Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 14 de 14
Filtrar
1.
Hormones (Athens) ; 23(2): 235-244, 2024 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-38564142

RESUMEN

PURPOSE: The immature and developing hypothalamic-pituitary-thyroid axis leads to different levels of thyroid function in twin neonates, including free thyroxine (FT4), free triiodothyronine (FT3), and thyroid stimulating hormone (TSH) levels. No reference intervals for twins have been established until now. To compensate for this lack, we collected data and established this standard across different gestational ages (GAs) and sexes. METHODS: A total of 273 pairs of neonates admitted to the NICU in Southeast China from 2015 to 2022 were included. Each pair was divided into Neonate A (relatively heavy birth weight (BW)) and Neonate B (relatively light BW). Their thyroid functions were analyzed to establish reference intervals and comparisons were made stratified by GA and sex. RESULTS: The FT3, FT4, and TSH reference intervals in twin neonates with a GA of 26-36 weeks were as follows: Neonate A and B: 3.59 ± 0.99 and 3.57 ± 1.00 pmol/L; Neonate A and B: 17.03 ± 5.16 and 16.77 ± 5.29 pmol/L; and Neonate A and B: 4.097 ± 3.688 and 4.674 ± 4.850 mlU/L, respectively. There were significant differences between serum FT3 and FT4 reference intervals and GA (p < 0.05). The serum FT3 and FT4 reference intervals for male neonates were lower than those for female neonates in the 29-32-week group (p < 0.05). CONCLUSION: This was the first study, to our knowledge, to establish reference intervals for thyroid function in twin neonates from the fifth to seventh day of life, which will be beneficial for the diagnosis and management of congenital hypothyroidism.


Asunto(s)
Recien Nacido Prematuro , Pruebas de Función de la Tiroides , Glándula Tiroides , Tirotropina , Tiroxina , Humanos , Recién Nacido , Femenino , Masculino , Estudios Retrospectivos , Embarazo , Valores de Referencia , Recien Nacido Prematuro/sangre , Pruebas de Función de la Tiroides/normas , Tirotropina/sangre , Tiroxina/sangre , Glándula Tiroides/fisiología , Embarazo Gemelar/sangre , Embarazo Gemelar/fisiología , Triyodotironina/sangre , Edad Gestacional
2.
J Steroid Biochem Mol Biol ; 232: 106347, 2023 09.
Artículo en Inglés | MEDLINE | ID: mdl-37331433

RESUMEN

Periodontitis is a chronic inflammatory disease caused by Porphyromonas gingivalis and other bacteria, and human periodontal ligament stem cells (hPDLSCs) are a promising candidate for the treatment of periodontal supporting tissue defects. This study aimed to investigate the effect of 1α,25-dihydroxyvitamin D3 [1,25(OH)2VitD3] on osteogenic differentiation of hPDLSCs in an in vitro periodontitis model and whether it can improve inflammatory status. hPDLSCs were in vitro isolated and identified. After treatment with 1,25(OH)2VitD3 and ultrapure pure Porphyromonas gingivalis lipopolysaccharide (LPS-G), the viability of hPDLSCs was detected using Cell Counting Kit-8, the expressions of osteogenic markers and inflammatory genes using Western blotting and quantitative reverse transcription PCR (qRT-PCR), the levels of inflammatory factors in cells using enzyme linked immunosorbent assay (ELISA), and the fluorescence signal intensity of osteoblastic markers and inflammatory genes in cells using immunofluorescence assay. It was found that 1,25(OH)2VitD3 reversed the inhibition of hPDLSCs proliferation by LPS-G; LPS-G exhibited inhibitory effect on ALP, Runx2, and OPN expressions, and such inhibitory effect was significantly weakened when co-acting with 1,25(OH)2VitD3. Meanwhile, LPS-G upregulated the expressions of inflammatory genes IL-1ß and Casp1, whereas 1,25(OH)2VitD3 antagonized such an effect and improved the inflammatory status. In conclusion, 1,25(OH)2VitD3 can reverse the inhibitory effect of LPS-G on hPDLSCs proliferation and osteogenic differentiation and suppress LPS-G-induced upregulation of inflammatory gene expressions.


