Physical activity-related mechanical loading may alter the structural and mechanical properties of the infrapatellar fat pad (IFP), a pain-sensitive tissue. Echo intensity and stiffness reflect the me Show more
Physical activity-related mechanical loading may alter the structural and mechanical properties of the infrapatellar fat pad (IFP), a pain-sensitive tissue. Echo intensity and stiffness reflect the mechanical properties of the IFP and are clinically relevant. This study aimed to investigate the associations between physical activity levels and ultrasound-derived properties of the IFP in older adults. Forty-six older adults participated in this cross-sectional study. Physical activity, including light physical activity (LPA) and moderate-to-vigorous physical activity (MVPA), was measured using a triaxial accelerometer. Echo intensity and stiffness of the IFP were assessed using ultrasound imaging and shear wave elastography. Simple and multiple linear regression analyses were conducted to examine associations between physical activity levels and IFP characteristics. MVPA was significantly negatively correlated with IFP echo intensity (r = -0.32), and LPA was significantly negatively correlated with IFP stiffness (r = -0.29). In multiple regression analyses, the association between LPA and IFP stiffness remained significant after adjusting for demographic variables. These findings suggest that physical activity influences the biological and mechanical properties of the IFP in older adults. Increasing both LPA and MVPA may help maintain or improve IFP condition, potentially contributing to better knee joint health. UMIN000053230. Show less
Ornithine transcarbamylase deficiency (OTCD) is an X-linked disorder. Several male patients with OTCD suffer from severe hyperammonemic crisis in the neonatal period, whereas others develop late-onset Show more
Ornithine transcarbamylase deficiency (OTCD) is an X-linked disorder. Several male patients with OTCD suffer from severe hyperammonemic crisis in the neonatal period, whereas others develop late-onset manifestations, including hyperammonemic coma. Females with heterozygous pathogenic variants in the Show less
Urea cycle disorders (UCDs) are inherited metabolic diseases that lead to hyperammonemia with variable clinical manifestations. Using data from a nationwide study, we investigated the onset time, gene Show more
Urea cycle disorders (UCDs) are inherited metabolic diseases that lead to hyperammonemia with variable clinical manifestations. Using data from a nationwide study, we investigated the onset time, gene variants, clinical manifestations, and treatment of patients with UCDs in Japan. Of the 229 patients with UCDs diagnosed and/or treated between January 2000 and March 2018, identified gene variants and clinical information were available for 102 patients, including 62 patients with ornithine transcarbamylase (OTC) deficiency, 18 patients with carbamoyl phosphate synthetase 1 (CPS1) deficiency, 16 patients with argininosuccinate synthetase (ASS) deficiency, and 6 patients with argininosuccinate lyase (ASL) deficiency. A total of 13, 10, 4, and 5 variants in the OTC, CPS1, ASS, and ASL genes were respectively identified as novel variants, which were neither registered in ClinVar databases nor previously reported. The onset time and severity in patients with UCD could be predicted based on the identified gene variants in each patient from this nationwide study and previous studies. This genetic information may help in predicting the long-term outcome and determining specific treatment strategies such as liver transplantation in patients with UCDs. Show less
We recently reported distinct nature of high-density lipoproteins (HDL) subgroup particles with apolipoprotein (apo) A-I but not apoA-II (LpAI) and HDL having both (LpAI:AII) based on the data from 31 Show more
We recently reported distinct nature of high-density lipoproteins (HDL) subgroup particles with apolipoprotein (apo) A-I but not apoA-II (LpAI) and HDL having both (LpAI:AII) based on the data from 314 Japanese. While plasma HDL level almost exclusively depends on concentration of LpAI having 3 to 4 apoA-I molecules, LpAI:AII appeared with almost constant concentration regardless of plasma HDL levels having stable structure with two apoA-I and one disulfide-dimeric apoA-II molecules (Sci. Rep. 6; 31,532, 2016). The aim of this study is further characterization of LpAI:AII with respect to its role in atherogenesis. Association of LpAI, LpAI:AII and other HDL parameters with apoB-lipoprotein parameters was analyzed among the cohort data above. ApoA-I in LpAI negatively correlated with the apoB-lipoprotein parameters such as apoB, triglyceride, nonHDL-cholesterol, and nonHDL-cholesterol + triglyceride, which are apparently reflected in the relations of the total HDL parameters to apoB-lipoproteins. In contrast, apoA-I in LpAI:AII and apoA-II positively correlated to the apoB-lipoprotein parameters even within their small range of variation. These relationships are independent of sex, but may slightly be influenced by the activity-related CETP mutations. The study suggested that LpAI:AII is an atherogenic indicator rather than antiatherogenic. These sub-fractions of HDL are to be evaluated separately for estimating atherogenic risk of the patients. Show less