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Genetic Evidence of Obesity-Induced Chronic Wounds Mediated by Inflammatory Biomarkers. 由炎症生物标志物介导的肥胖诱发慢性伤口的遗传证据
Pub Date : 2024-11-20 DOI: 10.1177/10998004241299375
Hai Xu, Sheyuan Ding, Yu Tong, Qiong Zhang

Background: Obese patients are increasingly recognized as being at higher risk for skin diseases, particularly chronic wounds. While the exact mechanisms remain unclear, obesity is suspected to influence the development of chronic injuries via inflammatory biomarkers. Single nucleotide polymorphisms (SNPs) may further influence gene expression, protein function, and levels of inflammatory biomarkers through various mechanisms, thereby modulating inflammatory responses that contribute to wound pathogenesis. Methods: A two-sample two-step Mendelian Randomization (MR) was employed to explore the causal relationship between obesity and chronic wounds, focusing on the mediating role of inflammatory biomarkers. SNPs were used as instrumental variables (IVs) to infer causality. Obesity-related genetic data were sourced from the UK Biobank and GIANT consortium. Genome-wide association studies provided data on 92 inflammatory biomarkers, involving 14,824 and 575,531 individuals. Pressure injuries, lower limb venous ulcers, and diabetic foot ulcer data were obtained from FinnGen R10 and the Pan-UK Biobank. Results: Obesity significantly increased the risk of pressure injuries, lower limb venous ulcers, and diabetic foot ulcers. CCL19, hGDNF, IL-12B, and TNFRSF9 were identified as mediators in obesity-induced lower limb venous ulcers. Conclusion: This study provides genetic evidence that obesity leads to lower limb venous ulcers via inflammatory biomarkers, suggesting potential therapeutic targets for intervention.

背景:越来越多的人认识到肥胖患者患皮肤病的风险较高,尤其是慢性伤口。虽然确切的机制尚不清楚,但人们怀疑肥胖会通过炎症生物标志物影响慢性损伤的发展。单核苷酸多态性(SNPs)可能会通过各种机制进一步影响基因表达、蛋白质功能和炎症生物标志物水平,从而调节炎症反应,导致伤口发病。研究方法采用两样本两步孟德尔随机法(MR)探讨肥胖与慢性伤口之间的因果关系,重点研究炎症生物标志物的中介作用。SNPs被用作推断因果关系的工具变量(IV)。与肥胖相关的基因数据来自英国生物库和 GIANT 联盟。全基因组关联研究提供了 92 个炎症生物标志物的数据,涉及 14,824 人和 575,531 人。压力伤害、下肢静脉溃疡和糖尿病足溃疡数据来自芬兰基因 R10 和泛英国生物库。结果显示肥胖会明显增加压力性损伤、下肢静脉溃疡和糖尿病足溃疡的风险。CCL19、hGDNF、IL-12B和TNFRSF9被确定为肥胖诱发下肢静脉溃疡的介质。结论本研究提供了肥胖通过炎症生物标志物导致下肢静脉溃疡的遗传证据,并提出了潜在的干预治疗靶点。
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引用次数: 0
Delayed Lactogenesis II in High-Risk Pregnancies: What Should We Care. 高危妊娠中的乳汁生成延迟 II:我们应该注意什么?
Pub Date : 2024-11-13 DOI: 10.1177/10998004241300477
Qianqian Liu, Hanxiang Lin

Background: The timely initiation of lactogenesis II is crucial for postpartum women, with delays having significant clinical implications. This study aimed to evaluate the determinants of delayed lactogenesis II (DOL II) in high-risk pregnant women to guide clinical interventions and postnatal care protocols. Methods: We conducted a study involving high-risk pregnant women who gave birth and were admitted to our hospital''s obstetric intensive care unit for postpartum surveillance and treatment from February 1, 2023, to April 30, 2024. We utilized Pearson correlation analysis and logistic regression to determine factors linked to DOL II. Results: Our study included 206 high-risk pregnant women, with 85 (41.26%) experiencing DOL II. Pearson correlation analysis indicated strong associations between DOL II and maternal age (r = 0.452), gestational hypertension (r = 0.514), gestational diabetes (r = 0.487), and delayed colostrum secretion (r = 0.506), all statistically significant (p < 0.05). Logistic regression analysis identified age 35 years or older (OR = 2.115, 95%CI: 1.785-2.466), gestational hypertension (OR = 2.404, 95%CI: 2.125-3.107), gestational diabetes (OR = 2.556, 95%CI: 2.008-2.879), and colostrum secretion later than one hour postpartum (OR = 3.126, 95%CI: 2.682-3.605) as independent risk factors for DOL II, all with p < 0.05. Conclusions: The incidence of DOL II is significantly elevated in high-risk pregnant women, especially those aged 35 or older, those with gestational diabetes and hypertension, and those who delay the initiation of breastfeeding. It is imperative that clinical practices prioritize enhanced prenatal care and health education, robust lactation support, and improved lactation awareness among postpartum women to reduce the prevalence of DOL II.

