Increased psychosocial risk, depression and reduced quality of life living with autosomal dominant polycystic kidney disease
- PMID: 26268712
- DOI: 10.1093/ndt/gfv299
Increased psychosocial risk, depression and reduced quality of life living with autosomal dominant polycystic kidney disease
Abstract
Background: The psychosocial impact of living with autosomal dominant polycystic kidney disease (ADPKD) is poorly understood. In this study, we assessed the overall quality of life (QOL), mood, perceived social support and psychosocial risk of having a diagnosis of ADPKD in a patient cohort from a major UK nephrology centre serving a large catchment population.
Methods: A postal questionnaire was sent to 349 patients registered at the Sheffield Kidney Institute with chronic kidney disease but not on renal replacement therapy (RRT). The questionnaire incorporated three validated forms: kidney disease quality-of-life short form (KDQOL SF1.3) to assess QOL; nine-item patient health questionnaire (PHQ9) to screen for depression; multidimensional scale of perceived social support (MSPSS) to evaluate perceived social support; as well as a novel genetic psychosocial risk instrument (GPRI-ADPKD) designed to study the specific psychosocial impact of coping with a diagnosis of ADPKD.
Results: The overall response rate was 53%. Patients with a lower estimated glomerular filtration rate (<30 mL/min) or larger kidneys (mean length on ultrasound ≥17 cm) reported reduced QOL and increased psychosocial risk. Clinically significant depression was reported in 22% and 62% felt guilty about passing ADPKD on to their children. In multivariate analysis, female gender was associated with overall poorer psychosocial well-being, whereas increasing age, lower kidney function, larger kidneys and loss of a first degree relative from ADPKD were additional risk factors for QOL, depression or psychosocial risk, respectively.
Conclusions: Our results reveal a significantly poorer QOL and increasing psychosocial risk with markers of disease progression in patients, particularly women, with ADPKD prior to starting RRT. The future management strategy of ADPKD should address these issues and provide for better individual and family support throughout the patient journey.
Keywords: ADPKD; depression; eGFR; psychosocial risk; quality of life; social support.
© The Author 2015. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved.
Similar articles
-
The relationship between depression, anxiety, quality of life levels, and the chronic kidney disease stage in the autosomal dominant polycystic kidney disease.Int Urol Nephrol. 2023 Apr;55(4):983-992. doi: 10.1007/s11255-022-03375-2. Epub 2022 Oct 2. Int Urol Nephrol. 2023. PMID: 36184721
-
Health-related quality of life in patients with autosomal dominant polycystic kidney disease and CKD stages 1-4: a cross-sectional study.Am J Kidney Dis. 2014 Feb;63(2):214-26. doi: 10.1053/j.ajkd.2013.08.017. Epub 2013 Nov 1. Am J Kidney Dis. 2014. PMID: 24183837 Free PMC article. Clinical Trial.
-
Development of the Autosomal Dominant Polycystic Kidney Disease Impact Scale: A New Health-Related Quality-of-Life Instrument.Am J Kidney Dis. 2018 Feb;71(2):225-235. doi: 10.1053/j.ajkd.2017.08.020. Epub 2017 Nov 14. Am J Kidney Dis. 2018. PMID: 29150246
-
Identifying and integrating consumer perspectives in clinical practice guidelines on autosomal-dominant polycystic kidney disease.Nephrology (Carlton). 2016 Feb;21(2):122-32. doi: 10.1111/nep.12579. Nephrology (Carlton). 2016. PMID: 26235729
-
Current diagnostic evaluation of autosomal dominant polycystic kidney disease.Pol Arch Med Wewn. 2008 Dec;118(12):767-73. Pol Arch Med Wewn. 2008. PMID: 19202957 Review.
Cited by
-
Mental Health and Autosomal Dominant Polycystic Kidney Disease: A Narrative Review.Kidney360. 2024 Aug 1;5(8):1200-1206. doi: 10.34067/KID.0000000000000504. Epub 2024 Jul 8. Kidney360. 2024. PMID: 38976329 Free PMC article. Review.
-
Developing a patient-centred tool for pain measurement and evaluation in autosomal dominant polycystic kidney disease.Clin Kidney J. 2021 Feb 8;14(11):2338-2348. doi: 10.1093/ckj/sfaa259. eCollection 2021 Nov. Clin Kidney J. 2021. PMID: 34754429 Free PMC article.
-
Is Autosomal Dominant Polycystic Kidney Disease Becoming a Pediatric Disorder?Front Pediatr. 2017 Dec 20;5:272. doi: 10.3389/fped.2017.00272. eCollection 2017. Front Pediatr. 2017. PMID: 29326910 Free PMC article. Review.
-
Disconnect in Assessments of Autosomal Dominant Polycystic Kidney Disease Burden Between Patients and Physicians: A Survey Study.Int J Nephrol Renovasc Dis. 2021 Apr 13;14:105-115. doi: 10.2147/IJNRD.S297491. eCollection 2021. Int J Nephrol Renovasc Dis. 2021. PMID: 33880055 Free PMC article.
-
Long-term effect of increasing water intake on repeated self-assessed health-related quality of life (HRQoL) in autosomal dominant polycystic kidney disease.Clin Kidney J. 2024 Jun 7;17(7):sfae159. doi: 10.1093/ckj/sfae159. eCollection 2024 Jul. Clin Kidney J. 2024. PMID: 39165901 Free PMC article.
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous