Migration choices of China's older adults and spatial patterns emerging therefrom (1995-2015).

The steady increase in China's ageing population and an upswing in migration among the country's population, on the whole, has caused a continuous expansion of the scale of older migrants. The migration of older adults not only directly affects the well-being of individual families but also significantly impacts the population structure and economic development of the places of origin and destination. Despite this, in China, the various relevant aspects concerning this age group and, in particular, its migration choices and the patterns thereof have only rarely been the subject of sound research. The study presented in this paper seeks to fill this gap; the present study makes use of the microdata obtained from the national population censuses of 2000 and 2010 and the 1% population sample surveys conducted nationally in 2005 and 2015. The findings of the present study were the following: ① During 1995-2015, the efficiency of older adults' migration was significantly higher in the eastern region than in the central and western regions. ② Older individuals migrating to urban areas are increasingly choosing, for their relocation, economically developed, urban areas such as the Yangtze River Delta, Pearl River Delta and Beijing-Tianjin-Hebei region. ③ Relocation of older adults to urban areas was much more than to rural areas. The latter group has a more diverse choice of destination, and the larger migration flow is primarily from developed provinces to relatively underdeveloped provinces. ④ The results of binary logit regression indicated that the factors that significantly and consistently influence the migration decisions of older adults were found to be the following: age, education level, health status, the primary financial resource, children aged ≤ 6 years being members of the household that would receive the migrants, and the average wage of employees. As for the geographical characteristics of the province to which the older adults migrate, a substantial difference was observed between the preferences of older adults migrating to urban regions and those of older adults relocating to rural areas. The findings of the present study provide further insight into the decision-making of older adults regarding migration. Further, these findings constitute an empirical basis for the local governments concerned to devise and implement policies to better cope with an ageing population.

Breast Carcinoma with a Special Histological Pattern of Sebaceous Differentiation and High-Frequency Microsatellite Instability: A Case Report and Review of the Literature.

The World Health Organization in its 2019 Classification of Breast Tumors termed breast sebaceous carcinoma as invasive breast carcinoma of no special type (IBC-NST), with a sebaceous pattern. Approximately 30 cases of IBC-NST with a sebaceous pattern have been reported in the literature, and in all cases the expression of mismatch repair proteins in tumors was normal. Here, we report a case of IBC-NST with a sebaceous pattern and high-frequency microsatellite instability (MSI-H). This case was a sporadic sebaceous pattern of IBC-NST with MSI-H and was unrelated to Muir-Torre syndrome. Its histopathological characteristics were similar to those of MSI-H-associated triple-negative breast carcinoma (TNBC) with a high histological grade but were without tumor-infiltrating lymphocytes (TILs). The tumor did not recur after 20 months of follow-up.

Heat shock factor 1-mediated transcription activation of Omi/HtrA2 induces myocardial mitochondrial apoptosis in the aging heart.

BACKGROUND: Increased cardiac apoptosis is a hallmark of the elderly, which in turn increases the risk for developing cardiac disease. The overexpression of Omi/HtrA2 mRNA and protein contributes to apoptosis in the aged heart. Heat shock factor 1 (HSF1) is a transcription factor that binds to the promoter of Omi/HtrA2 in the aging myocardium. However, whether HSF1 participates in cardiomyocyte apoptosis via transcriptional regulation of Omi/HtrA2 remains unclear. The present study was designed to investigate whether HSF1 plays a role in Omi/HtrA2 transcriptional regulation and myocardial apoptosis. METHODS AND RESULTS: Assessment of the hearts of mice of different ages was performed, which indicated a decrease in cardiac function reserve and an increase in mitochondrial apoptosis. Omi/HtrA2 overexpression in the elderly was negatively correlated with left ventricular function after exercise overload and positively correlated with myocardial Caspase-9 apoptosis. Chromatin immunoprecipitation (ChIP) of aging hearts and plasmid transfection/RNA interference of H9C2 cells revealed that enhancement of HSF1 expression promotes Omi/HtrA2 expression by inducing the promoter activity of Omi/HtrA2 while also increasing mitochondrial apoptosis by upregulating Omi/HtrA2 expression. CONCLUSIONS: HSF1 acts as a transcriptional factor that induces Omi/HtrA2 expression and Caspase-9 apoptosis in aged cardiomyocytes, while also decreasing cardiac function reserve.

p53 mediated transcription of Omi/HtrA2 in aging myocardium.

