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Calibration of 24-h urinary sodium excretion estimates from fasting morning urine in Chinese populations: a comparative analysis of 2 calibration models and a locally developed model. 校准中国人群空腹晨尿中 24 小时尿钠排泄量的估计值:两种校准模型与本地开发模型的比较分析》。
IF 6.5 1区 医学 Q1 NUTRITION & DIETETICS Pub Date : 2024-10-01 Epub Date: 2024-08-13 DOI: 10.1016/j.ajcnut.2024.08.007
Xiaofu Du, Jing Guo, Xiangyu Chen, Jie Zhang, Feng Lu, Jieming Zhong

Background: Spot urine collection offers a convenient alternative to the more cumbersome 24-h urine collection. However, the widely recognized estimation models, such as Tanaka and International Cooperative Study on Salt, Other Factors, and Blood Pressure (INTERSALT), have not been adequately adapted for widespread use in the general Chinese population.

Objectives: This study was designed to evaluate the precision of the Tanaka and INTERSALT calibration models, alongside a locally Zhejiang Province-formulated model, in predicting 24-h urinary sodium (24-hUNa) excretion among the Chinese population.

Methods: The study comprised 1424 participants, aged 18-69 y, who provided both comprehensive 24-h urine and fasting morning urine samples. The researchers assessed the accuracy of the measured 24-hUNa against the estimates obtained from the Tanaka, INTERSALT, and Zhejiang models. This evaluation was conducted at both population and individual levels, employing a range of statistical techniques, including bias analysis, correlation coefficients, intraclass correlation coefficients, receiver operating characteristic curves, Bland-Altman plots, as well as relative and absolute difference calculations, and misclassification rates.

Results: The measured average 24-hUNa excretion was found to be 165.7 ± 71.5 mmol/24-h. Notably, there was a significant deviation between the estimated and measured values for the Tanaka-adjusted model [-11.7 mmol, 95% confidence interval (CI): -16.7, -6.7 mmol/24-h], indicating a statistically significant difference. In contrast, the deviations for the INTERSALT-adjusted model (0.6 mmol, 95% CI: -4.2, 5.4 mmol/24-h) and the Zhejiang model (0.2 mmol, 95% CI: -4.6, 5.0 mmol/24-h) were nonsignificant. The correlation coefficients for the models were 0.303, 0.398, and 0.391, respectively, with the INTERSALT-adjusted and Zhejiang models showing superior performance at the population level.

Conclusions: The 3 evaluation models may serve as effective, low-burden alternatives for assessing urinary sodium levels in the population. However, to enhance the accuracy and reliability of predictions at the individual level, further repeated measurements are necessary to minimize measurement errors and augment the validity of the estimations.

背景:相对于繁琐的 24 小时尿液采集,定点尿液采集是一种便捷的替代方法。然而,被广泛认可的估算模型,如田中模型和 INTERSALT 模型,还没有被充分调整以在中国普通人群中广泛使用:本研究旨在评估田中和 INTERSALT 校准模型以及浙江省本地制定的模型在预测中国人群 24 小时尿钠(24-hUNa)排泄量方面的精确度:研究对象包括 1424 名 18 至 69 岁的参与者,他们提供了 24 小时尿液和空腹晨尿的综合样本。研究人员对照田中模型、INTERSALT 模型和浙江模型得出的估计值,评估了所测得的 24-hUNa 的准确性。评估在人群和个体两个层面进行,采用了一系列统计技术,包括偏差分析、相关系数、类内相关系数(ICC)、接收者操作特征曲线(ROC)、布兰登-阿尔特曼图、相对和绝对差异计算以及误分类率:测得的 24 小时平均UNa排泄量为 165.7 ± 71.5 mmol/24小时。值得注意的是,塔纳卡调整模型的估计值与测量值之间存在显著偏差(-11.7 毫摩尔,95% 置信区间(CI):-16.7,-6.7 毫摩尔/24 小时),表明两者之间存在显著的统计学差异。相比之下,INTERSALT 调整模型(0.6 毫摩尔,95% 置信区间:-4.2,5.4 毫摩尔/24 小时)和浙江模型(0.2 毫摩尔,95% 置信区间:-4.6,5.0 毫摩尔/24 小时)的偏差不显著。模型的相关系数分别为 0.303、0.398 和 0.391,INTERSALT 调整模型和浙江模型在人群水平上表现更优:结论:这三种评估模型可作为评估人群尿钠水平的有效、低负担的替代方法。然而,为了提高个体水平预测的准确性和可靠性,有必要进行进一步的重复测量,以尽量减少测量误差并提高估算的有效性。
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引用次数: 0
Effects of prenatal small-quantity lipid-based nutrient supplements on pregnancy, birth, and infant outcomes: a systematic review and meta-analysis of individual participant data from randomized controlled trials in low- and middle-income countries. 产前小剂量脂质营养补充剂对妊娠、分娩和婴儿结局的影响:对中低收入国家随机对照试验中个体参与者数据的系统回顾和荟萃分析。
IF 6.5 1区 医学 Q1 NUTRITION & DIETETICS Pub Date : 2024-10-01 Epub Date: 2024-08-16 DOI: 10.1016/j.ajcnut.2024.08.008
Kathryn G Dewey, K Ryan Wessells, Charles D Arnold, Seth Adu-Afarwuah, Benjamin F Arnold, Per Ashorn, Ulla Ashorn, Ana Garcés, Lieven Huybregts, Nancy F Krebs, Anna Lartey, Jef L Leroy, Kenneth Maleta, Susana L Matias, Sophie E Moore, Malay K Mridha, Harriet Okronipa, Christine P Stewart

