194 research outputs found
Association Between Chronic Exposure to Arsenic and Slow Nerve Conduction Velocity Among Adolescents in Taiwan
The association between chronic exposure to arsenic and peripheral
neuropathy has been controversial in previous studies, which may be due
to the influence of factors, such as age, gender, chronic diseases,
occupational injuries, and arsenic exposure. To clarify the question of
this association, a cross-sectional study was designed. In total, 130
junior high school students aged 12-14 years were included and
exami-ned for the motor and sensory nerve conduction velocity of
peripheral nerves in their right-upper and lower limbs. Concentrations
of arsenic in well-water and history of drinking well-water were
retrieved from a baseline database created in 1991. After adjustment
for gender and height, a significant odds ratio of 2.9 (95% confidence
interval [CI] 1.1-7.5) was observed for the development of slow nerve
conduction velocity of the sural sensory action potential (SAP) among
the study subjects with a cumulative arsenic dosage of >100.0 mg. In
addition, a borderline statistical significance with odds ratio of 7.8
(95% CI 1.001-69.5) for the development of slow nerve conduction
velocity of sural SAP was also observed among the study subjects who
drank well-water containing arsenic concentrations of >50.0
\u3bcg/L and with a cumulative arsenic dosage of >100.0 mg. The
study found that chronic exposure to arsenic might induce peripheral
neuropathy. It also found that the slowing of the nerve conduction
velocity of sural SAP might be an early marker of chronic arsenic
neuropathy
Rainfall Variation under Different Climate Change Scenarios Based on Cmip3 and Cmip5 Projections: a Case Study in Taiwan
Source: ICHE Conference Archive - https://mdi-de.baw.de/icheArchive
Bmi-1 Regulates Snail Expression and Promotes Metastasis Ability in Head and Neck Squamous Cancer-Derived ALDH1 Positive Cells
Recent studies suggest that ALDH1 is a putative marker for HNSCC-derived cancer
stem cells. However, the regulation mechanisms that maintain the stemness and metastatic capability
of HNSCC-ALDH1+ cells remain unclear. Initially, HNSCC-ALDH1+ cells from HNSCC patient showed
cancer stemness properties, and high expression of Bmi1 and Snail. Functionally, tumorigenic properties
of HNSCC-ALDH1+ cells could be downregulated by knockdown of Bmi-1. Overexpression of Bmi-1 altered in
expression property ALDH1− cells to that of ALDH1+ cells. Furthermore, knockdown of Bmi-1 enhanced
the radiosensitivity of radiation-treated HNSCC-ALDH1+ cells. Moreover, overexpression of Bmi-1 in
HNSCC-ALDH1− cells increased tumor volume and number of pulmonary metastatic lesions by xenotransplant
assay. Importantly, knock-down of Bmi1 in HNSCC-ALDH1+ cells significantly decreased distant metastases in
the lungs. Clinically, coexpression of Bmi-1/Snail/ALDH1 predicted the worst prognosis in HNSCC
patients. Collectively, our data suggested that Bmi-1 plays a key role in
regulating Snail expression and cancer stemness properties of HNSCC-ALDH1+ cells
Association between genetic variant on chromosome 12p13 and stroke survival and recurrence: a one year prospective study in Taiwan
<p>Abstract</p> <p>Background</p> <p>The association between ischemic stroke and 2 single nucleotide polymorphisms (SNPs) on chromosome 12p13, rs12425791 and rs11833579 appears inconsistent across different samples. These SNPs are close to the ninjurin2 gene which may alter the risk of stroke by affecting brain response to ischemic injury. The purpose of this study was to investigate the association between these two SNPs and ischemic stroke risk, as well as prognostic outcomes in a Taiwanese sample.</p> <p>Methods</p> <p>We examined the relations of these two SNPs to the odds of new-onset ischemic stroke, ischemic stroke subtypes, and to the one year risk of stroke-related death or recurrent stroke following initial stroke in a case-control study. A total of 765 consecutive patients who had first-ever ischemic stroke were compared to 977 stroke-free, age-matched controls. SNPs were genotyped by Taqman fluorescent allelic discrimination assay. The association between ischemic stroke and SNPs were analyzed by multivariate logistic regression. Cox proportional hazard model was used to assess the effect of individual SNPs on stroke-related mortality or recurrent stroke.</p> <p>Results</p> <p>There was no significant association between SNP rs12425791 and rs11833579 and ischemic stroke after multiple testing corrections. However, the marginal significant association was observed between SNP rs12425791 and large artery atherosclerosis under recessive model (OR, 2.30; 95%CI, 1.22-4.34; q-value = 0.062). Among the 765 ischemic stroke patients, 59 died or developed a recurrent stroke. After adjustment for age, sex, vascular risk factors and baseline stroke severity, Cox proportional hazard analysis indicated that the hazard ratios were 2.76 (95%CI, 1.34-5.68; q-value, 0.02) and 2.15 (95%CI, 1.15-4.02; q-value, 0.03) for individuals with homozygous variant allele of rs12425791 and rs11833579, respectively.</p> <p>Conclusions</p> <p>This is a precedent study that found genetic variants of rs12425791 and rs11833579 on chromosome 12p13 are independent predictors of stroke-related mortality or stroke recurrence in patients with incident ischemic stroke in Taiwan. Further study is needed to explore the details of the physiological function and the molecular mechanisms underlying the association of this genetic locus with ischemic stroke.</p
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Efficacy of pharmacologic treatment in tinnitus patients without specific or treatable origin: A network meta-analysis of randomised controlled trials
Background-
Although tinnitus has a prevalence between 20 and 42.8%, the currently recommended management for tinnitus, such as tinnitus support and psychologic therapies, are relatively time-consuming and expensive. Several new pharmacologic treatments designed for tinnitus patients without specific origin had been developed but their efficacy remains unclear.
