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1.
Front Endocrinol (Lausanne) ; 14: 1271395, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-38027198

RESUMO

Introduction: This study aimed to explore the impact of gonadotropin-releasing hormone agonists (GnRHa) on final adult height (FAH) in girls with early and fast puberty. Methods: A retrospective study was conducted by reviewing data from the medical records of the Pediatric Endocrinology Clinics between January 1, 2010, and December 31, 2020, at MacKay Children's Hospital. The treatment group included 109 patients who received 3.75 mg monthly for at least 1 year, whereas the control group consisted of 95 girls who received no treatment. Results: The treatment group was significantly older at the time of inclusion(chronological age (CA1), treatment vs. control, 8.7 vs. 8.4 years, p < 0.001), had a more advanced bone age (BA) (BA1, 11.5 vs. 10.8 years, p < 0.001), BA1-CA1 (2.7 vs. 2.2 years, p < 0.001), and shorter predicted adult height (PAH1) (153.3 vs. 157.1 cm, p = 0.005) that was significantly lower than their target height (Tht)(PAH1-Tht, -3.9 vs. -1.3 cm, p = 0.039). The FAHs of the GnRHa and the control group were similar (157.0 vs. 156.7 cm, p = 0.357) and were not significantly different from their Tht (FAH vs. Tht in the GnRHa group, 157.0 vs. 157.0 cm; control group, 156.7 vs. 157.0 cm). In the subgroup analysis, FAH was significantly higher after GnRHa treatment in those with PAH1 less than 153 cm and Tht (154.0 vs. 152.0 cm, p = 0.041), and those whose CA1 was between 8 and 9 years (158.0 vs. 155.4 cm, p = 0.004). We defined satisfactory FAH outcome as FAH-PAH1≥5 cm and significant factors were GnRHa therapy, PAH1 shorter than their Tht, age younger than 9 years, and faster growth velocity during the first year. Discussion: GnRHa is effective in restoring the Tht in some early and fast pubertal girls, especially in those with poorly PAH (PAH lower than 153 cm and shorter than their target height). A younger age at initiation of treatment and a faster growth velocity during treatment are associated with a better height gain.


Assuntos
Hormônio Liberador de Gonadotropina , Puberdade Precoce , Criança , Feminino , Humanos , Adulto , Hormônio Liberador de Gonadotropina/farmacologia , Puberdade Precoce/tratamento farmacológico , Estudos Retrospectivos , Estatura , Puberdade
2.
Bioresour Technol ; 384: 129277, 2023 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-37290703

RESUMO

The objective of this study was to explore the potential of utilizing Chlorella sorokiniana SU-1 biomass grown on dairy wastewater-amended medium as sustainable feedstock for the biosynthesis of ß-carotene and polyhydroxybutyrate (PHB) by Rhodotorula glutinis #100-29. To break down the rigid cell wall, 100 g/L of microalgal biomass was treated with 3% sulfuric acid, followed by detoxification using 5% activated carbon to remove the hydroxymethylfurfural inhibitor. The detoxified microalgal hydrolysate (DMH) was used for flask-scale fermentation, which yielded a maximum biomass production of 9.22 g/L, with PHB and ß-carotene concentration of 897 mg/L and 93.62 mg/L, respectively. Upon scaling up to a 5-L fermenter, the biomass concentration increased to 11.2 g/L, while the PHB and ß-carotene concentrations rose to 1830 mg/L and 134.2 mg/L. These outcomes indicate that DMH holds promise as sustainable feedstock for the production of PHB and ß-carotene by yeast.


Assuntos
Chlorella , Microalgas , Rhodotorula , beta Caroteno , Águas Residuárias , Biomassa
3.
Bioresour Technol ; 376: 128858, 2023 May.
Artigo em Inglês | MEDLINE | ID: mdl-36907225

RESUMO

A sequential anaerobic digestion and phycoremediation process was employed to recover nutrients and remove pollutants from dairy wastewater (DW), while simultaneously producing biomethane and biochemicals. Anaerobic digestion of 100% DW achieved a methane content and production rate of 53.7% and 0.17 L/L/d, respectively. This was accompanied by the removal of 65.5% chemical oxygen demand (COD), 86% total solid (TS), and 92.8% volatile fatty acids (VFAs). The anaerobic digestate was then used to grow Chlorella sorokiniana SU-1. Using 25% diluted digestate as the medium, SU-1 could reach 4.64 g/L biomass concentration, with total nitrogen (TN), total phosphorus (TP) and COD removal efficiencies of 77.6%, 87.1% and 70.4%, respectively. The obtained microalgal biomass (contained 38.5% carbohydrates, 24.9% proteins, 8.8% lipids) was used to co-digest with DW, resulting in good methane production performance. Co-digestion with 25% (w/v) algal biomass obtained a higher CH4 content (65.2%) and production rate (0.16 L/L/d) than other ratios.