Background: Undernutrition during pregnancy increases the risk of giving birth to a small vulnerable newborn. Small-quantity lipid-based nutrient supplements (SQ-LNSs) contain both macro- and micronutrients and can help prevent multiple nutritional deficiencies.

Objectives: We examined the effects of SQ-LNSs provided during pregnancy compared with 1) iron and folic acid or standard of care (IFA/SOC) or 2) multiple micronutrient supplements (MMSs) and identified characteristics that modified the estimates of effects of SQ-LNSs on birth outcomes.

Methods: We conducted a 2-stage meta-analysis of individual participant data from 4 randomized controlled trials of SQ-LNSs provided during pregnancy (n = 5273). We generated study-specific and subgroup estimates of SQ-LNS compared with IFA/SOC or MMS and pooled the estimates. In sensitivity analyses, we examined whether the results differed depending on methods for gestational age dating, birth anthropometry, or study design.

Results: SQ-LNSs (compared with IFA/SOC) increased birth weight [mean difference: +49 g; 95% confidence interval (CI): 26, 71 g] and all birth anthropometric z-scores (+0.10-0.13 standard deviation); they reduced risk of low birth weight by 11%, newborn stunting by 17%, newborn wasting by 11%, and small head size by 15%. Only 2 trials compared SQ-LNSs and MMSs; P values for birth outcomes were >0.10 except for head circumference (e.g., z-score for gestational age: +0.11; 95% CI: -0.01, 0.23). Effect estimates for SQ-LNSs compared with IFA/SOC were greater among female infants and, for certain outcomes, among mothers with body mass index <20 kg/m2, inflammation, malaria, or household food insecurity. Effect estimates for SQ-LNSs compared with MMSs were greater for certain outcomes among female infants, first-born infants, and mothers <25 y.

Conclusions: SQ-LNSs had positive impacts on multiple outcomes compared to IFA/SOC, but further research directly comparing SQ-LNSs and MMSs is needed. Targeting SQ-LNSs to vulnerable subgroups may be worth considering.

Clinical trial registry: This study was registered at PROSPERO as CRD42021283391.