AIMS: Omi/HtrA2 is a pro-apoptotic protein, increased mRNA and protein levels of Omi/HtrA2 in aging myocardium facilitates apoptosis and affects mitochondrial homeostasis. Our previous study found that p53 can bind to the Omi/HtrA2 promoter. The purpose of this study was to determine whether p53 participates in regulating the expression of Omi/HtrA2 in aging myocardium. METHODS AND RESULTS: we used Western blot to detect the expression of Omi/HtrA2 and p53 nucleoprotein, and then found that both of them were elevated in aging heart. Furthermore, we also observed the increased binding of p53 to Omi/HtrA2 promoter by chromatin immunoprecipitation. To initially explore the regulation mechanism of Omi/HtrA2, plasmid transfection and RNA interference in NIH3T3 cells were used to upregulate or knock down p53, respectively. The mRNA and protein levels of Omi/HtrA2 were increased with the overexpression of p53 by real-time PCR and Western blot, and Omi/HtrA2 promoter activity enhanced after transfected with pcDNA3.1-p53. The result from RNA interference was quite the contrary.Our study demonstrated that the binding ability of p53 to Omi/HtrA2 promoter was increased in aging myocardium, and increased p53 promoted the mRNA and protein levels of Omi/HtrA2 by enhancing the promoter activity of Omi/HtrA2. CONCLUSIONS: p53 acts as a transcriptional factor that induces Omi/HtrA2 expression in aged cardiomyocytes.These results provide a new way to explore the mechanism of increased Omi/HtrA2 in the aging process of heart.

Omi/HtrA2 Participates in Age-Related Autophagic Deficiency in Rat Liver.

Liver is a vital organ with many important functions, and the maintenance of normal hepatic function is necessary for health. As an essential mechanism for maintaining cellular homeostasis, autophagy plays an important role in ensuring normal organ function. Studies have indicated that the degeneration of hepatic function is associated with autophagic deficiency in aging liver. However, the underlying mechanisms still remain unclear. The serine protease Omi/HtrA2 belongs to the HtrA family and promotes apoptosis through either the caspase-dependent or caspase-independent pathway. Mice lacking Omi/HtrA2 exhibited progeria symptoms (premature aging), which were similar to the characteristics of autophagic insufficiency. In this study, we demonstrated that both the protein level of Omi/HtrA2 in liver and hepatic function were reduced as rats aged, and there was a positive correlation between them. Furthermore, several autophagy-related proteins (LC3II/I, Beclin-1 and LAMP2) in rat liver were decreased significantly with the increasing of age. Finally, inhibition of Omi/HtrA2 resulted in reduced autophagy and hepatic dysfunction. In conclusion, these results suggest that Omi/HtrA2 participates in age-related autophagic deficiency in rat liver. This study may offer a novel insight into the mechanism involved in liver aging.

Genetic variants in oxytocin receptor gene (OXTR) and childhood physical abuse collaborate to modify the risk of aggression in chinese adolescents.

BACKGROUND: Accumulating evidence suggests that genetic and environmental factors may influence aggression susceptibility. However, the etiology of aggressive behavior remains unknown. Compared to some extensively studied candidate genes of aggression, very little is known about the OXTR gene. The objective of this study was to determine whether OXTR genetic variants were associated with aggression risk and whether these polymorphisms showed interactive effects with childhood maltreatment on aggression in Chinese adolescents. METHODS: A total of 996 participants including 488 cases and 488 controls were selected in our study. Aggression, childhood maltreatment were measured by self-reported questionnaire. Buccal cells were collected. Genotyping was performed using SNPscan. Logistic regressions were used to estimate both main effects of OXTR polymorphisms and the interactive effects with childhood maltreatment on aggressive behavior. RESULTS: Participants who carried the rs237885 TT genotypes in OXTR had a higher risk of aggression compared to those who carried GG or GT genotypes under the recessive model (OR=1.40, 95% CI, 1.04-1.89) after controlling for potential confounders. In addition, we also found that the polymorphism had a synergic additive interaction with childhood physical abuse on the aggression risk. LIMITATIONS: The subjects in the present study were only males, thus our findings and conclusions could not be generalized to females. CONCLUSIONS: The present study provides evidence that OXTR genetic variants may contribute to aggression susceptibility. Moreover, this is the first study reporting significant interactive effects of OXTR polymorphism and childhood physical abuse on aggressive behavior in Chinese adolescents.

Association of genetic variations in the serotonin and dopamine systems with aggressive behavior in the Chinese adolescent population: Single- and multiple-risk genetic variants.