Assuntos
Chlorella , Microalgas , Águas Residuárias , Microalgas/metabolismo , Chlorella/metabolismo , Anaerobiose , Biomassa , Nitrogênio/metabolismo , Metano , Digestão
4.
Taiwan J Obstet Gynecol ; 61(5): 788-793, 2022 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-36088045

RESUMO

OBJECTIVE: In this study, we investigated various pubertal presentations and progressions before and after estrogen induction therapy and the correlations with Turner syndrome karyotypes. MATERIALS AND METHODS: We reviewed the medical records of patients with Turner syndrome diagnosed before the age of 18 years between 2000 and 2019. Sixty-six patients were enrolled and distributed into 45,X monosomy group, X chromosome structural abnormalities group and X mosaicism group. The pubertal presentations were classified into spontaneous puberty, arrested puberty and no spontaneous puberty. All patients' karyotypes, pubertal progressions and laboratory data were collected and analyzed. RESULTS: The karyotypes were highly correlated with pubertal presentations. No spontaneous puberty was noticed in 58.3% 45,X monosomy patients, 50% patients with X chromosome structural abnormalities had arrested puberty, whereas 70% patients with X mosaicism had spontaneous puberty. Estrogen induction therapy in patients with no spontaneous puberty could induce puberty and the tempo of puberty may approximate to the spontaneous puberty group (median, 2.3 vs. 2.2 years, P = 0.95). In both interventional groups, the FSH level was distinguishable before treatment (median, 65.1 vs. 100.4 mIU/mL, P = 0.02). After long term estrogen therapy, the FSH could be suppressed to similar level in both interventional groups (median, 37.5 vs 34.5 mIU/mL, P = 0.84). Neither LH nor E2 level provided valuable information before and after treatment. CONCLUSION: The karyotypes were highly correlated with pubertal presentations at Turner syndrome patients. The integrity of 2nd X chromosome plays an important role. Low dose estrogen could mimic the tempo of puberty even delay induction age at Taiwan. The FSH data could provide predictive information of pubertal induction for both interventional groups.


Assuntos
Síndrome de Turner , Adolescente , Estrogênios/uso terapêutico , Hormônio Foliculoestimulante , Humanos , Quimioterapia de Indução , Monossomia , Síndrome de Turner/tratamento farmacológico , Síndrome de Turner/genética
5.
IEEE Trans Cybern ; 52(8): 8258-8271, 2022 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-33531316

RESUMO

Aerial manipulators have the potential to perform various tasks with high agility and mobility, but the requirement of system parameters and the complicated dynamic model impede the implementation in practice. To deal with uncertain parameters and complexity of the coupled dynamic model, a decoupling approach is presented in this article by utilizing the adaptive/robust techniques and reinforcement learning approach for the tracking control of quadrotors with position control on the robotic arm. A reinforcement learning approach is proposed to control the robotic arm ensuring minimal effect on the quadrotor dynamics while following the desired trajectory. With the design of nominal inputs, the dynamic uncertainties from the quadrotor, robotic arm, and payload are coped with by utilizing the proposed adaptive algorithms. In addition, the residue of interactive force/torque after the use of DDPG is compensated by robust controllers so that the stability and tracking performance are guaranteed. Numerical examples and experiments are illustrated to demonstrate the efficacy of the presented aerial manipulator control structure and algorithms.


Assuntos
Algoritmos , Fenômenos Mecânicos , Simulação por Computador , Retroalimentação , Aprendizagem
6.
Chemosphere ; 291(Pt 1): 133057, 2022 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-34838828

RESUMO

Utilizing wastewaters as feedstock for microalgal cultivation has the dual benefits of water-saving and low nutrient costs, with simultaneous remediation of pollutants and generation of value-added biochemical products. This study employed two different strategies to treat raw dairy wastewaters with moderate and high chemical oxygen demand (COD) levels. For moderate-COD dairy wastewater, the wastewater was directly utilized as feedstock for algal cultivation, in which the effects of wastewater dilution ratios and algal inoculum sizes were investigated. The results show that the microalga strain used (Chlorella sorokiniana SU-1) was capable of obtaining a high biomass concentration of 3.2 ± 0.1 g/L, accompanied by 86.8 ± 6%, 94.6 ± 3%, and 80.7 ± 1%, removal of COD, total phosphorus (TP) and total nitrogen (TN), respectively. Meanwhile, the obtained microalgal biomass has lipids content of up to 12.0 ± 0.7% at a wastewater dilution ratio of 50% and an inoculum size of 2 g/L. For high-COD dairy wastewater, an integrated process of anaerobic digestion and microalgal phycoremediation was employed, and the effect of inoculum sizes was also studied. The inoculum size of 2 g/L gave highest biomass production of 4.25 ± 0.10 g/L with over 93.0 ± 2.0% removal of COD, TP, and TN. The harvested microalgal biomass has lipids and protein content of 12.5 ± 2.2% and 18.0 ± 2.2%, respectively. The present study demonstrated potential microalgal phycoremediation strategies for the efficient COD removal and nutrients recovery from dairy wastewater of different COD levels with simultaneous production of microalgal biomass which contains valuable components, such as protein and lipids.


