Vitamin B Complex

复合维生素 B
  • 文章类型: Journal Article
    探索叶酸代谢基因遗传多态性之间的联系(MTHFR,地铁,和MTRR)和心血管疾病(CVD),这项研究评估了B族维生素补充剂(叶酸甲酯,吡哆醛-5'-磷酸,和甲基钴胺)对高半胱氨酸和脂质水平,潜在的指导个性化CVD风险管理。在一个随机的,双盲,安慰剂对照试验,54名年龄在40-75岁的高半胱氨酸和中度LDL-C水平升高的患者根据MTHFR进行分组,地铁,和MTRR遗传多态性。超过六个月,他们接受了甲基叶酸的组合,P5P,和甲基钴胺,或者安慰剂.在6个月的随访中,治疗组的同型半胱氨酸水平显着降低了30.0%(95%CI:-39.7%至-20.3%),LDL-C显着降低了7.5%(95%CI:-10.3%至-4.7%),与安慰剂相比(全部p<0.01)。在亚组分析中,纯合子小等位基因携带者的同型半胱氨酸水平显着降低(48.3%,95%CI:-62.3%至-34.3%,p<0.01)与混合等位基因携带者(18.6%,95%CI:-25.6%至-11.6%,p<0.01),组间差异显著(29.7%,95%CI:-50.7%至-8.7%,p<0.01)。纯合携带者的LDL-C水平下降了11.8%(95%CI:-15.8%至-7.8%,p<0.01)和混合等位基因携带者的4.8%(95%CI:-6.8%至-2.8%,p<0.01),具有显著的组间差异(7.0%,95%CI:-13.0%至-1.0%,p<0.01)。叶酸甲酯,P5P,和甲基钴胺补充剂针对基因谱定制有效降低了特定MTHFR患者的同型半胱氨酸和LDL-C水平,地铁,和MTRR多态性,特别是具有纯合次要等位基因多态性。
    Exploring the link between genetic polymorphisms in folate metabolism genes (MTHFR, MTR, and MTRR) and cardiovascular disease (CVD), this study evaluates the effect of B vitamin supplements (methylfolate, pyridoxal-5\'-phosphate, and methylcobalamin) on homocysteine and lipid levels, potentially guiding personalized CVD risk management. In a randomized, double-blind, placebo-controlled trial, 54 patients aged 40-75 with elevated homocysteine and moderate LDL-C levels were divided based on MTHFR, MTR, and MTRR genetic polymorphisms. Over six months, they received either a combination of methylfolate, P5P, and methylcobalamin, or a placebo. At the 6 months follow-up, the treatment group demonstrated a significant reduction in homocysteine levels by 30.0% (95% CI: -39.7% to -20.3%) and LDL-C by 7.5% (95% CI: -10.3% to -4.7%), compared to the placebo (p < 0.01 for all). In the subgroup analysis, Homozygous Minor Allele Carriers showed a more significant reduction in homocysteine levels (48.3%, 95% CI: -62.3% to -34.3%, p < 0.01) compared to mixed allele carriers (18.6%, 95% CI: -25.6% to -11.6%, p < 0.01), with a notable intergroup difference (29.7%, 95% CI: -50.7% to -8.7%, p < 0.01). LDL-C levels decreased by 11.8% in homozygous carriers (95% CI: -15.8% to -7.8%, p < 0.01) and 4.8% in mixed allele carriers (95% CI: -6.8% to -2.8%, p < 0.01), with a significant between-group difference (7.0%, 95% CI: -13.0% to -1.0%, p < 0.01). Methylfolate, P5P, and methylcobalamin supplementation tailored to genetic profiles effectively reduced homocysteine and LDL-C levels in patients with specific MTHFR, MTR, and MTRR polymorphisms, particularly with homozygous minor allele polymorphisms.
