Early Detection, Prevention and Infections Branch, International Agency for Research On Cancer (IARC/WHO), Lyon, France.
Nutrition and Metabolism Branch, International Agency for Research on Cancer (IARC/WHO), Lyon, France.
Eur J Nutr. 2023 Aug;62(5):2129-2138. doi: 10.1007/s00394-023-03132-w. Epub 2023 Mar 24.
Gastric atrophy (GA), usually linked to chronic infection with Helicobacter pylori (H. pylori), may over time evolve into gastric malignancy. Besides H. pylori, high salt intake may play a role in GA development. This study evaluates cross sectionally the association between salt intake and GA in Chilean adults.
Population-based samples were recruited from two sites, Antofagasta and Valdivia, partaking in the Epidemiological Investigation of Gastric Malignancies. At recruitment, participants answered questionnaires and provided biospecimens. Salt intake (g/day) was estimated from casual spot urine samples using the Tanaka equation. GA was determined by serum pepsinogen levels. Only participants ≥ 40 to 70 years of age were considered in this analysis, n = 565. For the association between salt intake (as sex-specific quartiles) and GA, odds ratios (ORs) and the corresponding 95% confidence intervals (CI) were estimated through multivariable logistic regression.
In women, the multivariable-adjusted OR for GA comparing quartile 4 of the estimated salt intake (12.8 g/day) to quartile 1 (6.6 g/day) was 1.18 (95% CI 0.52-2.68, P-trend = 0.87). The corresponding OR in men was 0.49 (95% CI 0.19-1.27, P-trend = 0.17) with salt intakes of 12.8 g/day and 7.1 g/day for quartiles 4 and 1, respectively.
There was little evidence for an association between salt intake estimated from spot urine and GA risk in our cross-sectional analysis of middle aged and older adults in Chile. Reverse causation bias cannot be ruled out and the sample size was limited to provide more precise estimates.
胃萎缩(GA)通常与慢性幽门螺杆菌(H. pylori)感染有关,随着时间的推移可能会发展为胃癌。除了 H. pylori 之外,高盐摄入可能在 GA 发展中起作用。本研究评估了智利成年人中盐摄入量与 GA 之间的横断面关联。
本研究基于人群的样本来自安托法加斯塔和瓦尔迪维亚两个地点,参与了胃癌的流行病学调查。在招募时,参与者回答了问卷并提供了生物样本。盐摄入量(g/天)通过 Tanaka 方程从随机尿液样本中估算。GA 通过血清胃蛋白酶原水平确定。只有年龄在 40 至 70 岁以上的参与者被纳入本分析,n=565。为了评估盐摄入量(按性别分为四分位数)与 GA 之间的关联,通过多变量逻辑回归估计了比值比(OR)及其相应的 95%置信区间(CI)。
在女性中,与估计盐摄入量四分位数 1(6.6 g/天)相比,四分位数 4(12.8 g/天)患 GA 的多变量调整 OR 为 1.18(95%CI 0.52-2.68,P 趋势=0.87)。男性的相应 OR 为 0.49(95%CI 0.19-1.27,P 趋势=0.17),四分位数 4 和 1 的盐摄入量分别为 12.8 g/天和 7.1 g/天。
在我们对智利中年和老年人的横断面分析中,从随机尿液中估计的盐摄入量与 GA 风险之间几乎没有关联的证据。不能排除反向因果关系偏倚,而且样本量有限,无法提供更精确的估计。