Assuntos
Chlorella , Microalgas , Purificação da Água , Anaerobiose , Biomassa , Nitrogênio/análise , Águas Residuárias
7.
Front Endocrinol (Lausanne) ; 13: 1083690, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-36704033

RESUMO

Introduction: Autoimmune thyroid disease (AITD) is the most common associated autoimmune disorder in type 1 diabetes (T1D). Early detection of AITD is crucial to optimize glycemic control, growth, and intellectual development. In this prospective cohort study, we sought to characterize the prevalence, incident ages and risk factors of AITD in children and adolescents with T1D. Materials and methods: Patients with T1D diagnosed at ≤ 18 years at MacKay Children's Hospital, Taipei, from 1990 to 2019 underwent annual screening for AITD. Institutional Review Board-approved data on age, sex, and disease profile are collected. Statistical analysis was performed by using independent sample t test for continuous variables, chi-squared test for categorical variables, and Kaplan-Meier estimates of cumulative incidence of AITD were calculated. A p value of <0.05 was considered statistically significant. Results: We prospectively followed up 808 patients with T1D, 761 patients were included in the study. Of these patients, 197 (25.9%) of them had thyroid autoimmunity, meaning positivity of thyroid autoantibodies. Females had a higher prevalence of thyroid autoimmunity than males (59.9%, p = 0.012). Altogether, 5.5% patients developed AITD (4.1% had Graves disease; 1.4% had Hashimoto disease), at a mean age of 17.8 ± 8.5 years. The cumulative incidence of AITD at 30 years of disease duration was 0.29 in the total group and was significantly higher in females (0.39, n = 397) than in males (0.15, n = 364, p<0.001). Discussion: In Taiwan, the prevalence of AITD in pediatric population with T1D increases with age, a longer disease duration and female sex. For early detection of autoimmune thyroid disease in Taiwanese children and adolescents with T1D, an annual AITD screening program should be implemented.


Assuntos
Diabetes Mellitus Tipo 1 , Doença de Graves , Doença de Hashimoto , Masculino , Humanos , Criança , Feminino , Adolescente , Adulto Jovem , Adulto , Doença de Hashimoto/epidemiologia , Doença de Hashimoto/complicações , Diabetes Mellitus Tipo 1/complicações , Diabetes Mellitus Tipo 1/epidemiologia , Estudos Prospectivos , Autoanticorpos
8.
J Environ Manage ; 296: 113193, 2021 Oct 15.
Artigo em Inglês | MEDLINE | ID: mdl-34237671

RESUMO

Following the escalating human population growth and rapid urbanization, the tremendous amount of urban and industrial waste released leads to a series of critical issues such as health issues, climate change, water crisis, and pollution problems. With the advantages of a favorable carbon life cycle, high photosynthetic efficiencies, and being adaptive to harsh environments, algae have attracted attention as an excellent agent for pollution prevention and waste phycoremediation. Following the concept of circular economy and biorefinery for sustainable production and waste minimization, this review discusses the role of four different algal-based wastewater treatment technologies, including high-rate algal ponds (HRAPs), HRAP-absorption column (HRAP-AC), hybrid algal biofilm-enhanced raceway pond (HABERP) and algal turf scrubber (ATS) in waste management and resource recovery. In addition to the nutrient removal mechanisms and operation parameters, recent advances and developments have been discussed for each technology, including (1) Innovative operation strategies and treatment of emerging contaminants (ECs) employing HRAPs, (2) Biogas upgrading utilizing HRAP-AC system and approaches of O2 minimization in biomethane, (3) Operation of different HABERP systems, (4) Life-cycle and cost analysis of HRAPs-based wastewater treatment system, and (5) Value-upgrading for harvested algal biomass and life-cycle cost analysis of ATS system.