背景:及时启动泌乳功能 II 对产后妇女至关重要,延迟启动泌乳功能 II 会对临床产生重大影响。本研究旨在评估高危孕妇泌乳功能II(DOL II)延迟的决定因素,为临床干预和产后护理方案提供指导。研究方法我们对 2023 年 2 月 1 日至 2024 年 4 月 30 日期间分娩并入住本院产科重症监护室接受产后监测和治疗的高危孕妇进行了研究。我们利用皮尔逊相关分析和逻辑回归来确定与 DOL II 相关的因素。结果我们的研究包括 206 名高危孕妇,其中 85 人(41.26%)经历过 DOL II。皮尔逊相关分析表明,DOL II 与孕产妇年龄(r = 0.452)、妊娠高血压(r = 0.514)、妊娠糖尿病(r = 0.487)和初乳分泌延迟(r = 0.506)密切相关,均具有统计学意义(P 0.05)。逻辑回归分析发现,年龄在 35 岁或以上(OR = 2.115,95%CI:1.785-2.466)、妊娠高血压(OR = 2.404,95%CI:2.125-3.107)、妊娠糖尿病(OR = 2.556,95%CI:2.008-2.879)和初乳分泌晚于产后一小时(OR = 3.126,95%CI:2.682-3.605)是 DOL II 的独立风险因素,所有因素的 P 均为 0.05。结论高危孕妇的 DOL II 发生率明显升高,尤其是 35 岁或以上的孕妇、患有妊娠糖尿病和高血压的孕妇以及推迟开始母乳喂养的孕妇。临床实践中必须优先加强产前护理和健康教育,提供有力的哺乳支持,提高产后妇女的哺乳意识,以降低 DOL II 的发病率。
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引用次数: 0
Sex-Specific Impact of Serum Calcium Levels on Acute Coronary Syndrome Risk: A 19-Year Cohort Study in Korea. 血清钙水平对急性冠状动脉综合征风险的性别特异性影响:韩国一项为期 19 年的队列研究。
Pub Date : 2024-11-07 DOI: 10.1177/10998004241295360
Eujene Jung, Dong Ki Kim, Seok Jin Ryu, Hyun Ho Ryu

Background: This study aims to investigate the association between serum calcium levels and acute coronary syndrome (ACS) risk, examining whether this relationship differs by sex, given the known differences in calcium metabolism and hormonal influences between males and females. Methods: Utilizing the Korean Genome Epidemiology Study (KoGES) prospective cohort data, our primary exposure variables were serum calcium level and sex. The incidence of ACS served as the main outcome of interest. Hazard ratios (HRs) and 95% confidence intervals (CIs) were estimated using Cox regression analysis. An interaction analysis was conducted to assess the interaction effect of calcium level and sex on ACS incidence. Results: After adjusting for confounding variables, high calcium intake did not significantly increase ACS incidence, with a hazard ratio (HR) of 1.07 (95% CI: 0.90-1.26). There was also no significant difference in ACS risk between females and males (HR: 0.81, 95% CI: 0.61-1.04). However, interaction effect analysis revealed that higher calcium levels were associated with an increased risk of ACS only in females (HR: 1.24, 95% CI: 1.07-1.58), whereas the association in males was not statistically significant (HR: 0.90, 95% CI: 0.71-1.15). Conclusion: Our study results indicate that elevated serum calcium levels alone did not independently increase the risk of ACS; however, high serum calcium levels were associated with an increased risk of ACS in females but not in males, underscoring the importance of sex-specific factors in assessing and managing ACS risk and highlighting the necessity for personalized medical approaches to improve cardiovascular health outcomes for women.

