17 results match your criteria: "University of North Carolina Nutrition Research Institute[Affiliation]"

Genetic admixture predictors of fetal alcohol spectrum disorders (FASD) in a South African population.

Gene

December 2024

Department of Neurology and the Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Columbia University Vagelos College of Physicians and Surgeons, Columbia University Irving Medical Center, New York, NY, USA. Electronic address:

Article Synopsis
  • Ancestrally admixed populations, like the South African Cape Coloured (SACC), are underrepresented in genetic studies of complex diseases, which typically focus on European-descent populations, leading to a lack of understanding of their unique genetic features.
  • The study examined the genetic admixture and its associations with fetal alcohol spectrum disorders (FASD) in the SACC population, using data from two longitudinal birth cohorts that looked at prenatal alcohol exposure effects on development.
  • Findings revealed a high prevalence of rare genetic variants and significant associations between ancestry profiles and FASD outcomes, suggesting that the SACC population could provide insights for identifying disease-associated genetic loci in FASD and potentially other conditions.
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Differential effects of calorie restriction and rapamycin on age-related molecular and functional changes in skeletal muscle.

Exp Gerontol

August 2022

Department of Nutrition, University of North Carolina, Chapel Hill, NC, USA; Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA; University of North Carolina Nutrition Research Institute in Kannapolis, NC, USA.

Aging is a multifactorial process associated with progressive degradation of physiological integrity and function. One of the greatest factors contributing to the deleterious effects of aging is the decline of functional ability due to loss of muscle mass, strength, and function, a condition termed sarcopenia. Calorie restriction (CR) has consistently been shown to extend lifespan and delay the onset and progression of various age-related diseases, including sarcopenia.

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Background: This study aimed to develop an efficient and easily calculable risk score that can be used to identify an individual's risk of having been exposed to alcohol prenatally.

Methods: Data for this study were collected as part of the Collaborative Initiative on Fetal Alcohol Spectrum Disorders, Phases 2 and 3. Two cohorts (ages 5 to 17 years) completed a comprehensive neurobehavioral battery and a standard dysmorphology exam: a development cohort (DC; n = 325) and a comparative cohort (CC; n = 523).

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Background: Rating scales are designed to complement traditional performance-based measures, and both can provide useful information about the functioning of youth with histories of prenatal alcohol exposure. Few studies, however, have compared ratings from multiple informants or the relationship between these subjective rating scale scores and the objective results from laboratory performance-based scales.

Methods: The current study addressed both of these questions in 3 study groups: children with histories of prenatal alcohol exposure (n = 47), attention-deficit/hyperactivity disorder (ADHD; n = 41), and typically developing controls (CON; n = 73).

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Quantifying Medication Exposure in Very Low Birth Weight Neonates.

Am J Perinatol

March 2021

Department of Nutrition, University of North Carolina Nutrition Research Institute, University of North Carolina Chapel Hill, Kannapolis, North Carolina.

Objective: Very low birth weight (VLBW) infants are exposed to medications with insufficient evidence describing pharmacokinetics and safety. Objective was to quantify and identify risk factors associated with the highest quartile of medication exposure.

Study Design: Retrospective record review of VLBW infants admitted to a level-IV neonatal intensive care unit (NICU).

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A Unique Morphological Phenotype in Chemoresistant Triple-Negative Breast Cancer Reveals Metabolic Reprogramming and PLIN4 Expression as a Molecular Vulnerability.

Mol Cancer Res

December 2019

Segal Cancer Center, Lady Davis Institute for Medical Research, Sir Mortimer B. Davis Jewish General Hospital, McGill University, Montréal, Québec, Canada.

The major obstacle in successfully treating triple-negative breast cancer (TNBC) is resistance to cytotoxic chemotherapy, the mainstay of treatment in this disease. Previous preclinical models of chemoresistance in TNBC have suffered from a lack of clinical relevance. Using a single high dose chemotherapy treatment, we developed a novel MDA-MB-436 cell-based model of chemoresistance characterized by a unique and complex morphologic phenotype, which consists of polyploid giant cancer cells giving rise to neuron-like mononuclear daughter cells filled with smaller but functional mitochondria and numerous lipid droplets.