Assuntos
Microalgas , Purificação da Água , Biomassa , Humanos , Lagoas , Tecnologia , Eliminação de Resíduos Líquidos , Águas Residuárias
9.
Chemosphere ; 271: 129800, 2021 May.
Artigo em Inglês | MEDLINE | ID: mdl-33736224

RESUMO

Offering a potential solution for global food security and mitigating environmental issues caused by the expansion of land-based food production, the carbon-hunger and nutrient-rich microalgae emerged as a sustainable food source for both humans and animals. Other than as an alternative source for protein, microalgae offer its most valuable nutrients, omega-3 and 6 long-chain polyunsaturated fatty acids where the content can compete with that of marine fish with lower chemicals contamination and higher purity. Furthermore, the colorful pigments of microalgae can act as antioxidants together with many other health-improving properties as well as a natural colorant. In addition, the supplementation of algae as animal feed provides plentiful benefits, such as improved growth and body weight, reduced feed intake, enhanced immune response and durability towards illness, antibacterial and antiviral action as well as enrichment of livestock products with bioactive compounds. The significant breakthrough in algal biotechnology has made algae a powerful "cell factory" for food production and lead to the rapid growth of the algal bioeconomy in the food and feed industry. The first overview of this review was to present the general of microalgae and its potential capability. Subsequently, the nutritional compositions of microalgae were discussed together with its applications in human foods and animal feeds, followed by the exploration of their economic feasibility and sustainability as well as market trends. Lastly, both challenges and future perspectives were also discussed.


Assuntos
Ácidos Graxos Ômega-3 , Microalgas , Ração Animal , Animais , Biotecnologia , Ácidos Graxos , Humanos
10.
Pediatr Neonatol ; 62(2): 187-194, 2021 03.
Artigo em Inglês | MEDLINE | ID: mdl-33388255

RESUMO

BACKGROUND: The gonadotropin-releasing hormone (GnRH) stimulation test is the gold standard for confirming the activation of the hypothalamic-pituitary-gonadal axis in central precocious puberty (CPP). However, it is time-consuming and costly. Our aim was to search for a simpler diagnostic modality for CPP by 1) evaluating the performance of basal serum luteinizing hormone (LH), 2) constructing a practical scoring system, and 3) determining the optimal single sampling time for serum LH in the GnRH stimulation test. METHODS: Data of girls aged between 3 and 9 years at the time of the GnRH stimulation test, who attended our endocrine clinic at the MacKay Children's Hospital for signs of puberty between July 2014 and June 2019, were analyzed retrospectively. We recorded patients' age, height, weight, breast Tanner stage (BS), bone age, serum LH, and follicle-stimulating hormone (FSH). Receiver operating characteristic (ROC) curves and the Youden index were used to obtain the optimal basal serum LH level. Binary logistic regression was employed to construct a practical scoring system. Cross-sectional, cumulative frequency, and ROC curves were used to simplify the GnRH stimulation test. RESULTS: Overall, 381 sets of GnRH stimulation tests were performed in 313 patients. Basal serum LH ≥ 0.2 IU/L demonstrated 70% sensitivity and 70% specificity for predicting positive GnRH stimulation test results. The practical scoring system (3 × BS + 3 × LH + 4 × FSH) showed 76% sensitivity and 72% specificity. The serum LH level at 30 min after intravenous gonadorelin exhibited 99% sensitivity and 100% specificity. CONCLUSION: Single sampling of serum LH at 30th minute post-injection of GnRH demonstrated a diagnostic performance equivalent to the traditional GnRH stimulation test in diagnosing CPP. Therefore, this approach could become the simplest diagnostic modality.


Assuntos
Puberdade Precoce/diagnóstico , Criança , Pré-Escolar , Feminino , Hormônio Foliculoestimulante/sangue , Hormônio Liberador de Gonadotropina/administração & dosagem , Humanos , Hormônio Luteinizante/sangue , Puberdade Precoce/sangue , Estudos Retrospectivos , Sensibilidade e Especificidade
11.
PLoS One ; 15(10): e0239160, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-33027293

RESUMO

Diabetic ketoacidosis (DKA) is associated with dehydration and which can cause acute kidney injury (AKI). The proportion of AKI in children and adolescents with DKA has not been reported in East Asian population. This study aimed to identify the prevalence of AKI and to determine whether there is an association between AKI severity and recovery time from metabolic acidosis in children and adolescents with DKA. Medical records of children and adolescents (aged <18 years) presenting with type 1 or type 2 diabetes mellitus and DKA between 2000-2017 at the MacKay Children's Hospital were retrospectively reviewed. AKI was defined by an admission creatinine level >1.5 times the calculated expected baseline creatinine level. Patients were divided into three groups based on AKI severity: no AKI, mild AKI, and severe AKI. In total, 170 (56.5%) patients with DKA presented AKI (mild AKI, 116 [38.5%]; severe AKI, 54 [18.0%]). Heart rate and laboratory parameters related to dehydration, such as corrected sodium level and blood urea nitrogen, were strongly associated with AKI development (P<0.01). Blood pH, plasma glucose, and potassium levels were also associated with AKI. A negative correlation with borderline significance between the estimated glomerular filtration rate (eGFR) and recovery time from metabolic acidosis was observed in the severe AKI group. AKI was highly prevalent in children and adolescents with DKA. An association between AKI and biomarkers indicating dehydration was noted. The recovery time from metabolic acidosis following treatment may be longer in children with a decreased eGFR who present with severe AKI. AKI is a common complication in children with DKA.