研究背景本研究旨在调查血清钙水平与急性冠状动脉综合征(ACS)风险之间的关系,鉴于已知男性和女性在钙代谢和荷尔蒙影响方面存在差异,本研究将探讨这种关系是否因性别而异。研究方法利用韩国基因组流行病学研究(KoGES)的前瞻性队列数据,我们的主要暴露变量是血清钙水平和性别。ACS的发病率是我们关注的主要结果。我们使用 Cox 回归分析估算了危险比 (HR) 和 95% 置信区间 (CI)。还进行了交互作用分析,以评估钙水平和性别对 ACS 发病率的交互作用。结果显示在对混杂变量进行调整后,高钙摄入并不会显著增加 ACS 发病率,其危险比 (HR) 为 1.07(95% CI:0.90-1.26)。女性和男性的 ACS 风险也没有明显差异(HR:0.81,95% CI:0.61-1.04)。然而,交互效应分析表明,只有女性的钙水平越高,患 ACS 的风险越高(HR:1.24,95% CI:1.07-1.58),而男性的相关性在统计学上并不显著(HR:0.90,95% CI:0.71-1.15)。结论我们的研究结果表明,单纯的血清钙水平升高并不会独立地增加 ACS 风险;但是,高血清钙水平与女性 ACS 风险的增加有关,而与男性无关,这强调了性别特异性因素在评估和管理 ACS 风险中的重要性,并突出了采用个性化医疗方法改善女性心血管健康状况的必要性。
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引用次数: 0
Six Weeks to Wellness: The Role of Breathing Exercises Based on Motor Development Pattern in Improving Fitness and Quality of Life in Overweight Elderly Women. 六周健康:基于运动发展模式的呼吸练习在改善超重老年妇女的体能和生活质量中的作用》。
Pub Date : 2024-10-29 DOI: 10.1177/10998004241297403
Fatemeh Mohammad Rahimi, Mehdi Sohrabi, Alireza Saberi Kakhki, Nasser Mohammad Rahimi

Background: Being overweight is a major global health epidemic of the 20th and 21st centuries, which can affect the movement system function of older adult women. This study evaluated the effects of a breathing exercise based on motor development patterns on functional fitness and quality of life in overweight older adult women. Methods: A randomized controlled trial was conducted with 40 community-dwelling women aged 65-75. Participants were randomly assigned to an intervention group, which completed a 6-week breathing exercise program (three supervised and three home-based sessions per week), or a control group, which maintained usual routines. Outcome measures included cardiovascular fitness, upper and lower body flexibility, muscle strength, dynamic balance, and quality of life, assessed at baseline and post-intervention. Results: The intervention group showed significant improvements in cardiovascular fitness (p < .001, ES = 0.652), upper body flexibility (p < .001, ES = 0.652), lower body flexibility (p < .001, ES = 0.538), upper body strength (p < .001, ES = 0.538), lower body strength (p < .001, ES = 0.538), and dynamic balance (p < .001, ES = 0.475) compared to the control group. Quality of life also significantly improved in the intervention group (p < .001, ES = 0.475). Conclusion: Breathing exercises based on motor development patterns significantly enhance functional fitness and quality of life in overweight older adult women. Incorporating these exercises into regular physical activity routines may promote health and independence in older adults. Further research should explore long-term benefits and optimal exercise parameters for older adults.

背景:超重是 20 世纪和 21 世纪全球健康的主要流行病,会影响老年妇女的运动系统功能。本研究评估了基于运动发展模式的呼吸练习对超重老年妇女的功能性健身和生活质量的影响。方法:随机对照试验对 40 名 65-75 岁居住在社区的女性进行了随机对照试验。参与者被随机分配到干预组(完成为期 6 周的呼吸锻炼计划(每周 3 次有监督的训练和 3 次在家训练))或对照组(保持常规生活习惯)。结果测量包括心血管健康、上下肢灵活性、肌肉力量、动态平衡和生活质量,分别在基线和干预后进行评估。结果显示与对照组相比,干预组在心血管健康(p .001,ES = 0.652)、上半身柔韧性(p .001,ES = 0.652)、下半身柔韧性(p .001,ES = 0.538)、上半身力量(p .001,ES = 0.538)、下半身力量(p .001,ES = 0.538)和动态平衡(p .001,ES = 0.475)方面均有明显改善。干预组的生活质量也有明显改善(p .001,ES = 0.475)。结论基于运动发展模式的呼吸练习能显著提高超重老年妇女的功能性体能和生活质量。将这些练习纳入常规体育锻炼中可促进老年人的健康和独立性。进一步的研究应探讨对老年人的长期益处和最佳运动参数。
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引用次数: 0
Brain-Derived Neurotrophic Factor (BDNF) is Associated with Self-Reported Cognitive Function in Adults with HIV. 脑源性神经营养因子 (BDNF) 与艾滋病病毒感染者自述的认知功能有关。
Pub Date : 2024-10-28 DOI: 10.1177/10998004241296466
Joseph A Belloir, Thomas Myers, Scott Batey, Rebecca Schnall

Background: People with HIV (PWH) are at risk of developing HIV-associated neurocognitive disorder (HAND) despite receiving combination antiretroviral therapy. Brain-derived neurotrophic factor (BDNF) has been implicated in cognitive function and neuroplasticity, but its role in HIV-related neuroinflammation remains understudied. Methods: This study analyzed data from the CHAMPS study, assessing BDNF serum levels and cognitive function in 140 adults with HIV at baseline. Cognitive function was evaluated using the PROMIS Applied Cognition-Abilities 8-item questionnaire. BDNF levels (pg/ml) were measured using high sensitivity Enzyme-Linked Immunoassay (ELISA) kits. Linear regression analyses were conducted to explore the associations between BDNF levels, cognitive function, and AIDS diagnosis, adjusting for demographic variables. Results: A significant positive association was found between BDNF levels and cognitive function scores in PWH (p = .03). Additionally, PWH with a history of AIDS diagnosis showed significantly lower BDNF levels (p = .02). Other demographic factors did not significantly impact cognitive function or BDNF levels in this cohort. Conclusions: Our results highlight the potential of BDNF as a biomarker for cognitive decline in PWH and suggest its relevance in understanding HAND pathophysiology. Further research is warranted to explore the multifaceted interactions influencing cognitive outcomes in this population and to develop targeted interventions for improving cognitive health in PWH.

