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1.
Exp Lung Res ; 50(1): 127-135, 2024.
Artículo en Inglés | MEDLINE | ID: mdl-38973401

RESUMEN

INTRODUCTION: Bronchopulmonary dysplasia (BPD) impacts life expectancy and long-term quality of life. Currently, BPD mouse models exposed to high oxygen are frequently used, but to reevaluate their relevance to human BPD, we attempted an assessment using micro-computed tomography (µCT). METHODS: Newborn wildtype male mice underwent either 21% or 95% oxygen exposure for 4 days, followed until 8 wk. Weekly µCT scans and lung histological evaluations were performed independently. RESULTS: Neonatal hyperoxia for 4 days hindered lung development, causing alveolar expansion and simplification. Histologically, during the first postnatal week, the exposed group showed a longer mean linear intercept, enlarged alveolar area, and a decrease in alveolar number, diminishing by week 4. Weekly µCT scans supported these findings, revealing initially lower lung density in newborn mice, increasing with age. However, the high-oxygen group displayed higher lung density initially. This difference diminished over time, with no significant contrast to controls at 3 wk. Although no significant difference in total lung volume was observed at week 1, the high-oxygen group exhibited a decrease by week 2, persisting until 8 wk. CONCLUSION: This study highlights µCT-detected changes in mice exposed to high oxygen. BPD mouse models might follow a different recovery trajectory than humans, suggesting the need for further optimization.


Asunto(s)
Animales Recién Nacidos , Displasia Broncopulmonar , Hiperoxia , Pulmón , Oxígeno , Microtomografía por Rayos X , Animales , Microtomografía por Rayos X/métodos , Ratones , Masculino , Displasia Broncopulmonar/diagnóstico por imagen , Oxígeno/metabolismo , Hiperoxia/diagnóstico por imagen , Pulmón/diagnóstico por imagen , Modelos Animales de Enfermedad , Alveolos Pulmonares/diagnóstico por imagen , Ratones Endogámicos C57BL
2.
Pediatr Int ; 64(1): e15184, 2022 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-35727868

RESUMEN

BACKGROUND: In Japan, the definition and classification of neonatal chronic lung disease (CLD) used for its diagnosis are a combination of those used in Japan and abroad. METHODS: To clarify the current state of CLD diagnosis, a questionnaire survey was conducted. RESULTS: Half of the patients of the medical centers included in the study were diagnosed with CLD in real time, while the other half were diagnosed after discharge. In addition, in approximately 70% of the facilities, diagnosis was made after discussions various among medical teams. In approximately 80% of the centers, the chest radiography used for CLD diagnosis were evaluated by multiple doctors. Furthermore, some centers used chest X-rays that were taken at approximately 28 days of age for CLD diagnosis, whereas at other facilities, diagnosis was made regardless of time at which the chest radiography were obtained. Only a small number of centers have established criteria for determining the necessity of oxygen at the corrected age of 36 weeks, and the target saturation of peripheral oxygen levels also tend to vary for each facility. Whether the conditions wherein the patient receives respiratory support for apnea or respiratory tract diseases should be considered as CLD also differed among the facilities. CONCLUSIONS: It is necessary to reassess the definition and classification of CLD in Japan to accurately evaluate and improve the quality of respiratory management based on the long-term prognosis.


Asunto(s)
Enfermedades del Prematuro , Enfermedades Pulmonares , Enfermedad Crónica , Humanos , Lactante , Recién Nacido , Recien Nacido Prematuro , Japón , Enfermedades Pulmonares/diagnóstico , Oxígeno
3.
Sensors (Basel) ; 21(4)2021 Feb 16.
Artículo en Inglés | MEDLINE | ID: mdl-33669261

RESUMEN

This study aimed to evaluate the capability of a piezoelectric sensor to detect a heart murmur in patients with congenital heart defects. Heart sounds and murmurs were recorded using a piezoelectric sensor and an electronic stethoscope in healthy neonates (n = 9) and in neonates with systolic murmurs caused by congenital heart defects (n = 9) who were born at a hospital. Signal data were digitally filtered by high-pass filtering, and the envelope of the processed signals was calculated. The amplitudes of systolic murmurs were evaluated using the signal-to-noise ratio and compared between healthy neonates and those with congenital heart defects. In addition, the correlation between the amplitudes of systolic murmurs recorded by the piezoelectric sensor and electronic stethoscope was determined. The amplitudes of systolic murmurs detected by the piezoelectric sensor were significantly higher in neonates with congenital heart defects than in healthy neonates (p < 0.01). Systolic murmurs recorded by the piezoelectric sensor had a strong correlation with those recorded by the electronic stethoscope (ρ = 0.899 and p < 0.01, respectively). The piezoelectric sensor can detect heart murmurs objectively. Mechanical improvement and automatic analysis algorithms are expected to improve recording in the future.