Assuntos
Injúria Renal Aguda/etiologia , Diabetes Mellitus Tipo 1/complicações , Diabetes Mellitus Tipo 2/complicações , Cetoacidose Diabética/complicações , Injúria Renal Aguda/epidemiologia , Injúria Renal Aguda/metabolismo , Adolescente , Biomarcadores/metabolismo , Criança , Desidratação/complicações , Desidratação/metabolismo , Cetoacidose Diabética/metabolismo , Feminino , Humanos , Masculino , Prevalência , Estudos Retrospectivos , Fatores de Risco , Taiwan/epidemiologia
12.
Diabetes Res Clin Pract ; 170: 108485, 2020 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-33035596

RESUMO

AIMS: To test the reliability and validity of the Chinese version of the Insulin Treatment Appraisal Scale (ITAS) questionnaire in patients with type 2 diabetes mellitus (T2DM). METHODS: A total of 200 patients with T2DM were consecutively recruited from the outpatient clinic in Taiwan. The World Health Organization guideline was followed to translate the questionnaire. The internal consistency was assessed by Cronbach's α coefficient and item-total correlations. The construct validity was evaluated by using confirmatory factor analysis, convergent validity, and discriminate validity. RESULTS: The Cronbach's α coefficient for estimates of internal consistency of the total scale was 0.72, and ranged from 0.76 to 0.77 for the subscales. A value of ≥0.40 was considered being substantial. The item-total correlation values were 14 out of 20 items having substantial correlations (4 out of 4 items on the positive appraisal scale and 10 out of 16 items on the negative appraisal scale). The confirmatory factor analysis confirmed both positive and negative factors with total explained variance 33.9% (12.2% for positive subscale and 21.7% for negative subscale). The success rate, calculated from the item-total correlation values, was 70% for the convergent validity (100% for positive subscale and 63% for negative subscale) and 90% for discriminate validity (100% for positive subscale and 88% for negative subscale), respectively. Both the ceiling effect and floor effect were 0%. CONCLUSIONS: The Chinese version of the ITAS questionnaire is a valid and reliable instrument for measuring the perceptions of insulin injection in patients with T2DM.


Assuntos
Diabetes Mellitus Tipo 2/tratamento farmacológico , Diabetes Mellitus Tipo 2/psicologia , Hipoglicemiantes/uso terapêutico , Insulina/uso terapêutico , Inquéritos e Questionários/normas , Idoso , Instituições de Assistência Ambulatorial , Povo Asiático , Análise Fatorial , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Psicometria/normas , Reprodutibilidade dos Testes , Taiwan , Tradução , Organização Mundial da Saúde
13.
FASEB J ; 34(6): 8459-8474, 2020 06.
Artigo em Inglês | MEDLINE | ID: mdl-32362042

RESUMO

Human Leukocyte Antigen (HLA)-DQ2 and HLA-DQ8 are genetic risk factors for Type 1 Diabetes Mellitus (T1DM) and Celiac disease (CD) in Caucasians, but their association with Taiwanese Han population is unknown. We screened 532 Taiwanese T1DM patients for CD biomarkers including anti-tissue transglutaminase (TGM2), anti-gliadin and anti-neoepitope antibodies (Abs), sequencing DQB1 genotypes, and characterized the TGM2 Abs. We report that 3.76% of Taiwanese patients had TGM2-Abs and all had no CD's symptoms. In contrast to Caucasian's CD patients, DQ2/DQ8 only constituted ~4/5 of TGM2-Abs positive patients, while the other ~1/5 patients belonged to different HLA genotypes. Either anti-gliadin or anti-neoepitope Abs coexisted with ~3/4 of TGM2-Abs positive patients that were likely due to gluten-ingestion, while the cause of TGM2-Abs production for other ~1/4 of patients was unknown. Purified anti-TGM2 IgA (TGA) and anti-TGM2 IgG (TGG) could bind on endothelial cells surface, recognized native better than denatured forms of TGM2, and TGA inhibited TGM2's transamidation activity by up to 80% but TGG had no effects. Epitope mapping of all TGM2-Abs positive sera demonstrated that TGM2-Abs had heterogeneity in specificities. This is the first study on the differences between Taiwanese Han group and Caucasian in HLA genotypes and properties of TGM2-Abs.


