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1.
Transplant Proc ; 50(9): 2593-2596, 2018 Nov.
Article in English | MEDLINE | ID: mdl-30401357

ABSTRACT

BACKGROUND: The relationship between smoking cessation and weight gain is well recognized. Examining the link between smoking cessation and weight gain in donor candidates for living donor liver transplantation (LDLT) is an important topic because of the influence of weight gain on the liver. This study assessed body weight (BW) changes after smoking cessation in donor candidates for LDLT. METHODS: The 27 donor candidates were retrospectively analyzed. The smoking status was determined based on questionnaires administered at the initial presentation, and the candidates were divided into 2 groups: recent quitters and nonsmokers. The changes in BW were compared between the groups. RESULTS: The recent quitters group included 10 (37.0%) candidates, and the nonsmokers group included 17 (63.0%). In the nonsmokers group, 1 candidate had gained weight since the initial presentation. In contrast, in the recent quitters group, 70.0% of candidates had gained weight since the initial presentation (P < .01). The change in BW from the initial presentation was greater in recent quitters than in nonsmokers (+1.6 kg [+2.4%] vs -0.5 kg [-0.9%]; P < .01). Two candidates in the recent quitters group gained ≥ 5 kg [8%] of weight. One of these 2 candidates was judged to be in a donor-inadequate status because of the appearance of fatty liver. CONCLUSIONS: Weight gain due to smoking cessation was observed in donor candidates for LDLT. The amount of weight gain after smoking cessation is highly individualized, so everyone concerned with LDLT must be alert to its potential development.


Subject(s)
Liver Transplantation/methods , Living Donors , Smoking Cessation , Weight Gain , Adult , Body Weight , Female , Humans , Male , Middle Aged , Retrospective Studies , Surveys and Questionnaires
2.
Transplant Proc ; 50(9): 2723-2725, 2018 Nov.
Article in English | MEDLINE | ID: mdl-30348453

ABSTRACT

BACKGROUND: Living donor liver transplantation (LDLT) is a definitive procedure for splenomegaly caused by liver cirrhosis and portal hypertension, but splenomegaly persists in some patients. The aim of this study was to clarify the long-term changes in the spleen volume after LDLT. METHODS: The 13 pediatric patients who survived for >8 years after LDLT were retrospectively analyzed. We calculated the spleen volume/standard spleen volume (SV/SSV) ratio by automated computed tomography (CT) volumetry. We assessed the spleen volumes before LDLT, at roughly postoperative week (POW) 4, at postoperative year (POY) 1, at POY 5, and at POY 10. RESULTS: With regard to SV as evaluated by CT volumetry, there were no consistent trends, with median values as follows: before LDLT, 282.5 (71-641) cm3; POW 4, 252 (109-798) cm3; POY 1, 222.5 (97-948) cm3; POY 5, 263.5 (123-564) cm3; and POY 10, 377 (201-1080) cm3. In contrast, the SV/SSV ratio decreased chronologically as follows: before LDLT, 5.0 (0.7-6.0); POW 4, 3.7 (2.3-4.3); POY 1, 2.2 (1.7-6.3); POY 5, 1.7 (1.1-5.4); and POY 10, 1.4 (1.1-6.9). In the remote phase after LDLT, many cases showed a trend toward an improved SV/SSV ratio, but splenomegaly was prolonged without improvement in 3 cases (23.1%) with portal vein complications and advanced fibrosis. Furthermore, all 3 cases showed a decreased platelet count due to hypersplenism. CONCLUSION: Splenomegaly requires a long time to demonstrate an improvement. In cases without an improvement of splenomegaly, we should suspect abnormalities in the graft liver and portal hemodynamics.