Asunto(s)
Auscultación Cardíaca , Ruidos Cardíacos , Algoritmos , Auscultación , Soplos Cardíacos/diagnóstico , Humanos , Recién Nacido , Masculino
4.
Nihon Koshu Eisei Zasshi ; 68(9): 597-607, 2021 Sep 07.
Artículo en Japonés | MEDLINE | ID: mdl-34121058

RESUMEN

Objectives The COVID-19 pandemic spread rapidly across the globe during the first half of 2020. In Japan, a state of emergency was declared on April 7, 2020, which had a significant impact on the life of citizens. This study focused on behaviors like avoiding going out or coming in contact with others and frequent hand-washing to prevent the infection and the spread of COVID-19 among people living in Tokyo. We also examined the factors associated with these behaviors during the declaration of emergency.Methods An online survey was conducted from April 26 to 29, 2020, approximately 20 days after the declaration of the emergency, among men and women aged 20-69 years living in Tokyo. The study framework was based on the protection motivation theory, which explains the risk-reducing behaviors, and focus theory of normative conduct, which explains the effect of others' behavior on one's own behavior. The frequency of behaviors like avoiding going out or coming in contact with others and frequent hand-washing, as well as the perception of the risk of COVID-19 during the week preceding the survey, were assessed. Each preventive action was evaluated based on the following factors: perceived effectiveness (response efficacy), perceived practicability (self-efficacy), necessary cost (response cost), and perceptions of how much should be done (injunctive norm) and how well others are doing it (descriptive norm). Hierarchical multiple regression analysis with these behaviors as outcomes were performed.Results This study included 1,034 participants (50.3% male, mean age 44.82 years, standard deviation 14.00 years). The analyses of the frequency of avoiding going out or coming in contact with others showed that the injunctive norm was positively associated with the behavior (standardized partial regression coefficient (ß)=0.343, P<0.001), while the descriptive norm was negatively associated with the behavior (ß=-0.074, P=0.010). Furthermore, the two-way interaction between risk perception, response efficacy, and self-efficacy was significant (ß=0.129, P<0.001), indicating that risk perception was positively associated with the behavior only when either response efficacy or self-efficacy was low. A similar analysis conducted for hand-washing behavior revealed that injunctive norm (ß=0.256, P<0.001) and response efficacy (ß=0.132, P<0.001) were positively associated with the behavior, while the response cost (ß=-0.193, P<0.001) was negatively associated with the behavior.Conclusion Some variables in the protection motivation theory and the focus theory of normative conduct were related to the behavior for the prevention of COVID-19. The results suggest that the application of these theories is useful in future studies.


Asunto(s)
COVID-19/prevención & control , Conductas Relacionadas con la Salud , Salud Pública , Conducta de Reducción del Riesgo , Encuestas y Cuestionarios , Adulto , Anciano , Urgencias Médicas , Femenino , Humanos , Internet , Masculino , Persona de Mediana Edad , Tokio , Adulto Joven
5.
Acta Paediatr ; 109(4): 711-719, 2020 04.
Artículo en Inglés | MEDLINE | ID: mdl-31509290

