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1.
Pediatr Int ; 64(1): e15315, 2022 Jan.
Article in English | MEDLINE | ID: mdl-36331237

ABSTRACT

BACKGROUND: Ritodrine and magnesium sulfate are administered to prevent preterm labor. Magnesium sulfate is also administered to prevent preeclampsia. These drugs have been reported to increase potassium levels in pregnant women and neonates. The aim of this study was to investigate the relationship between potassium levels in preterm infants and antenatal treatment. METHODS: This prospective cohort study was conducted at Saiseikai Suita Hospital. Preterm infants born at <35 weeks' gestation between October 2012 and September 2014 were recruited and divided into four groups based on the antenatal treatment their mothers received. Serum and urine electrolyte levels at birth and serum potassium levels 1 day after birth were measured. RESULTS: The mothers of 16 infants received no antenatal treatment (condition C); the mothers of 29 infants received antenatal ritodrine (R); the mothers of seven infants received magnesium sulfate (M); and the mothers of 15 infants received both magnesium sulfate and ritodrine (M + R). At birth, potassium levels were similar among the four groups. However, potassium levels a day after birth were significantly higher in the M + R group than in the other groups: median (min.-max.) mEq/L 4.8 (3.8-6.2), 4.8 (3.6-6.0), and 4.4 (3.8-5.9) vs. 5.8 (4.9-7.2), in the C, R, and M groups versus the M + R group, respectively (P < 0.01). Significantly more infants in the M + R group exhibited a fractional excretion of potassium of <10% compared with those in the other groups. CONCLUSION: The increased potassium levels we observe in preterm infants of mothers who received antenatal magnesium sulfate and ritodrine administration on postnatal day 1 warrant monitoring by neonatologists.


Subject(s)
Ritodrine , Infant , Infant, Newborn , Female , Pregnancy , Humans , Ritodrine/therapeutic use , Infant, Premature , Magnesium Sulfate/therapeutic use , Sulfates , Cohort Studies , Prospective Studies , Potassium
2.
J Infect Chemother ; 20(9): 558-62, 2014 Sep.
Article in English | MEDLINE | ID: mdl-25009091

ABSTRACT

BACKGROUND: Candida species are clinically important causes of bloodstream infections because their mortality is very high. Given that some species of Candida are azole-resistant, identifying the distributions of Candida species could facilitate the formulation of an appropriate empirical antifungal therapy. It has been shown that the distribution varies depending on the continent, country, city, and hospital. In this paper, we describe the distributions of species in hospitals in northern Osaka, Japan. METHOD: We evaluated blood culture results obtained from six tertiary hospitals in the northern Osaka area between 2004 and 2011. We also obtained comorbidity information from the patients' hospital medical records. Kaplan-Meier curves were drawn to compare the risk of death related to the different species. RESULTS: Of the 165 cases of candidemia confirmed by blood culture, 66% were male and the mean age was 62 years (range = 0-96). Overall, Candida albicans comprised 70 cases (43%), followed by Candida parapsilosis with 36 cases (22%), Candida glabrata with 25 cases (15%), Candida tropicalis with 11 cases (7%), Candida krusei with 10 cases (6%), and other Candida species with 13 cases (8%). C. tropicalis had higher associated mortality than other species, although it was not statistically significant. CONCLUSIONS: C. albicans was the most frequently isolated species, but the proportion of non-albicans Candida species was not negligible. The relatively high frequency of non-albicans Candida species distinguished the Japanese distribution from other areas. This characteristic distribution may have important implications when formulating an empirical antifungal therapy for Japanese clinical practice.


Subject(s)
Candida/isolation & purification , Candidemia/microbiology , Candidiasis/blood , Candidiasis/microbiology , Adolescent , Adult , Aged , Aged, 80 and over , Antifungal Agents/therapeutic use , Candida/drug effects , Candidemia/drug therapy , Candidiasis/drug therapy , Candidiasis/epidemiology , Child , Child, Preschool , Cross Infection/blood , Cross Infection/drug therapy , Cross Infection/epidemiology , Cross Infection/microbiology , Female , Hospitals , Humans , Infant , Infant, Newborn , Japan , Male , Microbial Sensitivity Tests , Middle Aged , Young Adult
3.
Neonatology ; 99(4): 272-9, 2011.
Article in English | MEDLINE | ID: mdl-21109757