Asunto(s)
Osteogénesis , Periodontitis , Humanos , Ligamento Periodontal , Lipopolisacáridos/farmacología , Lipopolisacáridos/metabolismo , Periodontitis/metabolismo , Inflamación/metabolismo , Células Madre , Diferenciación Celular , Células Cultivadas
3.
J Matern Fetal Neonatal Med ; 36(1): 2183471, 2023 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-36822660

RESUMEN

BACKGROUND: Hypertensive disorders of pregnancy (HDP) is associated with an increased risk of adverse outcomes. The fetal middle cerebral artery (MCA) and umbilical artery (UA) blood flow detected by ultrasound are recommended to evaluate the oxygenation of the fetus. It is necessary to analyze the relationship between MCA & UA doppler indices or cerebroplacental ratio (CPR) and fetal outcomes and describe MCA and UA blood flow values across gestation. METHODS: Hospital-based retrospective case-control study during 2016 to 2020. 800 singleton pregnant women: 400 normotensive control, 219 gestational hypertension (GH), and 181 preeclampsia (PE)/eclampsia (EC). An analysis of the outcomes of mothers and neonates was performed. The fetal MCA and UA blood flow values across gestation were established, and MCA-resistance index (RI) and CPR were used to predict fetal distress and small for gestational age (SGA). RESULTS: In the normotensive control, GH and PE/EC groups, the mean gestational age (GA) was 38.9 ± 1.2 weeks, 39.0 ± 1.0 weeks, and 38.6 ± 1.3 weeks respectively, and the mean birth weight (BW) was 3.195 ± 0.387 kilograms, 3.198 ± 0.428 kilograms, and 2.987 ± 0.544 kilograms respectively. There were differences in GA, BW, fetal distress, SGA and intraventricular hemorrhage I-II between the hypertension group and normotensive control group (p < 0.05). The MCA-RI (sensitivity: 70.1%, specificity: 64.3%) and MCA-RI (sensitivity: 52.4%, specificity: 84.6%) were the best indices to predict fetal distress and SGA, respectively during GA of 35-40 weeks. CONCLUSIONS: Fetal MCA blood flow values and CPR are of great benefit for obstetricians to evaluate the status of fetus evidentially in singleton pregnancy.


Asunto(s)
Hipertensión Inducida en el Embarazo , Preeclampsia , Recién Nacido , Embarazo , Femenino , Humanos , Lactante , Arteria Cerebral Media/diagnóstico por imagen , Estudios Retrospectivos , Estudios de Casos y Controles , Arterias Umbilicales/diagnóstico por imagen , Sufrimiento Fetal , Feto/diagnóstico por imagen , Edad Gestacional , Retardo del Crecimiento Fetal , Peso al Nacer , Ultrasonografía Doppler , Ultrasonografía Prenatal
5.
Ann Med ; 53(1): 1722-1726, 2021 12.
Artículo en Inglés | MEDLINE | ID: mdl-34596490

RESUMEN

OBJECTIVE: Low triiodothyronine syndrome (LT3S) is a common endocrine disease in preterm neonates. Various serious acute or chronic diseases result in LT3S. Few studies have investigated the causal relationship between perinatal factors and LT3S in preterm neonates with a gestational age (GA) of 28-35 weeks. The present study comprehensively analyzed the perinatal factors of LT3S in preterm neonates. METHODS: This was a retrospective study of neonates with and without LT3S from January 2018 to November 2019. Compared to 206 preterm neonates without LT3S, 158 neonates were diagnosed with LT3S, excluding neonates with congenital malformations, other endocrine diseases, genetic diseases and inherited metabolic diseases. RESULTS: Five perinatal risk factors for LT3S were confirmed using univariate and multivariate analyses: smaller gestational age, lower birth weight, respiratory distress syndrome (RDS), neonatal sepsis, and dopamine use. CONCLUSIONS: LT3S in preterm neonates was associated with multiple perinatal factors, including smaller gestational age, lower birth weight, RDS, sepsis, and dopamine use. Preterm neonates with a GA of 28-35 weeks who are exposed to a series of high-risk perinatal factors must be closely observed, diagnosed early and treated for primary diseases promptly to reduce the occurrence of LT3S and improve the outcomes.Key Message:Few studies have investigated the relationship between perinatal factors and Low triiodothyronine syndrome (LT3S) in preterm neonates with a gestational age (GA) of 28-35 weeks.LT3S was associated with multiple perinatal factors, including smaller gestational age, lower birth weight, respiratory distress syndrome (RDS), sepsis, and dopamine use.