RESUMEN

AIM: Bubbly/cystic appearance on chest X-ray (CXR) is an important factor in cases of severe bronchopulmonary dysplasia (BPD). We aimed to determine whether CXR -based BPD classifications obtained in extremely preterm infants with oxygen dependency at 28 days after birth (BPD28) is associated with wheezing disorders. METHODS: This was a multicentre retrospective cohort study of population data from infants (body weight, <1500 g) enrolled in the Neonatal Research Network of Japan. Of the 15 480 infants born at <28 weeks of gestation between 2003 and 2012, 8979 met the BPD28 criteria, and 4007 were classified as the no BPD28 group. BPD28 infants were classified according to the bubbly/cystic or no bubbly/cystic appearance on CXR at postnatal ≧28 days. The effects on wheezing disorder at 3 years of age were analysed. RESULTS: Bubbly/cystic BPD28 infants showed higher rates of wheezing disorders compared with no BPD28 infants. Bubbly/cystic BPD28 (odds ratio 1.7; 95% confidence interval, 1.3-2.2) was a significant independent factor for wheezing disorders. CONCLUSION: A bubbly/cystic appearance on CXR with BPD28 was a potential risk factor of wheezing disorders at 3 years of age. This may be a useful early diagnostic tool at ≧28 postnatal days in extremely preterm infants.


Asunto(s)
Displasia Broncopulmonar , Displasia Broncopulmonar/diagnóstico por imagen , Displasia Broncopulmonar/epidemiología , Edad Gestacional , Humanos , Lactante , Recien Nacido Extremadamente Prematuro , Recién Nacido , Japón , Ruidos Respiratorios/etiología , Estudios Retrospectivos
6.
Tohoku J Exp Med ; 250(1): 5-11, 2020 01.
Artículo en Inglés | MEDLINE | ID: mdl-31941852

RESUMEN

Acid sphingomyelinase (ASM) is a lysosomal hydrolase that degrades sphingomyelin into ceramide and phosphocholine. Recent crystallographic studies revealed the functional role of the N-terminal ASM saposin domain. ASM deficiency due to mutations in the ASM-encoding sphingomyelin phosphodiesterase 1 (SMPD1) gene causes an autosomal recessive sphingolipid-storage disorder, known as Niemann-Pick disease Type A (NPA) or Type B (NPB). NPA is an early-onset neuronopathic disorder, while NPB is a late-onset non-neuronopathic disorder. A homozygous one-base substitution (c.398G>A) of the SMPD1 gene was identified in an infant with NPA, diagnosed with complete loss of ASM activity in the patient's fibroblasts. This mutation is predicted to substitute tyrosine for cysteine at amino acid residue 133, abbreviated as p.C133Y. The patient showed developmental delay, hepatosplenomegaly and rapid neurological deterioration leading to death at the age of 3 years. To characterize p.C133Y, which may disrupt one of the three disulfide bonds of the N-terminal ASM saposin domain, we performed immunoblotting analysis to explore the expression of a mutant ASM protein in the patient's fibroblasts, showing that the protein was detected as a 70-kDa protein, similar to the wild-type ASM protein. Furthermore, transient expression of p.C133Y ASM protein in COS-7 cells indicated complete loss of ASM enzyme activity, despite that the p.C133Y ASM protein was properly localized to the lysosomes. These results suggest that the proper three-dimensional structure of saposin domain may be essential for ASM catalytic activity. Thus, p.C133Y is associated with complete loss of ASM activity even with stable protein expression and proper subcellular localization.


Asunto(s)
Mutación/genética , Enfermedad de Niemann-Pick Tipo A/enzimología , Enfermedad de Niemann-Pick Tipo A/genética , Saposinas/química , Esfingomielina Fosfodiesterasa/química , Esfingomielina Fosfodiesterasa/genética , Edad de Inicio , Secuencia de Aminoácidos , Secuencia de Bases , Preescolar , Análisis Mutacional de ADN , ADN Complementario/genética , Resultado Fatal , Femenino , Fibroblastos/enzimología , Fibroblastos/patología , Humanos , Lactante , Dominios Proteicos
7.
Pediatr Int ; 61(3): 258-263, 2019 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-30636380