背景:孕期营养不良会增加产下弱小新生儿的风险。小量脂质营养补充剂(SQ-LNS)含有宏量和微量营养素,有助于预防多种营养缺乏症:我们研究了孕期提供的 SQ-LNS 与 a) 铁和叶酸或标准护理(IFA/SOC)或 b) 多种微量营养素补充剂(MMS)相比的效果,并确定了改变 SQ-LNS 对出生结果影响估计值的特征:我们对孕期提供 SQ-LNS 的 4 项随机对照试验(n = 5273)中的个体参与者数据进行了两阶段荟萃分析。我们得出了 SQ-LNS 与 IFA/SOC 或 MMS 相比的特定研究和亚组估计值,并对这些估计值进行了汇总。在敏感性分析中,我们研究了孕龄测定方法、出生人体测量或研究设计是否会导致结果不同:SQ-LNS(vs IFA/SOC)增加了出生体重(平均差异:+49g;95% CI:26, 71g)和所有出生人体测量Z值(+0.10-0.13 SD);降低了11%的低出生体重风险、17%的新生儿发育迟缓风险、11%的新生儿消瘦风险和15%的小头风险。只有 2 项试验对 SQ-LNS 和 MMS 进行了比较;除头围外,其他出生结局的 p 值均大于 0.10(例如,胎龄 Z 值 +0.11;95% CI:-0.01,0.23)。在女婴中,SQ-LNS 与 IFA/SOC 的效应估计值更大,在某些结果中,体重指数小于 20 kg/m2、患有炎症、疟疾或家庭粮食不安全的母亲的效应估计值更大。就某些结果而言,SQ-LNS 与 MMS 对女婴、头胎婴儿和年龄小于 25 岁的母亲的影响估计值更大:结论:与 IFA/SOC 相比,SQ-LNS 对多种结果都有积极影响,但还需要进一步研究直接比较 SQ-LNS 和 MMS。将 SQ-LNS 用于弱势亚群可能值得考虑。分析结果已登录 www.crd.york.ac.uk/PROSPERO (CRD42021283391)。系统综述或荟萃分析的注册表和注册号:于 2021 年 4 月 11 日在 www.crd.york.ac.uk/PROSPERO 注册为 CRD42021283391。
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引用次数: 0
Diet order significantly affects energy balance for diets varying in macronutrients but not ultraprocessing in crossover studies without a washout period. 在无冲淡期的交叉研究中,饮食顺序会显著影响宏量营养素不同的饮食的能量平衡,但不会影响超加工饮食的能量平衡。
IF 6.5 1区 医学 Q1 NUTRITION & DIETETICS Pub Date : 2024-10-01 Epub Date: 2024-08-18 DOI: 10.1016/j.ajcnut.2024.08.013
Christina M Sciarrillo, Juen Guo, Aaron Hengist, Valerie L Darcey, Kevin D Hall

Background: Crossover studies can induce order effects, especially when they lack a washout period.

Objectives: We performed secondary analyses comparing groups of subjects randomly assigned to different diet orders in 2 inpatient crossover studies originally designed to compare within-subject differences in ad libitum energy intake. One study compared minimally processed low-carbohydrate (LC) compared with low-fat (LF) diets, and the other matched macronutrients and compared minimally processed food (MPF) with ultraprocessed food (UPF) diets.

Methods: Diet order group comparisons of changes in body weight and body composition, and differences in energy expenditure and food intake were assessed over 4 wk in 20 adults randomly assigned to either the LC followed immediately by the LF diet (LC → LF) or the opposite order (LF → LC), and 20 adults randomly assigned to either the MPF followed by the UPF (MPF → UPF) diets or the opposite order (UPF → MPF).

Results: Subjects randomly assigned to LC → LF lost 2.9 ± 1.1 kg more body weight (P <0.001) and 1.5 ± 0.6 kg more body fat (P = 0.03) than the LF → LC group, likely because the LC → LF group consumed 921 ± 304 kcal/d less than the LF → LC group (P = 0.003). These energy intake differences were driven by the last 2 wk (-1610 ± 312 kcal/d; P < 0.0001), perhaps because of carryover effects of gut adaptations during the first 2 wk arising from large differences in the mass of food (1296 ± 215 g/d; P <0.00001) and fiber consumed (58 ± 6 g/d; P <0.00001). There were no significant diet order effects on energy intake, body weight, or body composition changes between UPF → MPF and MPF → UPF groups.

Conclusions: Diet order significantly affected energy intake, body weight, and body fat in a 4-wk crossover inpatient diet study varying in macronutrients, but not in a similarly structured study varying in ultraprocessed foods. This trial was registered at clinicaltrials.gov as NCT03407053 and NCT03878108.

