Mental Disorders Clinical Trial
Official title:
Biomarkers of Cardiometabolic Risk in Children Treated With Antipsychotics: A Preliminary Study of Direct Measures
The proposed study aims to begin the multi-step process of establishing the reliability and validity of hepatic triglyceride content (HTGC) and carotid artery intima-media thickness (IMT) as biomarkers of cardiometablic risk in children treated for mental illness. The distribution of HTGC and carotid IMT—proximate indicators of cardiometabolic risk—across a range of dual-energy X-ray absorptiometry (DEXA)-measured adiposity in children treated with antipsychotic agents will be characterized in comparison to healthy, untreated, non-psychiatric controls, in order to estimate effect sizes for future studies incorporating these markers. The ability of HTGC and IMT to predict cardiometabolic risk as measured by commonly-used laboratory tests, such as fasting lipids, liver function tests, C-reactive protein and serum fibrinogen, will be assessed.
Carotid artery intima media wall thickness (IMT) is one of the most developed biomarkers of
cardiometabolic risk, with established reliability and predictive validity, and has been
utilized as a surrogate endpoint for cardiovascular disease progression in FDA-reviewed
registration studies. This technique has also been used in children and adolescents without
psychiatric disorders, indicating that changes in IMT are positively correlated with
metabolic syndrome criteria. Magnetic Resonance Spectroscopy (1H MRS) to quantify hepatic
triglyceride content (HTGC) is a promising new marker of cardiometabolic risk, especially
given the importance of nocturnal circulating free fatty acids in the development of insulin
resistance leading to type 2 diabetes. Fatty liver, related in part to obesity, is the most
common liver abnormality found in children ages 2-19, with one in ten children manifesting
signs of macrovascular steatohepatitis. 1H MRS is a well-established methodology used to
measure HTGC that correlates well with liver biopsy results. This technique has been studied
in obese children without psychiatric disorders, and is widely considered to be the optimal
noninvasive means by which to measure HTGC. Unfortunately, neither of these promising methods
have been applied to the study of cardiometabolic risk in children with psychiatric
disorders.
It is important to now study these biomarkers in psychiatric populations, where individuals
are subject to treatments that can increase risk. Our group is experienced in the application
of sophisticated, gold standard techniques for measuring cardiometabolic risk in psychiatric
populations, and is—to our knowledge—the only group in the US using sensitive methodologies
like stable isotopomer euglycemic clamps to study the pathophysiology leading to diabetes and
cardiovascular disease in the mentally ill. An important goal of studying these biomarkers is
to ultimately determine which of the more commonly available conventional risk measures
(e.g., lipid profiles, adiposity measures) can be used alone or in combination to accurately
identify children at highest risk, to aid in the development and targeting of effective
interventions.
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