RESUMEN

BACKGROUND: Bubbly/cystic appearance on chest radiograph is an important factor in severe-type bronchopulmonary dysplasia (BPD) in Japan. The aim of this study was to determine the perinatal characteristics and neonatal complications of the bubbly/cystic(+) group in extremely preterm infants with BPD, that is, oxygen dependency at day 28 after birth (BPD28). METHODS: This was a multicenter retrospective cohort study of population data from infants (birthweight, <1,500 g) enrolled in the Neonatal Research Network of Japan. Of the 15 480 infants born at <28 weeks' gestational age (GA) between 2003 and 2012, 8,979 met the BPD28 criteria. The BPD28 infants were classified according to bubbly/cystic appearance on radiograph (±) at >28 postnatal days. RESULTS: The bubbly/cystic(+) group had lower GA and birthweight and required longer mechanical ventilation and oxygen dependency than the bubbly/cystic(-) group. After adjustment for confounding factors, bubbly/cystic appearance was an independent risk factor for home oxygen therapy at discharge. CONCLUSION: Bubbly/cystic appearance on chest radiograph was a predictor of short-term respiratory outcomes in infants with BPD28, which is diagnosed much earlier (≥28 postnatal days), and has a potentially different etiology to BPD36 (oxygen and/or positive pressure respiratory support dependency at 36 weeks' postmenstrual age).


Asunto(s)
Displasia Broncopulmonar/diagnóstico por imagen , Pulmón/diagnóstico por imagen , Displasia Broncopulmonar/complicaciones , Estudios de Cohortes , Bases de Datos Factuales , Femenino , Humanos , Recien Nacido Extremadamente Prematuro , Recién Nacido , Japón , Terapia por Inhalación de Oxígeno , Embarazo , Estudios Retrospectivos , Medición de Riesgo/métodos , Factores de Riesgo
8.
Bioorg Med Chem Lett ; 28(14): 2408-2412, 2018 08 01.
Artículo en Inglés | MEDLINE | ID: mdl-29934246

RESUMEN

We describe a medicinal chemistry approach to the discovery of a novel EP1 antagonist exhibiting high potency and good pharmacokinetics. Our starting point is 1, an EP1 receptor antagonist that exhibits pharmacological efficacy in cystometry models following intravenous administration. Despite its good potency in vitro, the high lipophilicity of 1 is a concern in long-term in vivo studies. Further medicinal chemistry efforts identified 4 as an improved lead compound with good in vitro ADME profile applicable to long term in vivo studies. A rat fracture study was conducted with 4 for 4 weeks to validate its utility in bone fracture healing. The results suggest that this EP1 receptor antagonist stimulates callus formation and thus 4 has potential for enhancing fracture healing.


Asunto(s)
Descubrimiento de Drogas , Curación de Fractura/efectos de los fármacos , Fracturas Óseas/tratamiento farmacológico , Subtipo EP1 de Receptores de Prostaglandina E/antagonistas & inhibidores , Tiazoles/farmacología , Animales , Modelos Animales de Enfermedad , Perros , Relación Dosis-Respuesta a Droga , Fracturas Óseas/metabolismo , Células de Riñón Canino Madin Darby/efectos de los fármacos , Células de Riñón Canino Madin Darby/metabolismo , Células de Riñón Canino Madin Darby/patología , Ratones , Ratones Noqueados , Estructura Molecular , Subtipo EP1 de Receptores de Prostaglandina E/deficiencia , Subtipo EP1 de Receptores de Prostaglandina E/metabolismo , Relación Estructura-Actividad , Tiazoles/química
10.
Mod Rheumatol ; 28(4): 721-723, 2018 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-26872497

RESUMEN

This report describes the case of a very low-birth-weight male infant with neonatal lupus erythematosus. His mother had Sjögren's syndrome, and her previous child had suffered a complete heart block. Accordingly, maternal steroid (betamethasone) therapy was administered to prevent a congenital heart block for 15 weeks (from 13 to 27 weeks' gestation). At 28 weeks' gestation, the mother was weaned off the steroid therapy, and an emergency cesarean section was carried out at 29 weeks and 6 days' gestation because of a nonreassuring fetal status (NRFS). At birth, the infant exhibited grade-III intraventricular hemorrhage (IVH). Although it is unclear why the infant developed a NRFS and IVH, the condition of the fetus should be carefully monitored during and after long-term maternal steroid treatment.


