Prevalence and Overlap of Malnutrition, Sarcopenia and Related Nutritional Syndromes in a Large Haemodialysis Population.

IF 9.1 1区 医学
Hanaa Noor, Subhashini Ganesan, Flavia Martinez Cantarutti, Ali Alharbi, Imed Helal, Joanne Reid, Adrian Slee
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引用次数: 0

Abstract

Background: Chronic kidney disease is a major global health burden linked to malnutrition, sarcopenia and related nutritional syndromes including protein-energy wasting (PEW)/cachexia and sarcopenic obesity (SO). Data from end-stage kidney disease (ESKD) populations in Saudi Arabia and the wider Middle East are scarce. This study assessed the prevalence and factors associated with malnutrition and sarcopenia risk in a large haemodialysis (HD) cohort and the co-occurrence of PEW/cachexia risk and SO.

Methods: Multicentre, cross-sectional study in 40 dialysis clinics across Saudi Arabia (June-August 2024). Adults on maintenance HD ≥ 90 days were screened using the malnutrition-inflammation score (MIS; high risk > 5), SARC-F (sarcopenia risk ≥ 4) high risk, calf circumference (CC; cut-offs ≤ 34-cm males, ≤ 33-cm females), CC adjusted for body mass index (BMI) and oedema (Adj. CC) and SARC-CalF (sarcopenia risk ≥ 11). SO was defined as sarcopenia risk by SARC-CalF (Adj. CC) plus BMI > 30 kg/m2. Routine blood chemistry (e.g., total iron-binding capacity [TIBC] and albumin) and screening tools were collected for physical function (Karnofsky), falls risk (Morse fall) and comorbidity (Charlson index). Univariate and multivariate logistic regression (adjusted for age, sex, diabetes, dialysis vintage and Kt/V) identified factors associated with each outcome.

Results: Of 3722 HD patients (56.8% male; age 53.6 ± 15.8 years; BMI 26.8 ± 6.4 kg/m2), 48% had diabetes and 35% had high/very high Charlson comorbidity index. High nutritional risk (MIS > 5) was found in 44.5% (n = 1657) and sarcopenia risk (SARC-CalF [Adj. CC]) in 53.1% (n = 1978); 31.6% (n = 1175) had combined malnutrition and sarcopenia (M + S) and 7.7% (n = 285) had SO. Versus the no-risk group, M + S patients had lower albumin, TIBC, Karnofsky score and higher comorbidity index and Morse fall risk score (all p < 0.001). Independent factors associated with high nutritional risk included lower BMI, higher Charlson index, longer dialysis vintage, lower serum creatinine and higher triglycerides (all p < 0.05). Shared independent factors for sarcopenia risk were older age, higher comorbidity index, longer dialysis duration, lower creatinine and higher triglycerides (all p < 0.05).

Conclusions: This is the first large-scale study to fully characterise a Saudi and Middle Eastern HD cohort. There was a very high risk of malnutrition and sarcopenia. Furthermore, a high number had both conditions and overlapping features of PEW/cachexia, which included high comorbidity and disability risk. Findings support routine, multitool nutritional and muscle screening in HD care, including younger patients.

大量血液透析人群中营养不良、肌肉减少和相关营养综合征的患病率和重叠。
背景:慢性肾脏疾病是与营养不良、肌肉减少症和相关营养综合征(包括蛋白质-能量消耗(PEW)/恶病质和肌肉减少性肥胖(SO))相关的主要全球健康负担。来自沙特阿拉伯和更广泛中东地区终末期肾病(ESKD)人群的数据很少。本研究评估了大型血液透析(HD)队列中营养不良和肌肉减少风险的患病率和相关因素,以及PEW/恶病质风险和SO的共同发生。方法:2024年6月- 8月在沙特阿拉伯40个透析诊所进行多中心横断面研究。采用营养不良-炎症评分(MIS,高风险bbbb5)、SARC-F(肌肉减少症风险≥4)高风险、小腿围(CC;临界值≤34 cm男性,≤33 cm女性)、体重指数(BMI)和水肿调整后的CC (Adj. CC)和SARC-CalF(肌肉减少症风险≥11)筛查维持HD≥90天的成年人。通过SARC-CalF (Adj. CC)和BMI bbb30 kg/m2将SO定义为肌少症风险。收集常规血化学指标(如总铁结合能力(TIBC)和白蛋白)和身体功能(Karnofsky)、跌倒风险(Morse跌倒)和合并症(Charlson指数)的筛查工具。单因素和多因素logistic回归(调整了年龄、性别、糖尿病、透析时间和Kt/V)确定了与每个结果相关的因素。结果:3722例HD患者(男性56.8%,年龄53.6±15.8岁,BMI 26.8±6.4 kg/m2)中,48%合并糖尿病,35%合并高/甚高Charlson合并症指数。高营养风险(MIS 5)者占44.5% (n = 1657),骨骼肌减少风险(SARC-CalF [Adj. CC])者占53.1% (n = 1978);31.6% (n = 1175)合并营养不良和肌肉减少症(M + S), 7.7% (n = 285)合并SO。与无风险组相比,M + S患者的白蛋白、TIBC、Karnofsky评分较低,合并症指数和Morse跌倒风险评分较高(均为p)。结论:这是首次全面表征沙特和中东HD队列的大规模研究。营养不良和肌肉减少症的风险非常高。此外,大量患者同时具有皮尤/恶病质的条件和重叠特征,包括高合并症和残疾风险。研究结果支持在包括年轻患者在内的HD护理中进行常规、多工具营养和肌肉筛查。
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来源期刊
Journal of Cachexia, Sarcopenia and Muscle
Journal of Cachexia, Sarcopenia and Muscle Medicine-Orthopedics and Sports Medicine
自引率
12.40%
发文量
0
期刊介绍: The Journal of Cachexia, Sarcopenia, and Muscle is a prestigious, peer-reviewed international publication committed to disseminating research and clinical insights pertaining to cachexia, sarcopenia, body composition, and the physiological and pathophysiological alterations occurring throughout the lifespan and in various illnesses across the spectrum of life sciences. This journal serves as a valuable resource for physicians, biochemists, biologists, dieticians, pharmacologists, and students alike.
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