| Literature DB >> 35215451 |
Hayato Fujioka1, Tsutomu Koike1, Teruhiko Imamura1, Fumihiro Tomoda2, Kota Kakeshita1, Hidenori Yamazaki1, Koichiro Kinugawa1.
Abstract
The prognostic impact of the combination of a geriatric nutritional risk index (GRNI) and modified creatinine index, both of which assess nutritious status in hemodialysis patients, has not yet been well investigated thus far. Patients receiving maintenance hemodialysis in our institutes between February 2011 and January 2017 were retrospectively included. The baseline GRNI and modified Creatinine index were calculated and the impact of their combination on 5-year all-cause mortality following the index hemodialysis was investigated. A total of 183 patients (68.3 ± 12.4 years, 98 men, hemodialysis duration 97 ± 89 months) were followed from the index hemodialysis for 5.5 years. Mean GNRI was 91.2 and mean modified Creatinine index was 22.2 in men and 19.6 in women. The 5-year survival was significantly stratified by the median values of GNRI and modified Creatinine index (p < 0.05 for both). Patients with low GNRI and a low modified Creatinine index had lower 5-year survival than those with the other three combination patterns (p < 0.05). A combination of GNRI and modified Creatinine index may be a promising tool to risk stratify mortality in dialysis patients.Entities:
Keywords: end-stage renal disease; inflammation; malnutrition
Mesh:
Substances:
Year: 2022 PMID: 35215451 PMCID: PMC8878210 DOI: 10.3390/nu14040801
Source DB: PubMed Journal: Nutrients ISSN: 2072-6643 Impact factor: 5.717
Baseline characteristics.
| N = 183 | |
|---|---|
| Demographics | |
| Males, | 98 (53.6) |
| Age, years | 68.3 ± 12.4 |
| Dialysis vintage, month | 97 ± 89 |
| Systolic blood pressure, mmHg | 150 ± 25 |
| Comorbidity | |
| Presence of diabetes, | 76 (41) |
| History of cardiovascular events, | 51 (27) |
| Charlson risk index | 3.5 ± 1.3 |
| Cause of end-stage renal disease | |
| Diabetic nephropathy, | 74 (40.4) |
| Chronic glomerulonephritis, | 48 (26.2) |
| Glomerulosclerosis, | 48 (26.2) |
| Polycystic disease, | 16 (8.7) |
| Others, | 16 (8.7) |
| Laboratory data | |
| Hemoglobin, g/dL | 10.0 ± 1.2 |
| Serum albumin, g/dL | 3.4 ± 0.4 |
| Serum urea nitrogen, mg/dL | 60.4 ± 14.5 |
| Serum creatinine, mg/dL | 10.6 ± 2.6 |
| Serum uric acid, mg/dL | 7.6 ± 1.2 |
| Corrected serum calcium, mg/dL | 9.3 ± 0.7 |
| Serum phosphate, mg/dL | 5.0 ± 1.2 |
| Serum C-reactive protein, mg/dL | 0.4 ± 0.7 |
| Serum total cholesterol, mg/dL | 148 ± 29 |
| Serum triglycerides, mg/dL | 109 ± 53 |
| Intact parathormone, pg/mL | 155 ± 167 |
| Kt/V ratio for urea | 1.43 ± 0.28 |
| Index | |
| GNRI | 91.2 ± 10.9 |
| Modified Cr index (male), mg/kg/day | 22.2 ± 2.5 |
| Modified Cr index (female), mg/kg/day | 19.6 ± 2.2 |
| Medication | |
| Angiotensin receptor blocker, | 81 (48) |
| Calcium channel blocker, | 101 (60) |
| Beta-blocker, | 34 (20) |
| Statin, | 25 (15) |
| Anti-platelets, | 82 (49) |
Cr, creatinine; GNRI, geriatric nutritional risk index.
Figure 1Five-year survival stratified by GNRI (A), modified Cr index (B), and a combination of both (C). Cr, creatinine; GNRI, geriatric nutritional risk index.
Prognostic impacts of each index.
| Unadjusted Model | Multivariable | Multivariable | Multivariable | |||||
|---|---|---|---|---|---|---|---|---|
| Hazard Ratio | Hazard Ratio | Hazard Ratio | Hazard Ratio | |||||
| GNRI | ||||||||
| High GNRI | 1.00 (reference) | - | 1.00 (reference) | - | 1.00 (reference) | - | 1.00 (reference) | - |
| Low GNRI | 2.59 (1.59–4.23) | <0.001 | 2.18 (1.31–3.64) | <0.01 | 2.19 (1.29–3.73) | <0.01 | 2.05 (1.17–3.60) | <0.05 |
| Modified Cr index | ||||||||
| High modified Cr index | 1.00 (reference) | - | 1.00 (reference) | - | 1.00 (reference) | - | 1.00 (reference) | - |
| Low modified Cr index | 3.15 (1.89–5.26) | <0.001 | 2.02 (1.11–3.68) | <0.05 | 1.81 (0.97–3.35) | 0.06 | 1.82 (0.94–3.50) | 0.07 |
Unadjusted and multivariable-adjusted HRs were analyzed by the Cox proportional hazards risk model with all-cause death. Multivariable-adjusted model 1 was adjusted for age and sex. Model 2 was adjusted for age, sex, dialysis vintage, the presence of diabetes and history of cardiovascular events. Model 3 was adjusted for age, sex, dialysis vintage, hemoglobin, log10 C-reactive protein, phosphate, total cholesterol, intact parathormone, the presence of diabetes, history of cardiovascular events and Charlson risk index. A two-tailed p-value < 0.05 was considered statistically significant. High GNRI means GNRI ≥ 91.6. High Cr index means Cr index ≥22.3 for males or ≥19.9 for females. CI, confidence interval; Cr, creatinine; GNRI, geriatric nutritional risk index.
Number of patients who were assigned to high/low indexes.
| Men | Women | Total | |
|---|---|---|---|
| High GNRI and high modified Cr index, | 32 (32.7) | 22 (25.9) | 54 (29.5) |
| High GNRI and low modified Cr index, | 24 (24.5) | 14 (16.5) | 38 (20.8) |
| Low GNRI and high modified Cr index, | 16 (16.3) | 16 (18.8) | 32 (17.5) |
| Low GNRI and low modified Cr index, | 26 (26.5) | 33 (38.8) | 59 (32.2) |
High GNRI means GNRI ≥91.6. High Cr index means Cr index ≥22.3 for males or ≥19.9 for females. Cr, creatinine; GNRI, geriatric nutritional risk index.
Figure 2Five-year freedom free from cardiovascular death (A), infection death (B), and cancer death (C) stratified by a combination of GNRI and modified Cr index. Cr, creatinine; GNRI, geriatric nutritional risk index.
Prognostic impacts of combination of both indexes.
| Unadjusted Model | Multivariable | Multivariable | Multivariable | |||||
|---|---|---|---|---|---|---|---|---|
| Hazard Ratio | Hazard Ratio | Hazard Ratio | Hazard Ratio | |||||
| All-cause death | ||||||||
| High GNRI and high modified Cr index | 1.00 (reference) | - | 1.00 (reference) | - | 1.00 (reference) | - | 1.00 (reference) | - |
| High GNRI and low modified Cr index | 1.48 | 0.34 | 0.92 | 0.84 | 0.73 | 0.62 | 0.69 | 0.42 |
| Low GNRI and high modified Cr index | 1.04 | 0.93 | 1.11 | 0.83 | 1.06 | 0.9 | 0.75 | 0.55 |
| Low GNRI and low modified Cr index | 4.60 | <0.001 | 2.83 | <0.01 | 2.54 | <0.05 | 2.33 | <0.05 |
| Cardiovascular death | ||||||||
| High GNRI and high modified Cr index | 1.00 (reference) | - | 1.00 (reference) | - | 1.00 (reference) | - | 1.00 (reference) | - |
| High GNRI and low modified Cr index | 1.54 | 0.50 | 1.43 | 0.57 | 1.41 | 0.59 | 1.49 | 0.54 |
| Low GNRI and high modified Cr index | 1.07 | 0.92 | 0.87 | 0.86 | 0.69 | 0.63 | 0.69 | 0.65 |
| Low GNRI and low modified Cr index | 4.30 | <0.01 | 3.46 | <0.05 | 3.08 | 0.07 | 3.14 | 0.07 |
| Infection-associated death | ||||||||
| High GNRI and high modified Cr index | 1.00 (reference) | - | 1.00 (reference) | - | 1.00 (reference) | - | 1.00 (reference) | - |
| High GNRI and low modified Cr index | 0.31 | 0.29 | 0.28 | 0.25 | 0.25 | 0.20 | 0.21 | 0.17 |
| Low GNRI and high modified Cr index | 1.08 | 0.92 | 0.80 | 0.76 | 0.70 | 0.65 | 1.35 | 0.74 |
| Low GNRI and low modified Cr index | 3.95 | <0.05 | 3.23 | 0.05 | 2.99 | 0.08 | 8.45 | <0.01 |
Unadjusted and multivariable-adjusted HRs were analyzed by the Cox proportional hazards risk model with all-cause death. Multivariable-adjusted model 1 was adjusted for age and sex. Model 2 was adjusted for age, sex, dialysis vintage, the presence of diabetes and history of cardiovascular events. Model 3 was adjusted for age, sex, dialysis vintage, hemoglobin, log10 C-reactive protein, phosphate, total cholesterol, intact parathormone, the presence of diabetes, history of cardiovascular events and Charlson risk index. A two-tailed p-value < 0.05 was considered statistically significant. High GNRI means GNRI ≥ 91.6. High Cr index means Cr index ≥22.3 for males or ≥19.9 for females. Cr, creatinine; GNRI, geriatric nutritional risk index.