Subject(s)
Liver Transplantation/adverse effects , Splenomegaly/etiology , Adolescent , Child , Child, Preschool , Female , Humans , Infant , Living Donors , Male , Retrospective Studies , Splenomegaly/epidemiology
3.
Transplant Proc ; 49(7): 1615-1618, 2017 Sep.
Article in English | MEDLINE | ID: mdl-28838450

ABSTRACT

When there is an anatomic anomaly in the biliary tract of the donor for living-donor liver transplantation, the risk of postoperative biliary tract complications increases in both the donor and the recipient. We studied a case of living-donor liver transplantation with a left hepatic lobe graft that had anatomic anomalies, in which the medial segmental branch (B4) joined the anterior segmental branch and the posterior segmental branch formed a common trunk with the lateral segmental branch. A 40-year-old man visited our institution as a candidate organ donor for his mother, who had end-stage liver failure. An anomaly of B4 connecting the anterior segmental branch was suspected on magnetic resonance cholangiopancreatography. On intraoperative cholangiography, confluence of B4 with the anterior segmental branch and connection of the posterior and lateral segmental branches forming a common trunk were confirmed. Accordingly, individual anastomoses of the lateral segmental branch and B4 with the recipient jejunum were planned, and a left-lobe graft was excised. The postoperative recovery was smooth, and the donor was discharged with no complications. Even when an anatomic anomaly is present in the donor bile duct, in urgent cases, accurate evaluation through the use of various modalities may enable living-donor liver transplantation with the use of a graft with an anatomic anomaly.


Subject(s)
Biliary Tract/abnormalities , Liver Transplantation/methods , Liver/abnormalities , Living Donors , Transplants/abnormalities , Adult , Bile Ducts/abnormalities , Bile Ducts/transplantation , Cholangiography , End Stage Liver Disease/surgery , Humans , Liver Transplantation/adverse effects , Male , Postoperative Complications/etiology , Transplants/transplantation
4.
J Anim Sci ; 93(1): 370-6, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25403197

ABSTRACT

The objective of this experiment was to determine the effects of in vitro fermentation of coconut endosperm fiber (CEF), chicory pulp (CHP), and selective blends of these substrates on SCFA production and changes in microbiota using canine fecal inocula. A total of 6 individual substrates, including short-chain fructooligosaccharide (scFOS; a well-established prebiotic source), pectin (PEC; used as a positive control), pelletized cellulose (PC; used as a negative control), beet pulp (BP; considered the gold standard fiber source in pet foods), CEF, and CHP, and 3 CEF:CHP blends (75:25% CEF:CHP [B1], 50:50% CEF:CHP [B2], and 25:75% CEF:CHP [B3]) were tested. Triplicate samples of each substrate were fermented for 0, 8, and 16 h after inoculation. A significant substrate × time interaction (P < 0.05) was observed for pH change and acetate, propionate, butyrate, and total SCFA concentrations. After 8 and 16 h, pH change was greatest for scFOS (-2.0 and -3.0, respectively) and smallest for PC (0.0 and -0.1, respectively). After 16 h, CEF had a greater butyrate concentration than CHP and all the CEF:CHP blends and it was not different than PEC. The substrate × time interaction was significant for bifidobacteria (P < 0.05) and lactobacilli (P < 0.05). After 8 h, bifidobacteria was greatest for BP and lowest for PC (12.7 and 10.0 log10 cfu/tube, respectively). After 16 h, PC had the lowest and scFOS had the greatest bifidobacteria (6.7 and 13.3 log10 cfu/tube, respectively). In general, CEF, CHP, and their blends had similar bifidobacteria populations after 8 and 16 h of fermentation when compared with BP and scFOS. After 16 h, lactobacilli populations were greatest for B1, B2, B3, BP, and scFOS, intermediate for PEC, and lowest for PC (P < 0.05). Overall, our data suggest that CEF had a butyrogenic effect and that CEF, CHP, and their blends had similar bifidobacteria and lactobacilli populations as popular prebiotic and fiber substrates. Future research should investigate the effects of CEF, CHP, and their blends on gastrointestinal health and fecal quality in dogs.