背景:艾滋病病毒感染者(PWH)尽管接受了抗逆转录病毒联合疗法,但仍有罹患艾滋病相关神经认知障碍(HAND)的风险。脑源性神经营养因子(BDNF)与认知功能和神经可塑性有关,但其在 HIV 相关神经炎症中的作用仍未得到充分研究。研究方法本研究分析了 CHAMPS 研究的数据,评估了 140 名成人 HIV 感染者基线时的 BDNF 血清水平和认知功能。认知功能采用 PROMIS 应用认知-能力 8 项问卷进行评估。BDNF水平(pg/ml)采用高灵敏度酶联免疫测定(ELISA)试剂盒进行测定。在对人口统计学变量进行调整后,进行了线性回归分析,以探讨 BDNF 水平、认知功能和艾滋病诊断之间的关联。结果发现发现BDNF水平与PWH的认知功能得分之间存在明显的正相关(p = .03)。此外,有艾滋病诊断史的艾滋病患者的 BDNF 水平明显较低(p = 0.02)。其他人口统计学因素对该人群的认知功能或 BDNF 水平没有明显影响。结论:我们的研究结果凸显了 BDNF 作为 PWH 认知功能下降生物标志物的潜力,并表明其与了解 HAND 病理生理学相关。有必要开展进一步研究,探索影响该人群认知结果的多方面相互作用,并制定有针对性的干预措施,以改善 PWH 的认知健康。
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引用次数: 0
Effect of Physical Function on Access to Repeat Kidney Transplantation. 身体机能对再次接受肾移植的影响。
Pub Date : 2024-10-25 DOI: 10.1177/10998004241271380
Jongwon Yoo

Background: The long-term success rate of kidney transplantation is disappointing, with repeat transplantation necessary for more than half of recipients. When a repeat kidney transplantation is needed, patients are often elderly and suffer from underlying advanced kidney disease, comorbidities, and adverse effects of immunosuppressants, leading to physical function limitations. Limited physical function is known to hinder access to an initial kidney transplantation, but there is no information about its impact on repeat transplantations. Objective: This study aimed to determine the effect of physical function on access to wait-listing for repeat transplantation. Methods: Data from the national registry was utilized to analyze 28,884 kidney transplant recipients. Physical function was assessed with Karnofsky scores, and patients were categorized into three strata: total assistance, some assistance, and no assistance. Logistic regression and multivariate Cox proportional hazard models were used to assess the impact of physical function on waiting list access and duration until wait-listing, respectively. Results: Patients with greater physical independence were more likely to be wait-listed for repeat kidney transplantation. Highly sensitized patients, those with diabetes, Black patients, and elderly individuals had a lower likelihood of access to wait-listing after kidney failure. Interestingly, those with limited physical function, provided they remained in the work-up process, experienced a relatively shorter duration to wait-listing after graft failure.Conclusions: These findings highlight the need to promote and support physical function throughout the kidney transplant journey to improve access to repeat transplantation and subsequent patient outcomes.

背景:肾移植的长期成功率令人失望,半数以上的受者需要重复移植。当需要再次进行肾移植时,患者通常是老年人,患有潜在的晚期肾病、合并症和免疫抑制剂的不良反应,导致身体功能受限。众所周知,身体功能受限会阻碍首次肾移植的进行,但目前还没有关于身体功能受限对重复肾移植的影响的信息。研究目的本研究旨在确定身体功能对获得重复移植等待名单的影响。研究方法:利用国家登记处的数据对 28,884 名肾移植受者进行了分析。身体功能以 Karnofsky 评分进行评估,并将患者分为三类:完全协助、部分协助和无协助。采用逻辑回归和多变量 Cox 比例危险模型分别评估了身体功能对进入候选名单和候选时间的影响。结果显示身体独立性较强的患者更有可能被列入重复肾移植的候选名单。高度敏感患者、糖尿病患者、黑人患者和老年人在肾衰竭后进入等待名单的可能性较低。有趣的是,身体功能受限的患者如果仍在接受检查,移植失败后等待移植的时间相对较短:这些发现强调了在整个肾移植过程中促进和支持身体功能的必要性,以改善重复移植的机会和患者的后续治疗效果。
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引用次数: 0
Preterm Birth in African American Women: A Multi-Omic Pilot Study in Early Pregnancy. 非裔美国妇女的早产问题:妊娠早期多血型试点研究。
Pub Date : 2024-10-23 DOI: 10.1177/10998004241275049
Alexandra L Nowak, Nadia Saadat, Jiao Sun, Anna M Forsman, Xiaoyu Liang, Cara Joyce, Jennifer Woo, Christopher G Engeland, Dawn P Misra, Carmen Giurgescu, Wei Zhang, Cindy M Anderson