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  • 文章类型: Journal Article
    两栖动物的大规模灭绝需要专门的计划来确保物种的生存。巴尔的摩的马里兰州动物园拥有极度濒危的巴拿马金蛙(Atelopuszeteki)的最大保证种群。然而,这个人群中的个体会经历类似于tetany的综合征,以四肢僵硬/位置不当和跳跃困难为特征,游泳,和扶正。在这项研究中,我们指定了综合征病例定义,并描述了相关的临床体征.然后,我们对四种不同的治疗方法进行了系统评估,以找到最有效的治疗方案,并开始阐明其根本原因.83只青蛙符合病例定义,用葡萄糖酸钙口服治疗14d,氯化镁,补充灌胃喂养,或钙的组合,镁,和复合维生素B.青蛙用定义的评估跳跃的协议进行了测试,Righting,游泳能力。在症状发作时进行测试,每周重复一次,直到出现缓解。分析表明,联合治疗在消除手提综合征的临床症状方面显着更有效。结果显示了治疗这种综合征最有效的方法,但无助于阐明根本原因。未来的工作将侧重于检查因素(例如,饮食,畜牧业),可能会引发该综合征,以便更全面地了解其病因。
    The mass extinction of amphibians necessitates specialized programs to ensure species\' survival. Maryland Zoo in Baltimore houses the largest assurance population of the critically endangered Panamanian golden frog (Atelopus zeteki). However, individuals in this population experience a tetany-like syndrome, characterized by rigid/inappropriately positioned limbs and difficulty hopping, swimming, and righting. In this study, a syndrome case definition was assigned and the associated clinical signs were described. Then, four different treatments were systematically assessed in order to find the most effective protocol for treatment and begin to elucidate its underlying causes. Eighty-three frogs fulfilled the case definition and were treated orally for 14 d with either calcium gluconate, magnesium chloride, supplemental gavage feeding, or combination of calcium, magnesium, and vitamin B complex. Frogs were tested with a defined protocol assessing hopping, righting, and swimming abilities. Testing was performed at symptom onset and repeated weekly until resolution occurred. Analyses revealed that combination treatment was significantly more effective in eliminating clinical signs of tetany syndrome. Results show the most effective way to treat this syndrome, but do not help elucidate the underlying cause. Future work will focus on examining factors (e.g., diet, husbandry) that may elicit the syndrome for a more complete understanding of its etiology.
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  • 文章类型: Journal Article
    背景:肌肉骨骼疾病是缺勤的重要原因。临床实践指南建议使用非甾体抗炎药(NSAIDs)治疗I-II级宫颈扭伤。已经使用了硫胺素+吡哆醇+氰钴胺维生素的组合,单独和与NSAIDs联合使用,肌肉骨骼疾病的疼痛和炎症。
    目的:本研究的目的是证明右酮洛芬的镇痛协同作用,和维生素硫胺素+吡哆醇+氰钴胺的组合在固定剂量组合(FDC)中用于治疗由I-II级宫颈扭伤引起的急性疼痛。
    方法:我们进行了多中心,prospective,随机化,双盲,IIIb期临床研究比较两个治疗组:(1)右酮洛芬25毫克/维生素B(硫胺素100毫克,吡哆醇50mg和氰钴胺0.50mg)在FDC(两种或更多种活性成分组合在一个单一的剂型)与(2)右酮洛芬25mg单药治疗(单一药物治疗特定的疾病),口服一个胶囊或片剂,每8小时7天。最终意味着,平均变化,和疼痛感知的百分比变化(使用视觉模拟评分[VAS]测量)与基线进行比较。P值<0.05被认为是统计学上显著的。使用SPSS软件进行分析,v.29.0.
    结果:与单药治疗相比,从FDC治疗的第三天开始观察到疼痛强度的统计学显着降低(-3.1±-1.5和-2.6±-1.1cm,分别)使用VAS(p=0.011)测量。关于残疾程度,使用NorthwickPark颈部疼痛问卷(NPQ),在最终测量中观察到统计学差异(7.5%,四分位数间距[IQR]2.5,10.5;vs.7.9%,IQR5.0,13.8;p=0.028)。使用FDC时报告的不良事件比例较低。
    结论:右酮洛芬/硫胺素+吡哆醇+氰钴胺维生素的FDC与右酮洛芬单药治疗I-II级宫颈扭伤患者的疼痛相比,显示出更好的疗效和更好的安全性。
    背景:NCT05001555,注册于2021年7月29日(https://clinicaltrials.gov/study/NCT05001555)。
    BACKGROUND: Musculoskeletal disorders are an important cause of work absence. Clinical practice guidelines recommend nonsteroidal anti-inflammatory drugs (NSAIDs) for grade I-II cervical sprains. The combination of thiamine + pyridoxine + cyanocobalamin vitamins has been used, alone and in combination with NSAIDs, for pain and inflammation in musculoskeletal disorders.
