The Relationship of Osmolality and Kidney Outcomes in Patients with Autosomal Dominant Polycystic Kidney Disease
Year: 2026
Type: article
Study design: Observational Study
Abstract: KEY POINTS: The causal relationship between serum osmolality and kidney outcome remained unclear in patients with autosomal dominant polycystic kidney disease. Serum osmolality may be a possible surrogate marker for the clinical monitoring of autosomal dominant polycystic kidney disease patients, especially when access to copeptin level is limited. High serum osmolality conveys possible detrimental effect on the kidney outcomes. BACKGROUND: Current treatment of autosomal dominant polycystic kidney disease (ADPKD) is mainly focused on inhibiting cystogenesis through arginine vasopressin suppression, and there has been interest in achieving similar vasopressin suppression by reduction of osmolality with increased water intake. However, the causal relationship between serum osmolality (sOSM) and kidney outcome remained unclear in patients with ADPKD. We aim to evaluate the relationship of sOSM and its effect on kidney outcome in patients with ADPKD. METHODS: Three hundred and eleven tolvaptan treatment-naïve patients with ADPKD were recruited prospectively from the CysticHK cohort, a territory-wide ADPKD registry across 12 tertiary hospitals in Hong Kong. Beside clinical data, serial measurement of serum, and urinary osmolality were obtained every 6 months over 5 years. All participants were treated according to the standard of clinical care. The primary outcome was the 40% decline from baseline eGFR. RESULTS: Patients with a high sOSM have a worse kidney outcome, as shown by the Kaplan-Meier plots (log-rank P ≤ 0.001) and the Cox regression model that showed a 5.91 times higher risk of reaching 40% eGFR decline compared with the top with bottom quartiles of osmolality ( P = 0.018). By contrast, there is an inverse relationship for urine osmolality. A receiver-operating characteristic analysis to assess the predictive efficacy of osmolality for identifying those at high risk of kidney decline also showed a good performance for sOSM (area under the curve, 0.81; 95% confidence interval, 0.73 to 0.89; P < 0.001). The urinary osmolality did not show a clinical meaningful predictive efficacy (area under the curve, 0.35; 95% confidence interval, 0.28 to 0.43; P = 0.003). CONCLUSIONS: sOSM may be a possible surrogate marker for the clinical monitoring of patients with ADPKD, especially when access to copeptin level is limited; and high sOSM conveys possible detrimental effect on the kidney outcomes.
Source: Kidney360
Authors: Winston Wing-Shing Fung, Cheuk-Chun Szeto, Kai-Ming Chow, Amelia Chien-Wei Chao, Vickie Wai-Ki Kwong, Sam Lik-Fung Lau, Wing-Fai Pang, Ho-Kwan Sin, Elaine Ho, Lorraine Pui-Yuen Kwan, Koon-Ming Chan, Gary Tung-Sen Shum, Anthony Kai-Ching Hau, Ka-Lok Chan, Ronald Chi-Chun Lin, Lap-Ming Kwok, Sze-Kit Yuen, Sing-Leung Lui, Samuel Ka-Shun Fung, Sunny Wong, Winnie Chiu-Wing Chu, Albert Chee Meng Ong, Olivier Devuyst, Philip Kam-Tao Li, On behalf of the CysticHK cohort collaborators
Institutions: Chinese University of Hong Kong, Prince of Wales Hospital, Kwong Wah Hospital, Tseung Kwan O Hospital, Tung Wah Hospital, United Christian Hospital, Queen Elizabeth Hospital, Princess Margaret Hospital, Tuen Mun Hospital, Caritas Medical Centre, Yan Chai Hospital, University of Sheffield, University of Zurich, UCLouvain
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: diamond
Funder: Hong Kong Society of Nephrology
OpenAlex ID: W7128689304
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