Preterm birth (PTB; <37 weeks completed gestation) is a devastating problem affecting over 13 million live births worldwide. In the U.S., African Americans experience significantly higher rates of PTB compared to non-Hispanic Whites. PTB disparities have been linked to social determinants of health (e.g., socioeconomic status, discrimination). However, the biological underpinnings related to these associations are unclear. DNA methylation (DNAm) is subject to environmental influences, and DNAm modifications are known to affect gene expression. Using a multi-omic approach, we examined differences in combined DNA methylation (DNAm) and messenger RNA (mRNA) transcriptomic data from 20 pregnant African American women (12 PTB; 8 term birth) early in pregnancy (8-18 weeks gestation). We found that the HLA-DQB2 gene was both differentially methylated (cg12296550; p = .02) and differentially expressed (p = .014; log2FC = 2.5) between women with PTB and term birth. Gene expression analysis showed HLA-DQB2 and HLA-DRB4 (p = .028; log2FC = -3.6) were the two most highly expressed genes. HLA-DQB2 expressed higher in PTB and HLA-DRB4 expressed higher in term birth. However, no genes remained significant (p < .05) after Bonferroni correction. HLA-DRB4 and AKR1C1 were identified as a potential biomarkers in dimensionality reduction models and are also important to immune function and allogenic breakdown. Altered gene expression may lead to inflammatory imbalances or allogenic intolerance resulting in PTB. This study provides proof-of-concept evidence for the feasibility and importance of future multi-omics studies with larger populations to further explore the genes and pathways identified here.

早产(PTB;HLA-DQB2 基因在早产和过期产妇女之间存在甲基化差异(cg12296550;p = .02)和表达差异(p = .014;log2FC = 2.5)。基因表达分析表明,HLA-DQB2 和 HLA-DRB4 (p = .028; log2FC = -3.6)是表达量最高的两个基因。HLA-DQB2 在 PTB 中表达较高,而 HLA-DRB4 在足月儿中表达较高。然而,经 Bonferroni 校正后,没有基因仍具有显著性(p < .05)。在降维模型中,HLA-DRB4 和 AKR1C1 被确定为潜在的生物标记物,它们对免疫功能和异体分解也很重要。基因表达的改变可能会导致炎症失衡或异基因不耐受,从而导致 PTB。这项研究提供了概念性证据,证明了未来利用更多人群进行多组学研究的可行性和重要性,以进一步探索在此发现的基因和通路。
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引用次数: 0
Heart Failure Symptoms Improve With More Intense Physical Activity. 加强体育锻炼可改善心衰症状
Pub Date : 2024-10-18 DOI: 10.1177/10998004241290827
Jonathan P Auld, Elaine A Thompson, Cynthia M Dougherty

Background: Little is known about how changes in physical activity (PA) over time may influence symptoms in people with heart failure (HF).

Methods: A secondary analysis was conducted with data from an RCT of an exercise intervention in patients with ICDs (implantable cardioverter defibrillator) and a HF diagnosis (n = 96). Data were collected at baseline and 2 months of PA intervention. Physical activity (PA Steps = mean steps/day; PA Intensity = mean steps/min for most intense 30 minutes/day) were measured over 5 days at each timepoint. Physical symptoms were measured using the Patient Concerns Assessment, the SF-36 Vitality, and Bodily Pain subscales for fatigue and pain. Psychological symptoms were assessed using the Patient Health Questionnaire-9, and the State-Trait Anxiety Index. Associations between PA and physical and psychological symptoms were analyzed with multivariate regression.

Results: Patients (n = 96) were predominately male (83%) and Caucasian (79%), aged 55.8 ± 12.3 years, BMI of 29.7 ± 5.1, with heart failure with reduced ejection fraction (HFrEF; 30.9 ± 9.9%). An increase in PA Steps was associated with improvement in anxiety (β = -1.178, p = .048). An increase in PA Intensity was associated with significant reductions in depression (β = -0.127, p = .021), anxiety (β = -0.234, p = .037), and fatigue (β = 0.528, p = .022). Decreases in PA Steps and PA Intensity were not associated with changes in any symptoms.