    OBJECTIVE: The objective of this study was to demonstrate the analgesic synergy of dexketoprofen, and the combination of vitamins thiamine + pyridoxine + cyanocobalamin in a fixed-dose combination (FDC) for the treatment of acute pain caused by grade I-II cervical sprains.
    METHODS: We conducted a multicentre, prospective, randomized, double-blind, phase IIIb clinical study comparing two treatment groups: (1) dexketoprofen 25 mg/vitamin B (thiamine 100 mg, pyridoxine 50 mg and cyanocobalamin 0.50 mg) in an FDC (two or more active ingredients combined in a single dosage form) versus (2) dexketoprofen 25 mg monotherapy (single drug to treat a particular disease), one capsule or tablet orally, every 8 h for 7 days. Final mean, average change, and percentage change in pain perception (measured using a visual analogue scale [VAS]) were compared with baseline between groups. A p value < 0.05 was considered statistically significant. Analyses were conducted using SPSS software, v.29.0.
    RESULTS: A statistically significant reduction in pain intensity was observed from the third day of treatment with the FDC compared with monotherapy (- 3.1 ± - 1.5 and - 2.6 ± - 1.1 cm, respectively) measured using the VAS (p = 0.011). Regarding the degree of disability, using the Northwick Park Neck Pain Questionnaire (NPQ), statistical difference was observed for the final measurement (7.5%, interquartile range [IQR] 2.5, 10.5; vs. 7.9%, IQR 5.0, 13.8; p = 0.028). A lower proportion of adverse events was reported when using the FDC.
    CONCLUSIONS: The FDC of dexketoprofen/thiamine + pyridoxine + cyanocobalamin vitamins demonstrated superior efficacy and a better safety profile compared with dexketoprofen monotherapy for pain treatment in patients with grade I-II cervical sprains.
    BACKGROUND: NCT05001555, registered 29 July 2021 ( https://clinicaltrials.gov/study/NCT05001555 ).
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  • 文章类型: Journal Article
    目的:喂养不耐受(FI)是晚期早产儿(34周≤胎龄<37周)的常见问题。本研究旨在评价酚妥拉明联合B族维生素治疗晚期早产儿FI的疗效和安全性,并探讨其对胃肠道症状的影响。炎症和并发症。
    方法:我们将118名有FI的晚期早产儿随机分为治疗组(n=56)或对照组(n=62)。治疗组静脉注射酚妥拉明和肌注B族维生素,而对照组仅接受基础治疗。我们测量了胃肠道症状消失的时间,基本达到的时间,住院时间,并发症的发生率,炎症标志物浓度和治疗总有效率。
    结果:治疗组胃肠道症状持续时间短于对照组(p<0.01)。与对照组相比,治疗组的炎症标志物浓度较低,总有效率较高(p<0.05)。两组的住院时间无差异,基础成就,体重恢复和并发症发生率(p>0.05)。
    结论:酚妥拉明和B族维生素可减轻晚期早产儿FI的胃肠道症状和炎症,但不影响并发症的发生。
    OBJECTIVE: Feeding intolerance (FI) is a common problem in late preterm infants (34 weeks ≤ gestational age < 37 weeks). This study aimed to evaluate the efficacy and safety of phentolamine combined with B vitamins in treating FI in late preterm infants and to explore its effects on gastrointestinal symptoms, inflammation and complications.
    METHODS: We randomly assigned 118 late preterm infants with FI to a treatment group (n = 56) or a control group (n = 62). The treatment group received intravenous phentolamine and intramuscular B vitamins, whereas the control group received basic treatment only. We measured the time of disappearance of gastrointestinal symptoms, the time of basal at-tainment, the time of hospitalisation, the incidence of complications, the concentrations of inflammatory markers and the overall effective rate of treatment.
    RESULTS: The treatment group had a shorter duration of gastrointestinal symptoms than did the control group (p < 0.01). The treatment group also had lower concentrations of inflammatory markers and a higher overall effective rate than did the control group (p < 0.05). There was no difference between the two groups in the time of hospitalisation, basal attainment, weight re-covery and the incidence of complications (p > 0.05).
    CONCLUSIONS: Phentolamine and B vitamins can reduce gastrointestinal symptoms and inflammation in late preterm infants with FI but do not affect the occurrence of complications.
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  • 文章类型: Journal Article
    背景:大量研究表明膳食微量营养素的摄入与便秘的发生之间存在相关性。然而,便秘与维生素B1之间的相关性仍未研究。这项研究的主要目的是研究国家健康与营养检查调查(NHANES)的成年参与者中慢性便秘与饮食中维生素B1消耗之间的关系。
    方法:这项研究使用了来自NHANES的数据,2005年至2010年进行的健康和营养调查。受访者的饮食信息是通过利用24小时饮食记录收集的。各种统计分析,如多元逻辑回归,亚组分析,和曲线拟合分析,研究了膳食摄入维生素B1与慢性便秘的相关性。
    结果:在试验中,有10371名参与者,其中1,123人(10.8%)被确定为患有慢性便秘。完全调整的多元logistic回归分析显示,增加维生素B1的饮食摄入量(OR=0.87,95%CI:0.77-0.99)与便秘风险降低显着相关。在对模型3中的多个变量进行调整后,第三个三分位数的比值比(OR)和95%置信区间(CI),与第一个三分位数(参照组)相比,为0.80(0.65,0.99)。此外,亚组分析和交互作用测试显示,维生素B1摄入量与便秘患病率之间存在显著的负相关,尤其是在男性中,非高血压,和非糖尿病个体(所有P值小于0.05)。
    结论:这项研究揭示了饮食中维生素B1的消耗与慢性便秘的发生之间的负相关。这种现象的一个潜在解释是,饮食中维生素B1的消耗与大便软化和结肠蠕动增加有关。需要进行更广泛的前瞻性研究,以彻底检查硫胺素在长期便秘中的重要性。
    BACKGROUND: Numerous researches have indicated a correlation between the intake of dietary micronutrients and the occurrence of constipation. Nevertheless, the correlation between constipation and vitamin B1 remains uninvestigated. The main aim of this research was to examine the association between chronic constipation and the consumption of vitamin B1 in the diet among adult participants of the National Health and Nutrition Examination Survey (NHANES).
    METHODS: This study used data from the NHANES, a survey on health and nutrition conducted between 2005 and 2010. The respondents\' dietary information was gathered by utilizing the 24-hour dietary records. Various statistical analyses, such as multiple logistic regression, subgroup analysis, and curve-fitting analysis, were employed to investigate the correlation between dietary intake of vitamin B1 and chronic constipation.
    RESULTS: In the trial, there were 10,371 participants, out of which 1,123 individuals (10.8%) were identified as having chronic constipation. Fully adjusted multiple logistic regression analyses showed that increasing dietary intake of vitamin B1 (OR = 0.87, 95% CI: 0.77-0.99) was significantly associated with a reduced risk of constipation. Following adjustment for multiple variables in Model 3, the odds ratio (OR) and 95% confidence interval (CI) for the third tertile, in comparison to the first tertile (reference group), was 0.80 (0.65, 0.99). In addition, subgroup analyses and interaction tests showed a significant inverse association between vitamin B1 intake and the prevalence of constipation, especially among men, non-hypertensive, and non-diabetic individuals (all P-values less than 0.05).
    CONCLUSIONS: This research uncovered an inverse correlation between the consumption of vitamin B1 in the diet and the occurrence of chronic constipation. One potential explanation for this phenomenon is that the consumption of vitamin B1 in one\'s diet is linked to the softening of stools and an augmented occurrence of colonic peristalsis. Additional extensive prospective research is required to thoroughly examine the significance of thiamine in long-term constipation.
