Cystatin C-derived measures of renal function as risk factors for mortality and renal replacement therapy in the critically ill – An analysis of the SWECRIT cohort
(2025) In Journal of Critical Care 89.- Abstract
Purpose: Assess if cystatin C-derived measures of kidney function are associated with mortality in septic- and non-septic intensive care unit (ICU) patients. Methods: Data from adult patients staying >24 h in four ICUs in Sweden from November 2015–December 2018 included. Outcomes were mortality and need for renal replacement therapy (RRT) due to acute kidney injury. Associations between cystatin C-estimated glomerular filtration rate (eGFRcys) and shrunken pore syndrome (SPS) and outcomes were assessed with Cox-regression in unadjusted and analyses adjusted for sex, age, illness severity, chronic kidney disease and creatinine. SPS was defined as a ratio between eGFRcys and eGFRcreatinine <0.6. Results: In total, 4455 patients were... (More)
Purpose: Assess if cystatin C-derived measures of kidney function are associated with mortality in septic- and non-septic intensive care unit (ICU) patients. Methods: Data from adult patients staying >24 h in four ICUs in Sweden from November 2015–December 2018 included. Outcomes were mortality and need for renal replacement therapy (RRT) due to acute kidney injury. Associations between cystatin C-estimated glomerular filtration rate (eGFRcys) and shrunken pore syndrome (SPS) and outcomes were assessed with Cox-regression in unadjusted and analyses adjusted for sex, age, illness severity, chronic kidney disease and creatinine. SPS was defined as a ratio between eGFRcys and eGFRcreatinine <0.6. Results: In total, 4455 patients were included in the analysis, of which 32 % had sepsis. SPS was present in 7.4 % of the cohort, and 90-day mortality was 30.8 %. In sepsis- and non-sepsis patients, SPS and eGFRcys were associated with 90-day-, 1-year mortality and RRT in unadjusted analyses. In an adjusted analysis, SPS was associated with 1-year mortality in sepsis patients (hazard ratio [HR] 1.4, 95 % CI 1.1–1.9, p = 0.021), and eGFRcys was associated with RRT in both sepsis and non-sepsis patients (HR 3.1, 95 % CI 1.6–6.0, p < 0.001, eGFRcys <20 vs ≥60 ml/min/1.73m2). No other associations between eGFRcys, SPS and mortality were detected in adjusted analyses. Conclusion: Our finding that SPS is more robustly associated with mortality in sepsis patients than in non-sepsis patients suggests that the association between SPS and mortality may depend on underlying pathophysiology. A cystatin C-based estimate of GFR is independently associated with RRT in sepsis and non-sepsis.
(Less)
- author
- Linné, Erik
LU
; Åkesson, Anna ; Lengquist, Maria LU
; Friberg, Hans LU ; Frigyesi, Attila LU ; Larsson, Anders O. ; Grubb, Anders LU
and Bentzer, Peter LU
- organization
-
- Anesthesiology and Intensive Care
- Center for cardiac arrest (research group)
- SWECRIT (research group)
- Intensive Care Epidemiology (research group)
- Cystatin C, renal disease, amyloidosis and antibiotics (research group)
- Fluid resuscitation in critical illness (research group)
- Anaesthesiology and Intensive Care Medicine (research group)
- publishing date
- 2025-10
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Critical care, Cystatin C, Renal function, Selective glomerular hypofiltration, Sepsis, Shrunken pore syndrome
- in
- Journal of Critical Care
- volume
- 89
- article number
- 155116
- publisher
- Elsevier
- external identifiers
-
- scopus:105004899853
- pmid:40373615
- ISSN
- 0883-9441
- DOI
- 10.1016/j.jcrc.2025.155116
- language
- English
- LU publication?
- yes
- id
- 34e20fb9-40e1-44aa-93cd-80d03311d981
- date added to LUP
- 2025-07-18 09:14:18
- date last changed
- 2025-07-19 03:27:51
@article{34e20fb9-40e1-44aa-93cd-80d03311d981, abstract = {{<p>Purpose: Assess if cystatin C-derived measures of kidney function are associated with mortality in septic- and non-septic intensive care unit (ICU) patients. Methods: Data from adult patients staying >24 h in four ICUs in Sweden from November 2015–December 2018 included. Outcomes were mortality and need for renal replacement therapy (RRT) due to acute kidney injury. Associations between cystatin C-estimated glomerular filtration rate (eGFRcys) and shrunken pore syndrome (SPS) and outcomes were assessed with Cox-regression in unadjusted and analyses adjusted for sex, age, illness severity, chronic kidney disease and creatinine. SPS was defined as a ratio between eGFRcys and eGFRcreatinine <0.6. Results: In total, 4455 patients were included in the analysis, of which 32 % had sepsis. SPS was present in 7.4 % of the cohort, and 90-day mortality was 30.8 %. In sepsis- and non-sepsis patients, SPS and eGFRcys were associated with 90-day-, 1-year mortality and RRT in unadjusted analyses. In an adjusted analysis, SPS was associated with 1-year mortality in sepsis patients (hazard ratio [HR] 1.4, 95 % CI 1.1–1.9, p = 0.021), and eGFRcys was associated with RRT in both sepsis and non-sepsis patients (HR 3.1, 95 % CI 1.6–6.0, p < 0.001, eGFRcys <20 vs ≥60 ml/min/1.73m<sup>2</sup>). No other associations between eGFRcys, SPS and mortality were detected in adjusted analyses. Conclusion: Our finding that SPS is more robustly associated with mortality in sepsis patients than in non-sepsis patients suggests that the association between SPS and mortality may depend on underlying pathophysiology. A cystatin C-based estimate of GFR is independently associated with RRT in sepsis and non-sepsis.</p>}}, author = {{Linné, Erik and Åkesson, Anna and Lengquist, Maria and Friberg, Hans and Frigyesi, Attila and Larsson, Anders O. and Grubb, Anders and Bentzer, Peter}}, issn = {{0883-9441}}, keywords = {{Critical care; Cystatin C; Renal function; Selective glomerular hypofiltration; Sepsis; Shrunken pore syndrome}}, language = {{eng}}, publisher = {{Elsevier}}, series = {{Journal of Critical Care}}, title = {{Cystatin C-derived measures of renal function as risk factors for mortality and renal replacement therapy in the critically ill – An analysis of the SWECRIT cohort}}, url = {{http://dx.doi.org/10.1016/j.jcrc.2025.155116}}, doi = {{10.1016/j.jcrc.2025.155116}}, volume = {{89}}, year = {{2025}}, }