Low intensity exercise linked to reduced depression, claims study

New research has found a significant association between participating in low to moderate intensity exercise and reduced rates of depression.

Researchers from Anglia Ruskin University (ARU) carried out an umbrella review of studies carried out across the world to examine the potential of physical activity as a mental health intervention.

The analysis, published in the journal Neuroscience and Biobehavioural Reviews, found that physical activity reduced the risk of depression by 23% and anxiety by 26%. A particularly strong association was found between low and moderate physical activity, which included activities such as gardening, golf and walking, and reduced risk of depression.

However, this was not strongly observed for high intensity exercise.

Physical activity was also significantly associated with reduced risk of severe mental health conditions, including a reduction in psychosis/schizophrenia by 27%.

The results were consistent in both men and women, and across different age groups and across the world.

Lead author Lee Smith, Professor of Public Health at Anglia Ruskin University (ARU), said: “Preventing mental health complications effectively has emerged as a major challenge, and an area of paramount importance in the realm of public health. These conditions can be complex and necessitate a multi-pronged approach to treatment, which may encompass pharmacological interventions, psychotherapy, and lifestyle changes.

“These effects of physical activity intensity on depression highlight the need for precise exercise guidelines. Moderate exercise can improve mental health through biochemical reactions, whereas high-intensity exercise may worsen stress-related responses in some individuals.

“Acknowledging differences in people’s response to exercise is vital for effective mental health strategies, suggesting any activity recommendations should be tailored for the individual.

“The fact that even low to moderate levels of physical activity can be beneficial for mental health is particularly important, given that these levels of activity may be more achievable for people who can make smaller lifestyle changes without feeling they need to commit to a high-intensity exercise programme.”

Reference:

Masoud Rahmati, San Lee, Dong Keon Yon, Seung Won Lee, Raphael Udeh, Mark McEvoy, Hans Oh, Laurie Butler, Helen Keyes, Yvonne Barnett, Ai Koyanagi, Jae Il Shin, Lee Smith. Physical activity and prevention of mental health complications: An umbrella review. Neuroscience & Biobehavioral Reviews, 2024; 160: 105641 DOI: 10.1016/j.neubiorev.2024.105641.

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Healthy lifestyle may offset effects of life-shortening genes by over 60%, reveals study

A healthy lifestyle may offset the effects of life-shortening genes by more than 60%, suggests an analysis of the findings from several large long term studies, published online in the journal BMJ Evidence Based Medicine.

While genes and lifestyle seem to have an additive effect on a person’s lifespan, an unhealthy lifestyle is independently linked to a 78% heightened risk of dying before one’s time, regardless of genetic predisposition, the research indicates.

The polygenic risk score (PRS) combines multiple genetic variants to arrive at a person’s overall genetic predisposition to a longer or shorter lifespan. And lifestyle-tobacco use, alcohol consumption, diet quality, sleep quota and physical activity levels-is a key factor.

But it’s not clear the extent to which a healthy lifestyle might offset genetic predisposition to a shortened lifespan, say the researchers.

To explore this further, they drew on a total of 353,742 adults, recruited to the UK Biobank between 2006 and 2010, and whose health was tracked up until 2021.

A polygenic risk score was derived for long (20% of participants), intermediate (60%), and short (20%) lifespan risks, using data from the LifeGen cohort study.

And a weighted healthy lifestyle score, to include no current smoking, moderate alcohol consumption, regular physical activity, healthy body shape, adequate sleep, and a healthy diet, was categorised into favourable (23% of participants), intermediate (56%), and unfavourable (22%) lifestyles, using data from the US NHANES study.

During an average tracking period of nearly 13 years, 24,239 participants died.

Those genetically predisposed to a short lifespan were 21% more likely to die early than those genetically predisposed to a long life, regardless of their lifestyle.

Similarly, those who had an unfavourable lifestyle were 78% more likely to die before their time than those with a favourable lifestyle, irrespective of their genetic predisposition.

And those at high genetic risk of a shortened lifespan and who had an unfavourable lifestyle were twice as likely to die as those genetically predisposed to a long life and who had a favourable lifestyle.

Four factors in particular seemed to make up the optimal lifestyle combination: not smoking; regular physical activity; adequate nightly sleep; and a healthy diet.

This is an observational study, and as such, no definitive conclusions can be reached about cause and effect, added to which the researchers acknowledge various limitations to their findings.

Lifestyle was assessed at only one point in time, for example, and lifestyle choices differ by age. Participants were also all of European ancestry, which may limit the generalisability of the findings, say the researchers.

Nevertheless, they suggest that their findings indicate that the genetic risk of a shorter lifespan or premature death might be offset by a favourable lifestyle by around 62%.

Those at high genetic risk of a shortened lifespan could extend their life expectancy by nearly 5.5 years at the age of 40 with a healthy lifestyle, they suggest, adding that given how lifestyle habits tend to be cemented before middle age, steps to mitigate genetic predisposition to a shortened life are needed before then.

“This study elucidates the pivotal role of a healthy lifestyle in mitigating the impact of genetic factors on lifespan reduction,” they conclude. “Public health policies for improving healthy lifestyles would serve as potent complements to conventional healthcare and mitigate the influence of genetic factors on human lifespan.”

Reference:

Bian Z, Wang L, Fan R, et alGenetic predisposition, modifiable lifestyles, and their joint effects on human lifespan: evidence from multiple cohort studiesBMJ Evidence-Based Medicine Published Online First: 29 April 2024. doi: 10.1136/bmjebm-2023-112583.

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Afib more common and dangerous in younger people than previously thought, claims study

Atrial fibrillation (Afib), a common type of arrhythmia that is on the rise in people under the age of 65, is more dangerous in this increasingly younger population than previously thought, according to a new study published today in Circulation Arrhythmia and Electrophysiology and authored by physician-scientists at the UPMC Heart and Vascular Institute.

The study, which is among the first to examine a large group of Afib patients younger than 65 in the U.S., found that these younger patients were more likely to be hospitalized for heart failure, stroke or heart attack and had significantly higher rates of comorbidity and mortality, compared to similarly aged and gender-matched people who do not have Afib.

“Common knowledge among cardiologists is that, in people under 65, Afib is extremely uncommon and not detrimental. But there really hasn’t been any data to back that up,” said lead author Dr. Aditya Bhonsale, M.D., M.H.S, a UPMC cardiac electrophysiologist in HVI’s Division of Cardiology who is also an assistant professor of medicine at the University of Pittsburgh.

“At UPMC, we’ve been seeing a lot more young patients with Afib in recent years and have been interested in understanding the real-world clinical course of these individuals. As a payer-provider with patient records across more than 40 hospitals, UPMC was uniquely positioned to ask this question, which no one has been able to ask before,” Bhonsale added.

Drawing from the electronic health records of 67,221 UPMC patients seeking care for Afib from 2010 through 2019, the researchers found that more than a quarter of them (17,335) were under the age of 65, a stark contrast to the 2% prevalence commonly estimated. The high proportion likely reflects an increasing burden of cardiovascular risk factors in younger Americans, said Bhonsale.

The UPMC team found that over the course of a decade, survival rates for those with the arrythmia were 1.3 to 1.5 times worse for men with Afib, and 1.82 to 3.16 times worse for women, compared to similarly aged patients who did not have Afib. The patients studied also had high rates of cardiovascular disease risk factors, including smoking, obesity, hypertension and sleep apnea, which contribute to damaging structural and electrical changes in the heart over time.

“We are optimistic that data from this study will foster future investigation to evaluate optimal therapies for patients with Afib,” said senior author Sandeep Jain, M.D., director of cardiac electrophysiology in HVI’s Division of Cardiology who is also a professor of medicine at the University of Pittsburgh.

Reference:

Aditya Bhonsale, Jianhui Zhu, Floyd Thoma, Steve Koscumb, Krishna Kancharla, Andrew Voigt, Jared Magnani, N.A. Estes, Samir Saba, Oscar Marroquin, Suresh Mulukutla and Sandeep Jain, Mortality, Hospitalization, and Cardiac Interventions in Patients With Atrial Fibrillation Aged <65 Years, Circulation: Arrhythmia and Electrophysiology, https://doi.org/10.1161/CIRCEP.123.012143.