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  • 文章类型: Journal Article
    背景:本研究的主要目的是评估吡哆醇延迟给药对诊断为吡哆醇依赖性癫痫(PDE)患者的神经系统后果。
    方法:我们回顾了29篇文章,包括52例基因诊断的PDE病例,确保数据同质性。另外3例病例来自圣马可医院普通儿科手术室。数据收集考虑了第一次癫痫发作时的年龄等因素,脑电图报告,遗传分析,还有更多.根据对一线抗癫痫药物的反应,患者分为4组.后续评估采用各种量表来确定神经系统,认知,和精神运动的发展。
    结果:我们的研究包括55名患者(28名男性和27名女性),其中15人因缺乏随访数据而被排除在外.21例患者被归类为“复发反应者”,11为“耐”,6为“吡哆醇第一方法”,和2作为“响应者”。神经系统结果显示37,5%没有神经系统影响,37,5%在两个发育区域出现并发症,15%,所有领域的10%。统计分析强调了首次癫痫发作后吡哆醇给药的时间与较差的神经系统结局之间的正相关。另一方面,发现延长的潜伏期(即,从首次发作到复发之间经过的时间)以及在随后的随访中发现的神经学评估评分不佳的患者的神经学结局较差。
    结论:该研究强调了早期识别和干预PDE的重要性。现有的医疗协议经常忽视PDE的及时诊断。立即服用吡哆醇,在存在典型症状的情况下进行快速诊断,可能会改善长期的神经系统结果,进一步的研究应评估及时接受吡哆醇治疗的PDE新生儿的结局。
    BACKGROUND: The main objective of this study was to evaluate the neurological consequences of delayed pyridoxine administration in patients diagnosed with Pyridoxin Dependent Epilepsies (PDE).
    METHODS: We reviewed 29 articles, comprising 52 genetically diagnosed PDE cases, ensuring data homogeneity. Three additional cases were included from the General Pediatric Operative Unit of San Marco Hospital. Data collection considered factors like age at the first seizure\'s onset, EEG reports, genetic analyses, and more. Based on the response to first-line antiseizure medications, patients were categorized into four distinct groups. Follow-up evaluations employed various scales to ascertain neurological, cognitive, and psychomotor developments.
    RESULTS: Our study includes 55 patients (28 males and 27 females), among whom 15 were excluded for the lack of follow-up data. 21 patients were categorized as \"Responder with Relapse\", 11 as \"Resistant\", 6 as \"Pyridoxine First Approach\", and 2 as \"Responders\". The neurological outcome revealed 37,5 % with no neurological effects, 37,5 % showed complications in two developmental areas, 15 % in one, and 10 % in all areas. The statistical analysis highlighted a positive correlation between the time elapsed from the administration of pyridoxine after the first seizure and worse neurological outcomes. On the other hand, a significant association was found between an extended latency period (that is, the time that elapsed between the onset of the first seizure and its recurrence) and worse neurological outcomes in patients who received an unfavorable score on the neurological evaluation noted in a subsequent follow-up.
    CONCLUSIONS: The study highlights the importance of early recognition and intervention in PDE. Existing medical protocols frequently overlook the timely diagnosis of PDE. Immediate administration of pyridoxine, guided by a swift diagnosis in the presence of typical symptoms, might improve long-term neurological outcomes, and further studies should evaluate the outcome of PDE neonates promptly treated with Pyridoxine.
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  • 文章类型: Journal Article
    本研究的目的是探讨牙周皮瓣手术后补充维生素B复合物对临床和微生物学参数的影响。
    对10例牙周炎患者进行分口设计的随机对照试验,以发现补充维生素B复合物并进行开放皮瓣清创对牙周伤口愈合的影响。在第0天和第90天使用龈下菌斑样品进行连翘单菌和牙龈卟啉单胞菌的多重聚合酶链反应(PCR)。
    结果显示临床(菌斑指数,牙龈指数,牙龈出血指数,探测袋深度,和相对附着水平)和两个治疗组的微生物概况,而在群体间分析中,在试验组中观察到所有临床参数的减少更多,但统计上,结果微不足道。
    UNASSIGNED: The purpose of this study is to explore the effect of vitamin B complex supplementation following periodontal flap surgery on clinical and microbiological parameters.
    UNASSIGNED: A randomized controlled trial on 10 patients with periodontitis in split-mouth design was undertaken to find the effect of vitamin B complex supplementation with open flap debridement on periodontal wound healing. Multiplex polymerase chain reaction (PCR) for Tannerella forsythus and Porphyromonas gingivalis was done using subgingival plaque samples at 0 and 90th day.
    UNASSIGNED: The results showed a significant reduction (P < 0.01) of clinical (plaque index, gingival index, gingival bleeding index, probing pocket depth, and relative attachment level) and microbial profile in both treatment groups, whereas on intergroup analysis, more reduction in all clinical parameters were observed in the test group, but statistically, the results were insignificant.