Subject(s)
Cichorium intybus , Cocos , Dietary Fiber/analysis , Dogs/microbiology , Endosperm/chemistry , Feces/microbiology , Animals , Beta vulgaris/metabolism , Bifidobacterium , Cellulose/metabolism , Fatty Acids, Volatile , Fermentation , Lactobacillus/metabolism , Oligosaccharides , Pectins , Propionates
5.
Transplant Proc ; 46(4): 1243-6, 2014 May.
Article in English | MEDLINE | ID: mdl-24815171

ABSTRACT

BACKGROUND: Recent study has demonstrated the important role of endothelial-mesenchymal interactions in 3-dimensional self-organization of immature progenitor populations with the use of mimicking of organogenesis. Here, we show that the same principle can be applicable to adult mature cells, ie, human adult hepatocytes (hAHs). METHODS: We cultivated hAHs with fluorescence-labeled human mesenchymal cells (hMSCs) and human umbilical vein endothelial cells (HUVECs) in micro-well culture plates and observed them for 9 days. Fluorescence microscopy imaging analyses were performed to evaluate the internal structures of generated 3-dimensional tissues. Maintenance of in vitro protein production capacity was examined with the use of enzyme-linked immunosorbent assay (ELISA). RESULTS: hAHs started to self-organize into 3-dimensional tissue with the use of coculturing with hMSCs and HUVECs. Live imaging analyses showed that endothelial cells started sprouting inside the generated tissues after 2 days of culture. ELISA showed that human albumin production capacity was improved with the use of coculture compared with hAHs-only culture after 9 days. CONCLUSIONS: We demonstrated that 3-dimensional vascularized hepatic tissue could be generated from hAHs by reconstituting endothelial-mesenchymal interactions. Future studies are needed to evaluate the therapeutic potential of vascularized hepatic tissue transplantation, and this may pave a new way to establish a new transplantation modality as an alternative to hepatocyte transplantation.


Subject(s)
Bioartificial Organs , Cell Communication , Hepatocytes/physiology , Human Umbilical Vein Endothelial Cells/physiology , Liver/blood supply , Liver/cytology , Neovascularization, Physiologic , Tissue Engineering/methods , Adult , Cell Culture Techniques , Cells, Cultured , Hepatocytes/metabolism , Hepatocytes/transplantation , Human Umbilical Vein Endothelial Cells/metabolism , Humans , Liver/metabolism , Liver Transplantation/methods , Luminescent Proteins/biosynthesis , Luminescent Proteins/genetics , Mesoderm/cytology , Microscopy, Fluorescence , Serum Albumin/metabolism , Serum Albumin, Human , Time Factors , Transfection , Red Fluorescent Protein
6.
Clin Microbiol Infect ; 20(3): 256-62, 2014 Mar.
Article in English | MEDLINE | ID: mdl-23829301

ABSTRACT

Factors that can interfere with the successful treatment of Mycobacterium avium lung infection have been inadequately studied. To identify a potent predictor of therapeutic responses of M. avium lung infection, we analyzed variable number tandem repeats (VNTR) at 16 minisatellite loci of M. avium clinical isolates. Associations between the VNTR profiling data and a therapeutic response were evaluated in 59 subjects with M. avium lung infection. M. avium lung infection of 30 subjects in whom clarithromycin-containing regimens produced microbiological and radiographic improvement was defined as responsive disease, while that of the remaining 29 subjects was defined as refractory disease. In phylogenetic analysis using the genotypic distance aggregated from 16-dimensional VNTR data, 59 M. avium isolates were divided into three clusters, which showed a nearly significant association with therapeutic responses (p 0.06). We then subjected the raw 16-dimensional VNTR data directly to principal component analysis, and identified the genetic features that were significantly associated with the therapeutic response (p <0.05). By further analysis of logistic regression with a stepwise variable-selection, we constructed the highest likelihood multivariate model, adjusted for age, to predict a therapeutic response, using VNTR data from only four minisatellite loci. In conclusion, we identified four mycobacterial minisatellite loci that together were associated with the therapeutic response of M. avium lung infections.


