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Published on: June 23, 2015
Risk of hypertension with multicystic kidney disease: a systematic review
1Paediatric Department, Sandwell General Hospital, West Bromwich B71 4HJ, UK. hassibnarchi@hotmail.com
Insights
The risk of hypertension in children with unilateral multicystic kidney disease (MCKD) is low, occurring in approximately 5.4 per 1000 children. Further research is needed to establish optimal follow-up strategies for blood pressure monitoring.
Area of Science:
- Pediatric Nephrology
- Clinical Epidemiology
Background:
- Children with multicystic kidney disease (MCKD) often receive conservative management.
- There is a recognized, yet poorly defined, risk of hypertension in these children.
- Current follow-up strategies may lack evidence-based justification.
Purpose of the Study:
- To estimate the probability of developing hypertension in children with unilateral MCKD.
- To inform evidence-based follow-up care for pediatric MCKD patients.
Main Methods:
- Systematic review of published prospective and retrospective cohort studies.
- Included children diagnosed with unilateral MCKD and managed conservatively.
- Excluded studies with bilateral MCKD or nephrectomy (not for hypertension).
Main Results:
- Six cases of hypertension observed in 1115 eligible children across 29 studies.
- The estimated mean probability of developing hypertension was 5.4 per 1000 (95% CI: 1.9–11.7 per 1000).
Conclusions:
- The risk of hypertension in pediatric unilateral MCKD is low.
- Current data are insufficient to recommend specific blood pressure monitoring frequency or duration.
- Large, long-term prospective cohort studies are required to guide follow-up protocols.
Background:
Children with multicystic kidney disease (MCKD) are increasingly managed conservatively, and are followed up throughout childhood because of the risk of hypertension highlighted in some reports. With this risk still poorly defined, the strategy and the duration of follow up do not seem to be based on evidence.
Methods:
Systematic review of the literature for all published cohort studies (prospective and retrospective) of children diagnosed to have unilateral MCKD and managed conservatively. Exclusion criteria were bilateral MCKD, and nephrectomy (not for hypertension) during the follow up period. For children with MCKD, the probability of developing hypertension during the follow up period was estimated.
Results:
From 29 reviewed studies, six cases of hypertension developed in 1115 eligible children. The mean probability of a child with unilateral MCKD developing hypertension was therefore 5.4 per 1000 (95% CI estimated at 1.9 to 11.7 per 1000).
Conclusion:
Although the risk of hypertension in MCKD is low, the results of this study do not allow firm recommendations on the frequency and duration of blood pressure measurement follow up for these children. Large prospective cohort studies with a very long duration of follow up are needed.
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