» Articles » PMID: 31977575

Long-term Blood Pressure Behavior and Progression to End-stage Renal Disease in Patients with Immunoglobulin A Nephropathy: a Single-center Observational Study in Italy

Overview
Journal J Hypertens
Date 2020 Jan 25
PMID 31977575
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Antihypertensive treatment by the use of RAAS inhibitors (RAAS-is) is of paramount importance in the management of slowly progressive IgA nephropathy (IgAN). With the aim of better understanding the relationship between BP behavior and progression, we looked at time-averaged SBP and time-averaged proteinuria and renal outcome in a single-center cohort of IgAN patients.

Methods: Among 248 consecutive patients referred to the Clinic of Nephrology of San Martino Hospital from 1996 to 2018 for native renal biopsy with a diagnosis of IgAN, we retrospectively analyzed 145 with available data at baseline and during follow-up. All patients received Supportive Care, 39% were on RAAS-is alone, 45% plus steroids, and 16% plus steroids and immunosuppressors. Renal replacing treatment (RRT) was the primary endpoint.

Results: During a mean follow-up of 67 ± 6 months, 23% of study patients (n = 33) progressed to RRT and 6% (n = 9) died. Patients who reached the renal endpoint, had lower baseline eGFR and higher proteinuria and proteinuria indexed at baseline. Moreover, they had higher TA-SBP (139 ± 17 vs. 130 ± 13, P = 0.0016). The incidence of RRT was higher in IgAN patients in the highest time-averaged SBP tertile as compared with the others (32 vs. 23 vs. 9%, χ 6.8, P = 0.033). After adjusting for baseline SBP, baseline and time-averaged proteinuria indexed, MEST-C score, and treatment, the association between TA-SBP and RRT persisted.

Conclusion: Time-averaged low BP values were independently associated to a decreased risk of renal progression in IgAN with no evidence of a J-curve relationship even at SBP levels below 125 mmHg.

Citing Articles

Blood and urine biomarkers of disease progression in IgA nephropathy.

Duan Z, Zhang C, Chen X, Cai G Biomark Res. 2024; 12(1):72.

PMID: 39075557 PMC: 11287988. DOI: 10.1186/s40364-024-00619-4.


Safety and feasibility of transcranial direct current stimulation in end-stage renal disease patients undergoing hemodialysis: an exploratory study.

Pegado R, Melo M, Oehmen T, Mastroianni Kirsztajn G, Silva-Filho E, Quintiliano A J Bras Nefrol. 2024; 46(4):e20240010.

PMID: 39051759 PMC: 11268524. DOI: 10.1590/2175-8239-JBN-2024-0010en.


Hyperuricemia is associated with the progression of IgA nephropathy in children.

Xu Y, Zheng X, Zhuang H, Liao H, Mo Y, Jiang X Pediatr Res. 2023; 94(3):1057-1066.

PMID: 36914808 DOI: 10.1038/s41390-023-02538-w.


Visit-to-visit variability in blood pressure and kidney disease progression in IgA nephropathy.

Tang C, Zhang X, Lv J, Shi S, Zhou X, Liu L Clin Kidney J. 2022; 15(12):2331-2339.

PMID: 36381367 PMC: 9664579. DOI: 10.1093/ckj/sfac200.


The epidemiology and evolution of IgA nephropathy over two decades: A single centre experience.

Storrar J, Chinnadurai R, Sinha S, Kalra P PLoS One. 2022; 17(9):e0268421.

PMID: 36048745 PMC: 9436111. DOI: 10.1371/journal.pone.0268421.