Subject(s)
Antitubercular Agents/therapeutic use , Genotype , Mycobacterium avium/genetics , Tuberculosis, Pulmonary/drug therapy , Tuberculosis, Pulmonary/microbiology , Aged , Animals , Antitubercular Agents/pharmacology , Cluster Analysis , DNA, Bacterial , Drug Resistance, Bacterial , Female , Genetic Loci , Humans , Male , Microbial Sensitivity Tests , Middle Aged , Minisatellite Repeats/genetics , Mycobacterium avium/drug effects , Odds Ratio , Phylogeny , Treatment Outcome , Tuberculosis, Pulmonary/diagnosis
7.
Article in English | MEDLINE | ID: mdl-24110686

ABSTRACT

Mu wave suppression is thought to accompany the activation of the mirror neuron system which occurs when a human observes or imitates the behavior of others. Our investigation indicates a possible difference in mirror neuron system activation between passive and more active observation as suggested by mu wave activation levels. Participants were asked to observe four different videos each 80 s in duration. Each video was repeated once after a 30 s interval. The first video was of visual white noise and participants were instructed to passively observe the video. This was identified as the Baseline condition and served as a mu activation level baseline. The second video was of simple bouncing balls and the observer was again asked to passively observe the video (Ball condition). The third video was of a moving hand (Observation condition). The forth video was of the same moving hand and participants also imagined executing the observed hand movement (Imagination condition). As hypothesized, the Imagination condition activated the greatest level of mu suppression, while the Ball condition activated the lowest level of mu wave suppression. The Observation condition produced a slightly larger level of mu wave suppression than the Ball condition. This progressive increase in mu wave suppression supports the hypothesis that the activation of the mirror neuron system increases as the level of active observation increases.


Subject(s)
Brain Waves/physiology , Imagination/physiology , Adolescent , Female , Hand/physiology , Humans , Male , Mirror Neurons/physiology , Photic Stimulation , Sensorimotor Cortex/physiology , Young Adult
8.
Br J Dermatol ; 165(6): 1290-2, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21801157

ABSTRACT

The palmoplantar keratodermas (PPKs) are a large group of genodermatoses comprising nearly 60 genetically distinct diseases. They are characterized by hyperkeratosis on the palms and soles with or without extrapalmoplantar hyperkeratotic lesions. Focal PPK is one of the hallmarks of pachyonychia congenita, a rare autosomal dominant disorder resulting from mutations in the keratin genes KRT6A, KRT6B, KRT16 or KRT17. Recently, in-frame deletion mutations of KRT6C have been identified in three families with focal PPK with slight or no nail changes. We report here a novel KRT6C mutation identified in a Japanese family with PPK with phenotypic heterogeneity, presenting with not only focal but also diffuse hyperkeratosis. The proband had diffuse hyperkeratosis on the soles and small focal hyperkeratoses on the palms, while the two other affected individuals showed focal hyperkeratoses on the soles. All three patients were heterozygotes for c.1414G>A in KRT6C, predicted to result in p.Glu472Lys. These findings strongly suggest that screening of patients with nonepidermolytic diffuse PPK, in whom the pathogenic mutations are yet to be determined, might identify mutations in KRT6C.