背景:交叉研究可能会产生顺序效应,尤其是在缺乏冲淡期的情况下:我们对两项住院病人交叉研究中被随机分配到不同饮食顺序的受试者群体进行了二次分析比较,这两项研究的初衷是比较受试者自由摄入能量的内部差异。其中一项研究比较了低碳水化合物(LC)和低脂肪(LF)饮食的微量加工饮食,另一项研究匹配了宏量营养素,并比较了微量加工食品(MPF)和超量加工食品(UPF)饮食:方法:对20名成人进行为期四周的体重和身体成分变化以及能量消耗和食物摄入差异的饮食顺序分组比较,这些成人被随机分配为先低脂饮食后低脂饮食(LC→LF)或相反顺序(LF→LC),以及20名成人被随机分配为先MPF后UPF(MPF→UPF)或相反顺序(UPF→MPF):与 LF→LC 组相比,随机采用 LC→LF 的受试者体重减少了 2.9 ± 1.1 千克(p < 0.001),体脂减少了 1.5 ± 0.6 千克(p = 0.03),这可能是因为 LC→LF 组比 LF→LC 组每天少摄入 921 ± 304 千卡(p = 0.003)。这些能量摄入差异是由最后两周造成的(-1610 ± 312 kcal/d;p < 0.0001),这可能是由于前两周食物量(1296 ± 215 g/d;p < 0.00001)和纤维摄入量(58 ± 6 g/d;p < 0.00001)的巨大差异导致的肠道适应性的延续效应。UPF→MPF组与MPF→UPF组之间的能量摄入、体重或身体成分变化没有明显的饮食顺序影响:在一项为期 4 周的住院病人交叉饮食研究中,饮食顺序对能量摄入、体重和体脂有明显影响,但在一项结构类似的研究中,饮食顺序对超标加工食品的影响不大:临床试验注册:NCT03407053 和 NCT03878108。
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引用次数: 0
Cardiovascular health, polygenic risk score, and cancer risk: a prospective cohort study. 心血管健康、多基因风险评分和癌症风险:一项前瞻性队列研究。
IF 6.5 1区 医学 Q1 NUTRITION & DIETETICS Pub Date : 2024-10-01 Epub Date: 2024-08-10 DOI: 10.1016/j.ajcnut.2024.07.033
Yu Peng, Peng Wang, Han Du, Fubin Liu, Xixuan Wang, Changyu Si, Jianxiao Gong, Huijun Zhou, Kexin Chen, Fangfang Song

Background: Cancer and cardiovascular disease share common lifestyle risk factors. However, it remains unclear whether cardiovascular health (CVH) evaluated by Life's Essential 8 can predict cancer risk, and attenuate the influence of genetic susceptibility on cancer.

Objectives: We aimed to evaluate independent and joint associations of CVH and polygenic risk score (PRS) with risks of overall and site-specific cancers.

Methods: We undertook a population-based cohort study based on the UK Biobank. The CVH score was constructed by physical activity, body mass index, nicotine exposure, sleep, diet, blood pressure, lipid profile, and blood glucose. PRSs were assessed individually for 18 cancer types by their independent single-nucleotide polymorphisms previously identified in genome-wide association studies. Multivariable Cox proportional-hazards models were applied to explore the independent and joint associations of CVH and PRS with cancer incidence risk. The results were displayed as hazard ratio (HR) and 95% confidence interval (CI).

Results: Compared with low CVH, high CVH was associated with decreased risks of overall cancer and the majority of common cancers, including digestive system [HRs (95% CI): 0.33 (0.23, 0.45)-0.66 (0.58, 0.75)], lung (HR: 0.25; 95% CI: 0.21, 0.31), renal (HR: 0.42; 95% CI: 0.32, 0.56), bladder (HR: 0.55; 95% CI: 0.44, 0.69), breast (HR: 0.83; 95% CI: 0.74, 0.92), and endometrial cancers (HR: 0.39; 95% CI: 0.30, 0.51). For overall cancer in males, there was an interaction between CVH and PRS. Notably, individuals with high CVH across all levels of PRS had lower risks of overall cancer for females and 8 site-specific cancers than those with low CVH and high PRS [HRs (95% CIs): 0.18 (0.12, 0.25)-0.79 (0.71, 0.87)].

Conclusions: High CVH was related to decreased risks of overall cancer and multiple cancers regardless of genetic predispositions. Our findings underscored the value of improving CVH for cancer prevention in the general population.