Assuntos
Autoanticorpos/genética , Diabetes Mellitus Tipo 1/genética , Proteínas de Ligação ao GTP/genética , Antígenos HLA-DQ/genética , Transglutaminases/genética , Adolescente , Doença Celíaca/genética , Criança , Pré-Escolar , Células Endoteliais/metabolismo , Feminino , Genótipo , Gliadina/genética , Humanos , Imunoglobulina A/genética , Lactente , Masculino , Proteína 2 Glutamina gama-Glutamiltransferase , Taiwan
14.
Pediatr Neonatol ; 61(3): 311-317, 2020 06.
Artigo em Inglês | MEDLINE | ID: mdl-31980413

RESUMO

BACKGROUND: Graves disease (GD) is the most common cause of thyrotoxicosis in children and adolescents, accounting for 15% of all thyroid diseases during childhood. Anti-thyroid drugs (ATD) are recommended as the first-line treatment in children and adolescents. However, the remission rate is lower in children than in adults, and the optimal treatment duration and favorable factors associated with remission remain unknown. We aimed to investigate long-term outcomes of pediatric GD patients receiving ATD. METHODS: We retrospectively reviewed medical charts of 396 GD subjects from 1985 to 2017 at MacKay Children's Hospital. Ninety-six patients were excluded from the analyses, including 71 patients followed for less than one year, 6 patients who received radioactive therapy and 19 patients who received surgery. The remaining 300 patients initially treated with ATD and followed up for more than 1 year constituted our study population. RESULTS: The 300 patients comprised 257 (85.7%) females and 43 (14.3%) males. Their median age at diagnosis was 11.6 (range 2.7-17.8) years with 11 patients (3.7%) younger than 5 years. Their median follow-up period was 4.7 (range 1.1-23.9) years. Overall, 122 patients achieved the criteria for discontinuing ATD treatment, and seventy-nine (39.9%) patients achieved remission, with a median follow-up period of 5.3 (range 1.5-20.1) years. Patients in the remission group were more likely to be aged <5 years (remission vs. relapse vs. ongoing ATD; 11.4 vs. 0 vs. 2.6%, P = 0.02), less likely to have a family history of thyroid disease (24.1 vs. 42.1 vs. 52.6%, P = 0.001), and had lower TSH receptor antibody (TRAb) levels (42.8 vs. 53.6 vs. 65.1%, P = 0.02) at the time of diagnosis. CONCLUSION: Long-term ATD remains an effective treatment option for GD in children. Pediatric GD patients aged <5 years, having no family history of thyroid disease and having initial lower TRAb levels were more likely to achieve remission.


Assuntos
Antitireóideos/uso terapêutico , Doença de Graves/tratamento farmacológico , Adolescente , Criança , Pré-Escolar , Feminino , Doença de Graves/genética , Humanos , Masculino , Estudos Retrospectivos
15.
Biochim Biophys Acta Mol Basis Dis ; 1865(2): 428-433, 2019 02 01.
Artigo em Inglês | MEDLINE | ID: mdl-30465894

RESUMO

Monogenic diabetes is caused by mutations that reduce ß-cell function. While Sanger sequencing is the standard method used to detect mutated genes. Next-generation sequencing techniques, such as whole exome sequencing (WES), can be used to find multiple gene mutations in one assay. We used WES to detect genetic mutations in both permanent neonatal (PND) and type 1B diabetes (T1BD). A total of five PND and nine T1BD patients were enrolled in this study. WES variants were assessed using VarioWatch, excluding those identified previously. Sanger sequencing was used to confirm the mutations, and their pathogenicity was established via the literature or bioinformatic/functional analysis. The PND and T1BD patients were diagnosed at 0.1-0.5 and 0.8-2.7 years of age, respectively. Diabetic ketoacidosis was present at diagnosis in 60% of PND patients and 44.4% of T1BD patients. We found five novel mutations in five different genes. Notably, patient 602 had a novel homozygous missense mutation c.1295C > A (T432 K) in the glucokinase (GCK) gene. Compared to the wild-type recombinant protein, the mutant protein had significantly lower enzymatic activity (2.5%, p = 0.0002) and Vmax (1.23 ±â€¯0.019 vs. 0.33 ±â€¯0.016, respectively; p = 0.005). WES is a robust technique that can be used to unravel the etiologies of genetically heterogeneous forms of diabetes. Homozygous inactivating mutations of the GCK gene may have a significant role in PND pathogenesis.