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  • 文章类型: Journal Article
    该研究旨在了解Chhukha一所中心学校的寄宿学生中发生的舌炎的原因,不丹,以及用复合维生素B片治疗15天后的结果。
    研究人员从2020年9月30日至2020年10月30日在寄宿学校接受舌炎治疗的患者的治疗记录中提取数据,并进行了回顾性描述性研究。研究中总共使用了97条记录:年龄,性别,向学校报告的日期,治疗,饮食偏好,和治疗结果。
    总之,63例(64.9%)患者为女性。在宿舍逗留时间较长的学生在患者中所占比例更高。用两剂一片复合维生素B片治疗15天后,约80%的患者主观改善。没有死亡。
    该研究无法确定寄宿学生舌炎的确切原因,但每天服用两剂32.5mg复合维生素B片剂后,80%的患者表现出主观改善。该研究建议进行前瞻性研究,以了解寄宿学生中舌炎的原因,以防止类似的未来爆发。
    UNASSIGNED: The study aimed to understand the cause of glossitis that occurred among boarding students in a central school in Chhukha, Bhutan, and the outcome after 15 days of treatment with a vitamin B complex tablet.
    UNASSIGNED: The researcher extracted data from the treatment records of patients treated for glossitis from 30 September 2020 to 30 October 2020 at the boarding school and conducted a retrospective descriptive study. A total of 97 records were used in the study: the age, gender,date of reporting to school, treatment, dietary preferences, and outcome of treatment.
    UNASSIGNED: In all, 63 (64.9%) patients were females. The students who were staying in the hostel for longer duration were more in proportion among the patients. About 80% of the patients had subjective improvement after treatment with two doses of one tablet of vitamin B complex tablet for 15 days. There were no deaths.
    UNASSIGNED: The study could not ascertain the definite cause of glossitis among boarding students but 80 % of the patients showed subjective improvement after treatment with daily two doses of 32.5 mg of vitamin B complex tablet. The study recommends a prospective study to understand the cause of glossitis among boarding students to prevent similar future outbreaks.
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  • 文章类型: Journal Article
    目的:目的是研究儿童饮食摄入B族维生素与10岁时胰岛自身免疫(IA)和1型糖尿病(T1D)进展风险之间的关系。
    方法:我们追踪了8500名在美国出生的T1D易感儿童,芬兰,瑞典,和德国在2004-2010年从Young糖尿病的环境决定因素(TEDDY)研究中,这是一个前瞻性观察出生队列。根据3个月时的24小时召回和6个月至10岁定期收集的3天食物记录,从食物和膳食补充剂中计算出7种B族维生素的饮食摄入量。Cox比例风险模型进行了能量调整,HLA基因型,与T1D的一级相对,性别,和国家。
    结果:共有778(9.2)名儿童出现了至少一种自身抗体(任何IA),335(3.9%)产生了多种自身抗体。280名(3.3%)儿童将IAA和319名(3.8%)GADA作为第一自身抗体。344名(44%)IA儿童进展为T1D。我们观察到,烟酸摄入量较高与每1mg/1000kcal摄入烟酸产生多种自身抗体(HR0.95;95%CI0.92,0.98)的风险降低相关。吡哆醇(HR0.66;95%CI0.46,0.96)和维生素B12(HR0.87;95%CI0.77,0.97)的较高摄入量与IAA首次自身免疫风险降低相关。较高的核黄素摄入量(HR1.38;95%CI1.05,1.80)与GADA-first自身免疫风险增加相关。任何B族维生素与结果“任何IA”和从IA到T1D的进展之间没有关联。结论:在这个跨国公司中,具有T1D遗传易感性的儿童的前瞻性出生队列,我们观察到不同B族维生素与IA风险之间存在一些正相关和负相关。
    OBJECTIVE: The aim was to study the association between dietary intake of B vitamins in childhood and the risk of islet autoimmunity (IA) and progression to type 1 diabetes (T1D) by the age of 10 years.
    METHODS: We followed 8500 T1D-susceptible children born in the U.S., Finland, Sweden, and Germany in 2004 -2010 from the Environmental Determinants of Diabetes in the Young (TEDDY) study, which is a prospective observational birth cohort. Dietary intake of seven B vitamins was calculated from foods and dietary supplements based on 24-h recall at 3 months and 3-day food records collected regularly from 6 months to 10 years of age. Cox proportional hazard models were adjusted for energy, HLA-genotype, first-degree relative with T1D, sex, and country.