Asunto(s)
Hemorragia Cerebral/patología , Enfermedades Fetales/patología , Recién Nacido de Bajo Peso , Lupus Eritematoso Sistémico/congénito , Síndrome de Sjögren/patología , Hemorragia Cerebral/etiología , Femenino , Enfermedades Fetales/etiología , Humanos , Recién Nacido , Lupus Eritematoso Sistémico/etiología , Lupus Eritematoso Sistémico/patología , Masculino , Embarazo , Síndrome de Sjögren/complicaciones
11.
Bioorg Med Chem Lett ; 27(21): 4828-4831, 2017 11 01.
Artículo en Inglés | MEDLINE | ID: mdl-28988762

RESUMEN

A series of indazole derivatives were identified as Sirt 1 activators though high-throughput screening. Optimization of each substituent on the indazole ring led to the identification of compound 13. Compound 13 appeared to give the best Sirt 1 activity of the compounds tested and also showed osteogenesis activity in a cell assay. Sirt 1 activators are therefore potential candidates for the treatment of osteoporosis.


Asunto(s)
Indazoles/química , Sirtuina 1/metabolismo , Acetilación/efectos de los fármacos , Diferenciación Celular/efectos de los fármacos , Línea Celular , Humanos , Indazoles/metabolismo , Indazoles/farmacología , Osteogénesis/efectos de los fármacos , Sirtuina 1/química , Relación Estructura-Actividad , Proteína p53 Supresora de Tumor/metabolismo
13.
Biomedicines ; 12(4)2024 Mar 27.
Artículo en Inglés | MEDLINE | ID: mdl-38672101

RESUMEN

BACKGROUND: Pyruvate dehydrogenase kinase isoform 4 (PDK4) plays a pivotal role in the regulation of cellular proliferation and apoptosis. The objective of this study was to examine whether the genetic depletion of the PDK4 gene attenuates hyperoxia-induced lung injury in neonatal mice. METHODS: Neonatal PDK4-/- mice and wild-type (WT) mice were exposed to oxygen concentrations of 21% (normoxia) and 95% (hyperoxia) for the first 4 days of life. Pulmonary histological assessments were performed, and the mRNA levels of lung PDK4, monocyte chemoattractant protein (MCP)-1 and interleukin (IL)-6 were assessed. The levels of inflammatory cytokines in lung tissue were quantified. RESULTS: Following convalescence from neonatal hyperoxia, PDK4-/- mice exhibited improved lung alveolarization. Notably, PDK4-/- mice displayed significantly elevated MCP-1 protein levels in pulmonary tissues following 4 days of hyperoxic exposure, whereas WT mice showed increased IL-6 protein levels under similar conditions. Furthermore, neonatal PDK4-/- mice subjected to hyperoxia demonstrated markedly higher MCP-1 mRNA expression at 4 days of age compared to WT mice, while IL-6 mRNA expression remained unaffected in PDK4-/- mice. CONCLUSIONS: Newborn PDK4-/- mice exhibited notable recovery from hyperoxia-induced lung injury, suggesting the potential protective role of PDK4 depletion in mitigating lung damage.

14.
J Matern Fetal Neonatal Med ; 37(1): 2332914, 2024 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-38522947

RESUMEN

BACKGROUND: Bronchopulmonary dysplasia (BPD) has a lasting effect on the respiratory function of infants, imposing chronic health burdens. BPD is influenced by various prenatal, postnatal, and genetic factors. This study explored the connection between BPD and home oxygen therapy (HOT), and then we examined the association between HOT and a specific single-nucleotide polymorphism (SNP) in the hyaluronan and proteoglycan link protein 1 (HAPLN1) gene among premature Japanese infants. MATERIALS AND METHODS: Prenatal and postnatal data from 212 premature infants were collected and analyzed by four SNPs (rs975563, rs10942332, rs179851, and rs4703570) around HAPLN1 using the TaqMan polymerase chain reaction method. The clinical characteristics and genotype frequencies of HAPLN1 were assessed and compared between HOT and non-HOT groups. RESULTS: Individuals with AA/AC genotypes in the rs4703570 SNP exhibited significantly higher HOT rates at discharge than those with CC homozygotes (odds ratio, 1.20, 95% confidence interval, 1.07-1.35, p = .038). A logistic regression analysis determined that CC homozygotes in the rs4703570 SNP did not show a statistically significant independent association with HOT at discharge. CONCLUSIONS: Although our study did not reveal a correlation between HAPLN1 and the onset of BPD, we observed that individuals with CC homozygosity at the rs4703570 SNP exhibit a reduced risk of HOT.


