Research Article

Differentiating AVP deficiency and primary polydipsia: a clinical and biochemical perspective

Volume: 7 Number: 5 September 15, 2025
TR EN

Differentiating AVP deficiency and primary polydipsia: a clinical and biochemical perspective

Abstract

Aims: The polyuria–polydipsia syndrome encompasses three major disorders—arginine vasopressin (AVP) deficiency, AVP resistance, and primary polydipsia. This study aimed to differentiate AVP deficiency from primary polydipsia by evaluating clinical features, biochemical markers, and anterior pituitary hormone levels, using the water deprivation test as the primary diagnostic modality. Methods: This retrospective observational study included 34 adult patients with polyuria–polydipsia syndrome who underwent a standardized inpatient water deprivation test. Patients were categorized into AVP deficiency (complete or partial) or primary polydipsia based on urine osmolality responses to dehydration and desmopressin. Clinical data, daily fluid intake, and nocturia frequency were recorded. Serum electrolytes and anterior pituitary hormones (LH, GH) were analyzed. Results: AVP deficiency was diagnosed in 76.4% of patients (58.8% complete, 17.6% partial), while 23.5% had primary polydipsia. LH and GH levels were significantly higher in the primary polydipsia group (p=0.011 and p=0.028, respectively), whereas AVP deficiency was associated with lower gonadotropin levels, especially in postoperative cases. Serum sodium, chloride, and magnesium levels were significantly lower in primary polydipsia (p<0.05), reflecting dilutional hyponatremia. Urine osmolality was significantly higher in primary polydipsia (p=0.011), indicating preserved concentrating ability. Nocturia occurred in 96.2% of patients with AVP deficiency versus 12.5% in primary polydipsia (p<0.001). Conclusion: The water deprivation test remains a valuable diagnostic tool for differentiating AVP deficiency from primary polydipsia. These retrospective findings may serve as predictive indicators in the differential diagnosis, particularly in clinical settings where water deprivation tests and copeptin testing are not readily available. Incorporating nocturia frequency, serum electrolytes, and anterior pituitary hormone levels particularly LH and GH may improve diagnostic precision and facilitate individualized management.

Keywords

Ethical Statement

This study was approved by the Ethics Committee of Ankara Bilkent City Hospital (E1-23-3947) and conducted in accordance with the Declaration of Helsinki.

References

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Details

Primary Language

English

Subjects

Endocrinology

Journal Section

Research Article

Publication Date

September 15, 2025

Submission Date

May 23, 2025

Acceptance Date

August 14, 2025

Published in Issue

Year 2025 Volume: 7 Number: 5

APA
Turan Erdoğan, B., Deniz, M. S., Tural Balsak, B. Ö., Keskin, Ç., Polat, B., Topaloğlu, O., Ersoy, R., & Çakır, B. (2025). Differentiating AVP deficiency and primary polydipsia: a clinical and biochemical perspective. Anatolian Current Medical Journal, 7(5), 576-582. https://doi.org/10.38053/acmj.1705329
AMA
1.Turan Erdoğan B, Deniz MS, Tural Balsak BÖ, et al. Differentiating AVP deficiency and primary polydipsia: a clinical and biochemical perspective. Anatolian Curr Med J / ACMJ / acmj. 2025;7(5):576-582. doi:10.38053/acmj.1705329
Chicago
Turan Erdoğan, Beril, Muzaffer Serdar Deniz, Belma Özlem Tural Balsak, et al. 2025. “Differentiating AVP Deficiency and Primary Polydipsia: A Clinical and Biochemical Perspective”. Anatolian Current Medical Journal 7 (5): 576-82. https://doi.org/10.38053/acmj.1705329.
EndNote
Turan Erdoğan B, Deniz MS, Tural Balsak BÖ, Keskin Ç, Polat B, Topaloğlu O, Ersoy R, Çakır B (September 1, 2025) Differentiating AVP deficiency and primary polydipsia: a clinical and biochemical perspective. Anatolian Current Medical Journal 7 5 576–582.
IEEE
[1]B. Turan Erdoğan et al., “Differentiating AVP deficiency and primary polydipsia: a clinical and biochemical perspective”, Anatolian Curr Med J / ACMJ / acmj, vol. 7, no. 5, pp. 576–582, Sept. 2025, doi: 10.38053/acmj.1705329.
ISNAD
Turan Erdoğan, Beril - Deniz, Muzaffer Serdar - Tural Balsak, Belma Özlem - Keskin, Çağlar - Polat, Burçak - Topaloğlu, Oya - Ersoy, Reyhan - Çakır, Bekir. “Differentiating AVP Deficiency and Primary Polydipsia: A Clinical and Biochemical Perspective”. Anatolian Current Medical Journal 7/5 (September 1, 2025): 576-582. https://doi.org/10.38053/acmj.1705329.
JAMA
1.Turan Erdoğan B, Deniz MS, Tural Balsak BÖ, Keskin Ç, Polat B, Topaloğlu O, Ersoy R, Çakır B. Differentiating AVP deficiency and primary polydipsia: a clinical and biochemical perspective. Anatolian Curr Med J / ACMJ / acmj. 2025;7:576–582.
MLA
Turan Erdoğan, Beril, et al. “Differentiating AVP Deficiency and Primary Polydipsia: A Clinical and Biochemical Perspective”. Anatolian Current Medical Journal, vol. 7, no. 5, Sept. 2025, pp. 576-82, doi:10.38053/acmj.1705329.
Vancouver
1.Beril Turan Erdoğan, Muzaffer Serdar Deniz, Belma Özlem Tural Balsak, Çağlar Keskin, Burçak Polat, Oya Topaloğlu, Reyhan Ersoy, Bekir Çakır. Differentiating AVP deficiency and primary polydipsia: a clinical and biochemical perspective. Anatolian Curr Med J / ACMJ / acmj. 2025 Sep. 1;7(5):576-82. doi:10.38053/acmj.1705329

 

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