背景:癌症和心血管疾病有着共同的生活方式风险因素。然而,通过 "生活必备 8 要素 "评估心血管健康(CVH)是否能预测癌症风险并减轻遗传易感性对癌症的影响仍不清楚:我们旨在评估 CVH 和多基因风险评分(PRS)与总体癌症和特定部位癌症风险的独立和联合关联:我们在英国生物库的基础上开展了一项基于人群的队列研究。CVH评分由体力活动、体重指数、尼古丁暴露、睡眠、饮食、血压、血脂和血糖构成。通过先前在全基因组关联研究中报告的独立单核苷酸多态性,对 18 种癌症类型的 PRSs 进行了单独评估。应用多变量 Cox 比例危险度模型探讨了 CVH 和 PRS 与癌症发病风险的独立和联合关联。结果显示为危险比(HR)和95%置信区间(CI):结果:与低 CVH 相比,高 CVH 与总体癌症和大多数常见癌症的发病风险降低相关,包括消化系统癌症[HRs (95% CI):0.33 (0.23, 0.45)-0.66 (0.58, 0.75)]、肺癌[HRs (95% CI):0.25(0.21,0.31)]、肾癌[HR(95% CI):0.42(0.32,0.56)]、膀胱癌[HR(95% CI):0.55(0.44,0.69)]、乳腺癌[HR(95% CI):0.83(0.74,0.92)]和子宫内膜癌[HR(95% CI):0.39(0.30,0.51)]。就男性总体癌症而言,CVH 与 PRS 之间存在交互作用。值得注意的是,与低 CVH 和高 PRS 的个体相比,在所有 PRS 水平上,高 CVH 的个体罹患女性总体癌症和八种特定部位癌症的风险较低[HRs (95%CIs): 0.18 (0.12, 0.25)-0.79 (0.71, 0.87)]:高CVH与总体癌症和多种癌症风险的降低有关,与遗传倾向无关。我们的研究结果强调了提高 CVH 对预防普通人群癌症的价值。
{"title":"Cardiovascular health, polygenic risk score, and cancer risk: a prospective cohort study.","authors":"Yu Peng, Peng Wang, Han Du, Fubin Liu, Xixuan Wang, Changyu Si, Jianxiao Gong, Huijun Zhou, Kexin Chen, Fangfang Song","doi":"10.1016/j.ajcnut.2024.07.033","DOIUrl":"10.1016/j.ajcnut.2024.07.033","url":null,"abstract":"<p><strong>Background: </strong>Cancer and cardiovascular disease share common lifestyle risk factors. However, it remains unclear whether cardiovascular health (CVH) evaluated by Life's Essential 8 can predict cancer risk, and attenuate the influence of genetic susceptibility on cancer.</p><p><strong>Objectives: </strong>We aimed to evaluate independent and joint associations of CVH and polygenic risk score (PRS) with risks of overall and site-specific cancers.</p><p><strong>Methods: </strong>We undertook a population-based cohort study based on the UK Biobank. The CVH score was constructed by physical activity, body mass index, nicotine exposure, sleep, diet, blood pressure, lipid profile, and blood glucose. PRSs were assessed individually for 18 cancer types by their independent single-nucleotide polymorphisms previously identified in genome-wide association studies. Multivariable Cox proportional-hazards models were applied to explore the independent and joint associations of CVH and PRS with cancer incidence risk. The results were displayed as hazard ratio (HR) and 95% confidence interval (CI).</p><p><strong>Results: </strong>Compared with low CVH, high CVH was associated with decreased risks of overall cancer and the majority of common cancers, including digestive system [HRs (95% CI): 0.33 (0.23, 0.45)-0.66 (0.58, 0.75)], lung (HR: 0.25; 95% CI: 0.21, 0.31), renal (HR: 0.42; 95% CI: 0.32, 0.56), bladder (HR: 0.55; 95% CI: 0.44, 0.69), breast (HR: 0.83; 95% CI: 0.74, 0.92), and endometrial cancers (HR: 0.39; 95% CI: 0.30, 0.51). For overall cancer in males, there was an interaction between CVH and PRS. Notably, individuals with high CVH across all levels of PRS had lower risks of overall cancer for females and 8 site-specific cancers than those with low CVH and high PRS [HRs (95% CIs): 0.18 (0.12, 0.25)-0.79 (0.71, 0.87)].</p><p><strong>Conclusions: </strong>High CVH was related to decreased risks of overall cancer and multiple cancers regardless of genetic predispositions. Our findings underscored the value of improving CVH for cancer prevention in the general population.</p>","PeriodicalId":50813,"journal":{"name":"American Journal of Clinical Nutrition","volume":null,"pages":null},"PeriodicalIF":6.5,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141972290","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Navigating complex nutritional challenges after bariatric surgery: malnutrition, multiple nutrient deficiencies, and gastrointestinal dysfunction in pregnancy. 应对减肥手术后的复杂营养挑战:妊娠期营养不良、多种营养缺乏和胃肠功能紊乱。
IF 6.5 1区 医学 Q1 NUTRITION & DIETETICS Pub Date : 2024-10-01 Epub Date: 2024-08-05 DOI: 10.1016/j.ajcnut.2024.07.027
Leen Z Hasan, David S Seres
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引用次数: 0
Plasma n6 polyunsaturated fatty acid levels and risk for total and cause-specific mortality: A prospective observational study from the UK Biobank. 血浆 n6 多不饱和脂肪酸水平与总死亡率和特定原因死亡率的风险:一项来自英国生物库的前瞻性观察研究。
IF 6.5 1区 医学 Q1 NUTRITION & DIETETICS Pub Date : 2024-10-01 Epub Date: 2024-08-22 DOI: 10.1016/j.ajcnut.2024.08.020
William S Harris, Jason Westra, Nathan L Tintle, Aleix Sala-Vila, Jason Hy Wu, Matti Marklund

