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1.
Asian Pac J Cancer Prev ; 17(3): 1313-23, 2016.
Article in English | MEDLINE | ID: mdl-27039765

ABSTRACT

To study the full health effects of parental radiation exposure on the children of the atomic bomb survivors, the Radiation Effects Research Foundation developed a cohort of 76,814 children born to atomic bomb survivors (F1 generation) to assess cancer incidence and mortality from common adult diseases. In analyzing radiationassociated health information, it is important to be able to adjust for sociodemographic and lifestyle variations that may affect health. In order to gain this and other background information on the F1 cohort and to determine willingness to participate in a related clinical study, the F1 Mail Survey Questionnaire was designed with questions corresponding to relevant health, sociodemographic, and lifestyle indicators. Between the years 2000 and 2006, the survey was sent to a subset of the F1 Mortality Cohort. A total of 16,183 surveys were completed and returned: 10,980 surveys from Hiroshima residents and 5,203 from Nagasaki residents. The response rate was 65.6%, varying somewhat across parental exposure category, city, gender, and year of birth. Differences in health and lifestyle were noted in several variables on comparison across city and gender. No major differences in health, lifestyle, sociodemographics, or disease were seen across parental exposure categories, though statistically significant tests for heterogeneity and linear trend revealed some possible changes with dose. The data described herein provide a foundation for studies in the future.


Subject(s)
Neoplasms, Radiation-Induced/epidemiology , Neoplasms, Radiation-Induced/etiology , Nuclear Warfare , Postal Service , Radiation Exposure/adverse effects , Survivors/statistics & numerical data , Adolescent , Adult , Case-Control Studies , Female , Follow-Up Studies , Health Status , Health Surveys , Humans , Incidence , Japan/epidemiology , Life Style , Male , Middle Aged , Neoplasms, Radiation-Induced/mortality , Pregnancy , Prenatal Exposure Delayed Effects , Prognosis , Risk Factors , Socioeconomic Factors , Survival Rate , Young Adult
2.
Steroids ; 99(Pt A): 49-55, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25304359

ABSTRACT

Epidemiological studies have examined breast cancer risk in relation to sex hormone concentrations measured by different methods: "extraction" immunoassays (with prior purification by organic solvent extraction, with or without column chromatography), "direct" immunoassays (no prior extraction or column chromatography), and more recently with mass spectrometry-based assays. We describe the associations of estradiol, estrone and testosterone with both body mass index and breast cancer risk in postmenopausal women according to assay method, using data from a collaborative pooled analysis of 18 prospective studies. In general, hormone concentrations were highest in studies that used direct assays and lowest in studies that used mass spectrometry-based assays. Estradiol and estrone were strongly positively associated with body mass index, regardless of the assay method; testosterone was positively associated with body mass index for direct assays, but less clearly for extraction assays, and there were few data for mass spectrometry assays. The correlations of estradiol with body mass index, estrone and testosterone were lower for direct assays than for extraction and mass spectrometry assays, suggesting that the estimates from the direct assays were less precise. For breast cancer risk, all three hormones were strongly positively associated with risk regardless of assay method (except for testosterone by mass spectrometry where there were few data), with no statistically significant differences in the trends, but differences may emerge as new data accumulate. Future epidemiological and clinical research studies should continue to use the most accurate assays that are feasible within the design characteristics of each study.


Subject(s)
Body Mass Index , Breast Neoplasms/etiology , Estradiol/blood , Estrone/blood , Postmenopause/blood , Testosterone/blood , Female , Humans , Prospective Studies , Risk Factors
3.
J Viral Hepat ; 19(2): e126-33, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22239510

ABSTRACT

Obesity and insulin resistance have been reported as negative predictors for sustained virological response (SVR) in hepatitis C virus (HCV) genotype 1 infected patients treated with pegylated interferon-α plus ribavirin. They are also known to affect serum levels of several cytokines including adipocytokines. But the association between these cytokines and treatment outcome has not been fully elucidated. We examined pretreatment serum levels of 14 cytokines among 190 patients who were treated with pegylated interferon-α-2b plus ribavirin for chronic HCV-1b infection with high viral load (≥ 5 log IU/mL) and analyzed their contribution to treatment response. Plasminogen activator inhibitor-1 (PAI-1), vascular endothelial growth factor, and 11 clinical factors showed significant association with SVR in univariate logistic regression analysis. Four significant factors in multivariate analysis; serum PAI-1 (odds ratio [OR] = 15.42), body mass index (OR = 4.56), rs8099917 (OR = 4.95) and fibrosis stage (OR = 5.18) were identified as independent predictors. We constructed a simple and minimally invasive prediction score for SVR based on the presence of these factors except for fibrosis stage. The accuracy of this score was 73%, and was confirmed using an independent validation cohort consisting of 31 patients (68%). The strongest correlation was between PAI-1 level and platelet count (r = 0.38, P = 1.8 × 10(-7)), and PAI-1 level was inversely correlated with fibrosis stage. Serum PAI-1 is a novel predictor for the response to combination therapy against chronic HCV-1b infection and may be associated with liver fibrosis.