Asunto(s)
Síndromes del Eutiroideo Enfermo/diagnóstico , Recien Nacido Prematuro/sangre , Triyodotironina/sangre , Peso al Nacer , Dopamina , Síndromes del Eutiroideo Enfermo/sangre , Femenino , Edad Gestacional , Humanos , Lactante , Recién Nacido , Embarazo , Síndrome de Dificultad Respiratoria del Recién Nacido/epidemiología , Síndrome de Dificultad Respiratoria del Recién Nacido/etiología , Estudios Retrospectivos , Sepsis/epidemiología , Pruebas de Función de la Tiroides
6.
Int Breastfeed J ; 16(1): 59, 2021 08 21.
Artículo en Inglés | MEDLINE | ID: mdl-34419090

RESUMEN

BACKGROUND: Oropharyngeal administration of colostrum (OAC) may provide immunoprotective and anti-inflammatory effects that potentially reduce the incidence of necrotizing enterocolitis (NEC) and late-onset sepsis and improve short-term outcomes. Our objective was to evaluate the role of OAC in the early prevention of NEC and late-onset sepsis in preterm infants with gestational age (GA) ≤ 32 weeks. METHODS: A pilot, single-center, 1:1 parallel randomized controlled trial was conducted in a 40-bed tertiary neonatal intensive care unit (NICU) in China from 1 January 2019 to 30 September 2020. Preterm infants were randomly divided into two groups with GA ≤ 32 weeks. The OAC group included preterm infants who received 0.4 ml of maternal colostrum via the oropharyngeal route every 3 h for 10 days beginning within the first 48 h after birth, and the control group included preterm infants who received normal saline instead. Data from the two groups were collected and compared. RESULTS: A total of 127 infants in the OAC group and 125 infants in the control group were enrolled. The incidence of NEC (Bell stage 2 or 3) and late-onset sepsis were lower in the OAC group [2.36% vs. 10.40%, relative risk (RR) 0.23 (95% confidence interval (CI) 0.07, 0.78), adjusted RR 0.23 (95% CI 0.06, 0.84); 4.72% vs. 13.60%, RR 0.35 (95% CI 0.14, 0.85), adjusted RR 0.36 (95% CI 0.14, 0.95)]. In addition, the incidence of proven sepsis and intraventricular hemorrhage (IVH) (stage 3 or 4) were lower in the OAC group [2.36% vs. 8.80%, RR 0.27 (95% CI 0.08, 0.94); 1.57% vs. 7.20%, RR 0.22 (95% CI 0.05, 0.99)], and the time to achieve full enteral feeding was shorter (23.13 ± 9.45 days vs. 28.50 ± 14.80 days). No adverse reactions were observed in either group. CONCLUSIONS: Oropharyngeal administration of colostrum is a safe and simple NICU procedure that may yield a potential effect in decreasing the incidences of NEC, late-onset sepsis, and severe IVH and shorten the time to achieve full enteral feeding in preterm infants with GA ≤ 32 weeks. TRIAL REGISTRATION: Chinese Clinical Trial Registry, ChiCTR1900023697 , Registered 8 June 2019, retrospectively registered.


Asunto(s)
Enterocolitis Necrotizante , Sepsis , Calostro , Enterocolitis Necrotizante/epidemiología , Enterocolitis Necrotizante/prevención & control , Femenino , Edad Gestacional , Humanos , Lactante , Recién Nacido , Recien Nacido Prematuro , Embarazo , Sepsis/epidemiología , Sepsis/prevención & control
7.
Front Pediatr ; 9: 683510, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-34195163