Subject(s)
Foot Dermatoses/genetics , Hand Dermatoses/genetics , Keratin-6/genetics , Keratoderma, Palmoplantar/genetics , Mutation/genetics , Adult , Female , Heterozygote , Humans , Male , Pedigree
11.
Br J Dermatol ; 163(4): 704-10, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20518783

ABSTRACT

BACKGROUND: Vascular-type Ehlers-Danlos syndrome (vEDS) is a severe autosomal dominant inherited disorder resulting from mutations within the α1 type III collagen gene (COL3A1). The majority of published mutations are base changes leading to the substitution of single glycine residues within the triple-helical domain of type III collagen. Although clinical characteristics and mutations in the COL3A1 gene have been analysed for some patients from Europe and America, similar analyses have not yet been performed for Japanese patients with vEDS. OBJECTIVES: To analyse the genetic and phenotypic findings in Japanese patients with vEDS. METHODS: We analysed the clinical features of 20 unrelated individuals with vEDS. To quantify type III collagen production, the fibroblasts were cultured with (3) H-proline, and the radiolabelled collagenous proteins were analysed using sodium dodecyl sulphate-polyacrylamide gel electrophoresis and fluorography. Mutations in COL3A1 were detected by sequence analysis of cDNA from patients' fibroblasts and subsequently by a genomic DNA sequence analysis. RESULTS: Thin and translucent skin with extensive bruising and hypermobility of the small joints were observed in about 90% of the patients, whereas the prevalence of serious clinical findings such as rupture/dissection/aneurysm of the arteries (30%) or rupture of the gastrointestinal tract (25%) was relatively low. Sequence analyses of the COL3A1 gene demonstrated heterozygous point mutations leading to glycine substitution in only nine patients (45%), while heterozygous splice-site mutations at the junction of the triple-helical exons were observed in the remaining 11 patients (55%). The average type III collagen production level in the cultured dermal fibroblasts was 14·6% of the normal value. The types of complication were not associated with specific mutations in COL3A1. CONCLUSION: The analysis in the present series revealed a low frequency of patients presenting with serious clinical findings such as arterial rupture/arterial dissection/aneurysm and perforation or rupture of the gastrointestinal tract, and revealed a higher prevalence of splice-site mutations at the junction of the triple-helical exons than of glycine substitution mutations in COL3A1.


Subject(s)
Ehlers-Danlos Syndrome/genetics , Skin Diseases, Vascular/genetics , Adolescent , Adult , Cells, Cultured , Collagen Type III/biosynthesis , Collagen Type III/genetics , DNA Mutational Analysis/methods , Ehlers-Danlos Syndrome/diagnosis , Ehlers-Danlos Syndrome/metabolism , Female , Fibroblasts/metabolism , Humans , Male , Point Mutation , Skin/metabolism , Skin Diseases, Vascular/diagnosis , Skin Diseases, Vascular/metabolism , Young Adult
12.
J Anim Physiol Anim Nutr (Berl) ; 94(3): 287-92, 2010 Jun.
Article in English | MEDLINE | ID: mdl-19364373

ABSTRACT

For the purpose of investigating the mechanism of obesity-induction/re-induction including weight-cycling in beagles, a study was conducted using commercially available dog food combined with human food to mimic at home-snacking and diet-supplementation behaviours. Adult female beagles, which had free access to water and exercise, were used (n = 9). All dogs were initially offered two times their daily calculated number of calories using a dry extruded diet plus blend of canola and soybean oils and allowed to eat ad libitum. After 3 weeks, Pecan shortbread cookies were added to the diet mixture. Obesity was induced during a 19-week period with 1875-2250 kcal/day consumed, on average, during this period. The dogs were then subjected to a weight-loss regimen while consuming 490-730 kcal/day. After weight loss, a similar degree of obesity was re-induced for 17 weeks even though dogs consumed only 1125-1250 kcal/day. Body weight, body condition scores, kcal consumption and food efficiency were recorded. Results indicated that less time and fewer kcal were required to re-induce the same degree of obesity compared with the initial obesity induction. Human snack foods appeared to stimulate appetite and thus contribute to the obese state. Food efficiency was also increased during the obesity-reinduction period compared with the induction period. This information may help pet owners better understand the need to limit table scraps and human-type food snacks in dogs prone to obesity as well as weight maintenance after weight loss.