Conclusion: For HF patients with an ICD, more intense PA over 2 months was associated with improved psychological symptoms and reduced fatigue. Decreases in PA (total and intensity) were not associated with changes in symptoms. Interventions promoting increasing the intensity of PA over time may be an effective approach to reduce some HF symptoms.

背景:人们对体力活动(PA)随时间的变化如何影响心衰患者的症状知之甚少:人们对体力活动(PA)随时间的变化如何影响心力衰竭(HF)患者的症状知之甚少:我们对一项针对植入式心律转复除颤器(ICD)和心力衰竭诊断患者(n = 96)的运动干预 RCT 数据进行了二次分析。基线数据和 PA 干预 2 个月的数据均已收集。在每个时间点测量了 5 天的体力活动(体力活动步数 = 平均步数/天;体力活动强度 = 最激烈的 30 分钟/天的平均步数/分钟)。身体症状采用患者关注问题评估、SF-36 活力和身体疼痛分量表(疲劳和疼痛)进行测量。心理症状采用患者健康问卷-9 和状态-特质焦虑指数进行评估。通过多变量回归分析了 PA 与身体和心理症状之间的关系:患者(n = 96)主要为男性(83%)和白种人(79%),年龄为(55.8 ± 12.3)岁,体重指数为(29.7 ± 5.1),患有射血分数降低型心力衰竭(HFrEF;30.9 ± 9.9%)。PA Steps 的增加与焦虑症的改善有关(β = -1.178, p = .048)。PA 强度的增加与抑郁(β = -0.127,p = .021)、焦虑(β = -0.234,p = .037)和疲劳(β = 0.528,p = .022)的显著降低有关。PA Steps 和 PA Intensity 的减少与任何症状的变化均无关联:结论:对于患有 ICD 的高血压患者来说,在 2 个月内进行强度更大的 PA 与心理症状的改善和疲劳的减轻有关。PA(总量和强度)的减少与症状的变化无关。随着时间的推移,增加体力活动强度的干预措施可能是减轻某些高血压症状的有效方法。
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引用次数: 0
The Moderating Role of Genetics on the Effectiveness of the Mindfulness-Based Stress Reduction for Breast Cancer (MBSR(BC)) Program on Cognitive Impairment. 遗传对乳腺癌正念减压疗法(MBSR(BC))效果的调节作用认知障碍计划
Pub Date : 2024-10-16 DOI: 10.1177/10998004241289629
Jong Y Park, Cecile A Lengacher, Carmen S Rodriguez, Hongdao Meng, Kevin E Kip, Sandra Morgan, Anisha Joshi, Gizem Hueluer, Julia R Wang, Sara Tinsley, Charles Cox, John Kiluk, Kristine A Donovan, Manolete Moscoso, Elizabeth Bornstein, Jean M Lucas, Tamela Fonseca, Mahathi Krothapalli, Lynne S Padgett, Sreenidhi Nidamanur, Estella Hornback, Diya Patel, Ramya Chamkeri, Richard R Reich

Background: Genetics may influence symptoms experienced by breast cancer survivors (BCS) by moderating the effects of stress-reducing interventions, including the Mindfulness-Based Stress Reduction (MBSR(BC)) program, to reduce symptom severity. As part of a larger clinical trial, the aim of this study was to evaluate genetic variants as moderators of MBSR(BC) on improvements among BCS in cognitive functioning and symptoms.

Methods: BCS (n = 128) were randomized to MBSR(BC) or the Breast Cancer Education Support Program. Objective neuropsychological and subjective measures of cognitive performance, and psychological and physical symptoms were collected at baseline, 6, 12, and 26 weeks. Linear mixed models were implemented to identify MBSR(BC)'s effects over time. A total of 22 single nucleotide polymorphisms (SNPs) from 20 genes known to be related to these symptoms were investigated using genomic DNA. These SNPs were tested as moderators of MBSR(BC) program effects.

Results: Results showed MBSR(BC) participants experienced significantly greater benefits in cognitive functioning, however, the level of benefit varied based on one's genetic profile. Effects sizes, consistency across similar measures were investigated. Among 22 candidate SNPs, rs4680 in COMT, rs1800497 in ANKK1, and rs6277 in DRD2 demonstrated the strongest, most consistent positive effects in moderating MBSR(BC)'s impact on cognitive outcomes.

Conclusions: Although the effects were small, this translational research may potentially identify BCS with genotypes that would be most influenced by the MBSR(BC) program. These results may be used to develop personalized intervention programs tailored to the genetic profile of each breast cancer survivor who received chemotherapy or chemotherapy and radiation.

Trial registration: ClinicalTrials.gov, https://www.ClinicalTrials.gov Registration Number: NCT02786797.

