scholarly journals Effects of a medium chain triglyceride oil mixture and α-lipoic acid diet on body composition, antioxidant status, and plasma lipid levels in the Golden Syrian hamster

2004 ◽  
Vol 15 (7) ◽  
pp. 402-410 ◽  
Author(s):  
Stephanie D Wollin ◽  
Yanwen Wang ◽  
Stan Kubow ◽  
Peter J.H Jones
2009 ◽  
Vol 161 (6) ◽  
pp. 845-852 ◽  
Author(s):  
Labros Melistas ◽  
Christos S Mantzoros ◽  
Meropi Kontogianni ◽  
Smaragdi Antonopoulou ◽  
Jose M Ordovas ◽  
...  

ObjectiveWe explored potential associations of two single nucleotide polymorphisms (SNPs) in the adiponectin gene (ADIPOQ; +45T>G, rs2241766 and +276G>T, rs1501299) with circulating total and high-molecular weight (HMW) adiponectin, insulin resistance (IR), and markers of obesity in a healthy Greek female population.Design and methodsThe two SNPs were genotyped in 349 women without diabetes (mean age: 47.0±12.1 years, mean body mass index: 28.9±5.6 kg/m2). Total and HMW adiponectin concentrations, body composition variables, IR parameters, and plasma lipid levels were determined.ResultsIn single SNP analysis adjusting for several potential confounders, SNP +276G>T was associated with higher fasting insulin levels (P=0.01) and higher homeostasis model assessment index for IR (HOMA-IR; P=0.009), and SNP +45T>G was associated with lower insulin levels and HOMA-IR (P=0.05 and P=0.07 respectively). No association with total or HMW adiponectin, plasma lipid levels, and body composition variables was observed; however, haplotype analysis revealed that subjects homozygous for the most common +45T/+276G haplotype had lower total adiponectin levels than did noncarriers of this haplotype (P=0.02). The observed differences in HOMA-IR were very significant among women with a higher body fat (BF) percentage (≥ the population median of 41%; all P≤0.005), but not among leaner individuals (P for interactions 0.01–0.07), thus suggesting that ADIPOQ effects on insulin sensitivity may depend upon BF status.ConclusionOur data suggest a significant role of ADIPOQ variants at positions +45 and +276 in the development of IR in healthy Greek women possibly through an interaction with BF.


Aquaculture ◽  
2012 ◽  
Vol 368-369 ◽  
pp. 29-35 ◽  
Author(s):  
M.T. Kütter ◽  
J.M. Monserrat ◽  
E.G. Primel ◽  
S.S. Caldas ◽  
M.B. Tesser

2003 ◽  
Vol 112 (5-6) ◽  
pp. 610-616 ◽  
Author(s):  
Coleen M. Damcott ◽  
Eleanor Feingold ◽  
Susan P. Moffett ◽  
M. Michael Barmada ◽  
Julie A. Marshall ◽  
...  

2003 ◽  
Vol 133 (6) ◽  
pp. 1815-1820 ◽  
Author(s):  
Marie-Pierre St-Onge ◽  
Benoı̂t Lamarche ◽  
Jean-François Mauger ◽  
Peter J. H. Jones

2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Ammu Thampi Susheela ◽  
Padmesh Vadakapet ◽  
Lekshmi Pillai ◽  
Susheela Thampi

Abstract Background Familial chylomicronemia is an extremely rare disease. Lipoprotein lipase deficiency, lipoprotein defect or lipoprotein receptor defect are the main genetic causes of familial chylomicronemia. Case presentation We report a rare case of hypertriglyceridemia which was diagnosed at 24 days after birth. A newborn south east Asian baby born for G3P2A1 mother was presented with hematuria at 24 days at the hospital. The patient's family history is significant for pink blood in an elder sibling who died within a few months of birth without a proper diagnosis. Physical examination was not significant for any findings. Urinalysis revealed numerous RBC in the urine. Blood draw to perform renal function test revealed a characteristic pink blood. Baby’s blood was normal and red in color at the time of birth. During the present visit, although most of the blood test were not able to be carried out by the regular laboratory instruments, the patient’s lipid profile was alarmingly high with triglyceride levels over 4000 mg/dL. Due to a very high triglyceride level in a neonate and a significant familial history, a genetic cause of hypertriglyceridemia is suspected. Upon diagnosis, baby was discontinued of breast feeding completely and was given a special diet devoid of triglyceride and containing medium chain fatty acid diet and was also started with fenofibrate. After a month and a half, follow up tests were conducted which showed the triglyceride level was reduced to 1300 and a reversal of the blood color from pink to red. Since the imported diet was extremely expensive for the family, the patient was put on skimmed milk with medium-chain triglyceride (MCT) oil. With 6 weeks of treatment, baby’s condition has improved and is thriving well. Conclusions Our case reports an extremely rare and fatal condition and illustrated the significance of timely diagnosis and intervention for saving the life of the baby.


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