BACKGROUND: Genetic predisposition is an important factor leading to aggressive behavior. However, the relationship between genetic polymorphisms and aggressive behavior has not been elucidated. METHODS: We identified candidate genes located in the dopaminergic and serotonin system (DRD3, DRD4, and FEV) that had been previously reported to be associated with aggressive behavior. We investigated 14 tag single-nucleotide polymorphisms (SNPs) using a multi-analytic strategy combining logistic regression (LR) and classification and regression tree (CART) to explore higher-order interactions between these SNPs and aggressive behavior in 318 patients and 558 controls. RESULTS: Both LR and CART analyses suggested that the rs16859448 polymorphism is the strongest individual factor associated with aggressive behavior risk. In CART analysis, individuals carrying the combined genotypes of rs16859448TT/GT-rs11246228CT/TT-rs3773679TT had the highest risk, while rs16859448GG-rs2134655CT had the lowest risk (OR = 5.25, 95% CI: 2.53-10.86). CONCLUSION: This study adds to the growing evidence on the association of single- and multiple-risk variants in DRD3, DRD4, and FEV with aggressive behavior in Chinese adolescents. However, the aggressive behavior scale used to diagnose aggression in this study did not account for comorbid conditions; therefore, further studies are needed to confirm our observations.

Possible association between SIRT1 single nucleotide polymorphisms and predisposition to antisocial personality traits in Chinese adolescents.

Accumulating evidence suggests an association between the SIRT1 gene and human psychiatric disorders. The aim of the study was to investigate the association between SIRT1 and predisposition to antisocial personality traits (ASP) in Chinese adolescents. Participants consisted of 327 controls and 261 juvenile offenders who were diagnosed with predisposition to ASP according to the Personality Diagnostic Questionnaire. Four tag single nucleotide polymorphisms (tagSNPs) of SIRT1, namely rs12778366, rs7896005, rs10823112, and rs4746720, were genotyped. Association analysis between individual SNPs and ASP risk revealed the CC genotype of rs4746720 to be significantly associated with reduced risk of ASP (OR = 0.51, 95% CI = 0.33-0.77, adjusted P = 0.007). Haplotype analysis showed the TAAC haplotype was associated with reduced susceptibility to ASP (OR = 0.72, 95% CI = 0.57-0.91, P = 0.005). Moreover, rs4746720 variants were found to not only have a direct impact on ASP susceptibility but also modulate the effect of alcohol consumption (Y = 0.022X + 0.431 vs. Y = -0.066X + 0.387). The present study is the first to report a significant association between SIRT1 polymorphisms and ASP in adolescents. This finding is expected to aid in the development of effective interventions for this socially and personally costly disorder.

[Aerobic power of students aged 13-15 years in Wuhan City].

OBJECTIVE: To measure the maximal capacity of students aged 13- 15 years by graded exercise test, and establish a model to indirect predict VO2 max. METHODS: A total of 31 school-aged students in Wuhan participated in the study. Maximal oxygen uptake was obtained from a graded maximal exercise test, the anthropometric variables including height, weight, vital capacity( VC), resting heart rate, fat mass were measured and body mass index( BMI), body fat percentage( FAT%) was calculated. The relationships between maximal oxygen uptake and anthropometric characteristics were investigated in partial correlation analysis and a linear multiple regression model was established. RESULTS: There was a significant difference in mass-relative VO_(2max)[( 48. 00± 5. 80) L / min vs( 39. 79 ± 6. 37) L / min, P < 0. 001], absolute VO_(2max)[( 2. 66 ± 0. 29)m L /( kg·min) vs( 2. 02 ± 0. 36) m L /( kg·min), P < 0. 001], pulse oxygen [( 13. 33 ±1. 28) m L / beat vs( 10. 34 ± 1. 70) m L / beat, P < 0. 001] between the boys and girls respectively. And a statistically significant negative correlation was observed between values of maximal oxygen uptake and weight, BMI, FAT% and resting heart rate( P <0. 05), while lean body mass was positive with VO_(2max)( P < 0. 05). Multiple regression analysis suggested that the best VO_(2max) predictive model of boys was VO_(2max)= 0. 856 +0. 044 × lean body mass- 0. 011 × resting heart rate + 0. 0002 × vital capacity( R =0. 903, R~2= 0. 816), and the prediction equation of girls was follows: VO_(2max)= 4. 769 +0. 044 × lean body mass- 0. 020 × resting heart rate- 0. 254 × age( R = 0. 813, R~2=0. 662). CONCLUSION: The present study suggests that anthropometric characteristics might be closely related with maximal aerobic capacity and can effectively predict the maximal aerobic power.