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Choline has been recognized as an essential nutrient by the Food and Nutrition Board of the National Academies of Medicine since 1998. Its metabolites have structural, metabolic, and regulatory roles within the body. Humans can endogenously produce small amounts of choline via the hepatic phosphatidylethanolamine -methyltransferase pathway.

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Background: Adaptive function and general intellectual function are two important and often correlated domains. While youth with prenatal alcohol exposure frequently demonstrate impairments in both domains, it is not clear whether the relation between these domains is consistent across levels of ability or whether, for example, adaptive function is less affected by intellectual function at higher ability levels. The aim of the current study was to test this relation in youth with and without prenatal alcohol exposure.

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Obesity is associated with increased risk and poor prognosis of many types of cancers. Several obesity-related host factors involved in systemic metabolism can influence tumor initiation, progression, and/or response to therapy, and these have been implicated as key contributors to the complex effects of obesity on cancer incidence and outcomes. Such host factors include systemic metabolic regulators including insulin, insulin-like growth factor 1, adipokines, inflammation-related molecules, and steroid hormones, as well as the cellular and structural components of the tumor microenvironment, particularly adipose tissue.

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The Latino Eyelid: Anthropometric Analysis of a Spectrum of Findings.

Ophthalmic Plast Reconstr Surg

November 2017

*Department of Ophthalmology, The University of Texas Health Science Center at San Antonio, San Antonio, Texas; †Department of Ophthalmology, Tulane University, New Orleans, Louisiana; ‡Department of Genetics, Texas Biomedical Research Institute, San Antonio, Texas; §Department of Epidemiology and Biostatistics, The University of Texas Health Science Center at San Antonio, San Antonio, Texas; ‖Department of Nutrition and University of North Carolina Nutrition Research Institute, University of North Carolina at Chapel Hill, Kannapolis, North Carolina; and ¶Department of Ophthalmology, The University of Tennessee Health Science Center at Memphis, Memphis, Tennessee, U.S.A.

Purpose: Published anthropometric measurements of the Latino eyelid are limited. This study describes features spanning the morphologic range from non-Latino whites to East Asians in the spectrum of the Latino eyelid.

Methods: A cross-sectional study of 68 people (32 Latinos, 18 non-Latino whites, and 18 East Asians, ages 18-39), approved by the Institutional Review Board and HIPAA-compliant, was performed.

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A Decision Tree to Identify Children Affected by Prenatal Alcohol Exposure.

J Pediatr

October 2016

Center for Behavioral Teratology, Department of Psychology, San Diego State University, San Diego, CA. Electronic address:

Objective: To develop and validate a hierarchical decision tree model that combines neurobehavioral and physical measures to identify children affected by prenatal alcohol exposure even when facial dysmorphology is not present.

Study Design: Data were collected as part of a multisite study across the US. The model was developed after we evaluated more than 1000 neurobehavioral and dysmorphology variables collected from 434 children (8-16 years of age) with prenatal alcohol exposure, with and without fetal alcohol syndrome, and nonexposed control subjects, with and without other clinically-relevant behavioral or cognitive concerns.

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The objective of this study is to identify genetic factors associated with chronic kidney disease (CKD) and related cardiometabolic phenotypes among participants of the Genetics of Kidney Disease in Zuni Indians study. The study was conducted as a community-based participatory research project in the Zuni Indians, a small endogamous tribe in rural New Mexico. We recruited 998 members from 28 extended multigenerational families, ascertained through probands with CKD who had at least one sibling with CKD.

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Mechanism of choline deficiency and membrane alteration in postural orthostatic tachycardia syndrome primary skin fibroblasts.