Asunto(s)
Displasia Broncopulmonar , Proteínas de la Matriz Extracelular , Ácido Hialurónico , Recién Nacido , Lactante , Femenino , Humanos , Embarazo , Displasia Broncopulmonar/genética , Displasia Broncopulmonar/terapia , Japón , Recien Nacido Prematuro , Proteoglicanos/genética , Oxígeno
15.
Psychooncology ; 22(10): 2339-46, 2013 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-23661593

RESUMEN

OBJECTIVES: This study aimed to develop a structural model for mammography adoption in Japanese middle-aged women by using constructs from the transtheoretical model (TTM), the theory of planned behavior (TPB), implementation intentions, and cancer worry. METHODS: Questionnaires based on items including TTM, TPB, implementation intentions, cancer worry-related variables, and demographic variables were distributed to 1000 adult women aged 40 to 59 years, with 641 subjects being used in the final analysis (response rate = 64.1%). RESULTS: Regarding the stage of adoption, 79 participants (12.3%) were at the precontemplation stage, 30 (4.7%) were at the relapse stage, 142 (22.2%) were at the contemplation stage, 88 (13.7%) were at the action stage, and 302 (47.1%) were at the maintenance stage. Our model, derived from structural equation modeling, revealed that the stage of mammography adoption was significantly affected by goal intentions, implementation intentions, perceived barriers, history of breast cancer screening, and relative risk. A logistic regression analysis revealed that goal intentions and implementation intentions significantly predicted mammography uptake within 1 year. CONCLUSION: This study developed an integrated model constructed from TTM, TPB, implementation intentions, and cancer worry to account for mammography adoption in Japan, and also confirmed the predictive validity of the model.


Asunto(s)
Ansiedad/psicología , Neoplasias de la Mama/psicología , Detección Precoz del Cáncer/psicología , Intención , Mamografía/psicología , Aceptación de la Atención de Salud/psicología , Adulto , Actitud Frente a la Salud , Neoplasias de la Mama/diagnóstico por imagen , Detección Precoz del Cáncer/estadística & datos numéricos , Femenino , Humanos , Japón , Modelos Logísticos , Mamografía/estadística & datos numéricos , Persona de Mediana Edad , Modelos Psicológicos , Teoría Psicológica
16.
Endocr J ; 60(4): 403-8, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23197114

RESUMEN

Beckwith-Wiedemann syndrome (BWS) is the most common congenital overgrowth syndrome involving tumor predisposition. BWS is caused by various epigenetic or genetic alterations that disrupt the imprinted genes on chromosome 11p15.5 and the clinical findings of BWS are highly variable. Hyperinsulinemic hypoglycemia is reported in about half of all babies with BWS. We identified an infant with diazoxide-unresponsive congenital hyperinsulinism (HI) without any apparent clinical features suggestive of BWS, but diagnosed BWS by molecular testing. The patient developed severe hyperinsulinemic hypoglycemia within a few hours after birth, with macrosomia and mild hydronephrosis. We excluded mutations in the K(ATP) channel genes on chromosome 11p15.1, but found a rare homozygous single nucleotide polymorphism (SNP) of ABCC8. Parental SNP pattern suggested paternal uniparetal disomy in this region. By microsatellite marker analysis on chromosome 11p15, we could diagnose BWS due to the mosaic of paternal uniparental disomy. Our case suggests that some HI of unknown genetic etiology could involve undiagnosed BWS with no apparent clinical features, which might be diagnosed only by molecular testing.


Asunto(s)
Síndrome de Beckwith-Wiedemann/diagnóstico , Disomía Uniparental/diagnóstico , Transportadoras de Casetes de Unión a ATP/química , Transportadoras de Casetes de Unión a ATP/genética , Síndrome de Beckwith-Wiedemann/tratamiento farmacológico , Síndrome de Beckwith-Wiedemann/genética , Síndrome de Beckwith-Wiedemann/fisiopatología , Cromosomas Humanos Par 11/genética , Hiperinsulinismo Congénito/genética , Hiperinsulinismo Congénito/prevención & control , Monitoreo de Drogas , Femenino , Humanos , Hidronefrosis/etiología , Hidronefrosis/prevención & control , Hipoglucemia/etiología , Hipoglucemia/prevención & control , Recién Nacido , Antagonistas de Insulina/administración & dosificación , Antagonistas de Insulina/uso terapéutico , Mosaicismo , Octreótido/administración & dosificación , Octreótido/uso terapéutico , Polimorfismo de Nucleótido Simple , Canales de Potasio de Rectificación Interna/química , Canales de Potasio de Rectificación Interna/genética , Receptores de Droga/química , Receptores de Droga/genética , Índice de Severidad de la Enfermedad , Receptores de Sulfonilureas , Resultado del Tratamiento , Disomía Uniparental/genética , Disomía Uniparental/fisiopatología
18.
Health Commun ; 28(7): 709-17, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23356504