Assuntos
Diabetes Mellitus Tipo 1/enzimologia , Diabetes Mellitus Tipo 1/genética , Sequenciamento do Exoma , Glucoquinase/genética , Glucoquinase/metabolismo , Mutação/genética , Feminino , Humanos , Lactente , Recém-Nascido , Cinética , Masculino
16.
J Hazard Mater ; 357: 180-186, 2018 09 05.
Artigo em Inglês | MEDLINE | ID: mdl-29886363

RESUMO

This study evaluated the methanogens responsible for methanogenic degradation of tetramethylammonium hydroxide (TMAH) in a continuous flow bioreactor. The enriched methanogens attained an estimated maximum specific TMAH degradation rate and half-saturation constant of 39.5 mg TMAH/gVSS/h and 820 mg/L, following the Monod-type kinetic expression for methanogenic TMAH degradation. Presence of sulfide more than 20 mg/L significantly extended lag period and slowed down specific TMAH degradation rates. The results of terminal restriction fragment length polymorphism (T-RFLP), cloning/sequencing, and quantitative real-time PCR analyses targeting on the methyl coenzyme M reductase alpha subunit (mcrA) genes retrieved from the bioreactor and batch experiments indicated that Methanomethylovorans species were the dominant methanogens responsible for methanogenic degradation of TMAH. The isolated TMAH-degrading methanogen from the bioreactor, however, was identified closely related to Methanosarcina mazei. It is likely that a very low TMAH environment in the bioreactor favored the growth of Methanomethylovorans hollandica, while the much higher TMAH in the isolation growth medium proliferated Methanosarcina mazei.


Assuntos
Reatores Biológicos/microbiologia , Metano/metabolismo , Methanosarcinaceae/metabolismo , Compostos de Amônio Quaternário/metabolismo , Proteínas de Bactérias/genética , Biodegradação Ambiental , Methanosarcinaceae/genética , Oxirredutases/genética
17.
Oncotarget ; 9(23): 16275-16283, 2018 Mar 27.
Artigo em Inglês | MEDLINE | ID: mdl-29662644

RESUMO

We investigated the prevalence of glutamic acid decarboxylase 65 autoantibody (GADA), insulinoma-associated protein 2 autoantibody (IA2A), and insulin autoantibody (IAA) in 750 children with type 1 diabetes (T1D) living in Taiwan. GADA, IA2A, and IAA were measured by radioimmunoassay. The data were assessed by χ2 test, binary logistic regression, and Spearman rank correlation. Of the 750 T1D patients, 66.3% had GADA, 65.3% IA2A, 35.7% IAA, and 17.2% no autoantibodies. The prevalence of GADA and IA2A significantly decreased along T1D duration. The positivity of either GADA or IA2A was 89.4% within the first year of disease and decreased to 36.7% after 9 years (P = 1.22 × 10-20). Female patients had significantly higher prevalence of GADA compared with male patients (72.3% vs. 59.7%, P = 0.00027). The patients diagnosed before 12 years of age had a positive rate of 92.2% for either GADA or IA2A. Patients diagnosed at age 12 or above had a significantly lower positive rate of 81.6% (P = 0.011). GADA and IA2A significantly correlated with each other (rs = 0.245, P = 1.09 × 10-11). We concluded that autoantibodies were detectable in 89.4% of T1D patients within one year after diagnosis. Their prevalence declined with disease duration. GADA was more prevalent in female patients. GADA and IA2A weakly correlated with each other.

18.
J Formos Med Assoc ; 116(12): 924-932, 2017 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-29070437

RESUMO

BACKBROUD/PURPOSE: Microalbuminuria and macroalbuminuria are markers of diabetic nephropathy (DN). The purpose of this study was to unravel the risk factors for DN in the young patients with type 1 diabetes (T1D). METHODS: 341 patients (160 males) with T1D diagnosed at the age 7.6 ± 4.0 years with disease duration 11.5 ± 6.5 years were assessed. Among them, 185 were young adults (aged 18.0-36.2 years). Urinary albumin creatinine ratio (UACR) was checked on morning spot urine. Microalbuminuria and macroalbuminuria were defined as a UACR of 30-300 mg/g and >300 mg/g, respectively, in at least 2 consecutive specimens. RESULTS: 50 (14.7%) patients were classified as microalbuminuria and 13 (3.8%) as macroalbuminuria. In all patients, multivariate logistic regression revealed that the most significant risk factors were average HbA1c (%), OR (95% CI) = 1.76 (1.37-2.25), P = 0.002); and male sex, OR = (odd ratio 2.31 (1.19-4.46), P = 0.013). In adult patients, the most significant factors were average HbA1c, OR = 1.74 (1.32-2.31), P = 0.003; and systolic blood pressure, OR = 1.06 (1.01-1.11), P = 0.011. Survival analysis showed average HbA1c levels significantly influenced the development of DN. CONCLUSION: The most important risk factors for DN were average HbA1c and age. When microalbuminuria is detected, proper treatment with ACEIs or ARBs and improving glycemic control can delay progression of DN.


