preclinical
studies, but this concept has not been investigated in human trials. Uric acid may lead to SSBP via changes in
klotho and the renin-angiotensin system, notably increased angiotensin II and decreased angiotensin-(1-7) in
the renal proximal tubules. In individuals born preterm compared to those born at full term, higher uric acid
correlates with higher blood pressure, altered renal sodium handling, decreased klotho, increased angiotensin
II, and decreased angiotensin-(1-7). Thus, the proposed study will determine the prevalence of SSBP in young
adults born preterm versus full-term and will initiate (a) a clinical trial testing the effect of blocking uric acid
production with allopurinol on SSBP, and (b) a mechanistic study evaluating uric acid's effects on the renin-
angiotensin system and klotho in human renal proximal tubule cells. We hypothesize that (i) more young adults
with SSBP will have been born preterm versus full-term; (ii) mitigation of uric acid levels will reduce the
proportion of young adults born preterm with SSBP, vascular stiffness, and autonomic dysfunction; and (iii) uric
acid will promote oxidative stress within human proximal tubule cells, resulting greater angiotensin II relative to
angiotensin-(1-7) and diminished klotho. Our team is co-led by experienced and senior investigators with
extensive experience in the preterm and term cohort, the influence of programing events on hypertension and
internationally recognized expertise in the renin-angiotensin system and renal models of hypertensive disease.
Our results will establish the role of uric acid in SSBP among individuals born preterm, thus providing evidence
for the mechanisms behind the increased risk of hypertension and cardiovascular disease in individuals born
prematurely.
Terms: <12-20 years old><21+ years old><ACE2><Address><Adolescence><Adolescent and Young Adult><Adult><Adult Human><Affect><Allopurinol><Ang I (1-7)><AngII><Angiotensin II><Angiotensinogen><Attenuated><Autonomic Dysfunction><Baroreceptor Reflex><Baroreflex><Biological Markers><Birth Rate><Blood><Blood Plasma><Blood Pressure><Blood Reticuloendothelial System><Blood Serum><Blood Vessels><CD10 Antigens><Cardiovascular Diseases><Cause of Death><Cell Body><Cells><Childhood><Clinical><Clinical Trials><Data><Development><Diuresis><Doctor of Philosophy><Dysfunction><Endogenous Nitrate Vasodilator><Endothelium-Derived Nitric Oxide><Enkephalinase><Epithelial Cells><Event><Exhibits><Frequencies><Functional disorder><Future><Generations><Hour><Human><Hydrogen Oxide><Hypertensinogen><Hypertension><Impairment><Incidence><Individual><Infant><Intermediary Metabolism><International><Investigators><Kidney><Kidney Urinary System><Lead><Life><Link><Low-Salt Diet><Low-Sodium Diet><Mediating><Membrane Metalloendopeptidase><Metabolic Processes><Metabolism><Modeling><Modern Man><Monitor><Mononitrogen Monoxide><Na element><Natriuresis><Neprilysin><Neutral Endopeptidase><Nitric Oxide><Nitrogen Monoxide><Nitrogen Protoxide><Oxidative Stress><Participant><Pb element><Ph.D.><PhD><Physiologic pulse><Physiopathology><Plasma><Plasma Serum><Premature Birth><Prematurely delivering><Preterm Birth><Prevalence><Preventative strategy><Prevention><Prevention strategy><Preventive strategy><Proangiotensin><Production><Proteins><Proximal Kidney Tubules><Pulse><Receptor Protein><Renin-Angiotensin System><Renin-Substrate><Research><Research Personnel><Researchers><Reticuloendothelial System, Serum, Plasma><Risk><Risk Factors><Role><Serum><Sigapurol><Sodium><Sodium Chloride><Sodium-Restricted Diet><System><Testing><Trioxopurine><Tubular><Tubular formation><Uric Acid><Urine><Urine Urinary System><Vascular Hypertensive Disease><Vascular Hypertensive Disorder><Water><adolescence (12-20)><adult youth><adulthood><angiotensin I (1-7)><angiotensin converting enzyme 2><angiotensin converting enzyme II><angiotensin-(1-7)><anti aging><anti aging drug><anti aging medicine><antiaging><antiaging drug><antiaging medicine><arm><bio-markers><biologic marker><biomarker><blood pressure elevation><cardiovascular disorder><cardiovascular risk><cardiovascular risk factor><cohort><developmental><early adulthood><elevated blood pressure><emerging adult><endothelial cell derived relaxing factor><experience><experiment><experimental research><experimental study><fetal><heart rate variability><heavy metal Pb><heavy metal lead><high blood pressure><high risk><human data><hyperpiesia><hyperpiesis><hypertensive disease><hypertensive disorder><improved><increase in blood pressure><increased blood pressure><indexing><individual response><individualized response><neural mechanism><neuromechanism><new drug treatments><new drugs><new therapeutics><new therapy><next generation therapeutics><novel drug treatments><novel drugs><novel therapeutics><novel therapy><pathophysiology><pediatric><peer><pre-clinical study><preclinical study><premature><premature childbirth><premature delivery><prematurity><pressure><preterm delivery><prevent><preventing><programs><prospective><receptor><renal><renal epithelium><renal proximal tubule><response><response to therapy><response to treatment><salt><salt intake><social role><therapeutic response><therapy response><treatment response><treatment strategy><urinary><vascular><young adult><young adulthood>