RESUMEN

Objectives: Portal venous gas (PVG) was an important clinical sign in stage II or III necrotizing enterocolitis (NEC) in preterm neonates. Not a proper predictive indicator was found to predict the diseases (NEC with the presence of PVG) up to now. There is a need to put forward predictive indicators and compare the predictive effects among them. Methods: We conducted a retrospective study of preterm neonates with NEC-PVG (n = 61) or NEC-non PVG (n = 62) from 2014 to 2021. Predictive indicators were put forward and determined by receiver operating characteristic curve analysis. An analysis of the surgical interventions and their outcomes was performed. Results: The incidence rate of NEC among preterm neonates was 4.99%; surgical and conservative interventions accounted for 20.47 and 75.07%, and the mortality rate was 0.03%. The composition ratio of shock in the NEC-PVG group increased 13.2% (P = 0.029). C-reactive protein, fibrinogen degradation product, and blood glucose had better predictive effects in the predictive indicators (P < 0.05). Intestinal necrosis and subependymal hemorrhage in the outcomes of surgical interventions had a strong relationship with the presence of PVG in NEC II/III (P < 0.05). Conclusion: Early and reasonable use of antibiotics, improvement of coagulation function, rectification of acidosis, and decreased blood glucose could cut down the occurrence of the disease (NEC with the presence of PVG). Except for subependymal hemorrhage and intestinal necrosis, NEC with the presence of PVG did not increase the occurrence of other outcomes after surgery.

8.
Clin Biochem ; 95: 54-59, 2021 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-34077759

RESUMEN

BACKGROUND: Due to the lack of reference intervals for serum free triiodothyronine (FT3), free thyroxine (FT4) and thyroid stimulating hormone (TSH) in preterm neonates during the 5th to 7th day of life, we performed a retrospective study using the chemiluminescence immunoassay system. METHODS: A total of 2040 preterm neonates with a gestational age (GA) of 26-35 weeks in the neonatal intensive care unit from 2014 to 2019 were included. Their serum FT3, FT4 and TSH values were calculated and analyzed to establish reference intervals for preterm neonates stratified by GA. The comparisons of FT3, FT4 and TSH were made by sex (males and females) and gestational age (26-28 weeks; 29-32 weeks; 33-35 weeks). RESULTS: The reference intervals for FT3, FT4 and TSH in preterm neonates with a GA of 26-35 weeks were (1.65~5.21) pmol/L, (8.64~25.41) pmol/L, and (0.406~12.468) mlU/L, respectively. There were significant differences between serum FT3 and FT4 values and GA, while TSH levels were not significantly different (P < 0.01). The serum FT3 values of males were lower than those of females, especially in the 29-32 weeks group. No significant differences in serum values between sexes were found in FT4 or TSH (P > 0.05). CONCLUSION: Reference intervals of thyroid function tests were established to determine the early diagnostic criteria of thyroid diseases for neonates with a GA of 26-35 weeks and to avoid unnecessary retesting and interventions. The reference intervals of FT4 can be used as an indicator to regulate the doses of thyroid hormone supplement in the treatments of congenital hypothyroidism.


Asunto(s)
Glándula Tiroides/fisiología , Tirotropina/normas , Tiroxina/normas , Triyodotironina/normas , Femenino , Edad Gestacional , Humanos , Inmunoensayo , Recién Nacido , Recien Nacido Prematuro , Mediciones Luminiscentes , Masculino , Valores de Referencia , Estudios Retrospectivos , Caracteres Sexuales , Enfermedades de la Tiroides/sangre , Enfermedades de la Tiroides/diagnóstico , Pruebas de Función de la Tiroides , Tirotropina/sangre , Tiroxina/sangre , Triyodotironina/sangre
9.
J Matern Fetal Neonatal Med ; 34(1): 12-23, 2021 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-30700176

