ArticleEXCLI journal2017
Postmenopausal hormone and the risk of nephrolithiasis: A meta-analysis.
Article in EXCLI journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
3 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.
- A holistic guide to effective prevention and treatment for kidney stones: a systematic review exploring anti-urolithiasis approaches.Naunyn-Schmiedeberg's archives of pharmacology · 2026Pooled it
- Article
- Incorporation of osteopontin peptide into kidney stone-related calcium oxalate monohydrate crystals: a quantitative study.Urolithiasis · 2019Article
Corrections and comments
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Authors and funding
2 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Menopause is reported to be associated with increased urinary calcium excretion, which may enhance the risk for the development of calcium kidney stones. However, it remains controversial about whether high level of postmenopausal hormone (PMH) is a risk factor for formation of nephrolithiasis. Several observational studies have shown that PMH is protective based on 24-hour urinary parameters. Recent clinical trials provided evidence to conclude that estrogen therapy increases the risk of nephrolithiasis in healthy postmenopausal women. Our study aimed to comprehensively assess clinical evidence on the relationship between postmenopausal hormone level and risk of nephrolithiasis. To conduct systematic review, we pooled total 98 potentially related articles in Cochrane library, Medline, and Embase. Three studies with a total of 71101 study participants that included two clinical trials, 4 stratified and potentially usable results by the status of menopause and type of PMH use derived from one prospective cohort study, and one case-control studies were selected to pool relative risk using random-effect model. How the difference in menopause status, whether naturally menopausal or surgically menopausal, influenced the pooled relative risk was included in the subgroup analysis. The study population aged from 45 to 70 years old. The follow-up year and adjusted confounders differed across different studies. The pooled relative risk for the 7 stratified studies was 0.91 (95 % confidence interval (CI): [0.72, 1.14]). In the menopausal status-specific analysis, the pooled relative risk for naturally menopausal women was 0.92 (95 % CI, [0.64, 1.27]; I
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