Methods-
The current Network Meta-Analysis (NMA) of randomised controlled trials (RCTs) was conducted to evaluate the efficacy of different pharmacologic treatments for tinnitus management in tinnitus patients without specific or treatable origin (i.e. primary tinnitus). Databases were searched from inception to April 5th, 2021. All network meta-analytic procedures were conducted under the frequentist model. We calculated the effect size of outcomes with different rating scales with standardized mean difference. PROSPERO registration: CRD42020177742.
Findings-
Overall, 36 RCTs were included with 2,761 participants. The main results revealed that pharmacologic interventions with brain-acting effect (for example, amitriptyline, acamprosate, and gabapentin) and those with anti-inflammation/anti-oxidant effect (for example, intra-tympanic dexamethasone injection plus oral melatonin) were associated with superior improvement in tinnitus severity and response rate compared to placebo/control. Oral amitriptyline were associated with the highest improvement in tinnitus severity and the fourth highest response rate. None of the investigated interventions was associated with different changes in quality of life compared to placebo/control. All the investigated treatments were associated with similar drop-out rate to placebo/control.
Interpretation-
The current NMA suggests a potential role for treatments with brain-acting effect (for example, amitriptyline, acamprosate, and gabapentin) or anti-inflammation/anti-oxidant effect (for example, intra-tympanic dexamethasone injection plus oral melatonin) as the preferable effective treatments for tinnitus without specific or treatable origin
An evolutionary approach to rehabilitation patient scheduling: A case study
Focusing on real settings, this study aimed to develop an evolutionary approach based on genetic algorithm for solving the problem of rehabilitation patient scheduling to increase service quality by reducing patient waiting time and improve operation efficiency by increasing the therapy equipment utilization. Indeed, due to partial precedence constraints of rehabilitation therapies, the problem can be structured as a hybrid shop scheduling problem that has received little attention to date. In addition, a mixed integer programming model was also constructed as a benchmark to validate the solution quality with small problems. Based on empirical data from a Medical Center in Taiwan, several experiments were conducted to estimate the validity of the proposed algorithm. The results showed that the proposed algorithm can reduce patient waiting time and enhance resource utilization and thus demonstrated the practicality of the proposed algorithm. Indeed, a decision support system embedded with the developed algorithm has been implemented in this medical center.
Association Between Chronic Exposure to Arsenic and Slow Nerve Conduction Velocity Among Adolescents in Taiwan
The association between chronic exposure to arsenic and peripheral
neuropathy has been controversial in previous studies, which may be due
to the influence of factors, such as age, gender, chronic diseases,
occupational injuries, and arsenic exposure. To clarify the question of
this association, a cross-sectional study was designed. In total, 130
junior high school students aged 12-14 years were included and
exami-ned for the motor and sensory nerve conduction velocity of
peripheral nerves in their right-upper and lower limbs. Concentrations
of arsenic in well-water and history of drinking well-water were
retrieved from a baseline database created in 1991. After adjustment
for gender and height, a significant odds ratio of 2.9 (95% confidence
interval [CI] 1.1-7.5) was observed for the development of slow nerve
conduction velocity of the sural sensory action potential (SAP) among
the study subjects with a cumulative arsenic dosage of >100.0 mg. In
addition, a borderline statistical significance with odds ratio of 7.8
(95% CI 1.001-69.5) for the development of slow nerve conduction
velocity of sural SAP was also observed among the study subjects who
drank well-water containing arsenic concentrations of >50.0
μg/L and with a cumulative arsenic dosage of >100.0 mg. The
study found that chronic exposure to arsenic might induce peripheral
neuropathy. It also found that the slowing of the nerve conduction
velocity of sural SAP might be an early marker of chronic arsenic
neuropathy
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