RESUMEN

Objective: The association between a (GT)n dinucleotide length polymorphism in the promoter region of heme oxygenase 1 (HMOX1) and the risk of neonatal hyperbilirubinemia remains controversial. This meta-analysis was, therefore, performed with aims to examine the correlation between the HMOX1 (GT)n repeat length polymorphism and neonatal hyperbilirubinemia susceptibility.Materials and methods: We searched the databases including PubMed, Embase, Cochrane Library, China national knowledge infrastructure (CNKI), and Wanfang Data, with all reviewed studies published before 28 June 2018. After the evaluation of quality, we used RevMan to perform the meta-analyses. Pooled odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to assess the effect of HMOX1 gene promoter polymorphisms on the risk of neonatal hyperbilirubinemia.Results: Seven studies, involving 584 patients with neonatal hyperbilirubinemia and 1655 controls, were included. A statistically significant association was found between the HMOX1 (GT)n repeat length polymorphism and risk of neonatal hyperbilirubinemia under the allele (allele S vs. allele L: OR = 1.81, 95% CI = 1.22-2.67, p = .003), recessive (genotype SS vs. genotypes LS + LL: OR = 1.38, 95% CI = 1.02-1.86, p = .04), dominant (genotypes SS + LS vs. LL: OR = 1.37, 95% CI = 1.01-1.76, p = .01), and homozygous genetic models (genotype SS vs. genotype LL: OR = 1.47, 95% CI = 1.02-2.11, p = .003), but not under the heterozygous genetic model. Interestingly, subgroup analysis revealed that the cutoffs of the S allele < 25 showed significant associations in any of the five genetic models (allele S vs. allele L: OR = 2.26, 95% CI = 1.68-3.05, p < .00001; genotype SS vs. genotypes LS + LL: OR = 2.56, 95% CI = 1.41-4.65, p = .002; genotypes SS + LS vs. genotype LL: OR = 1.82, 95% CI = 1.28-2.59, p = .0009; genotype SS vs. genotype LL: OR = 3.09, 95% CI = 1.50-6.36, p = .002; genotype LS vs. genotype LL: OR = 1.64, 95% CI = 1.11-2.42, p = .01); however, this association was not observed in the cutoffs of the S allele ≥25.Conclusion: The results of this study indicate that there is a significant association between the HMOX1 (GT)n repeat length polymorphism and susceptibility to neonatal hyperbilirubinemia. Newborns carrying shorter (GT)n repeats in the HMOX1 gene promoter may have a higher risk of neonatal hyperbilirubinemia.


Asunto(s)
Hemo-Oxigenasa 1 , Hiperbilirrubinemia Neonatal , China , Predisposición Genética a la Enfermedad , Genotipo , Hemo-Oxigenasa 1/genética , Hemo-Oxigenasa 1/metabolismo , Humanos , Hiperbilirrubinemia Neonatal/genética , Recién Nacido , Polimorfismo Genético , Regiones Promotoras Genéticas
10.
Eur J Endocrinol ; 178(6): 623-633, 2018 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-29650690

RESUMEN

OBJECTIVE: Congenital hypothyroidism (CH), the most common neonatal metabolic disorder, is characterized by impaired neurodevelopment. Although several candidate genes have been associated with CH, comprehensive screening of causative genes has been limited. DESIGN AND METHODS: One hundred ten patients with primary CH were recruited in this study. All exons and exon-intron boundaries of 21 candidate genes for CH were analyzed by next-generation sequencing. And the inheritance pattern of causative genes was analyzed by the study of family pedigrees. RESULTS: Our results showed that 57 patients (51.82%) carried biallelic mutations (containing compound heterozygous mutations and homozygous mutations) in six genes (DUOX2, DUOXA2, DUOXA1, TG, TPO and TSHR) involved in thyroid hormone synthesis. Autosomal recessive inheritance of CH caused by mutations in DUOX2, DUOXA2, TG and TPO was confirmed by analysis of 22 family pedigrees. Notably, eight mutations in four genes (FOXE1, NKX2-1, PAX8 and HHEX) that lead to thyroid dysgenesis were identified in eight probands. These mutations were heterozygous in all cases and hypothyroidism was not observed in parents of these probands. CONCLUSIONS: Most cases of congenital hypothyroidism in China were caused by thyroid dyshormonogenesis rather than thyroid dysgenesis. This study identified previously reported causative genes for 57/110 Chinese patients and revealed DUOX2 was the most frequently mutated gene in these patients. Our study expanded the mutation spectrum of CH in Chinese patients, which was significantly different from Western countries.


