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1.
Clin Genet ; 92(1): 52-61, 2017 Jul.
Article in English | MEDLINE | ID: mdl-28039895

ABSTRACT

Advanced cholestatic liver disease is a leading referral to pediatric liver transplant centers. Recent advances in the genetic classification of this group of disorders promise a highly personalized management although the genetic heterogeneity also poses a diagnostic challenge. Using a next-generation sequencing-based multi-gene panel, we performed retrospective analysis of 98 pediatric patients who presented with advanced cholestatic liver disease. A likely causal mutation was identified in the majority (61%), spanning many genes including ones that have only rarely been reported to cause cholestatic liver disease, e.g. TJP2 and VIPAS39. We find no evidence to support mono-allelic phenotypic expression in the carrier parents despite the severe nature of the respective mutations, and no evidence of oligogenicity. The high-carrier frequency of the founder mutations identified in our cohort (1 in 87) suggests a minimum incidence of 1:7246, an alarmingly high disease burden that calls for the primary prevention through carrier screening.


Subject(s)
Cholestasis/genetics , Liver Diseases/genetics , Vesicular Transport Proteins/genetics , Zonula Occludens-2 Protein/genetics , Adolescent , Child , Child, Preschool , Cholestasis/diagnosis , Cholestasis/enzymology , Cholestasis/pathology , Female , Gene Expression Regulation , Genetic Predisposition to Disease , High-Throughput Nucleotide Sequencing , Humans , Infant , Infant, Newborn , Liver Diseases/diagnosis , Liver Diseases/enzymology , Liver Diseases/pathology , Male , Mutation , Young Adult
2.
J Appl Physiol (1985) ; 63(1): 285-91, 1987 Jul.
Article in English | MEDLINE | ID: mdl-3305468

ABSTRACT

Distribution of muscle blood flow has not been measured in man during prolonged exercise, but progressive elevations in skin flow coupled with constant cardiac output (QT) have suggested muscle blood flow may be compromised. However, previous experiments with rats demonstrated progressive increases in muscle blood flow over time during prolonged submaximal exercise. The present study was performed to study muscle blood flow in miniature swine during long-term exercise to shed light on this apparent anomaly. QT and distribution of QT were studied with radiolabeled microspheres while pigs ran on a level treadmill at a speed (10.5 km/h) requiring 71 +/- 4% of maximal O2 consumption (VO2 max). QT increased 23% from the 5th to the 30th min of exercise, whereas total skeletal muscle flow increased by 49%. Increases in flow in the muscles resulted from decreased resistance, since mean arterial pressure declined over this time period (-7%). In addition, the proportional increases in muscle flow were similar within synergistic muscle groups independent of fiber type composition (e.g., elbow extensors: 59-78%; elbow flexors: 26-40%). The factor that limited continued exercise appeared to be body temperature. Colonic temperature rose in linear fashion over time; the animals became exhausted at approximately 42 degrees C. These flow data are similar to previous findings in rats and indicate that during prolonged treadmill locomotion in quadrupedal animals muscle blood flow increases over time to near maximal levels.


Subject(s)
Muscles/blood supply , Physical Exertion , Regional Blood Flow , Animals , Blood Pressure , Cardiac Output , Female , Heart Rate , Muscles/physiology , Organ Specificity , Oxygen Consumption , Swine , Swine, Miniature
3.
J Appl Physiol (1985) ; 62(3): 1285-98, 1987 Mar.
Article in English | MEDLINE | ID: mdl-3106313

ABSTRACT

The purpose of this study was to determine how the distribution of blood flow within and among the skeletal muscles of miniature swine (22 +/- 1 kg body wt) varies as a function of treadmill speed. Radiolabeled microspheres were used to measure cardiac output (Q) and tissue blood flows in preexercise and at 3-5 min of treadmill exercise at 4.8, 8.0, 11.3, 14.5, and 17.7 km/h. All pigs (n = 8) attained maximal O2 consumption (VO2max) (60 +/- 4 ml X min-1 X kg-1) by the time they ran at 17.7 km/h. At VO2max, 87% of Q (9.9 +/- 0.5 l/min) was to skeletal muscle, which constituted 36 +/- 1% of body mass. Average total muscle blood flow at VO2max was 127 +/- 14 ml X min-1 X 100 g-1; average limb muscle flow was 135 +/- 17 ml X min-1 X 100 g-1. Within the limb muscles, blood flow was distributed so that the deep red parts of extensor muscles had flows about two times higher than the more superficial white portions of the same muscles; the highest muscle blood flows occurred in the elbow flexors (brachialis: 290 +/- 44 ml X min-1 X 100 g-1). Peak exercise blood flows in the limb muscles were proportional (P less than 0.05) to the succinate dehydrogenase activities (r = 0.84), capillary densities (r = 0.78), and populations of oxidative (slow-twitch oxidative + fast-twitch oxidative-glycolytic) fiber types (r = 0.93) in the muscles. Total muscle blood flow plotted as a function of exercise intensity did not peak until the pigs attained VO2max, although flows in some individual muscles showed a plateau in this relationship at submaximal exercise intensities. The data demonstrate that blood flow in skeletal muscles of miniature swine is distributed heterogeneously and varies in relation to fiber type composition and exercise intensity.


Subject(s)
Cardiovascular Physiological Phenomena , Muscles/blood supply , Physical Exertion , Regional Blood Flow , Animals , Blood Pressure , Body Temperature , Carbon Dioxide/blood , Cardiac Output , Female , Heart Rate , Hydrogen-Ion Concentration , Male , Muscles/physiology , Oxygen/blood , Partial Pressure , Swine , Swine, Miniature
4.
Clin Chem ; 31(5): 782, 1985 May.
Article in English | MEDLINE | ID: mdl-3987010
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