Subject(s)
Dogs/physiology , Energy Intake/physiology , Obesity/metabolism , Weight Gain/physiology , Animal Feed , Animal Nutritional Physiological Phenomena , Animals , Diet/veterinary , Diet, Reducing , Female , Time Factors , Weight Loss/physiology
15.
Interv Neuroradiol ; 15(1): 73-6, 2009 Mar 31.
Article in English | MEDLINE | ID: mdl-20465932

ABSTRACT

SUMMARY: We describe a very rare case of anomalous origin of the anterior choroidal artery. In our case the anterior choroidal artery arises from the internal carotid artery proximal to the posterior communicating artery.

16.
AJNR Am J Neuroradiol ; 28(6): 1179-84, 2007.
Article in English | MEDLINE | ID: mdl-17569984

ABSTRACT

BACKGROUND AND PURPOSE: The inferior petrosal sinus (IPS) is the main transvenous access route used to examine or treat lesions involving the cavernous sinus. To carry out these procedures successfully, one must have a detailed knowledge of the anatomy of the venous system around the junction of the IPS and the internal jugular vein (IJV). MATERIALS AND METHODS: Eighty-three sides in 63 patients (26 men, 37 women; mean, 56.5 years of age) were examined by using 3D rotational venography (3DRV). RESULT: The drainage patterns of the IPS could be classified into the following 6 types, with emphasis on the level of IPS-IJV junction: type A, the IPS drains into the jugular bulb in 1/83 sides (1.2%); type B, the IPS drains into the IJV at the level of the extracranial opening of the hypoglossal canal in 29/83 sides (34.9%); type C, the IPS drains into the lower extracranial IJV in 31/83 sides (37.3%); type D, the IPS forms a plexus and has multiple junctions to the IJV near the jugular foramen in 5/83 sides (6.0%); type E, the IPS drains directly into the vertebral venous plexus (VVP) with no connection to the IJV in 3/83 sides (3.6%); and type F, the IPS is absent in 14/83 sides (16.9%). Each type is also characterized by the way of anastomosis with the VVP. CONCLUSION: This classification seemed to be rational from the embryologic viewpoint, and it may be useful in establishing treatment strategies that involve endovascular manipulation via the IPS.


Subject(s)
Cranial Sinuses/anatomy & histology , Cranial Sinuses/diagnostic imaging , Imaging, Three-Dimensional/methods , Phlebography/methods , Radiographic Image Interpretation, Computer-Assisted/methods , Adult , Aged , Female , Humans , Male , Middle Aged , Reproducibility of Results , Rotation , Sensitivity and Specificity
19.
Int J Gynaecol Obstet ; 94(1): 62-6, 2006 Jul.
Article in English | MEDLINE | ID: mdl-16782101

ABSTRACT

Buerger's disease is an inflammatory occlusive vascular disorder involving small- and medium-sized arteries in the distal extremities and is usually complicated with thrombophlebitis. Since Buerger's disease develops most frequently in men who smoke, pregnancy complicated with this disease is extremely rare. Only three pregnancies have been reported previously. All cases indicate that Buerger's disease worsens during pregnancy. However, anti-coagulant therapy appeared to be effective in this case. Accordingly, careful observation is mandatory in pregnancies complicated with Buerger's disease.


Subject(s)
Pregnancy Complications, Cardiovascular , Thromboangiitis Obliterans , Adult , Anticoagulants/administration & dosage , Female , Heparin/administration & dosage , Humans , Placenta/pathology , Pregnancy , Pregnancy Complications, Cardiovascular/drug therapy , Pregnancy Complications, Cardiovascular/pathology , Pregnancy Complications, Cardiovascular/physiopathology , Thromboangiitis Obliterans/drug therapy , Thromboangiitis Obliterans/pathology , Thromboangiitis Obliterans/physiopathology , Umbilical Cord/pathology
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