Asunto(s)
Pueblo Asiatico/genética , Hipotiroidismo Congénito/genética , China , Oxidasas Duales/genética , Femenino , Factores de Transcripción Forkhead/genética , Estudios de Asociación Genética , Secuenciación de Nucleótidos de Alto Rendimiento , Proteínas de Homeodominio/genética , Humanos , Lactante , Recién Nacido , Yoduro Peroxidasa/genética , Masculino , Proteínas de la Membrana/genética , Mutación , Factor de Transcripción PAX8/genética , Linaje , Receptores de Tirotropina/genética , Análisis de Secuencia de ADN , Tiroglobulina/genética , Disgenesias Tiroideas/genética , Factor Nuclear Tiroideo 1/genética , Factores de Transcripción/genética
11.
Pediatr Neonatol ; 58(6): 509-515, 2017 12.
Artículo en Inglés | MEDLINE | ID: mdl-28528756

RESUMEN

BACKGROUND: We retrospectively investigated incidence, morbidity, and mortality of neonatal necrotizing enterocolitis in China, with special emphasis on determining the predictors of necrotizing enterocolitis associated mortality. METHODS: We identified neonates as having necrotizing enterocolitis if they met the accepted diagnostic criterion. Data pertaining to antenatal period, labor and birth, and the postnatal course of illness were collected. Multivariate analysis and logistic regression were used to analyze the risk factors. RESULTS: There were 1167 cases of necrotizing enterocolitis identified from the 95 participating NICUs in mainland China in 2011, with the incidence of 2.50% and 4.53% in LBW (birth weight <2500 g) and VLBW (birth weight <1500 g) infants, respectively. Stage 1, 2 and 3 diseases were noted in 51.1%, 30.3% and 18.6% of cases respectively. The mortality from stage 2 and 3 necrotizing enterocolitis in this cohort was 41.7%. In VLBW infants, the important risk factors for mortality were small for gestation age (OR: 5.02, 95% CI 1.73-14.6; P = 0.003) and stage 3 NEC (OR: 8.09, 95% CI 2.80-23.3, P < 0.001). In moderate LBW infants (birth weight 1500-2499 g), the risk factors identified for mortality were sepsis during hospitalization (OR: 2.59, 95% CI 1.57-4.28, P < 0.001) and stage 3 NEC (OR: 5.37, 95% CI 3.24-8.90; P < 0.001). CONCLUSIONS: Necrotizing enterocolitis remains an important cause of morbidity and mortality in prematurely born neonates in Chinese neonatal units. Awareness of the associated risk factors and appropriate interventions may improve the outcome of necrotizing enterocolitis in different birth weight subgroup.


Asunto(s)
Peso al Nacer , Enterocolitis Necrotizante/mortalidad , Estudios de Cohortes , Femenino , Humanos , Lactante , Recién Nacido de Bajo Peso , Recién Nacido , Recién Nacido de muy Bajo Peso , Modelos Logísticos , Masculino , Estudios Retrospectivos , Factores de Riesgo
12.
Shanghai Kou Qiang Yi Xue ; 21(5): 506-10, 2012 Oct.
Artículo en Chino | MEDLINE | ID: mdl-23135178

RESUMEN

PURPOSE: To investigate the relationship between diabetes mellitus and pulposis and the pathogenesis of diabetes mellitus pulposis, via comparing the pulp tissue conditions and ultramicrostructures of capillary vessels in pulp tissues of diabetes mellitus patients and normal control. METHODS: Pulp tissues were obtained from clinically extracted human third molars with impaction (control group, 30 cases) and intact third molars with impaction (non-insulin dependent diabetes patients) whilst without pulposis symptom (diabetic group, 30 cases). The pathological changes of two groups' pulp tissues were evaluated under light microscope and electron microscopy. The thickness of pulp capillary basement membrane and their anionic sites were quantitatively analyzed by electron microscopy and special staining. Statistical analysis was performed using SAS6.12 software package. RESULTS: The tricked blood capillary wall was observed in diabetic pulp under light microscope. The thickened blood capillary wall and constrictive lumen were observed in diabetic pulp under electron microscope, accompanied with vascular endothelial cell swelling and structural destruction and thickened basement membrane (P<0.01). The decrease of anionic sites of capillary basement membrane was observed in diabetic pulp under specially stained electron microscope (P<0.01). CONCLUSIONS: Inflammatory reaction existed in the pulp of intact teeth of DM patients without symptoms. The changes observed in diabetic vessels may occur in the dental pulp. Diabetes mellitus is closely related to pulposis.


