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1.
Prog Lipid Res ; 74: 87-102, 2019 04.
Article in English | MEDLINE | ID: mdl-30822462

ABSTRACT

Dietary plant sterols and stanols as present in our diet and in functional foods are well-known for their inhibitory effects on intestinal cholesterol absorption, which translates into lower low-density lipoprotein cholesterol concentrations. However, emerging evidence suggests that plant sterols and stanols have numerous additional health effects, which are largely unnoticed in the current scientific literature. Therefore, in this review we pose the intriguing question "What would have occurred if plant sterols and stanols had been discovered and embraced by disciplines such as immunology, hepatology, pulmonology or gastroenterology before being positioned as cholesterol-lowering molecules?" What would then have been the main benefits and fields of application of plant sterols and stanols today? We here discuss potential effects ranging from its presence and function intrauterine and in breast milk towards a potential role in the development of non-alcoholic steatohepatitis (NASH), cardiovascular disease (CVD), inflammatory bowel diseases (IBD) and allergic asthma. Interestingly, effects clearly depend on the route of entrance as observed in intestinal-failure associated liver disease (IFALD) during parenteral nutrition regimens. It is only until recently that effects beyond lowering of cholesterol concentrations are being explored systematically. Thus, there is a clear need to understand the full health effects of plant sterols and stanols.


Subject(s)
Asthma/drug therapy , Cardiovascular Diseases/drug therapy , Inflammatory Bowel Diseases/drug therapy , Non-alcoholic Fatty Liver Disease/drug therapy , Phytosterols/pharmacology , Sitosterols/pharmacology , Asthma/metabolism , Cardiovascular Diseases/metabolism , Cholesterol/metabolism , Cholesterol, LDL/antagonists & inhibitors , Cholesterol, LDL/metabolism , Humans , Inflammatory Bowel Diseases/metabolism , Intestinal Absorption/drug effects , Non-alcoholic Fatty Liver Disease/metabolism , Phytosterols/administration & dosage , Sitosterols/administration & dosage
2.
J Neonatal Perinatal Med ; 8(3): 243-50, 2015.
Article in English | MEDLINE | ID: mdl-26518407

ABSTRACT

OBJECTIVE: To determine the predictive ability of cord blood bilirubin (CBB) for hyperbilirubinemia in a population at risk for maternal-fetal blood group incompatibility and hemolytic disease of the newborn. STUDY DESIGN: This is a single center retrospective case-control study. Cases received phototherapy; controls did not. Cases were matched 1:3 to controls by gender and treating physician. Inclusion criteria included: ≥35 weeks gestation, CBB, and one or more total serum bilirubin (TSB) concentrations. The primary outcome was CBB. Secondary outcomes were a TSB >75th percentile, length of stay, and neonatal intensive care unit admission. The prognostic ability of CBB for phototherapy and TSB >75th percentile was assessed using area under the receiver operating characteristic (ROC) curve. Logistic regression analyses were performed to determine predictors for phototherapy and TSB >75th percentile. RESULT: When compared to controls (n = 142), cases (n = 54) were more likely to have a positive Coombs' test (82% vs. 41% , p <  0.001) and TSB >75th percentile (85% vs. 21% , p <  0.001). When compared to controls, cases had a higher mean (±SD) CBB (2.5 ± 0.5 vs. 1.8 ± 0.4 mg/dL, p <  0.001). The area under the ROC curve (±SEM) for CBB for phototherapy and TSB >75th percentile was 0.87 ± 0.03 (p <  0.001, 95% CI 0.82, 0.93) and 0.87 ± 0.03 (p <  0.001, 95% CI 0.82, 0.92), respectively. CONCLUSION: In this study, the mean CBB concentration was higher in neonates who received phototherapy compared to those who did not. CBB concentrations may help predict severe hyperbilirubinemia and phototherapy in a population at risk for hemolytic disease of the newborn.


Subject(s)
ABO Blood-Group System , Bilirubin/blood , Hyperbilirubinemia/blood , Hyperbilirubinemia/diagnosis , Neonatal Screening/instrumentation , Case-Control Studies , Female , Humans , Infant, Newborn , Male , Predictive Value of Tests , Reproducibility of Results , Retrospective Studies , Risk Assessment
3.
Am J Emerg Med ; 16(7): 708-9, 1998 Nov.
Article in English | MEDLINE | ID: mdl-9827755
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