Kidney Stones: A Fetal Origins Hypothesis

被引:4
作者
Howles, Sarah A. [1 ,2 ]
Edwards, Mark H. [3 ]
Cooper, Cyrus [3 ,4 ]
Thakker, Rajesh V. [1 ,2 ]
机构
[1] Univ Oxford, Nuffield Dept Clin Med, Oxford OX3 7LJ, England
[2] Univ Oxford, Radcliffe Dept Med, Oxford OX3 7LJ, England
[3] Univ Southampton, Univ Hosp Southampton NHS Fdn Trust, MRC, Lifecourse Epidemiol Unit, Southampton, Hants, England
[4] Univ Oxford, Nuffield Dept Orthopaed Rheumatol & Musculoskelet, Oxford OX3 7LJ, England
基金
英国医学研究理事会;
关键词
KIDNEY STONES; LOW BIRTH WEIGHT; FETAL ORIGINS; OSTEOPOROSIS; METABOLIC SYNDROME; LOW-BIRTH-WEIGHT; COHORT PROFILE; CORTISOL; CALCIUM; GROWTH; NEPHROLITHIASIS; HYPERTENSION; PREVALENCE; PREGNANCY; OBESITY;
D O I
10.1002/jbmr.1993
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Kidney stones are common, with a multifactorial etiology involving dietary, environmental, and genetic factors. In addition, patients with nephrolithiasis are at greater risk of hypertension, diabetes mellitus, metabolic syndrome, and osteoporosis, although the basis for this is not fully understood. All of these renal stone-associated conditions have also been linked with adverse early-life events, including low-birth weight, and it has been suggested that this developmental effect is due to excess exposure to maternal glucocorticoids in utero. This is proposed to result in long-term increased hypothalamic-pituitary-axis activation; there are mechanisms through which this effect could also promote urinary lithogenic potential. We therefore hypothesize that the association between renal stone disease and hypertension, diabetes mellitus, metabolic syndrome, and osteoporosis may be related by a common pathway of programming in early life, which, if validated, would implicate the developmental origins hypothesis in the etiology of nephrolithiasis. (c) 2013 American Society for Bone and Mineral Research.
引用
收藏
页码:2535 / 2539
页数:5
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