RESUMEN

We examined the predictive validity of a segmentation strategy based on intention and cancer worry for mammography adoption and explored key factors for promoting mammography adoption in each segment. A questionnaire survey was completed by 641 women aged 40-59 years. Among them, 559 answered a follow-up survey after 15 months. They were categorized into five segments: maintenance group (S5), higher implementation intention group (S4), higher goal intention group (S3), higher worry group (S2), or lower worry group (S1). The odds of participants in each segment adopting mammography during the follow-up period were calculated. Logistic regression analysis was conducted to identify psychological predictors (five attitudes to mammography and perceived health competence) of transition to upper segments (S1 vs. S2, S2 vs. S3, S3 vs. S4, S4 vs. S5). Compared to S5, other segments did not undertake mammography at significant rates during the follow-up. The following were significant predictors for inclusion in upper segments: Lack of importance and perceived health competence were associated with inclusion in S2; lack of importance and barriers to screening were associated with inclusion in S3; perceived health competence was associated with inclusion in S4; and lack of importance was associated with inclusion in S5. These results confirm the predictive validity of a segmentation strategy, and indicate that there might be specific key factors for each segment in promoting mammography adoption.


Asunto(s)
Ansiedad , Promoción de la Salud/métodos , Intención , Mamografía/psicología , Aceptación de la Atención de Salud , Encuestas y Cuestionarios/normas , Adulto , Femenino , Humanos , Japón , Modelos Logísticos , Estudios Longitudinales , Persona de Mediana Edad
19.
Front Psychol ; 14: 1239103, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-37637897

RESUMEN

The present study examined how the importance of values and perceived value congruence with families, friends, and country would be associated with the risk factors of passive suicide ideation. Specifically, the study investigated the associations that the values and perceived congruence had with thwarted belongingness and perceived burdensomeness during the COVID-19 pandemic after controlling for the impact of depression levels. The data from the US and Japan demonstrated that the values such as cherishing family and friends and value congruence played a protective factor for Japanese participants; however, the associations differed among those in the US. Values such as enduring challenges played a protective factor for perceived burdensomeness in Japan whereas values such as cherishing family and friends played a protective factor and improving society was a risk factor for thwarted belongingness for those in the US. These results can be used to further understand the roles of values in mental health.

20.
Biomedicines ; 11(2)2023 Feb 14.
Artículo en Inglés | MEDLINE | ID: mdl-36831089

RESUMEN

BACKGROUND: Over the years, bronchopulmonary dysplasia (BPD) affects the pulmonary function of infants, resulting in chronic health burdens for infants and their families. The aim of this scoping review was to screen available evidence regarding perinatal risk factors associated with the development and severity of BPD. METHODS: The eligibility criteria of the studies were year of publication between 2016 and 2021; setting of a developed country; English or Japanese as the study language; and randomized controlled, cohort, or case-control design. The titles and abstracts of the studies were screened by independent reviewers. RESULTS: Of 8189 eligible studies, 3 were included for severe BPD and 26 were included for moderate BPD. The risk factors for severe BPD were male sex, iatrogenic preterm birth, maternal hypertensive disorders of pregnancy (HDP), low gestational age, small-for-gestational-age (SGA) birth weight, mechanical ventilation on day 1, and need for patent ductus arteriosus (PDA) management. The risk factors for moderate or severe BPD included male sex, premature rupture of membranes, clinical chorioamnionitis, maternal HDP, SGA birth weight, bubbly/cystic appearance on X-ray, and PDA management. CONCLUSIONS: We identified several risk factors for BPD. We plan to confirm the validity of the new classification using the existing dataset.

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