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Current State and Future Perspectives in the Diagnosis of Diabetes Insipidus: A Clinical Review
被引:120
|作者:
Fenske, Wiebke
[1
]
Allolio, Bruno
[1
]
机构:
[1] Univ Hosp Wurzburg, Dept Internal Med 1, Endocrine & Diabet Unit, D-97080 Wurzburg, Germany
关键词:
POSTERIOR PITUITARY-FUNCTION;
HYPERTONIC SALINE INFUSIONS;
COMPULSIVE WATER DRINKING;
SIGNAL PEPTIDE MUTATION;
INDUCED DOWN-REGULATION;
RAT-KIDNEY MEDULLA;
DIFFERENTIAL-DIAGNOSIS;
VASOPRESSIN SECRETION;
ANTIDIURETIC HORMONE;
PRIMARY POLYDIPSIA;
D O I:
10.1210/jc.2012-1981
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Context: The differential diagnosis of diabetes insipidus (DI) is often challenging but essential, because treatment may vary substantially. This article analyzes the database and performance of currently used differential diagnostic tests for DI and discusses future perspectives for diagnostic improvement. Evidence Acquisition: A review of electronic and print data comprising original and review articles retrieved from the PubMed or Cochrane Library database up to January 2012 was conducted. The search term "polyuria polydipsia syndrome" was cross-referenced with underlying forms of disease and associated clinical, diagnostic, and therapeutic MeSH terms. In addition, references from review articles and textbook chapters were screened for papers containing original data. Search results were narrowed to articles containing primary data with a description of criteria for the differential diagnosis of DI. Evidence Synthesis: Fifteen articles on differential diagnosis of DI were identified, mainly consisting of small series of patients, and mostly covering only part of the differential diagnostic spectrum of DI. Test protocols differed, and prospective validation of diagnostic criteria was consistently missing. Inconsistent data were reported on the diagnostic superiority of direct plasma arginine vasopressin determination over the indirect water deprivation test. Both test methods revealed limitations, especially in the differentiation of disorders with a milder phenotype. Conclusion: The available data demonstrate limitations of current biochemical tests for the differential diagnosis of DI, potentially leading to incorrect diagnosis and treatment. The newly available assay for copeptin, the C terminus of the vasopressin precursor, holds promise for a higher diagnostic specificity and simplification of the differential diagnostic protocol in DI. (J Clin Endocrinol Metab 97: 3426-3437, 2012)
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页码:3426 / 3437
页数:12
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