背景:遗传可能会影响乳腺癌幸存者(BCS)所经历的症状,从而调节减压干预措施(包括正念减压(MBSR(BC))计划)对减轻症状严重程度的影响。作为一项大型临床试验的一部分,本研究旨在评估基因变异对MBSR(BC)改善BCS认知功能和症状的调节作用:乳腺癌患者(n = 128)被随机分配到 MBSR(BC)或乳腺癌教育支持计划中。在基线、6周、12周和26周收集了认知功能、心理和身体症状的客观神经心理学和主观测量数据。采用线性混合模型来确定 MBSR(BC) 随时间变化的影响。利用基因组 DNA 对已知与这些症状相关的 20 个基因中的 22 个单核苷酸多态性 (SNP) 进行了调查。这些SNPs作为MBSR(BC)项目效果的调节因子进行了测试:结果表明,MBSR(BC)参与者在认知功能方面的获益明显增加,但获益程度因个人遗传特征而异。研究还调查了效应大小以及类似测量的一致性。在 22 个候选 SNPs 中,COMT 的 rs4680、ANKK1 的 rs1800497 和 DRD2 的 rs6277 在调节 MBSR(BC)对认知结果的影响方面表现出最强、最一致的积极效应:虽然影响很小,但这项转化研究有可能识别出受 MBSR(BC)计划影响最大的 BCS 基因型。这些结果可用于为每位接受化疗或化疗和放疗的乳腺癌幸存者量身定制个性化干预方案:ClinicalTrials.gov, https://www.ClinicalTrials.gov 注册号:NCT02786797。
{"title":"The Moderating Role of Genetics on the Effectiveness of the Mindfulness-Based Stress Reduction for Breast Cancer (MBSR(BC)) Program on Cognitive Impairment.","authors":"Jong Y Park, Cecile A Lengacher, Carmen S Rodriguez, Hongdao Meng, Kevin E Kip, Sandra Morgan, Anisha Joshi, Gizem Hueluer, Julia R Wang, Sara Tinsley, Charles Cox, John Kiluk, Kristine A Donovan, Manolete Moscoso, Elizabeth Bornstein, Jean M Lucas, Tamela Fonseca, Mahathi Krothapalli, Lynne S Padgett, Sreenidhi Nidamanur, Estella Hornback, Diya Patel, Ramya Chamkeri, Richard R Reich","doi":"10.1177/10998004241289629","DOIUrl":"https://doi.org/10.1177/10998004241289629","url":null,"abstract":"<p><strong>Background: </strong>Genetics may influence symptoms experienced by breast cancer survivors (BCS) by moderating the effects of stress-reducing interventions, including the Mindfulness-Based Stress Reduction (MBSR(BC)) program, to reduce symptom severity. As part of a larger clinical trial, the aim of this study was to evaluate genetic variants as moderators of MBSR(BC) on improvements among BCS in cognitive functioning and symptoms.</p><p><strong>Methods: </strong>BCS (<i>n</i> = 128) were randomized to MBSR(BC) or the Breast Cancer Education Support Program. Objective neuropsychological and subjective measures of cognitive performance, and psychological and physical symptoms were collected at baseline, 6, 12, and 26 weeks. Linear mixed models were implemented to identify MBSR(BC)'s effects over time. A total of 22 single nucleotide polymorphisms (SNPs) from 20 genes known to be related to these symptoms were investigated using genomic DNA. These SNPs were tested as moderators of MBSR(BC) program effects.</p><p><strong>Results: </strong>Results showed MBSR(BC) participants experienced significantly greater benefits in cognitive functioning, however, the level of benefit varied based on one's genetic profile. Effects sizes, consistency across similar measures were investigated. Among 22 candidate SNPs, rs4680 in COMT, rs1800497 in ANKK1, and rs6277 in DRD2 demonstrated the strongest, most consistent positive effects in moderating MBSR(BC)'s impact on cognitive outcomes.</p><p><strong>Conclusions: </strong>Although the effects were small, this translational research may potentially identify BCS with genotypes that would be most influenced by the MBSR(BC) program. These results may be used to develop personalized intervention programs tailored to the genetic profile of each breast cancer survivor who received chemotherapy or chemotherapy and radiation.</p><p><strong>Trial registration: </strong>ClinicalTrials.gov, https://www.ClinicalTrials.gov Registration Number: NCT02786797.</p>","PeriodicalId":93901,"journal":{"name":"Biological research for nursing","volume":" ","pages":"10998004241289629"},"PeriodicalIF":0.0,"publicationDate":"2024-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142482958","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Multivariate Bayesian Analyses in Nursing Research: An Introductory Guide. 护理研究中的多变量贝叶斯分析:护理研究中的多变量贝叶分析:入门指南》。
Pub Date : 2024-10-16 DOI: 10.1177/10998004241292644
Lacey W Heinsberg, Tara S Davis, Dylan Maher, Catherine M Bender, Yvette P Conley, Daniel E Weeks