Subject(s)
Antiviral Agents/administration & dosage , Biomarkers/blood , Hepatitis C, Chronic/drug therapy , Interferon-alpha/administration & dosage , Plasminogen Activator Inhibitor 1/blood , Polyethylene Glycols/administration & dosage , Ribavirin/administration & dosage , Aged , Female , Hepacivirus/isolation & purification , Humans , Interferon alpha-2 , Male , Middle Aged , Prognosis , Recombinant Proteins/administration & dosage , Serum/chemistry , Treatment Outcome , Viral Load
4.
Radiat Res ; 170(4): 451-7, 2008 Oct.
Article in English | MEDLINE | ID: mdl-19024652

ABSTRACT

The first study to examine whether parental radiation exposure leads to increased heritable risk of common adult-onset multifactorial diseases (i.e., hypertension, diabetes mellitus, hypercholesterolemia, ischemic heart disease, and stroke) was conducted among 11,951 participants in the clinical examination program out of a potential of 24,673 mail survey subjects who were offspring of survivors born from May 1946 through December 1984. Logistic regression analyses demonstrated no evidence of an association between the prevalence of multifactorial diseases in the offspring and parental radiation exposure, after adjusting for age, city, gender and various risk factors. The odds ratio (OR) for a paternal dose of 1 Gy was 0.91 [95% confidence interval (CI) 0.81-1.01, P = 0.08], and that for a maternal dose of 1 Gy was 0.98 (95% CI 0.86-1.10, P = 0.71). There was no apparent effect of parental age at exposure or of elapsed time between parental exposure and birth, but male offspring had a low odds ratio (OR = 0.76 at 1 Gy) for paternal exposure, but cautious interpretation is needed for this finding. The clinical assessment of nearly 12,000 offspring of A-bomb survivors who have reached a median age of about 50 years provided no evidence for an increased prevalence of adult-onset multifactorial diseases in relation to parental radiation exposure.


Subject(s)
Adult Children , Cardiovascular Diseases/epidemiology , Diabetes Mellitus/epidemiology , Hypercholesterolemia/epidemiology , Maternal Exposure/adverse effects , Nuclear Weapons , Paternal Exposure/adverse effects , Adult , Age of Onset , Cardiovascular Diseases/genetics , Diabetes Mellitus/genetics , Female , Genetic Predisposition to Disease , Humans , Hypercholesterolemia/genetics , Japan/epidemiology , Logistic Models , Male , Middle Aged , Prevalence , Radiation Dosage , Risk , Survivors , Young Adult
5.
Diabetes Res Clin Pract ; 81(3): 381-5, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18653258

ABSTRACT

AIMS: Recent evidence indicates that oxidative stress may play an important role in the pathogenesis of insulin resistance and that gene polymorphism (Ala16Val) of manganese superoxide dismutase (MnSOD) may protect against reactive oxygen species (ROS) function. We aimed to test the hypothesis that the Ala16Val variant could be associated with the development of type 2 diabetes. METHODS: We examined 523 nondiabetic Japanese-Americans who underwent a 75g oral glucose tolerance test (OGTT) and were followed for an average of 9.9 years. Cox proportional hazard analysis, stratified by category of OGTT, was used to determine whether the Ala16Val polymorphism was a risk factor in the development of type 2 diabetes. RESULTS: During the follow-up period, 65 subjects developed type 2 diabetes. Compared with Ala allele carriers, subjects with a Val homozygote showed significantly higher risk for developing diabetes (stratified hazard ratio=2.05 [95% confidence interval 1.03-4.08]; P=0.041) after adjustment for age, gender, systolic blood pressure, total cholesterol, body mass index, and homeostasis model assessment. CONCLUSIONS: We demonstrated that the MnSOD Ala16Val polymorphism might be associated with development of type 2 diabetes among Japanese-Americans. These results suggest that insufficient ROS scavenging might be associated with a susceptibility to glucose intolerance.


Subject(s)
Amino Acid Substitution , Diabetes Mellitus, Type 2/genetics , Glucose Intolerance/genetics , Superoxide Dismutase/genetics , Alanine , Diabetes Mellitus, Type 2/blood , Diabetes Mellitus, Type 2/enzymology , Female , Glucose Intolerance/blood , Glucose Tolerance Test , Humans , Insulin/blood , Insulin Resistance/genetics , Japan/ethnology , Male , Middle Aged , Polymorphism, Genetic , Reactive Oxygen Species/metabolism , United States , Valine
6.
Scand J Gastroenterol ; 38(8): 894-900, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12940445

ABSTRACT

BACKGROUND: It is difficult to study the long-term outcome of hepatitis C virus (HCV) infection because chronic infection is often asymptomatic and duration of the disease is prolonged. The clinical outcome of HCV infection remains unclear in patients of advanced age. METHODS: Among 575 patients consecutively diagnosed with hepatocellular carcinoma (HCC) from 1988 to 1999 at Hiroshima University, we examined 430 with HCV. We studied the differences between males and females in the following characteristics: age at first diagnosis of HCC, Child grade, various tumour factors, history of blood transfusion, duration to development of HCC, and history of alcohol intake. RESULTS: The incidence of HCC patients with HCV increased in elderly persons, including female patients. Background liver function was significantly better for female patients (P < 0.001). In both genders, the duration between blood transfusion and diagnosis of HCC was significantly shorter when the patients received blood transfusion at an older age (P < 0.001). In habitual drinkers, the average age at first diagnosis of HCC was significantly younger (P < 0.001), and duration to development of HCC significantly shorter (P < 0.05). The percentage of atomic bomb survivors among HCV-positive HCC patients was significantly higher than that among HCV-negative HCC patients (P < 0.05). CONCLUSIONS: Patients with HCV might exhibit slow disease progression and develop HCC finally with aging regardless of gender. Patients of advanced age with HCV, even female patients, should therefore be closely followed.


Subject(s)
Aging/physiology , Carcinoma, Hepatocellular/etiology , Carcinoma, Hepatocellular/physiopathology , Hepatitis C/complications , Liver Neoplasms/etiology , Liver Neoplasms/physiopathology , Adult , Age of Onset , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Risk Factors , Sex Factors , Time Factors
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