    RESULTS: A total of 778 (9.2) children developed at least one autoantibody (any IA), and 335 (3.9%) developed multiple autoantibodies. 280 (3.3%) children had IAA and 319 (3.8%) GADA as the first autoantibody. 344 (44%) children with IA progressed to T1D. We observed that higher intake of niacin was associated with a decreased risk of developing multiple autoantibodies (HR 0.95; 95% CI 0.92, 0.98) per 1 mg/1000 kcal in niacin intake. Higher intake of pyridoxine (HR 0.66; 95% CI 0.46, 0.96) and vitamin B12 (HR 0.87; 95% CI 0.77, 0.97) was associated with a decreased risk of IAA-first autoimmunity. Higher intake of riboflavin (HR 1.38; 95% CI 1.05, 1.80) was associated with an increased risk of GADA-first autoimmunity. There were no associations between any of the B vitamins and the outcomes \"any IA\" and progression from IA to T1D.  CONCLUSION: In this multinational, prospective birth cohort of children with genetic susceptibility to T1D, we observed some direct and inverse associations between different B vitamins and risk of IA.
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  • 文章类型: Journal Article
    目的:在高风险环境中,基于对治疗性硫胺素的反应,建立有硫胺素缺乏症(TDD)体征或症状的住院婴幼儿的硫胺素反应性疾病(TRD)的预测模型。
    方法:在老挝北部地区住院的21天至<18个月有症状或体征提示TDD的儿童,除常规护理外,接受肠外硫胺素(每天100mg)治疗≥3天。开始硫胺素后72小时,经常进行身体检查和恢复评估。个别病例报告由三名指定TRD状态(TRD或非TRD)的儿科医生独立审查,它在逻辑回归模型中用作因变量,以确定TRD的预测因子。模型性能通过接收器工作特征曲线下的经验面积(AUROC)量化。
    结果:449名儿童(中位[Q1,Q3]2.9[1.7,5.7]个月;70.3%完全/主要是母乳喂养)入选;60.8%患有TRD。在52个候选变量中,最能预测TRD的是纯母乳喂养/主要母乳喂养,声音嘶哑/失去声音,紫癜,在过去的2周内没有眼睛接触和腹泻。AUROC(95%CI)为0.82(0.78,0.86)。
    结论:在这项研究中,大多数有TDD体征或症状的儿童对硫胺素反应良好.虽然有五个特定特征可以预测TRD,TRD的高患病率提示,在类似高危环境中,所有出现与TDD一致的体征或症状的婴儿和儿童均应服用硫胺素.预测模型在其他情况下的有用性值得进一步探索和完善。
    OBJECTIVE: To develop a predictive model for thiamine responsive disorders (TRDs) among infants and young children hospitalized with signs or symptoms suggestive of thiamine deficiency disorders (TDDs) based on response to therapeutic thiamine in a high-risk setting.
    METHODS: Children aged 21 days to <18 months hospitalized with signs or symptoms suggestive of TDD in northern Lao People\'s Democratic Republic were treated with parenteral thiamine (100 mg daily) for ≥3 days in addition to routine care. Physical examinations and recovery assessments were conducted frequently for 72 hours after thiamine was initiated. Individual case reports were independently reviewed by three pediatricians who assigned a TRD status (TRD or non-TRD), which served as the dependent variable in logistic regression models to identify predictors of TRD. Model performance was quantified by empirical area under the receiver operating characteristic curve.
    RESULTS: A total of 449 children (median [Q1, Q3] 2.9 [1.7, 5.7] months old; 70.3% exclusively/predominantly breastfed) were enrolled; 60.8% had a TRD. Among 52 candidate variables, those most predictive of TRD were exclusive/predominant breastfeeding, hoarse voice/loss of voice, cyanosis, no eye contact, and no diarrhea in the previous 2 weeks. The area under the receiver operating characteristic curve (95% CI) was 0.82 (0.78, 0.86).
    CONCLUSIONS: In this study, the majority of children with signs or symptoms of TDD responded favorably to thiamine. While five specific features were predictive of TRD, the high prevalence of TRD suggests that thiamine should be administered to all infants and children presenting with any signs or symptoms consistent with TDD in similar high-risk settings. The usefulness of the predictive model in other contexts warrants further exploration and refinement.
    BACKGROUND: Clinicaltrials.gov NCT03626337.
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