Background: The potential role of n-6 PUFAs in major health outcomes remains controversial.

Objectives: To examine the relationship between the major plasma n6 PUFA, linoleic acid (LA), as well as the non-LA n6 PUFAs, and total and cause-specific mortality.

Methods: This was a prospective, observational, biomarker-based study in the UK Biobank. Individuals with complete information on baseline demographic, covariate and plasma PUFA levels (percent ot total fatty acids) and mortality outcomes were included (n=257,925). Multivariable-adjusted, Cox-proportional hazards models were used to predict risk of death from all-causes, and from cardiovascular disease (CVD), cancer, and other causes as a function of plasma LA and non-LA n6 levels, both continuously and by PUFA quintile (Q).

Results: Comparing LA Q5 to Q1, the hazard ratio (HR, 95% CI) for total mortality was 0.80 (0.76, 0.84; p<0.001), and this was similar for all three cause-specific death categories. On the other hand, mortality HR for non-LA n6 was 1.12 (1.08,1.17; p<0.001), and this was primarily due to increased risk for non-CVD, noncancer deaths [HR 1.29 (1.19,1.40; p<0.001)]. Exploratory analyses among the eight next most common other causes of death suggested that both the decreased risk associated with higher LA and the increased risk associated with non-LA n6 were confined to deaths from respiratory and digestive diseases.

Conclusions: These findings highlight the profound differences in mortality risk related to LA and non-LA n6 PUFA levels and underscore the inappropriateness of treating n-6 PUFAs as a homogenous class with respect to health outcomes. They also support recommendations to maintain (if not increase) current LA intakes.

目的研究血浆中主要的 n6 PUFA--亚油酸(LA)以及非 n6 PUFA--亚油酸与总死亡率和特定病因死亡率之间的关系:前瞻性、观察性、基于生物标志物的研究:参与者研究对象:具有完整基线人口统计学信息、协变量和血浆 PUFA 水平以及死亡率结果的个体(n=257,925):方法: 使用多变量调整的 Cox 比例危险模型预测所有原因的死亡风险,以及心血管疾病(CVD)、癌症和其他原因的死亡风险,并将其作为血浆 LA 和非 LA n6 水平的函数,既连续预测,也按 PUFA 五分位数(Q)预测:结果:将 LA Q5 与 Q1 相比较,总死亡率的危险比(HR,95% CI)为 0.80(0.76,0.84;p结论:这些研究结果突显了健康状况的深刻差异:这些研究结果突显了与 LA 和非 LA n6 PUFA 水平相关的健康相关结果的巨大差异,并强调了在健康结果方面将 n-6 PUFA 作为同质类别处理是不恰当的。这些研究还支持维持(如果不是增加)当前 LA 摄入量的建议。
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引用次数: 0
Food is Medicine National Summit: Transforming Health Care. 食物即药物全国峰会:转变医疗保健。
IF 6.5 1区 医学 Q1 NUTRITION & DIETETICS Pub Date : 2024-10-01 DOI: 10.1016/j.ajcnut.2024.09.027
Ronit A Ridberg, Melissa Maitin-Shepard, Katie Garfield, Hilary K Seligman, Pamela M Schwartz, Jean Terranova, Amy L Yaroch, Dariush Mozaffarian