In the era of precision health, nursing research has increasingly focused on the analysis of large, multidimensional data sets containing multiple correlated phenotypes (e.g., symptoms). This presents challenges for statistical analyses, especially in genetic association studies. For example, the inclusion of multiple symptoms within a single model can raise concerns about multicollinearity, while individual SNP-symptom analyses may obscure complex relationships. As such, many traditional statistical approaches often fall short in providing a comprehensive understanding of the complexity inherent in many nursing-focused research questions. Multivariate Bayesian approaches offer the unique advantage of allowing researchers to ask questions that are not feasible with traditional approaches. Specifically, these methods support the simultaneous exploration of multiple phenotypes, accounting for the underlying correlational structure between variables, and allow for formal incorporation of existing knowledge into the statistical model. By doing so, they may provide a more realistic view of statistical relationships within a biological system, potentially uncovering new insights into well-established and undiscovered connections, such as the probabilities of association and direct versus indirect effects. This valuable information can help us better understand our phenotypes of interest, leading to more effective nurse-led intervention and prevention programs. To illustrate these concepts, this paper includes an application section covering two specific multivariate Bayesian analysis software programs, bnlearn and mvBIMBAM, with an emphasis on interpretation and extension to nursing research. To complement the paper, we provide access to a detailed online tutorial, including executable R code and a synthetic data set, so the concepts can be more easily extended to other research questions.

在精准健康时代,护理研究越来越注重分析包含多种相关表型(如症状)的大型多维数据集。这给统计分析带来了挑战,尤其是在遗传关联研究中。例如,在单一模型中包含多种症状可能会引发多重共线性问题,而单个 SNP-症状分析可能会掩盖复杂的关系。因此,许多传统的统计方法往往无法全面了解许多以护理为重点的研究问题的内在复杂性。多变量贝叶斯方法具有独特的优势,允许研究人员提出传统方法无法解决的问题。具体来说,这些方法支持同时探索多种表型,考虑变量之间的潜在相关结构,并允许将现有知识正式纳入统计模型。通过这样做,这些方法可以更真实地反映生物系统内的统计关系,并有可能揭示已建立和未发现的联系的新见解,如关联概率和直接效应与间接效应。这些宝贵的信息可以帮助我们更好地了解我们感兴趣的表型,从而制定出更有效的由护士主导的干预和预防计划。为了说明这些概念,本文包括一个应用部分,涉及两个特定的多元贝叶斯分析软件程序:bnlearn 和 mvBIMBAM,重点是解释和推广到护理研究中。作为本文的补充,我们提供了详细的在线教程,包括可执行的 R 代码和合成数据集,以便更轻松地将这些概念推广到其他研究问题中。
{"title":"Multivariate Bayesian Analyses in Nursing Research: An Introductory Guide.","authors":"Lacey W Heinsberg, Tara S Davis, Dylan Maher, Catherine M Bender, Yvette P Conley, Daniel E Weeks","doi":"10.1177/10998004241292644","DOIUrl":"https://doi.org/10.1177/10998004241292644","url":null,"abstract":"<p><p>In the era of precision health, nursing research has increasingly focused on the analysis of large, multidimensional data sets containing multiple correlated phenotypes (e.g., symptoms). This presents challenges for statistical analyses, especially in genetic association studies. For example, the inclusion of multiple symptoms within a single model can raise concerns about multicollinearity, while individual SNP-symptom analyses may obscure complex relationships. As such, many traditional statistical approaches often fall short in providing a comprehensive understanding of the complexity inherent in many nursing-focused research questions. Multivariate Bayesian approaches offer the unique advantage of allowing researchers to ask questions that are not feasible with traditional approaches. Specifically, these methods support the simultaneous exploration of multiple phenotypes, accounting for the underlying correlational structure between variables, and allow for formal incorporation of existing knowledge into the statistical model. By doing so, they may provide a more realistic view of statistical relationships within a <i>biological system</i>, potentially uncovering new insights into well-established and undiscovered connections, such as the probabilities of association and direct versus indirect effects. This valuable information can help us better understand our phenotypes of interest, leading to more effective nurse-led intervention and prevention programs. To illustrate these concepts, this paper includes an application section covering two specific multivariate Bayesian analysis software programs, <i>bnlearn</i> and <i>mvBIMBAM</i>, with an emphasis on interpretation and extension to nursing research. To complement the paper, we provide access to a detailed online tutorial, including executable R code and a synthetic data set, so the concepts can be more easily extended to other research questions.</p>","PeriodicalId":93901,"journal":{"name":"Biological research for nursing","volume":" ","pages":"10998004241292644"},"PeriodicalIF":0.0,"publicationDate":"2024-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142482957","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Biological research for nursing
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