Assuntos
Albuminúria/urina , Creatinina/urina , Diabetes Mellitus Tipo 1/complicações , Nefropatias Diabéticas/fisiopatologia , Hemoglobinas Glicadas/análise , Adolescente , Adulto , Fatores Etários , Biomarcadores/análise , Pressão Sanguínea , Criança , Pré-Escolar , Feminino , Humanos , Modelos Logísticos , Masculino , Análise Multivariada , Fatores de Risco , Análise de Sobrevida , Taiwan/epidemiologia , Adulto Jovem
19.
PLoS One ; 11(4): e0154394, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27111218

RESUMO

Autoimmune thyroid disease (AITD), including Graves disease (GD) and Hashimoto disease (HD), is an organ-specific autoimmune disease with a strong genetic component. Although the cytotoxic T-lymphocyte-associated protein 4 (CTLA4) polymorphism has been reported to be associated with AITD in adults, few studies have focused on children. The aim of our study was to investigate whether the CTLA4 polymorphisms, including -318C/T (rs5742909), +49A/G (rs231775), and CT60 (rs3087243), were associated with GD and HD in Han Chinese adults and children. We studied 289 adult GD, 265 pediatric GD, 229 pediatric HD patients, and 1058 healthy controls and then compared genotype, allele, carrier, and haplotype frequencies between patients and controls. We found that CTLA4 SNPs +49A/G and CT60 were associated with GD in adults and children. Allele G of +49A/G was significantly associated with GD in adults (odds ratio [OR], 1.50; 95% confidence interval [CI], 1.21-1.84; corrected P value [Pc] < 0.001) and children (OR, 1.42; 95% CI, 1.15-1.77; Pc = 0.002). Allele G of CT60 also significantly increased risk of GD in adults (OR, 1.63; 95% CI, 1.27-2.09; Pc < 0.001) and GD in children (OR, 1.58; 95% CI, 1.22-2.04; Pc < 0.001). Significant linkage disequilibrium was found between +49A/G and CT60 in GD and control subjects (D' = 0.92). Our results showed that CTLA4 was associated with both GD and HD and played an equivalent role in both adult and pediatric GD in Han Chinese population.


Assuntos
Antígeno CTLA-4/genética , Predisposição Genética para Doença , Doença de Graves/genética , Doença de Hashimoto/genética , Polimorfismo de Nucleotídeo Único , Adolescente , Adulto , Idoso , Alelos , Povo Asiático , Antígeno CTLA-4/imunologia , Estudos de Casos e Controles , Criança , Pré-Escolar , Feminino , Expressão Gênica , Frequência do Gene , Doença de Graves/etnologia , Doença de Graves/imunologia , Doença de Graves/patologia , Haplótipos , Doença de Hashimoto/etnologia , Doença de Hashimoto/imunologia , Doença de Hashimoto/patologia , Heterozigoto , Humanos , Desequilíbrio de Ligação , Masculino , Pessoa de Meia-Idade , Razão de Chances , Linfócitos T Citotóxicos/imunologia , Linfócitos T Citotóxicos/patologia
20.
Chemosphere ; 150: 605-614, 2016 May.
Artigo em Inglês | MEDLINE | ID: mdl-26899855

RESUMO

A p-n junction Cu2O doped TiO2 nanotube arrays (Cu2O/TNAs) were synthesized by square wave voltammetry electrochemical (SWVE) deposition method and employed as the working anode. The crystalline, optical properties, surface morphology, and structure of the Cu2O/TNAs were characterized by XRD, UV-vis absorbance edges, SEM, and XPS. Results showed that the Cu2O/TNAs were dominated by anatase phase after sintering at 450 °C with significant visible light response. XPS finding confirmed XRD results that the copper element in Cu2O/TNAs was Cu (I) instead of Cu (II). SEM images illustrated the diameter and the length of supported TiO2 nanotubes was approximately 100 nm and 2.75-4.34 µm, respectively. After Cu2O doping, the nano-tubular structure of TiO2 nanotube kept its integrity with no significant morphological change, which was beneficial for PEC applications. The photocurrent of Cu2O/TNAs was 1.45 times larger than that of TNAs, implying that Cu2O doping significantly enhanced electron mobility by reducing the recombination of electron-hole pairs. In addition, electrochemical impedance spectroscopy (EIS) measurements revealed that the recombination of photogenerated electron-hole pairs was inhibited as the bias potential was applied. Results of Bode plot further demonstrated that the electron lifetime τel of Cu2O/TNAs-20 (30.79 ms), under 0.5 V bias potential, was about 2.23 times higher than that of pure TNAs (13.82 ms). Results of electron spin resonance (ESR) analyses demonstrate that the hydroxyl radicals (OH) are responsible for the PEC decomposition of Ibuprofen.


Assuntos
Cobre/química , Técnicas Eletroquímicas/métodos , Hidrogênio/química , Ibuprofeno/química , Nanotubos/química , Titânio/química , Catálise , Espectroscopia Dielétrica , Técnicas Eletroquímicas/instrumentação , Eletrodos , Espectroscopia de Ressonância de Spin Eletrônica , Ibuprofeno/efeitos da radiação , Luz , Oxirredução , Fotoquímica , Propriedades de Superfície
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