Food Is Medicine (FIM) interventions reflect the critical links between food security, nutrition security, health, and health equity, integrated into health care delivery. They comprise programs that provide nutritionally-tailored food, free of charge or at a discount, to support disease management, disease prevention, or optimal health, linked to the health care system as part of a patient's treatment plan. Such programs often prioritize health equity. On April 26-27, 2023, Tufts University's Gerald J. and Dorothy R. Friedman School of Nutrition Science and Policy and Food & Nutrition Innovation Institute held a two-day National Food is Medicine Summit with leaders, practitioners, and individuals with diverse lived experiences in health care, research, government, advocacy, philanthropy, and the private sector to identify challenges and opportunities to sustainably incorporate FIM services into the health care system and at scale. This report of a meeting describes key themes of the Summit, based on presentations and discussions on momentum around FIM, incorporating FIM in health care, tradeoffs and unintended consequences of various FIM models, scaling of programs, financing and payment mechanisms, educating and engaging the health care workforce, and federal and state government actions and opportunities on FIM. Speakers highlighted examples of recent public and private sector actions on FIM and innovative cross-sector partnerships, including state Medicaid waivers, academic and philanthropic research initiatives, health care system screenings and interventions, and collaborations including community-based organizations and/or entities outside of the food and health care sectors. Challenges and opportunities to broader implementation and scaling of FIM programs identified include incorporating FIM into health care business models, educating the health care workforce, and sustainably scaling FIM programs while leveraging the local connections of community-based organizations. This meeting report highlights recent advances, best practices, challenges, and opportunities discussed at the National Summit to inform future actions on FIM.

