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本文引用的文献

1
Birth weight and systemic lupus erythematosus.出生体重与系统性红斑狼疮
Lupus. 2005;14(7):526-8. doi: 10.1191/0961203305lu2152oa.
2
Perinatal characteristics and risk of developing primary Sjögren's syndrome: a case-control study.围产期特征与原发性干燥综合征的发病风险:一项病例对照研究。
J Rheumatol. 2005 Apr;32(4):665-8.
3
Is there a gender difference in the associations of birthweight and adult hypothalamic-pituitary-adrenal axis activity?出生体重与成人下丘脑 - 垂体 - 肾上腺轴活动之间的关联是否存在性别差异?
Eur J Endocrinol. 2005 Feb;152(2):249-53. doi: 10.1530/eje.1.01846.
4
Growth patterns and the risk of breast cancer in women.女性的生长模式与患乳腺癌风险
N Engl J Med. 2004 Oct 14;351(16):1619-26. doi: 10.1056/NEJMoa040576.
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Birth weight as a risk factor for childhood leukemia: a meta-analysis of 18 epidemiologic studies.出生体重作为儿童白血病的一个风险因素:18项流行病学研究的荟萃分析
Am J Epidemiol. 2003 Oct 15;158(8):724-35. doi: 10.1093/aje/kwg210.
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Perinatal characteristics and risk of rheumatoid arthritis.围产期特征与类风湿关节炎风险
BMJ. 2003 May 17;326(7398):1068-9. doi: 10.1136/bmj.326.7398.1068.
7
Fetal origins of adult disease: strength of effects and biological basis.成人疾病的胎儿起源:效应强度与生物学基础。
Int J Epidemiol. 2002 Dec;31(6):1235-9. doi: 10.1093/ije/31.6.1235.
8
Size at birth and coronary artery disease in a population with high birth weight.高出生体重人群的出生时体重与冠状动脉疾病
Am J Clin Nutr. 2002 Dec;76(6):1290-4. doi: 10.1093/ajcn/76.6.1290.
9
Fetal programming of coronary heart disease.冠心病的胎儿编程
Trends Endocrinol Metab. 2002 Nov;13(9):364-8. doi: 10.1016/s1043-2760(02)00689-6.
10
The role of neuroendocrine system in the pathogenesis of rheumatic diseases (minireview).神经内分泌系统在风湿性疾病发病机制中的作用(综述)
Endocr Regul. 2002 Jun;36(2):95-106.

出生体重与类风湿关节炎风险有关吗?一项大型队列研究的数据。

Is birthweight associated with risk of rheumatoid arthritis? Data from a large cohort study.

作者信息

Mandl L A, Costenbader K H, Simard J F, Karlson E W

机构信息

Division of Rheumatology, Hospital for Special Surgery, Weill Cornell Medical College, New York City, New York 10021, USA.

出版信息

Ann Rheum Dis. 2009 Apr;68(4):514-8. doi: 10.1136/ard.2007.080937. Epub 2008 Jul 1.

DOI:10.1136/ard.2007.080937
PMID:18593757
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2748398/
Abstract

OBJECTIVES

The "fetal origins of adult disease" hypothesis suggests the uterine environment can influence the susceptibility of a fetus to future disease. We examine whether the fetal environment, as reflected by birthweight, could modulate an individual's future risk of rheumatoid arthritis (RA).

METHODS

The relationship between birthweight and the risk of incident RA was studied in 87 077 women followed prospectively in the Nurses' Health Study cohort. New cases of RA diagnosed between 1976 and 2002 were confirmed in 619 women. The association between birthweight and the future development of RA was studied in age-adjusted and Cox proportional hazard models adjusting for age and potential confounders, including history of maternal diabetes, childhood socioeconomic status, prematurity, maternal and paternal smoking, as well as additionally adjusting for risk factors for RA including smoking, age at menarche, use of oral contraceptives, use of post-menopausal hormones, total lifetime breastfeeding, and body mass index (BMI) at age 18.

RESULTS

In an age-adjusted model, birthweight >4.54 kg vs birthweight 3.2-3.85 kg was associated with a two-fold increased risk of RA (relative risk (RR) = 2.1, 95% CI 1.4 to 3.3). Further adjusting for potential confounders and risk factors did not change this relationship (RR = 2.0, 95% CI 1.3 to 3.0). Findings were similar when we limited cases to those with rheumatoid factor positive RA (RR = 2.1, 95% CI = 1.2 to 3.6).

CONCLUSIONS

In this large prospective cohort, birthweight >4.54 kg was associated with a two-fold increased risk of adult onset RA, compared with those of average birthweight. Further study of this observation may provide insight into the pathogenesis of RA.

摘要

目的

“成人疾病的胎儿起源”假说表明子宫环境会影响胎儿未来患疾病的易感性。我们研究出生体重所反映的胎儿环境是否会调节个体未来患类风湿关节炎(RA)的风险。

方法

在护士健康研究队列中对87077名女性进行前瞻性随访,研究出生体重与RA发病风险之间的关系。1976年至2002年间确诊的619名女性为RA新发病例。在年龄调整和Cox比例风险模型中研究出生体重与RA未来发病的关联,该模型对年龄和潜在混杂因素进行了调整,包括母亲糖尿病史、儿童期社会经济状况、早产、母亲和父亲吸烟情况,此外还对RA的风险因素进行了调整,包括吸烟、初潮年龄、口服避孕药的使用、绝经后激素的使用、终生母乳喂养总量以及18岁时的体重指数(BMI)。

结果

在年龄调整模型中,出生体重>4.54 kg与出生体重3.2 - 3.85 kg相比,RA风险增加两倍(相对风险(RR)= 2.1,95%可信区间1.4至3.3)。进一步对潜在混杂因素和风险因素进行调整并没有改变这种关系(RR = 2.0,95%可信区间1.3至3.0)。当我们将病例限制为类风湿因子阳性的RA患者时,结果相似(RR = 2.1,95%可信区间 = 1.2至3.6)。

结论

在这个大型前瞻性队列中,与平均出生体重的人相比,出生体重>4.54 kg的人成年后患RA的风险增加两倍。对这一观察结果的进一步研究可能有助于深入了解RA的发病机制。