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Cystic fibrosis patients may have a high prevalence of developmental defect of enamel, reveals study

Cystic fibrosis patients may have a high prevalence of developmental defects of enamel, according to a study published in the Journal of Dentistry.

Cystic Fibrosis is an autosomal recessive condition. It is a multisystem disease treated with a broad range of pharmacological therapies, diet and nutrition, and physiotherapy. Previous studies suggest that people with cystic fibrosis have a higher prevalence of developmental defects of enamel which may place this population at a greater risk of developing oral diseases such as caries. This study aimed to assess a cohort of people with cystic fibrosis (PwCF) for the presence of developmental defects of enamel and compare the results with a control group of people without cystic fibrosis. A cross-sectional study involving 92 participants with cystic fibrosis and 92 controls was conducted in XXXXXXXXXXXXXXX. All participants completed a detailed questionnaire before undergoing a full clinical examination. The Developmental Defect of Enamel Index was used as a measurement index. All data was statistically analysed with the help of statisticians from Cystic Fibrosis Registry XXXXX.

Results: 64% (n=59) of PwCF had enamel defects compared to just 30% (n=28) of people without cystic fibrosis. The median number of teeth affected by enamel defects in the study group was 1.5, compared to 0 in the control group. In this study the cohort of PwCF had more enamel defects than people without CF. Further research is required to investigate the aetiology of these findings. Clinicians should be vigilant after teeth have erupted in PwCF as they may have an increased susceptibility to developmental defects of enamel.

Reference:

Fiona O’Leary, Niamh Coffey, Francis M Burke, Anthony Roberts, Paul O’Regan, Laura Kirwan, Barry Plant, Martina Hayes. The Prevalence of Developmental Defects of Enamel in a Cohort of Adults with Cystic Fibrosis – A Cross Sectional Study, Journal of Dentistry,

2024, 104893, ISSN 0300-5712, https://doi.org/10.1016/j.jdent.2024.104893.

(https://www.sciencedirect.com/science/article/pii/S0300571224000630)

Keywords:

Cystic fibrosis patients, high prevalence, developmental defect, enamel, study, Journal of Dentistry, Cystic Fibrosis; Developmental Defects of Enamel; Preventative Care; Policy; Oral Health, Fiona O’Leary, Niamh Coffey, Francis M Burke, Anthony Roberts, Paul O’Regan, Laura Kirwan, Barry Plant, Martina Hayes

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Prenatal exposure to smoking may raise risk of autism and attention-deficit disorders in newborns: Study

Japan: A recent study published in Cells has identified prenatal nicotine exposure (PNE) to be a risk factor for comorbidity with attention-deficit/hyperactive disorder (ADHD) and autism spectrum disorder (ASD) in newborns. 

Previous studies have linked smoking during pregnancy with neurodevelopmental disorders, the results of behavioral experiments in mice prenatally exposed to nicotine have been inconsistent. In the new study, scientists from Japan developed a deep learning-based framework to automatically observe and classify mice behavior in such experiments, producing more accurate and unbiased results. 

The fact that smoking is a risk factor for several diseases, including cancer, stroke, and diabetes, has been known for approximately half a century. However, over the past few decades, scientists have brought to light many of the detrimental effects of smoking during pregnancy, linking this habit to high infant mortality, failed delivery, and low body weight at birth. In addition, recent studies suggest that prenatal nicotine exposure (PNE) may be related to neurodevelopmental disorders, such as attention deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD).

For a long time now, scientists have used animal models (like rodents) to understand how PNE leads to neurodevelopmental disorders. By carefully analyzing the behavior of rodents, they can infer whether PNE is causing neurological changes and the brain regions affected by it; this can later be confirmed through histological analyses.

Unfortunately, thus far, studies on behavioral changes induced by PNE in mice have shown varied results, some of which are contradictory. Although there could be multiple reasons behind these discrepancies, human error and bias are prime suspects. In general, the assessment of complex animal behaviors, especially social interactions, relies on the efforts of human observers, which introduces a baseline level of subjectivity that is hard to dispel. But what if we can leverage artificial intelligence (AI) to produce more accurate and unbiased results from observations of PNE mice behavior?

In the study, researchers from the Department of Molecular and Cellular Physiology at the Shinshu University School of Medicine, including graduate student Mengyun Zhou, Assistant Professor Takuma Mori, and Professor Katsuhiko Tabuchi, developed and trained a deep learning-based system to automatically analyze footage from behavioral experiments on mice. They used this tool to explore the behavioral changes induced by PNE in mice without observer biases, seeking to shed light on the link between nicotine and neurodevelopmental disorders.

The proposed AI-based framework relied on a combination of two well-established open-source toolkits, namely DeepLabCut and Simple Behavioral Analysis (SimBA). “AI tools can label the body parts of animals in a markerless video footage and precisely estimate their poses using supervised machine learning,” explains Prof. Tabuchi. “Since animal behaviors are defined as a specific arrangement of body parts over a short period of time, deep-learning toolkits like SimBA can use the pose estimations obtained with DeepLabCut to classify different types of animal behaviors.”

After reaching an optimal training protocol for their framework using manually labeled data, the researchers conducted several experiments using PNE and control mice, looking for indicators of ADHD- and ASD-like behaviors. First, they carried out cliff avoidance reaction tests, which are used to test impulsivity. In these tests, they placed the subject mouse on top of a slightly elevated platform and took note—both manually and with the AI system—of how long the mouse waited before jumping down the platform. The test results suggested that PNE mice are more impulsive, a behavioral feature of ADHD in humans.

They also tested the working memory of mice using a Y-shaped maze and counted the number of times each mouse spontaneously switched from one arm of the maze to another. “We observed a decrease in the spontaneous alteration in PNE mice, suggesting that their working memory was altered, which is another behavioral feature of ADHD,” comments Mengyun Zhou. “These results suggest prenatal exposure to nicotine may cause ADHD in mice, which is consistent with clinical reports in humans.”

Finally, the researchers conducted open-field and social-interaction experiments, which represented the main challenge for their AI-based system. In these experiments, the researchers observed either one or two mice behaving freely in a large enclosure and looked for indicators of anxiety and social behaviors, such as grooming and following. Interestingly, PNE mice exhibited social behavioral deficits and increased anxiety which are features of ASD. Subsequent histological analysis of hippocampal brain tissue confirmed decreased neurogenesis, a hallmark of ASD. Thus, it appears that smoking may not only increase the risk of ADHD, but also ASD.

Worth noting, the results obtained using the AI-based system were highly reliable, as Prof. Tabuchi highlights: “We validated the accuracy of our behavioral analysis framework by drawing a careful comparison between the results generated by the model and behavior assessments made by multiple human annotators, which is considered the gold standard.” These analyses cement the potential of the proposed approach and showcase its capabilities for many types of behavioral studies.

With any luck, further efforts will pave the way to a solid understanding of mechanisms behind neurodevelopmental disorders like ASD and ADHD, ultimately leading to better diagnostic tools and therapeutic methods.

Reference:

Zhou, M.; Qiu, W.; Ohashi, N.; Sun, L.; Wronski, M.-L.; Kouyama-Suzuki, E.; Shirai, Y.; Yanagawa, T.; Mori, T.; Tabuchi, K. Deep-Learning-Based Analysis Reveals a Social Behavior Deficit in Mice Exposed Prenatally to Nicotine. Cells 2024, 13, 275. https://doi.org/10.3390/cells13030275.

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Individuals with NALFD more than twice as likely to have osteoarthritis, study finds

USA: A US nationwide survey has shown a positive correlation between non-alcoholic fatty liver disease (NAFLD) and osteoarthritis (OA). The findings published in Arthritis Research & Therapy suggest that clinicians should screen for NAFLD in arthritis patients and intervene early, given the current pandemic of NAFLD and OA.

“Individuals with NALFD were more than twice as likely to have osteoarthritis, even after adjusting for various factors (OR = 2.05),” the researchers reported.

“The correlation persisted across subgroups of age & metabolic syndrome, but importantly, the association was more pronounced in non-obese individuals, females and those without heightened C-reactive protein levels.”

Previous studies have suggested that low-grade inflammation and metabolic derangements may at least be involved in the occurrence of osteoarthritis and NAFLD, implying that these two diseases have similar causative factors. However, few studies have explored the correlation between NAFLD and OA. Hence, Ting Li, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China, and colleagues investigated the association between NAFLD and OA in US adults.

For this purpose, the researchers performed a cross-sectional study on participants in the 2017–2018 National Health and Nutrition Examination Survey (NHANES) cycle. The diagnosis of osteoarthritis was based on self-reported data. NALFD was defined by the vibration-controlled transient elastography.

To explore the relationship and verify the stability of the conclusions, the research team performed logistic regression models and stratified analyses. They also performed propensity score matching (PSM) and sensitivity analysis using multiple imputations for missing data.

The study included 2622 participants [47.8% males] with a mean age of 48.1 years old, containing 317 OA patients and 1140 NAFLD patients. Based on the study, the researchers reported the following findings:

  • A logistic regression indicated a significant association between NAFLD and OA without adjustment [odds ratio (OR) = 2.05]. The association remained stable after adjustment for covariates (OR = 1.72).
  • Sensitivity analysis of missing data with multiple interpolations and PSM found similar results.
  • A significant and consistent association of NAFLD with OA was still observed in each subgroup stratified by age and metabolic syndrome (MetS).
  • Stratified by obesity, sex, and sensitivity c-reactive protein (hs-CRP) category, a statistically significant association was only shown in females, those without obesity, and those without hyper hs-CRP.
  • The results illustrated that the relationship between NAFLD and OA was stable in all subgroups and had no interaction.

Using large-scale cross-sectional data from NHANES, the study clarified the relationship between NAFLD and OA. Compared to NALFD patients, those without showed a lower likelihood of OA.

“Given the current pandemic of NAFLD and OA, clinicians should screen for NAFLD in arthritis patients and intervene early, the research team concluded.

Reference:

Lu, Y., Zhang, J., Li, H. et al. Association of non-alcoholic fatty liver disease with self-reported osteoarthritis among the US adults. Arthritis Res Ther 26, 40 (2024). https://doi.org/10.1186/s13075-024-03272-2

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Antibiotic Use in early infancy Linked to Increased Risk of Atopic Dermatitis, claims study

Researchers have found that the use of antibiotics early in life is linked to an increased risk of developing atopic dermatitis, a chronic inflammatory skin condition, likely due to gut microbiome disruption. This association was observed in data from the Canadian CHILD birth cohort study. This study was published in The Journal of Allergy and Clinical Immunology by Hoskinson C. and colleagues.

Atopic dermatitis (AD) is a common chronic inflammatory skin disease that affects both children and adults, often driven by genetic and environmental factors. Early exposure to antibiotics is believed to disrupt the gut microbiome, which can influence the development of allergic conditions such as AD.

The study involved a longitudinal analysis of data from the Canadian CHILD birth cohort, which tracked infants from birth to 5 years of age and beyond. The cohort included 3,455 eligible infants with no congenital abnormalities who were born at a minimum of 34 weeks of gestation.

The researchers examined the association between antibiotic use in the first year of life and the development of AD by the age of 5 years. They collected stool samples from a subset of infants and analyzed microbial features sensitive to antibiotic exposure.

The key findings of the study were:

  • Use of systemic antibiotics during the first year of life was associated with an increased risk of AD (adjusted OR 1.81, 95% CI 1.28-2.57, P<0.001).

  • The risk was not significant when antibiotics were used after 1 year of age.

  • A dose-response-like relationship was observed between the number of antibiotic courses and the increased risk of AD (one course: aOR 1.67, 95% CI 1.17-2.38; two or more courses: aOR 2.16, 95% CI 1.30-3.59).

  • The study found that 18 species of 72 tested were significantly altered in those with AD, while 15 species were altered by antibiotic exposure.

  • Four overlapping species were significantly altered in patients with both antibiotic exposure during the first year of life and AD at 5 years: Bifidobacterium bifidum (mean relative abundance 5.03%), Bifidobacterium longum (14.87%), Eubacterium rectale (1.17%), and Tyzzerella nexilis (0.20%).

The study suggests that early-life exposure to antibiotics may disrupt the gut microbiome, potentially leading to the development of AD. This underscores the importance of cautious antibiotic use in infancy.

Early antibiotic use is linked to an increased risk of atopic dermatitis, emphasizing the need for careful consideration of antibiotic prescriptions in infancy. Stool microbiome analysis may provide insights into predicting and managing the risk of AD and other allergic conditions in children.

Reference:

Hoskinson, C., Medeleanu, M. V., Reyna, M. E., Dai, D. L. Y., Chowdhury, B., Moraes, T. J., Mandhane, P. J., Simons, E., Kozyrskyj, A. L., Azad, M. B., Petersen, C., Turvey, S. E., & Subbarao, P. (2024). Antibiotics within first year are linked to infant gut microbiome disruption and elevated atopic dermatitis risk. The Journal of Allergy and Clinical Immunology. https://doi.org/10.1016/j.jaci.2024.03.025

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Excessive screen time in children impacted vocalizations and communication: JAMA

A recent study published in the recent edition of Journal of American Medical Association looked into the intricate relationship between screen time and its impact on parent-child communication, highlight on the concerning phenomenon known as technoference.

This study was conducted in Australia investigated the longitudinal association between screen time and three crucial measures of parent-child talk: adult words, child vocalizations and conversational turns. This study spanned from January 2018 to December 2021 and the data was collected from 220 families every six months by offering valuable insights into the critical early years of child development.

The study used innovative Language Environment Analysis (LENA) technology and meticulously examined the screen time exposure of children and their home language environment comprising an average 16-hour day. The outcomes of this comprehensive analysis underlined the profound impact of screen time on parent-child interactions.

After rigorous statistical analysis, the results unveiled a increase in screen time that was consistently associated with decreased in measures of parent-child talk across various age intervals, with the most significant declines observed at 36 months of age. Also, each additional minute of screen time translated to a reduction in adult words, child vocalizations and conversational turns that highlights the detrimental effects of excessive screen exposure on language development.

These findings emphasize the crucial role of a language-rich home environment in nurturing the linguistic skills of children during their formative years. The concept of technoference rings alarm bells for modern-day households with increasing screen time habits. Educating the families about the potential repercussions of excessive screen time is a compelling imperative that can help empower them with strategies to prioritize meaningful interactions amidst digital distractions.

Reference:

Brushe, M. E., Haag, D. G., Melhuish, E. C., Reilly, S., & Gregory, T. (2024). Screen Time and Parent-Child Talk When Children Are Aged 12 to 36 Months. In JAMA Pediatrics. American Medical Association (AMA). https://doi.org/10.1001/jamapediatrics.2023.6790

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Night sweats may be associated with severity of sleep apnea, claims study

A collaborative effort between the University of Córdoba and IMIBIC uses, for the first time, changes in sweat metabolism to diagnose the severity of sleep apnea.

In Greek, apnea (ἄπνοια) denotes the “absence of breathing.” Hence, obstructive sleep apnea is a disease defined by interruptions in breathing, which recurs while the person suffering from it is asleep. A feeling of breathlessness, fatigue and drowsiness are symptoms that patients suffer. This disease is also related to the incidence of cardiovascular disorders, so to deal with these related problems, adequate diagnosis of the severity of the disease is necessary.

Alterations in the metabolism of people with sleep apnea are key to determining the severity of the disease. These changes are usually analyzed in blood or urine. However, in search of a less invasive and more accessible alternative, a team from the Department of Analytical Chemistry at the University of Córdoba and the Maimonides Institute for Biomedical Research in Córdoba (IMIBIC), formed by researchers Laura Castillo, Mónica Calderón, Feliciano Priego and Bernabé Jurado, has verified, for the first time, the potential of sweat samples to ascertain the severity of sleep apnea.

“By analyzing sweat metabolome and its alterations, mainly at night, we were able to see what stage of the disease the patients were in,” explains Laura Castillo, the study’s lead author. For her, the advantages of using sweat over other samples are clear: “it is a non-invasive and clean sample since, unlike the case with blood, we don’t have to remove proteins, and it’s much easier to analyze and detect metabolites.”

In this study, sweat samples from before and after sleep were analyzed from a series of individuals with sleep apnea at different stages, as well as from a control group without the disease.

In these samples, using the gas chromatography technique, coupled with high-resolution mass spectrometry, 78 metabolites were identified and their changes were studied, mostly related to energy production and oxidative stress. “We could see how the sweat metabolism itself indicates those alterations during sleep as a result of which the person’s energy production worsens and their oxidative stress increases,” says Castillo. Thus, with a personalized follow-up using the sweat excreted during the sleep of a person with the disease, its development can be tracked, and its possible effects, such as cardiovascular problems, can be monitored. This metabolomic profile also made it possible, in the trial, to distinguish between those who suffered from the disease and those who did not have it and belonged to the control group.

An index to learn more about the disease

In addition to establishing sweat as a good sentinel when it comes to determining the stage of the disease, this work also reveals the importance of taking into account the oxygen desaturation index when diagnosing it.

The diagnosis of sleep apnea is currently based on the Apnea-Hypopnea Index (AHI), which measures sleep apnea based on the episodes of shortness of breath one suffers per hour (for example, the disease is severe when one has 30 or more episodes per hour). According to the team, this index “does not provide all the information about the disease or the patient’s situation at a given time” since it counts how many events there are, but not their severity.

Therefore, in their study they also verify the importance of using the oxygen desaturation index, which shows how serious the episodes are by measuring the number of events in which oxygen saturation has decreased by more than 3%. After verifying the linear relationship between this index and the AHI, its validity has been confirmed, since, in addition to the data provided by the AHI, it also measures severity, taking into account oxygen saturation loss.

Reference:

Laura S. Castillo-Peinado, Mónica Calderón-Santiago, Bernabé Jurado-Gámez, Feliciano Priego-Capote, Changes in human sweat metabolome conditioned by severity of obstructive sleep apnea and intermittent hypoxemia, Journal of Sleep Research, https://doi.org/10.1111/jsr.14075.

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Non-Invasive Predictive Model may Help in Early Detection of Endometriosis in Infertile Women: Study

A recent study by Jie Zhang and team have successfully crafted a non-invasive predictive model to identify minimal or mild endometriosis in patients who struggle with infertility. The findings were published in the Journal of Minimally Invasive Gynecology.

Infertility affects millions worldwide and identifying the underlying causes is a persistent challenge. By recognizing the significance of early detection in endometriosis-related infertility the team sought to develop a predictive model. This retrospective study was conducted at a tertiary referral center and enrolled a total of 1365 infertility patients who underwent laparoscopy between January 2013 and August 2020.

The study divided patients into a training set (n=910) for model development and a validation set (n=455) for confirmation. This in depth evaluation included sensitivities, specificities, AUCs, the Hosmer-Lemeshow goodness of fit test, NRIs, and IDIs. The final model demonstrated high accuracy by incorporating BMI, dysmenorrhea, dyspareunia, uterosacral tenderness, and serum CA-125. Sensitivities of 87.7% and 93.3%, specificities of 68.6% and 66.4%, and AUCs of 0.84 and 0.85 were recorded for the training and validation sets, respectively.

Uterosacral tenderness emerged as a pivotal predictor and the nomogram underscored good calibration and clinical value. This innovative model promises a cost-effective and less invasive means of identifying minimal or mild endometriosis, a significant factor in infertility.

This study delivers a reliable tool for clinicians as a crucial step towards personalized infertility care. Early identification is a key to prompt intervention which potentially revolutionize the landscape of infertility treatment. This is a significant advancement in empowering healthcare providers with a tool to enhance the diagnosis and treatment of infertility in women.

Source:

Zhang, J., Wang, J., Zhang, J., Liu, J., Xu, Y., Zhu, P., Dai, L., Shu, L., Liu, J., Hou, Z., Diao, F., Liu, J., & Mao, Y. (2023). Developing a predictive model for minimal or mild endometriosis as a clinical screening tool in infertile women: uterosacral tenderness as a key predictor. In Journal of Minimally Invasive Gynecology. Elsevier BV. https://doi.org/10.1016/j.jmig.2023.12.008

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