食品是药(FIM)干预措施反映了食品安全、营养安全、健康和健康公平之间的重要联系,并与医疗保健服务相结合。它们包括免费或以折扣价提供营养定制食品的计划,以支持疾病管理、疾病预防或最佳健康,并作为病人治疗计划的一部分与医疗保健系统联系起来。此类计划通常优先考虑健康公平。2023 年 4 月 26-27 日,塔夫茨大学杰拉尔德-弗里德曼(Gerald J. and Dorothy R. Friedman)营养科学与政策学院和食品与营养创新研究所举办了为期两天的全国 "食品即医学 "峰会,来自医疗保健、研究、政府、宣传、慈善事业和私营部门的领导者、从业人员和具有不同生活经历的个人参加了此次峰会,共同探讨将 "食品即医学 "服务可持续地纳入医疗保健系统并扩大其规模所面临的挑战和机遇。本会议报告介绍了本次峰会的主要议题,这些议题基于以下方面的演讲和讨论:围绕家庭综合管理的发展势头、将家庭综合管理纳入医疗保健、各种家庭综合管理模式的权衡和意外后果、项目的规模、融资和支付机制、教育和吸引医疗保健队伍,以及联邦和州政府在家庭综合管理方面的行动和机遇。发言者重点介绍了近期公共和私营部门在食品添加剂使用方面的行动以及创新的跨部门合作,包括州医疗补助豁免、学术和慈善研究计划、医疗保健系统筛查和干预,以及包括食品和医疗保健部门以外的社区组织和/或实体在内的合作。在更广泛地实施和推广 FIM 计划方面所面临的挑战和机遇包括:将 FIM 纳入医疗保健业务模式、教育医疗保健人员以及在利用社区组织的地方联系的同时可持续地推广 FIM 计划。本会议报告重点介绍了全国峰会上讨论的最新进展、最佳实践、挑战和机遇,为未来的 FIM 行动提供参考。
{"title":"Food is Medicine National Summit: Transforming Health Care.","authors":"Ronit A Ridberg, Melissa Maitin-Shepard, Katie Garfield, Hilary K Seligman, Pamela M Schwartz, Jean Terranova, Amy L Yaroch, Dariush Mozaffarian","doi":"10.1016/j.ajcnut.2024.09.027","DOIUrl":"https://doi.org/10.1016/j.ajcnut.2024.09.027","url":null,"abstract":"<p><p>Food Is Medicine (FIM) interventions reflect the critical links between food security, nutrition security, health, and health equity, integrated into health care delivery. They comprise programs that provide nutritionally-tailored food, free of charge or at a discount, to support disease management, disease prevention, or optimal health, linked to the health care system as part of a patient's treatment plan. Such programs often prioritize health equity. On April 26-27, 2023, Tufts University's Gerald J. and Dorothy R. Friedman School of Nutrition Science and Policy and Food & Nutrition Innovation Institute held a two-day National Food is Medicine Summit with leaders, practitioners, and individuals with diverse lived experiences in health care, research, government, advocacy, philanthropy, and the private sector to identify challenges and opportunities to sustainably incorporate FIM services into the health care system and at scale. This report of a meeting describes key themes of the Summit, based on presentations and discussions on momentum around FIM, incorporating FIM in health care, tradeoffs and unintended consequences of various FIM models, scaling of programs, financing and payment mechanisms, educating and engaging the health care workforce, and federal and state government actions and opportunities on FIM. Speakers highlighted examples of recent public and private sector actions on FIM and innovative cross-sector partnerships, including state Medicaid waivers, academic and philanthropic research initiatives, health care system screenings and interventions, and collaborations including community-based organizations and/or entities outside of the food and health care sectors. Challenges and opportunities to broader implementation and scaling of FIM programs identified include incorporating FIM into health care business models, educating the health care workforce, and sustainably scaling FIM programs while leveraging the local connections of community-based organizations. This meeting report highlights recent advances, best practices, challenges, and opportunities discussed at the National Summit to inform future actions on FIM.</p>","PeriodicalId":50813,"journal":{"name":"American Journal of Clinical Nutrition","volume":null,"pages":null},"PeriodicalIF":6.5,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142373497","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Beyond isocaloric models: enhancing dietary research for severe liver disease. 超越等热量模型:加强严重肝病的饮食研究。
IF 6.5 1区 医学 Q1 NUTRITION & DIETETICS Pub Date : 2024-10-01 Epub Date: 2024-08-19 DOI: 10.1016/j.ajcnut.2024.06.026
Peng Yang, Zhihui Yang, Zhansheng Yao
{"title":"Beyond isocaloric models: enhancing dietary research for severe liver disease.","authors":"Peng Yang, Zhihui Yang, Zhansheng Yao","doi":"10.1016/j.ajcnut.2024.06.026","DOIUrl":"https://doi.org/10.1016/j.ajcnut.2024.06.026","url":null,"abstract":"","PeriodicalId":50813,"journal":{"name":"American Journal of Clinical Nutrition","volume":null,"pages":null},"PeriodicalIF":6.5,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142373498","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Reply to P Yang et al. 对 P Yang 等人的答复
IF 6.5 1区 医学 Q1 NUTRITION & DIETETICS Pub Date : 2024-10-01 Epub Date: 2024-08-19 DOI: 10.1016/j.ajcnut.2024.07.018
Michael Fridén, Eva Warensjö Lemming, Lars Lind, Johan Vessby, Fredrik Rosqvist, Ulf Risérus
{"title":"Reply to P Yang et al.","authors":"Michael Fridén, Eva Warensjö Lemming, Lars Lind, Johan Vessby, Fredrik Rosqvist, Ulf Risérus","doi":"10.1016/j.ajcnut.2024.07.018","DOIUrl":"https://doi.org/10.1016/j.ajcnut.2024.07.018","url":null,"abstract":"","PeriodicalId":50813,"journal":{"name":"American Journal of Clinical Nutrition","volume":null,"pages":null},"PeriodicalIF":6.5,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142373502","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Reply to Zhang et al. and Tang et al. 对 Zhang 等人和 Tang 等人的答复
IF 6.5 1区 医学 Q1 NUTRITION & DIETETICS Pub Date : 2024-10-01 Epub Date: 2024-08-28 DOI: 10.1016/j.ajcnut.2024.07.030
Lisa M Bodnar, Kari Johansson, Jennifer A Hutcheon
{"title":"Reply to Zhang et al. and Tang et al.","authors":"Lisa M Bodnar, Kari Johansson, Jennifer A Hutcheon","doi":"10.1016/j.ajcnut.2024.07.030","DOIUrl":"https://doi.org/10.1016/j.ajcnut.2024.07.030","url":null,"abstract":"","PeriodicalId":50813,"journal":{"name":"American Journal of Clinical Nutrition","volume":null,"pages":null},"PeriodicalIF":6.5,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142373503","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
American Journal of Clinical Nutrition
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