FASEB J

May 2015

*Department of Human Health and Nutritional Sciences, University of Guelph, Guelph, Ontario, Canada; University of North Carolina Nutrition Research Institute, Kannapolis, North Carolina, USA; Department of Nutrition, University of North Carolina, Chapel Hill, Chapel Hill, North Carolina, USA; Toxicology Services Incorporated, Chapel Hill, North Carolina, USA; and The Laboratory of Molecular Biology, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland, USA

Fibroblasts from a patient with postural orthostatic tachycardia syndrome (POTS), who presented with low plasma choline and betaine, were studied to determine the metabolic characteristics of the choline deficiency. Choline is required for the synthesis of the phospholipid phosphatidylcholine (PC) and for betaine, an important osmoregulator. Here, choline transport, lipid homeostasis, and mitochondria function were analyzed in skin fibroblasts from POTS and compared with control cells.

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Both rare and common variants in PCSK9 influence plasma low-density lipoprotein cholesterol level in American Indians.

J Clin Endocrinol Metab

February 2015

Departments of Epidemiology (C.-W.T., A.T., T.H.B., A.N.-A., W.H.L.K.) and Environmental Health Sciences (A.N.-A.), Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland; Department of Epidemiology (K.E.N., N.F.), University of North Carolina, Chapel Hill, North Carolina; Department of Genetics (K.H., S.L., J.W.M.), Texas Biomedical Research Institute, San Antonio, Texas; Department of Nutrition and University of North Carolina Nutrition Research Institute (V.S.V.), University of North Carolina at Chapel Hill, Kannapolis, North Carolina; Center for American Indian Health Research (Y.Z.), University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma; Missouri Breaks Industries Research, Inc. (L.G.B.), Timber Lake, South Dakota; The Welch Center for Prevention (A.N.-A., W.H.L.K.), Epidemiology and Clinical Research, Johns Hopkins Medical Institutions, Baltimore, Maryland; MedStar Health Research Institute (B.V.H.), Hyattsville, Maryland; Georgetown and Howard Universities Center for Clinical and Translational Science (B.V.H.), Washington, D.C.; Kidney Institute and Division of Nephrology, Department of Internal Medicine (C.-W.T.), China Medical University Hospital, Taichung, Taiwan.

Context: Elevated LDL cholesterol (LDL-C) is an important risk factor for atherosclerosis and cardiovascular disease. Variants in the proprotein convertase subtilisin/kexin type 9 (PCSK9) gene have been associated not only with plasma LDL-C concentration, but also with ischemic heart disease. Little is known about the genetic architecture of PCSK9 and its influence on LDL-C in American Indians.

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Prenatal alcohol exposure and attention-deficit/hyperactivity disorder (ADHD) result in behavioral issues related to poor executive function (EF). This overlap may hinder clinical identification of alcohol-exposed children. This study examined the relation between parent and neuropsychological measures of EF and whether parent ratings aid in differential diagnosis.

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Previous studies indicated that the intake of α-linolenic acid (ALA) can alter the concentration of both ω-6 and ω-3 fatty acids in both mother and offspring, with consequences on postnatal brain development. This study describes the association between maternal ALA availability during gestation and lactation, and alterations in the Fads2 DNA methylation in both maternal and offspring livers, at the end of lactation period. Both Fads2 promoter and intron 1 DNA methylation were increased in the groups receiving postnatal flaxseed oil containing 50% ALA (mothers or pups), while bivariate analysis indicated a significant association of the Fads2 epigenetic status in the liver between each mother and its offspring.

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Maternal dietary choline deficiency alters angiogenesis in fetal mouse hippocampus.

Proc Natl Acad Sci U S A

July 2010

University of North Carolina Nutrition Research Institute at Kannapolis, University of North Carolina at Chapel Hill, Kannapolis, NC 28081, USA.

We examined whether maternal dietary choline modulates angiogenesis in fetal brain. Pregnant C57BL/6 mice were fed either a choline-deficient (CD), control (CT), or choline-supplemented diet (CS) from days 12 to 17 (E12-17) of pregnancy and then fetal brains were studied. In CD fetal hippocampus, proliferation of endothelial cells (EC) was decreased by 32% (p < 0.

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