ABSTRACT

BACKGROUND: Persistent pulmonary hypertension of the newborn is often associated with meconium aspiration syndrome (MAS) or perinatal asphyxia. OBJECTIVE: To determine the effect of meconium or asphyxia on pulmonary arterial pressure and circulating levels of vasoactive substances, we conducted a prospective study of 54 term infants, including infants with meconium-stained amniotic fluid with normal (MSAF) or abnormal (MAS) chest X-ray findings, infants with perinatal asphyxia, and controls. The purpose of this study was to determine the group most likely to have elevated pulmonary arterial pressure and a disturbed balance between vasoactive substances. METHODS: To estimate the pulmonary arterial pressure by echocardiography, we used the ratio of the right to left systolic ventricular pressure (RVP/LVP ratio). We measured the plasma concentrations of endothelin-1 (ET-1), cyclic guanosine monophosphate (cGMP) as an indicator of nitric oxide (NO) production, and 6-keto-prostaglandin F(1)α (6-keto-PGF(1)α) for the estimation of prostacyclin concentration. We also measured KL-6 as a marker of lung injury. RESULTS: The RVP/LVP ratio was significantly higher in the MAS group than the other groups on day 0. Although ET-1 and 6-keto-PGF(1)α levels were comparable among all groups, the cGMP level on days 3-5 and the KL-6 level throughout the first postnatal week were significantly higher in the MAS group. CONCLUSIONS: It is possible that meconium aspiration delays normal decline of pulmonary vascular resistance shortly after birth through lung parenchymal injury. The subsequent increase of cGMP in MAS may be an adaptive response to prevent further elevation of pulmonary arterial pressure by inducing NO.


Subject(s)
Lung Injury/etiology , Meconium Aspiration Syndrome/complications , Parturition/physiology , Vascular Resistance/physiology , Asphyxia Neonatorum/blood , Asphyxia Neonatorum/epidemiology , Asphyxia Neonatorum/physiopathology , Asphyxia Neonatorum/therapy , Blood Pressure/physiology , Down-Regulation , Fetal Blood/chemistry , Fetal Blood/metabolism , Gestational Age , Humans , Infant, Newborn , Lung/cytology , Lung/physiology , Lung Injury/blood , Lung Injury/epidemiology , Meconium Aspiration Syndrome/epidemiology , Natriuretic Peptide, Brain/analysis , Natriuretic Peptide, Brain/blood , Pulmonary Artery/physiopathology , Time Factors
4.
Pediatr Res ; 60(5): 613-8, 2006 Nov.
Article in English | MEDLINE | ID: mdl-16988187

ABSTRACT

Circulating KL-6 is a specific indicator of pulmonary injury affecting the alveolar epithelium and interstitium. Our preliminary study suggested the usefulness of plasma KL-6 as a marker of bronchopulmonary dysplasia (BPD). To confirm the diagnostic value of KL-6 for BPD as well as to determine the reference range, we conducted a larger prospective study in 135 preterm infants <32 wk GA. Among the infants without oxygen dependence at a postconceptional age of 36 wk, the plasma KL-6 level showed no significant association with GA at any time. Among 42 infants <28 wk GA, plasma KL-6 levels were significantly higher in those with moderate/severe BPD compared with those with no/mild BPD. A plasma level of 199 U/mL at 1 wk or 232 U/mL at 2 wk was an excellent predictor of moderate/severe BPD <28 wk GA (positive predictive value of 83% and 80%, respectively). Unlike nonspecific markers of inflammation or fibrosis, KL-6 objectively reflects the severity of pulmonary injury irrespective of the treatment or the radiographic changes. Therefore, not only as a good marker, measurement of KL-6 may also help to provide new insights into the pathogenesis of BPD.


Subject(s)
Antigens, Neoplasm/blood , Bronchopulmonary Dysplasia/blood , Bronchopulmonary Dysplasia/diagnosis , Mucins/blood , Biomarkers/blood , Female , Fetal Blood/chemistry , Gestational Age , Humans , Infant, Newborn , Infant, Premature , Male , Mucin-1 , Predictive Value of Tests , Pregnancy , ROC Curve , Reference Values , Reproducibility of Results
5.
Pediatr Res ; 53(4): 594-9, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12612209

ABSTRACT

Among various hypothetical mechanisms for the in vivo production of reactive oxygen species, transition metal-catalyzed reactions in cooperation with a biologic reducing agent like ascorbic acid or superoxide may be some of the most important. In the present study, we retrospectively examined the existence of non-protein-bound metal ions, an essentially hazardous pro-oxidant form of various transition metals, and the occurrence of metal-catalyzed reactive oxygen species production in cerebrospinal fluid (CSF) of 10 infants with hypoxic ischemic encephalopathy (HIE) subsequent to perinatal asphyxia and 12 control infants within 72 h of birth. Non-protein-bound iron was detected in eight out of 10 CSF samples from the HIE infants and its level was significantly correlated with Sarnat's clinical stage, whereas none of the control infants had detectable non-protein-bound iron levels. Non-protein-bound copper was below the detection limit in all CSF samples from both groups. Ascorbic acid was significantly increased in the CSF of HIE infants when compared with that of controls (means, 664.9 versus 449.4 microM, p = 0.008). ortho-Tyrosine and meta-tyrosine, which are highly specific and sensitive markers of protein oxidation induced by hydroxyl radicals, were significantly higher in HIE infants than in controls when evaluated by the ratio relative to their source amino acid, phenylalanine [means, 110.5 versus 75.4, p = 0.018 for ortho-tyrosine/phenylalanine; 104.6 versus 67.7 (nM/microM x 10(2)), p = 0.048 for meta-tyrosine/phenylalanine]. Both ratios were significantly correlated with non-protein-bound iron, but not with ascorbic acid. Our preliminary observations provide direct evidence that hydroxyl radicals are generated in the CNS during asphyxiation. Iron chelation therapy could be worth developing as a neuroprotective strategy for perinatal asphyxia.


Subject(s)
Copper/cerebrospinal fluid , Hypoxia-Ischemia, Brain/cerebrospinal fluid , Iron/cerebrospinal fluid , Allantoin/cerebrospinal fluid , Ascorbic Acid/cerebrospinal fluid , Biomarkers , Dehydroascorbic Acid/cerebrospinal fluid , Female , Humans , Hydroxyl Radical/cerebrospinal fluid , Infant, Newborn , Male , Oxidative Stress , Protein Binding , Reactive Oxygen Species/cerebrospinal fluid
6.
Free Radic Res ; 36(9): 933-8, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12448818

ABSTRACT

alpha-Tochopherol transfer protein (alpha TTP), a 32 kDa protein exclusively expressed in liver cytosol, has a high binding affinity for alpha-tochopherol. The factors that regulate the expression of hepatic alpha TTP are not clearly understood. In this study, we investigated whether or not exposure to hyperoxia (> 95% O2 for 48 h) could alter the expression of hepatic alpha TTP. We also examined the association between the expression of antioxidant enzymes (hepatic glutathione peroxidase (GPX) and Mn-superoxide dismutase (Mn-SOD)) and the expression of hepatic alpha TTP. The levels of thiobarbituric acid-reactive substances (TBARS) in both plasma and liver were significantly higher after rats were exposed to hyperoxia for 48 h when compared with the levels in control rats. Northern blotting showed a decrease in the expression of alpha TTP messenger RNA (mRNA) after hyperoxia, although the alpha TTP protein level remained constant. Expression of Mn-SOD mRNA and protein, as well as the expression of GPX mRNA, were stable after hyperoxia. These findings indicate that mRNA for hepatic alpha TTP, rather than Mn-SOD or GPX, may be highly responsive to oxidative stress.


Subject(s)
Carrier Proteins/metabolism , Hyperoxia/metabolism , Liver/metabolism , RNA, Messenger/metabolism , alpha-Tocopherol/metabolism , Alanine Transaminase/metabolism , Animals , Blotting, Northern , Blotting, Western , Carrier Proteins/genetics , Glutathione Peroxidase/metabolism , Lipid Peroxidation , Liver/cytology , Liver Extracts , Male , Oxidative Stress/physiology , Rats , Rats, Wistar , Superoxide Dismutase/metabolism
7.
J Nutr Sci Vitaminol (Tokyo) ; 48(1): 6-9, 2002 Feb.
Article in English | MEDLINE | ID: mdl-12026191

ABSTRACT

We administered high-dose vitamin E to healthy adult male volunteers and assessed the safety of such supplementation. Fourteen volunteers received daily 1,200 IU of vitamin E (800 mg of D-alpha-tocopherol) for 28 d and eight controls were also enrolled. The volunteers treated with vitamin E showed no abnormalities during the study period. The alpha-tocopherol concentrations of plasma and platelets were markedly elevated by vitamin E treatment, but there were no significant differences in platelet aggregation, coagulation, and the clinical parameters between the two groups. In conclusion, a high dose of vitamin E for 28 d had no adverse effects in healthy men.


Subject(s)
Antioxidants/adverse effects , Coronary Artery Disease/prevention & control , Dietary Supplements , Vitamin E/adverse effects , Adult , Antioxidants/administration & dosage , Blood Cell Count , Blood Coagulation/drug effects , Cholesterol/blood , Chromatography, High Pressure Liquid , Humans , Japan , Male , Platelet Aggregation/drug effects , Time Factors , Vitamin E/administration & dosage , Vitamin E/blood , alpha-Tocopherol/blood
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