scholarly journals Beta-2 microglobulin and all-cause mortality in the era of high-flux hemodialysis: results from the Dialysis Outcomes and Practice Patterns Study

2020 ◽  
Author(s):  
Eiichiro Kanda ◽  
Daniel Muenz ◽  
Brian Bieber ◽  
Aleix Cases ◽  
Francesco Locatelli ◽  
...  

Abstract Background Beta-2 microglobulin (β2M) accumulates in hemodialysis (HD) patients, but its consequences are controversial, particularly in the current era of high-flux dialyzers. High-flux HD treatment improves β2M removal, yet β2M and other middle molecules may still contribute to adverse events. We investigated patient factors associated with serum β2M, evaluated trends in β2M levels and in hospitalizations due to dialysis-related amyloidosis (DRA), and estimated the effect of β2M on mortality. Methods We studied European and Japanese participants in the Dialysis Outcomes and Practice Patterns Study. Analysis of DRA-related hospitalizations spanned 1998–2018 (n = 23 976), and analysis of β2M and mortality in centers routinely measuring β2M spanned 2011–18 (n = 5332). We evaluated time trends with linear and Poisson regression and mortality with Cox regression. Results Median β2M changed nonsignificantly from 2.71 to 2.65 mg/dL during 2011–18 (P = 0.87). Highest β2M tertile patients (>2.9 mg/dL) had longer dialysis vintage, higher C-reactive protein and lower urine volume than lowest tertile patients (≤2.3 mg/dL). DRA-related hospitalization rates [95% confidence interval (CI)] decreased from 1998 to 2018 from 3.10 (2.55–3.76) to 0.23 (0.13–0.42) per 100 patient-years. Compared with the lowest β2M tertile, adjusted mortality hazard ratios (95% CI) were 1.16 (0.94–1.43) and 1.38 (1.13–1.69) for the middle and highest tertiles. Mortality risk increased monotonically with β2M modeled continuously, with no indication of a threshold. Conclusions DRA-related hospitalizations decreased over 10-fold from 1998 to 2018. Serum β2M remains positively associated with mortality, even in the current high-flux HD era.

2018 ◽  
Vol 33 (3) ◽  
pp. 542-542
Author(s):  
Maria-Eleni Roumelioti ◽  
Gregory Trietley ◽  
Thomas D Nolin ◽  
Yue-Harn Ng ◽  
Zhi Xu ◽  
...  

2008 ◽  
Vol 17 (9) ◽  
pp. 758-763 ◽  
Author(s):  
Jong Lian ◽  
Chi Hung Cheng ◽  
Yen Lin Chagn ◽  
Cheng Hwae Hsiong ◽  
†Chau Jen Lee

ASAIO Journal ◽  
1994 ◽  
Vol 40 (1) ◽  
pp. 62-66
Author(s):  
CHAU JEN LEE ◽  
CHENG HUEI HSIONG ◽  
YEN LIN CHANG ◽  
CHI HUNG CHENG ◽  
JONG DA LIAN

2017 ◽  
Vol 33 (6) ◽  
pp. 1025-1039 ◽  
Author(s):  
Maria-Eleni Roumelioti ◽  
Gregory Trietley ◽  
Thomas D Nolin ◽  
Yue-Harn Ng ◽  
Zhi Xu ◽  
...  

Blood ◽  
1993 ◽  
Vol 81 (12) ◽  
pp. 3382-3387 ◽  
Author(s):  
PR Greipp ◽  
JA Lust ◽  
WM O'Fallon ◽  
JA Katzmann ◽  
TE Witzig ◽  
...  

The plasma cell labeling index (PCLI) and serum beta 2-microglobulin (beta 2M) are independent prognostic factors in multiple myeloma (MM). Recently, levels of thymidine kinase (TK) and C-reactive protein (CRP) have been shown to have prognostic value. We studied 107 patients with newly diagnosed myeloma to determine whether TK and CRP values added prognostic information not already available using the PCLI and beta 2M. Univariate survival analysis showed prognostic significance for the PCLI, TK, beta 2M, age, serum albumin, and CRP. Multivariate analysis showed that only PCLI and beta 2M have independent prognostic significance. The survival curves were better separated using the PCLI and beta 2M than with other combinations of variables. Among nine patients under age 65 with low PCLI and low beta 2M, eight were alive almost 6 years after starting chemotherapy. These good-risk patients could not be identified by standard clinical features. Although creatinine and calcium were normal, other features such as bone lesions, osteoporosis, fracture, and anemia were present and stage distribution was similar to other patients in the study. In conclusion, PCLI and beta 2M measured at diagnosis are independent prognostic factors. They must be considered when interpreting the results of clinical trials and should be helpful in counseling patients and in designing new trials. When the PCLI and beta 2M values are known, the TK and CRP values do not add useful additional prognostic information.


2016 ◽  
Vol 70 (5) ◽  
pp. 348 ◽  
Author(s):  
Valdete TopciuShufta ◽  
Ram Miftari ◽  
Valdete Haxhibeqiri ◽  
Shpend Haxhibeqiri

Author(s):  
Suguru Yamamoto ◽  
Douglas S Fuller ◽  
Hirotaka Komaba ◽  
Takanobu Nomura ◽  
Ziad A Massy ◽  
...  

Abstract Background Uremic toxins are associated with various chronic kidney disease-related comorbidities. Indoxyl sulfate (IS), a protein-bound uremic toxin, reacts with vasculature, accelerating atherosclerosis and/or vascular calcification in animal models. Few studies have examined the relationship of IS with clinical outcomes in a large cohort of hemodialysis (HD) patients. Methods We included 1170 HD patients from the Japan Dialysis Outcomes and Practice Patterns Study Phase 5 (2012–15). We evaluated the associations of serum total IS (tIS) levels with all-cause mortality and clinical outcomes including cardiovascular (CV)-, infectious- and malignancy-caused events using Cox regressions. Results The median (interquartile range) serum tIS level at baseline was 31.6 μg/mL (22.6–42.0). Serum tIS level was positively associated with dialysis vintage. Median follow-up was 2.8 years (range: 0.01–2.9). We observed 174 deaths (14.9%; crude rate, 0.06/year). Serum tIS level was positively associated with all-cause mortality [adjusted hazard ratio per 10 μg/mL higher, 1.16; 95% confidence interval (CI) 1.04–1.28]. Association with cause-specific death or hospitalization events, per 10 μg/mL higher serum tIS level, was 1.18 (95% CI 1.04–1.34) for infectious events, 1.08 (95% CI 0.97–1.20) for CV events and 1.02 (95% CI 0.87–1.21) for malignancy events after adjusting for covariates including several nutritional markers. Conclusions In a large cohort study of HD patients, serum tIS level was positively associated with all-cause mortality and infectious events.


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