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1.
JAMA Netw Open ; 7(5): e2410248, 2024 May 01.
Article in English | MEDLINE | ID: mdl-38717777

ABSTRACT

This cohort study investigates the risk of alcohol-related death among US health care workers compared with non­health care workers.


Subject(s)
Health Personnel , Humans , Health Personnel/statistics & numerical data , United States/epidemiology , Male , Female , Adult , Middle Aged , Alcohol Drinking/mortality , Alcohol Drinking/adverse effects , Alcohol Drinking/epidemiology , Cause of Death
2.
Sci Rep ; 14(1): 10390, 2024 05 06.
Article in English | MEDLINE | ID: mdl-38710935

ABSTRACT

The kidney cancer (KC) burden measures have changed dramatically in recent years due to changes in exposure to the determinants over time. We aimed to decompose the difference in the KC burden measures between 1990 and 2019. This ecological study included data on the KC burden measures as well as socio-demographic index (SDI), behavioral, dietary, and metabolic risk factors from the global burden of disease study. Non-linear multivariate decomposition analysis was applied to decompose the difference in the burden of KC. Globally, ASIR, ASMR, and ASDR of KC increased from 2.88 to 4.37, from 1.70 to 2.16, and from 46.13 to 54.96 per 100,000 people between 1990 and 2019, respectively. The global burden of KC was more concentrated in developed countries. From 1990 to 2019, the burden of KC has increased the most in Eastern European countries. More than 70% of the difference in the KC burden measures between 1990 and 2019 was due to changes in exposure to the risk factors over time. The SDI, high body mass index (BMI), and alcohol use had the greatest contribution to the difference in the KC burden measures. Changes in characteristics over time, including SDI, high BMI, and alcohol consumption, appear to be important in the evolving landscape of KC worldwide. This finding may help policymakers design policies and implement prevention programs to control and manage KC.


Subject(s)
Global Burden of Disease , Kidney Neoplasms , Humans , Kidney Neoplasms/epidemiology , Risk Factors , Male , Female , Middle Aged , Body Mass Index , Global Health , Adult , Aged , Alcohol Drinking/adverse effects , Alcohol Drinking/epidemiology
3.
BMC Public Health ; 24(1): 1238, 2024 May 06.
Article in English | MEDLINE | ID: mdl-38711042

ABSTRACT

BACKGROUND: We conducted this meta-analysis to investigate the potential association between maternal smoking, alcohol and caffeinated beverages consumption during pregnancy and the risk of childhood brain tumors (CBTs). METHODS: A thorough search was carried out on PubMed, Embase, Web of Science, Cochrane Library, and China National Knowledge Internet to identify pertinent articles. Fixed or random effects model was applied to meta-analyze the data. RESULTS: The results suggested a borderline statistically significant increased risk of CBTs associated with maternal smoking during pregnancy (OR 1.04, 95% CI 0.99-1.09). We found that passive smoking (OR 1.12, 95% CI 1.03-1.20), rather than active smoking (OR 1.00, 95% CI 0.93-1.07), led to an increased risk of CBTs. The results suggested a higher risk in 0-1 year old children (OR 1.21, 95% CI 0.94-1.56), followed by 0-4 years old children (OR 1.12, 95% CI 0.97-1.28) and 5-9 years old children (OR 1.11, 95% CI 0.95-1.29). This meta-analysis found no significant association between maternal alcohol consumption during pregnancy and CBTs risk (OR 1.00, 95% CI 0.80-1.24). An increased risk of CBTs was found to be associated with maternal consumption of caffeinated beverages (OR 1.16, 95% CI 1.07-1.26) during pregnancy, especially coffee (OR 1.18, 95% CI 1.00-1.38). CONCLUSIONS: Maternal passive smoking, consumption of caffeinated beverages during pregnancy should be considered as risk factors for CBTs, especially glioma. More prospective cohort studies are warranted to provide a higher level of evidence.


Subject(s)
Alcohol Drinking , Brain Neoplasms , Caffeine , Observational Studies as Topic , Prenatal Exposure Delayed Effects , Humans , Pregnancy , Female , Alcohol Drinking/adverse effects , Alcohol Drinking/epidemiology , Prenatal Exposure Delayed Effects/epidemiology , Brain Neoplasms/epidemiology , Brain Neoplasms/chemically induced , Brain Neoplasms/etiology , Child , Child, Preschool , Caffeine/adverse effects , Infant , Infant, Newborn , Smoking/epidemiology , Smoking/adverse effects , Risk Factors , Beverages/adverse effects
4.
Transl Psychiatry ; 14(1): 220, 2024 May 28.
Article in English | MEDLINE | ID: mdl-38806472

ABSTRACT

Heavy maternal alcohol drinking during pregnancy has been associated with altered neurodevelopment in the child but the effects of low-dose alcohol drinking are less clear and any potential safe level of alcohol use during pregnancy is not known. We evaluated the effects of prenatal alcohol on reward-related behavior and substance use in young adulthood and the potential sex differences therein. Participants were members of the European Longitudinal Study of Pregnancy and Childhood (ELSPAC) prenatal birth cohort who participated in its neuroimaging follow-up in young adulthood. A total of 191 participants (28-30 years; 51% men) had complete data on prenatal exposure to alcohol, current substance use, and fMRI data from young adulthood. Maternal alcohol drinking was assessed during mid-pregnancy and pre-conception. Brain response to reward anticipation and reward feedback was measured using the Monetary Incentive Delay task and substance use in young adulthood was assessed using a self-report questionnaire. We showed that even a moderate exposure to alcohol in mid-pregnancy but not pre-conception was associated with robust effects on brain response to reward feedback (six frontal, one parietal, one temporal, and one occipital cluster) and with greater cannabis use in both men and women 30 years later. Moreover, mid-pregnancy but not pre-conception exposure to alcohol was associated with greater cannabis use in young adulthood and these effects were independent of maternal education and maternal depression during pregnancy. Further, the extent of cannabis use in the late 20 s was predicted by the brain response to reward feedback in three out of the nine prenatal alcohol-related clusters and these effects were independent of current alcohol use. Sex differences in the brain response to reward outcome emerged only during the no loss vs. loss contrast. Young adult men exposed to alcohol prenatally had significantly larger brain response to no loss vs. loss in the putamen and occipital region than women exposed to prenatal alcohol. Therefore, we conclude that even moderate exposure to alcohol prenatally has long-lasting effects on brain function during reward processing and risk of cannabis use in young adulthood.


Subject(s)
Alcohol Drinking , Brain , Magnetic Resonance Imaging , Prenatal Exposure Delayed Effects , Reward , Humans , Female , Pregnancy , Prenatal Exposure Delayed Effects/physiopathology , Male , Adult , Alcohol Drinking/psychology , Alcohol Drinking/adverse effects , Longitudinal Studies , Brain/diagnostic imaging , Brain/drug effects , Brain/physiopathology , Sex Factors
6.
Ugeskr Laeger ; 186(19)2024 May 06.
Article in Danish | MEDLINE | ID: mdl-38808766

ABSTRACT

This review investigates that, in 2023, fatty liver disease underwent a name change to "steatotic liver disease" (SLD). SLD now includes metabolic dysfunction-associated steatotic liver disease (MASLD), alcohol-related liver disease (ALD), and metabolic and alcohol-related liver disease (MetALD). The renaming aims to better incorporate alcohol intake and metabolic risk factors into disease classification and to diminish the stigma associated with the previous nomenclature. Early identification of the patient's aetiology is important for the prognosis which can be improved by interventions against the causative risk factors.


Subject(s)
Terminology as Topic , Humans , Risk Factors , Fatty Liver/classification , Fatty Liver/diagnosis , Fatty Liver, Alcoholic/classification , Fatty Liver, Alcoholic/diagnosis , Alcohol Drinking/adverse effects , Non-alcoholic Fatty Liver Disease/classification , Non-alcoholic Fatty Liver Disease/diagnosis , Liver Diseases, Alcoholic/classification
7.
BMC Pediatr ; 24(1): 320, 2024 May 09.
Article in English | MEDLINE | ID: mdl-38724982

ABSTRACT

BACKGROUND: Alcohol consumption by children and adolescents is receiving increasing attention. It may cause dyslipidemia, a risk factor for cardiovascular disease. However, the association between alcohol consumption and blood lipids in children and adolescents is unclear, and so we aimed to characterize this association. METHODS: Data from the China Health and Nutrition Survey were extracted from children and adolescents aged 7-18 years for whom information was available on alcohol consumption. The population was divided into drinking and nondrinking groups. The χ2, Student's t, or Mann-Whitney U test was used to compare groups. Univariate and multivariate linear regression and propensity score matching (PSM) analysis were used to identify the association between alcohol consumption and blood lipids. RESULTS: This study included 408 children and adolescents with 35 drinkers and 373 nondrinkers. The drinkers had significantly lower values of total cholesterol (TC) (3.8 mmol/L for nondrinkers versus 3.5 mmol/L for drinkers, p = 0.002) and high-density lipoprotein cholesterol (HDL-C) (1.3 mmol/L for nondrinkers versus 1.2 mmol/L for drinkers, p = 0.007), but not for low-density lipoprotein cholesterol (LDL-C) (2.1 mmol/L for nondrinkers versus 2.0 mmol/L for drinkers, p = 0.092) or triglyceride (TG) (0.9 mmol/L for nondrinkers versus 0.8 mmol/L for drinkers, p = 0.21). The univariate and multivariate analyses led to the same conclusions. After PSM there was still a significant negative association between alcohol consumption and TC or HDL-C. CONCLUSION: Alcohol consumption in children and adolescents exhibited significant negative associated with TC and HDL-C, but not with LDL-C or TG. These findings need to be confirmed in future prospective research, and the health effects of blood lipid changes caused by drinking in children and adolescents need to be clarified.


Subject(s)
Alcohol Drinking , Nutrition Surveys , Humans , Adolescent , Child , Male , Female , China/epidemiology , Alcohol Drinking/epidemiology , Alcohol Drinking/adverse effects , Lipids/blood , Cholesterol, HDL/blood , Cross-Sectional Studies , Triglycerides/blood , Cholesterol, LDL/blood , Dyslipidemias/blood , Dyslipidemias/epidemiology , Dyslipidemias/etiology , Cholesterol/blood , Risk Factors , East Asian People
8.
Nutrients ; 16(10)2024 May 17.
Article in English | MEDLINE | ID: mdl-38794754

ABSTRACT

Alcohol consumption significantly impacts disease burden and has been linked to various diseases in observational studies. However, comprehensive meta-analyses using Mendelian randomization (MR) to examine drinking patterns are limited. We aimed to evaluate the health risks of alcohol use by integrating findings from MR studies. A thorough search was conducted for MR studies focused on alcohol exposure. We utilized two sets of instrumental variables-alcohol consumption and problematic alcohol use-and summary statistics from the FinnGen consortium R9 release to perform de novo MR analyses. Our meta-analysis encompassed 64 published and 151 de novo MR analyses across 76 distinct primary outcomes. Results show that a genetic predisposition to alcohol consumption, independent of smoking, significantly correlates with a decreased risk of Parkinson's disease, prostate hyperplasia, and rheumatoid arthritis. It was also associated with an increased risk of chronic pancreatitis, colorectal cancer, and head and neck cancers. Additionally, a genetic predisposition to problematic alcohol use is strongly associated with increased risks of alcoholic liver disease, cirrhosis, both acute and chronic pancreatitis, and pneumonia. Evidence from our MR study supports the notion that alcohol consumption and problematic alcohol use are causally associated with a range of diseases, predominantly by increasing the risk.


Subject(s)
Alcohol Drinking , Genetic Predisposition to Disease , Mendelian Randomization Analysis , Humans , Male , Alcohol Drinking/adverse effects , Alcohol Drinking/genetics , Alcoholism/genetics , Arthritis, Rheumatoid/genetics , Colorectal Neoplasms/genetics , Colorectal Neoplasms/epidemiology , Colorectal Neoplasms/etiology , Head and Neck Neoplasms/genetics , Head and Neck Neoplasms/epidemiology , Parkinson Disease/genetics , Parkinson Disease/epidemiology , Parkinson Disease/etiology , Risk Factors , Female
10.
Acta Derm Venereol ; 104: adv18487, 2024 May 17.
Article in English | MEDLINE | ID: mdl-38757177

ABSTRACT

An association between psoriasis and cancer risk has been suggested in prior studies, but few have focused on head and neck cancers. Using the Korean National Health Insurance Service database, the relevance between psoriasis and head and neck cancer risks was investigated in a cross-sectional study of 3,869,264 individuals over 20 years of age, who received general health examination in 2009 and were followed until 2020. Head and neck cancer incidence rates were compared between individuals with and without psoriasis, and contributing factors were analysed. The head and neck cancer risk was significantly increased in the psoriasis group compared with the non-psoriasis group (hazard ratio [HR] 1.36; 95% confidence interval [CI] 1.07-1.74; p = 0.01) after adjusting for age, sex, body mass index, income, smoking, alcohol, exercise, diabetes mellitus, hypertension and dyslipidaemia. The risk was especially elevated for nasopharyngeal (HR 2.04; 95% CI 1.12-3.70; p = 0.02) and salivary gland cancer (HR 1.96; 95% CI 1.08-3.56; p = 0.03). Alcohol consumption significantly influenced the risk, particularly for oropharyngeal and oral cavity cancer. Our study provides insights into the potential risks of head and neck cancer in patients with psoriasis, which could aid in refining patient management strategies.


Subject(s)
Head and Neck Neoplasms , Psoriasis , Humans , Psoriasis/epidemiology , Psoriasis/complications , Male , Female , Head and Neck Neoplasms/epidemiology , Middle Aged , Cross-Sectional Studies , Republic of Korea/epidemiology , Risk Factors , Adult , Incidence , Aged , Risk Assessment , Databases, Factual , Alcohol Drinking/epidemiology , Alcohol Drinking/adverse effects , Young Adult , Time Factors
11.
Eur Respir Rev ; 33(172)2024 Apr 30.
Article in English | MEDLINE | ID: mdl-38719738

ABSTRACT

INTRODUCTION: The health effects of alcohol are well established but the influence on pulmonary function remains debated. Studies indicate that small amounts of alcohol are beneficial and heavy consumption is harmful, suggesting a U-shaped association. Our objective is to determine whether there is an association between alcohol intake and changes in pulmonary function parameters, exploring the potential protective effect of moderate alcohol consumption and the harm caused by heavy drinking. METHODS: A comprehensive search from PubMed, Embase, Cochrane and CINAHL was carried out, and studies were evaluated using the JBI methodological framework for scoping reviews. Two independent reviewers conducted parallel screening and data extraction. A data extraction form was utilised to organise key themes, with qualitative analysis and visual representation of the results. RESULTS: Among 4427 screened abstracts, 179 underwent full-text review, resulting in 30 eligible studies. Of these, 10 showed a negative effect, nine reported no impact, nine exhibited a positive effect and two indicated a nonlinear U-shaped association between alcohol consumption and pulmonary function parameters. CONCLUSION: While the U-shaped curve hypothesis remains unconfirmed by the current literature, there are notable associations. Heavy alcohol consumption appears to negatively affect pulmonary function, while low to moderate intake shows a positive influence in included studies. However, the diversity in study quality, the nonstandardised alcohol intake quantification and the confounding role of smoking challenge definitive conclusions. The need for consistent, long-term international studies is evident to further explore this relationship while addressing the complex interplay between alcohol and smoking.


Subject(s)
Alcohol Drinking , Lung , Respiratory Function Tests , Humans , Alcohol Drinking/adverse effects , Alcohol Drinking/epidemiology , Lung/physiopathology , Lung/drug effects , Risk Factors , Male , Female , Adult , Middle Aged , Risk Assessment , Aged , Young Adult , Lung Diseases/physiopathology , Lung Diseases/epidemiology , Lung Diseases/etiology , Lung Diseases/diagnosis , Adolescent
12.
Pan Afr Med J ; 47: 90, 2024.
Article in English | MEDLINE | ID: mdl-38737219

ABSTRACT

Introduction: alcohol and other psychoactive substances have adverse health effects, particularly on young people. This study determined the prevalence of alcohol and other psychoactive substance abuse and its association with depression among Niger Delta University, Bayelsa State, Nigeria, medical students. Methods: a cross-sectional study involving 243 medical students who completed a patient-rated version of the Mini International Neuropsychiatric Interview (MINI-PR). For analyzing the data, descriptive and inferential statistics were employed. Results: most respondents were 18 to 24 years old (67.1%), and 52.7% were male; the prevalence of major depressive episodes (current) and lifetime alcohol and other psychoactive use was 30.5%, 25.5%, and 21%, respectively. Also, the prevalence of current alcohol abuse and dependence was 5.8% and 4.9%, respectively. Alcohol use (χ2: 12.57, p = 0.001) and abuse (χ2: 22.33, p = 0.001) were significantly associated with depression. Psychoactive substance use was significantly associated with depression (χ2: 12.91, p = 0.001). The odds of having depression increased with the use of alcohol (OR: 3.54; 95% CI: 1.71-7.33) and psychoactive substances (OR: 4.52; 95% CI: 1.88-10.88). Conclusion: alcohol and psychoactive substance use were significantly associated with depression. Organizing interventions to reduce such unhealthy social practices among medical students is necessary.


Subject(s)
Alcoholism , Psychotropic Drugs , Students, Medical , Substance-Related Disorders , Humans , Nigeria/epidemiology , Male , Cross-Sectional Studies , Students, Medical/statistics & numerical data , Students, Medical/psychology , Female , Prevalence , Young Adult , Substance-Related Disorders/epidemiology , Adolescent , Alcoholism/epidemiology , Psychotropic Drugs/administration & dosage , Psychotropic Drugs/adverse effects , Adult , Universities , Depressive Disorder, Major/epidemiology , Depression/epidemiology , Alcohol Drinking/epidemiology , Alcohol Drinking/adverse effects
13.
Hepatol Commun ; 8(6)2024 Jun 01.
Article in English | MEDLINE | ID: mdl-38727677

ABSTRACT

BACKGROUND: Polygenic Risk Scores (PRS) based on results from genome-wide association studies offer the prospect of risk stratification for many common and complex diseases. We developed a PRS for alcohol-associated cirrhosis by comparing single-nucleotide polymorphisms among patients with alcohol-associated cirrhosis (ALC) versus drinkers who did not have evidence of liver fibrosis/cirrhosis. METHODS: Using a data-driven approach, a PRS for ALC was generated using a meta-genome-wide association study of ALC (N=4305) and an independent cohort of heavy drinkers with ALC and without significant liver disease (N=3037). It was validated in 2 additional independent cohorts from the UK Biobank with diagnosed ALC (N=467) and high-risk drinking controls (N=8981) and participants in the Indiana Biobank Liver cohort with alcohol-associated liver disease (N=121) and controls without liver disease (N=3239). RESULTS: A 20-single-nucleotide polymorphisms PRS for ALC (PRSALC) was generated that stratified risk for ALC comparing the top and bottom deciles of PRS in the 2 validation cohorts (ORs: 2.83 [95% CI: 1.82 -4.39] in UK Biobank; 4.40 [1.56 -12.44] in Indiana Biobank Liver cohort). Furthermore, PRSALC improved the prediction of ALC risk when added to the models of clinically known predictors of ALC risk. It also stratified the risk for metabolic dysfunction -associated steatotic liver disease -cirrhosis (3.94 [2.23 -6.95]) in the Indiana Biobank Liver cohort -based exploratory analysis. CONCLUSIONS: PRSALC incorporates 20 single-nucleotide polymorphisms, predicts increased risk for ALC, and improves risk stratification for ALC compared with the models that only include clinical risk factors. This new score has the potential for early detection of heavy drinking patients who are at high risk for ALC.


Subject(s)
Genome-Wide Association Study , Liver Cirrhosis, Alcoholic , Multifactorial Inheritance , Polymorphism, Single Nucleotide , White People , Humans , Liver Cirrhosis, Alcoholic/genetics , Male , Female , Middle Aged , White People/genetics , Aged , Risk Assessment , Alcohol Drinking/adverse effects , Alcohol Drinking/genetics , Adult , Risk Factors , Genetic Predisposition to Disease , United Kingdom , Genetic Risk Score
14.
BMC Oral Health ; 24(1): 535, 2024 May 06.
Article in English | MEDLINE | ID: mdl-38711116

ABSTRACT

BACKGROUND: Periodontitis is a complex chronic inflammatory disease that is particularly associated with health-related conditions such as smoking, excessive drinking and depression. This research aimed to investigate the interaction between these lifestyles factors on periodontitis risk. METHODS: This study included participants who participated in the National Health and Nutrition Examination Survey in the United States between 2009 and 2014. They had completed oral health-periodontal examination, Smoking-Cigarette Use Questionnaire, Alcohol Use Questionnaire, and Patient Health Questionnaire. Periodontal clinical attachment loss (CAL) of 3 mm or more and Patient Health Questionnaire-9 (PHQ-9) of 10 scores or more were used to identify periodontitis and depression, respectively. Daily alcohol consumption in the past year was classified into three levels: low (1 drink or less), moderate (between 1 and 3 drinks), and heavy drinking (4 drinks or more), while smoking was defined as having smoked at least 100 cigarettes in one's lifetime. Then, the logistic regression combined with interaction models were used to analyze the independent and combined effects of smoking, drinking and depression on periodontitis risk. RESULTS: The results indicated a statistically significant multiplicative interaction between smoking and depression in relation to the development of periodontitis, both in the overall population (P = 0.03) and among male participants (P = 0.03). Furthermore, among individuals experiencing depression, smoking was found to significantly increase the prevalence of periodontitis by 129% in the younger age group compared to non-smokers (odds ratio [OR]: 2.29; 95% confidence interval [CI]: 1.10 to 4.76). However, the interaction between smoking and alcohol consumption was only significant among females (P < 0.05). There was a dose-dependent relationship between drinking frequency and smoking on periodontitis prevalence. In the smoking population, occasional drinking (OR: 1.70; 95% CI: 1.22 to 2.37) and regular drinking (OR: 2.28; 95% CI: 1.68 to 3.11) significantly increased the prevalence of periodontitis compared to individuals without these two factors. CONCLUSION: These results suggested that there were interactive effects between smoking, drinking and depression on periodontitis risk and policies aimed at healthy behaviours and mental health may be beneficial for our oral health.


Subject(s)
Alcohol Drinking , Depression , Smoking , Humans , Male , Female , Alcohol Drinking/adverse effects , Alcohol Drinking/epidemiology , Smoking/adverse effects , Smoking/epidemiology , Middle Aged , Adult , Depression/epidemiology , United States/epidemiology , Risk Factors , Periodontitis/epidemiology , Nutrition Surveys , Aged , Periodontal Diseases/epidemiology , Young Adult , Surveys and Questionnaires
15.
Nutrients ; 16(10)2024 May 11.
Article in English | MEDLINE | ID: mdl-38794688

ABSTRACT

This article reports the results of an ecological study of cancer incidence rates by state in the US for the period 2016-2020. The goals of this study were to determine the extent to which solar UVB doses reduced cancer risk compared to findings reported in 2006 for cancer mortality rates for the periods 1950-1969 and 1970-1794 as well as cancer incidence rates for the period 1998-2002 and to determine which factors were recently associated with cancer risk. The cancer data for non-Hispanic white (European American) men and women were obtained from the Centers for Disease Control and Prevention. Indices were obtained for solar UVB at the surface for July 1992, and alcohol consumption, diabetes, and obesity prevalence near the 2016-2020 period. Lung cancer incidence rates were also used in the analyses as a surrogate for smoking, diet, and air pollution. The cancers for which solar UVB is significantly associated with reduced incidence are bladder, brain (males), breast, corpus uteri, esophageal, gastric, non-Hodgkin's lymphoma, pancreatic, and renal cancer. Lung cancer was significantly associated with colorectal, laryngeal, and renal cancer. Diabetes was also significantly associated with breast, liver, and lung cancer. Obesity prevalence was significantly associated with breast, colorectal, and renal cancer. Alcohol consumption was associated with bladder and esophageal cancer. Thus, diet has become a very important driver of cancer incidence rates. The role of solar UVB in reducing the risk of cancer has been reduced due to people spending less time outdoors, wearing sunscreen that blocks UVB but not UVA radiation, and population increases in terms of overweight and obese individuals, which are associated with lower 25-hydroxyvitamin D concentrations and the generation of systemic inflammation, which is a risk factor for cancer. A dietary approach that would reduce the risk of diabetes, obesity, lung cancer, and, therefore, cancer, would be one based mostly on whole plants and restrictions on red and processed meats and ultraprocessed foods. Solar UVB exposure for a few minutes before applying sunscreen and taking vitamin D supplements would also help reduce the risk of cancer.


Subject(s)
Alcohol Drinking , Diabetes Mellitus , Lung Neoplasms , Obesity , Ultraviolet Rays , Humans , Male , Female , Alcohol Drinking/epidemiology , Alcohol Drinking/adverse effects , Lung Neoplasms/epidemiology , Lung Neoplasms/etiology , Incidence , Obesity/epidemiology , United States/epidemiology , Prevalence , Ultraviolet Rays/adverse effects , Diabetes Mellitus/epidemiology , Risk Factors , Neoplasms/epidemiology , Neoplasms/etiology , Neoplasms/prevention & control , Sunlight
16.
An Acad Bras Cienc ; 96(2): e20240014, 2024.
Article in English | MEDLINE | ID: mdl-38747842

ABSTRACT

Despite the prevalence of substance use during pregnancy, studies focusing exclusively on Neonatal Intensive Care Units (NICU) admissions remain limited. This study investigates the impact of maternal use of tobacco, alcohol, and/or crack, on neonatal outcomes among infants admitted to three Brazilian NICUs. Additionally, the investigation explores the impact of substance use on DNA damage in newborns. Over a one-year period, data from 254 newborns were collected through medical records, accompanied by blood samples. Findings revealed that 16.1% of newborns had mothers reporting substance use during pregnancy. Significant associations were found between maternal substance use and adverse neonatal outcomes, including low birth weight, preterm birth, and sexually transmitted infections. Maternal variables linked to substance use encompassed non-white skin color, low education, non-masonry housing, lower income, diseases in other children, and fewer prenatal consultations. Notably, neonatal DNA damage showed no significant association with substance use. Our results underscore the substantial impact of maternal substance use on NICU-admitted infants, emphasizing the necessity for targeted interventions that address both neonatal health and maternal well-being, thereby underscoring the crucial role of comprehensive care in NICU settings.


Subject(s)
Alcohol Drinking , Intensive Care Units, Neonatal , Humans , Pregnancy , Female , Infant, Newborn , Brazil/epidemiology , Adult , Alcohol Drinking/adverse effects , Pregnancy Complications , Male , Young Adult , Pregnancy Outcome , Infant, Low Birth Weight , Crack Cocaine/adverse effects , Cocaine-Related Disorders/epidemiology , Risk Factors , Socioeconomic Factors , DNA Damage , Prenatal Exposure Delayed Effects
17.
Gene ; 916: 148437, 2024 Jul 20.
Article in English | MEDLINE | ID: mdl-38582264

ABSTRACT

Biallelic variants in PPA2 gene cause a rare but lethal mitochondrial disorder. We describe the first four cases reported in Spain of PPA2 disease in two unrelated families. We have conducted a revision of the clinical history, necropsies, and postmortem genetic testing from probands, and clinical evaluation, genetic testing and blood transcript analysis in family members. All the cases harbored biallelic PPA2 variants in compound heterozygous status. Two brothers from family 1 suffered sudden death after a small first intake of alcohol in 2013 and 2022. The sister remains alive but affected with cardiomyopathy, extensive scar on cardiac imaging, and high sensitivity to alcohol intake. The three siblings carried PPA2 c.290A > G (p.Glu97Gly) novel missense variant and PPA2 c.513C > T (p.Cys171 = ) altering splicing site variant, both probably leading to mRNA degradation based on in-silico and transcript analyses. A teenager from family 2 suffered sudden death after a small intake of alcohol in 2018 and carried PPA2 c.683C > T (p.Pro228Leu) missense and PPA2 c.980_983del (p.Gln327fs) novel frameshift variant, both probably leading to abnormal protein structure. All cases were asymptomatic until adolescence. Furthermore, the sister in family 1 has survived as an asymptomatic adult. PPA2 disease can manifest as cardiac arrest in the young, especially after alcohol exposure. Our results show that PPA2 deficiency can be related to different pathogenicity mechanisms such as abnormal protein structure but also mRNA decay caused by synonymous or missense variants. Strict avoidance of alcohol consumption and early defibrillator implantation might prevent lethal arrhythmias in patients at risk.


Subject(s)
Alcohol Drinking , Death, Sudden, Cardiac , Pedigree , Humans , Male , Death, Sudden, Cardiac/etiology , Female , Alcohol Drinking/genetics , Alcohol Drinking/adverse effects , Adolescent , Adult , Mutation, Missense , Mutation , Spain
18.
Alcohol Alcohol ; 59(3)2024 Mar 16.
Article in English | MEDLINE | ID: mdl-38678371

ABSTRACT

AIMS: To examine the relationship between prenatal alcohol exposure (PAE) and children's behavioural and emotional development in a large generalizable sample of women and their children in Aotearoa New Zealand. METHODS: Using data from the Growing Up in New Zealand longitudinal cohort, we investigated the relationship between maternal PAE and behavioural and emotional development in 8-year-old children. We explored secondary outcomes including measures of language, executive function, academic achievement, and adaptive behaviour. RESULTS: We found no significant differences in the measures of behavioural and emotional development in children 8 years old based on alcohol consumption. No significant differences in behavioural and emotional development were found based on amount of PAE and when PAE occurred, despite controlling for a range of potential confounding factors, such as neighbourhood deprivation and maternal health measures. PAE was associated with significantly higher scores for parent-rated oral language indicating better oral language. In Maori mothers, PAE was significantly associated with an increased risk of higher scores on two of the Strengths and Difficulties Questionnaire subscales. CONCLUSIONS: We did not find an association between PAE and behavioural and emotional development in children aged 8 years. PAE and behavioural and emotional development are difficult to measure accurately, and the moderating variables between them are complex. Future analyses will require larger cohorts of mothers and their children using precise measures of PAE and outcomes to enable more precise estimates of association.


Subject(s)
Alcohol Drinking , Child Behavior , Child Development , Emotions , Prenatal Exposure Delayed Effects , Humans , Female , New Zealand/epidemiology , Child , Prenatal Exposure Delayed Effects/psychology , Prenatal Exposure Delayed Effects/epidemiology , Pregnancy , Male , Longitudinal Studies , Emotions/drug effects , Child Development/drug effects , Alcohol Drinking/adverse effects , Alcohol Drinking/epidemiology , Alcohol Drinking/psychology , Child Behavior/drug effects , Child Behavior/psychology , Adult , Cohort Studies , Executive Function/drug effects
19.
BMC Oral Health ; 24(1): 506, 2024 Apr 29.
Article in English | MEDLINE | ID: mdl-38685000

ABSTRACT

PURPOSE: Almost 200,000 tongue cancers were diagnosed worldwide in 2020. The aim of this study was to describe occupational risk variation in this malignancy. METHODS: The data are based on the Nordic Occupational Cancer (NOCCA) study containing 14.9 million people from the Nordic countries with 9020 tongue cancers diagnosed during 1961-2005. The standardized incidence ratio (SIR) of tongue cancer in each occupational category was calculated using national incidence rates as the reference. RESULTS: Among men, the incidence was statistically significantly elevated in waiters (SIR 4.36, 95% confidence interval (CI) 3.13--5.92), beverage workers (SIR 3.42, 95% CI 2.02-5.40), cooks and stewards (SIR 2.55, 95% CI 1.82-3.48), seamen (SIR 1.66, 95% CI 1.36-2.00), journalists (SIR 1.85, 95% CI 1.18-2.75), artistic workers (SIR 2.05, 95% CI 1.54-2.66), hairdressers (SIR 2.17, 95% CI 1.39-3.22), and economically inactive persons (SIR 1.57, 95% CI 1.42-1.73). Among women, the SIR was statistically significantly elevated only in waitresses (SIR 1.39, 95% CI 1.05-1.81). Statistically significant SIRs ≤ 0.63 were observed in male farmers, gardeners, forestry workers and teachers, and in female launderers. CONCLUSIONS: These findings may be related to consumption of alcohol and tobacco, but the effect of carcinogenic exposure from work cannot be excluded.


Subject(s)
Occupational Diseases , Occupations , Tongue Neoplasms , Humans , Male , Tongue Neoplasms/epidemiology , Female , Scandinavian and Nordic Countries/epidemiology , Occupational Diseases/epidemiology , Incidence , Occupations/statistics & numerical data , Middle Aged , Adult , Risk Factors , Occupational Exposure/adverse effects , Occupational Exposure/statistics & numerical data , Aged , Sex Factors , Alcohol Drinking/epidemiology , Alcohol Drinking/adverse effects
20.
J Neonatal Perinatal Med ; 17(2): 217-224, 2024.
Article in English | MEDLINE | ID: mdl-38640173

ABSTRACT

BACKGROUND: Exposure to toxins during pregnancy is the main modifiable behavior that affects the placenta and, consequently, the fetus. In particular, smoking is a recognized risk factor for negative outcomes. Our study pretended to examine gross and microscopic placental features in women who reported exposure to tobacco, alcohol, or other psychoactive substances. METHODS: In this observational case-control study, we collected 706 placentas to assess precise substance exposure histological-interaction features of in the placenta. We examined gross and microscopic placental features, and then recorded maternal and newborn clinical conditions. RESULTS: We found that 4.8% of mothers admitted to consumption of some type of (harmful) substance. The most common pre-existing maternal condition was obesity (20.3%); predominant complications included amniotic infection (32.3%), urinary tract infection (14.5%) and hypertensive disorders of pregnancy (14.5%). In newborns, we discovered positive associations as respiratory distress syndrome. Macroscopically, exposed mothers had heavier placentas, more true knots, and single umbilical artery; microscopically, they were more likely to exhibit fetal vascular malperfusion (FVM). CONCLUSIONS: Until our present study, no research linked umbilical cord defects to toxic substance exposure; our study results do confirm association with adverse outcomes in neonates and alterations in the neuro-cardio-placental circuit through FVM. IMPLICATIONS: The results are confirming the importance of this modifiable risk factor and how its presence may potentially affect the course of pregnancy, as well as the health of both mother and child.


Subject(s)
Placenta , Pregnancy Complications , Substance-Related Disorders , Humans , Female , Pregnancy , Placenta/pathology , Infant, Newborn , Case-Control Studies , Adult , Pregnancy Complications/epidemiology , Substance-Related Disorders/epidemiology , Substance-Related Disorders/complications , Alcohol Drinking/adverse effects , Alcohol Drinking/epidemiology , Smoking/adverse effects , Smoking/epidemiology , Risk Factors
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