Asunto(s)
Pulpa Dental , Diabetes Mellitus , Membrana Basal , Capilares , Estudios de Casos y Controles , Células Endoteliales , Humanos , Inflamación , Microscopía Electrónica
13.
Chin Med J (Engl) ; 124(8): 1156-63, 2011 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-21542988

RESUMEN

BACKGROUND: Hypoxemic respiratory failure (HRF) is one of the most common causes for neonatal infants requiring aggressive respiratory support. Inhaled nitric oxide (iNO) has been established routinely as an adjunct to conventional respiratory support in developed countries. The aim of this study was to investigate effects of iNO in neonates with HRF in resource limited condition with no or limited use of surfactant, high frequency oscillatory ventilation (HFOV) and extracorporeal membrane oxygenation. METHODS: A non-randomized, open, controlled study of efficacy of iNO was conducted over 18 months. Eligible term and near-term neonates from 28 hospitals with HRF (oxygenation index > 15) were enrolled prospectively into two groups as either iNO or control. Oxygenation improvement and mortality as primary endpoint were determined in relation with dosing and timing of iNO, severity of underlying diseases, complications and burden. Intention-to-treat principle was adopted for outcome assessment. Response to iNO at 10 or 20 parts per million (ppm) was determined by oxygenation in reference to the control (between-group) and the baseline (within-group). RESULTS: Compared to 93 controls, initial dose of iNO at 10 ppm in 107 treated infants significantly improved oxygenation from first hour (P = 0.046), with more partial- and non-responders improved oxygenation with subsequent 20 ppm NO (P = 0.018). This effect persisted on days 1 and 3, and resulted in relatively lower mortalities (11.2% vs. 15%) whereas fewer were treated with surfactant (10% vs. 27%), HFOV (< 5%) or postnatal corticosteroids (< 10%) in both groups. The overall outcomes at 28 days of postnatal life in the iNO-treated was not related to perinatal asphyxia, underlying diseases, severity of hypoxemia, or complications, but to the early use of iNO. The cost of hospital stay was not significantly different in both groups. CONCLUSIONS: With relatively limited use of surfactant and/or HFOV in neonatal HRF, significantly more responders were found in the iNO-treated patients as reflected by improved oxygenation in the first three days over the baseline level. It warrants a randomized, controlled trial for assessment of appropriate timing and long-term outcome of iNO.


Asunto(s)
Hipoxia/tratamiento farmacológico , Óxido Nítrico/administración & dosificación , Óxido Nítrico/uso terapéutico , Insuficiencia Respiratoria/tratamiento farmacológico , Administración por Inhalación , Femenino , Humanos , Hipoxia/fisiopatología , Recién Nacido , Masculino , Embarazo , Insuficiencia Respiratoria/fisiopatología
14.
Shanghai Kou Qiang Yi Xue ; 17(1): 15-9, 2008 Feb.
Artículo en Chino | MEDLINE | ID: mdl-18360661

RESUMEN

PURPOSE: To compare the young permanent teeth enamel demineralization after immersion in different kinds of soft drinks; to compare the degree of enamel demineralization caused by the different immersion time and frequency of beverages. METHODS: The change of young permanent teeth enamel surface microhardness was measured by a leitzs microhardness tester. The change of calcium and phosphate in the different drinks after immersion of the enamel was analyzed by Roche Biochemical analyzer. Two-way ANOVA in SPSS 15.0 software package was used for statistical analysis. RESULTS: The dissolution of calcium and phosphate in young permanent teeth enamel was caused by all kinds of soft drinks the surface microhardness of enamel was decreased by these drinks. There were great significant differences in the demineralization abilities among different beverages (P<0.05).The enamel demineralization was increased when prolonging the immersion time and frequency. CONCLUSIONS: The enamel demineralization can be caused by orange juice and carbonic acid drinks. The enamel remineralization can be increased by tea drink, which is an ideal healthy beverage. Supported by Excellent Middle-aged Science Foundation of School of Medicine,Shanghai Jiao Tong University (Grant No.040407).


Asunto(s)
Bebidas Gaseosas , Erosión de los Dientes , Calcio , China , Esmalte Dental , Humanos , Concentración de Iones de Hidrógeno
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA