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营养对镰状细胞病成人患者疾病严重程度及健康相关生活质量的影响:一项前瞻性研究。

Influence of Nutrition on Disease Severity and Health-related Quality of Life in Adults with Sickle Cell Disease: A Prospective Study.

作者信息

Kamal Sanaa, Naghib Moheyeldeen Mohamed, Al Zahrani Jamaan, Hassan Huda, Moawad Karim, Arrahman Omar

机构信息

Department of Medicine, Prince Sattam Bin Abdul Aziz College of Medicine, Kingdom of Saudi Arabia.

Department of Medicine, Ain Shams Faculty of Medicine, Cairo, Egypt.

出版信息

Mediterr J Hematol Infect Dis. 2021 Jan 1;13(1):e2021007. doi: 10.4084/MJHID.2021.007. eCollection 2021.

Abstract

BACKGROUND & AIMS: Sickle cell disease (SCD), a genetic disorder resulting from the presence of a mutated hemoglobin S (HbS), has a worldwide distribution and causes significant morbidity and mortality in children and adults. Few studies addressed the determinants of SCD severity in adults; therefore, we investigated the impact of nutrition on the outcome of SCD and health-related quality of life (HRQoL) in adult patients.

METHODS

In this longitudinal study, we recruited and prospectively followed 62 adults with SCD (aged ≥18 years) for a median of 93 months. At entry and follow-up, patients provided medical and dietary history, had a physical examination and anthropometric measurements, assessed protein-energy intake, measurement of micronutrient levels, estimation of SCD severity score, and determination of the HRQoL (SF-26v2). The study outcome was a composite of hospitalization due to SCD crises or death.

RESULTS

At baseline, 42 (67.74%) patients had macro and, or micro-undernutrition (Group A), and 20 (32.26%) were well nourished. (Group B). The BMI and most anthropometric measurements were significantly lower in SCD patients compared to control subjects. Seventy percent of SCD patients had vitamin D, vitamin B12, and zinc deficiencies. Thirty-six under-nourished patients (86%) had gastrointestinal disorders. During follow-up, 46 patients (74.19%) developed one or more vaso-occlusive pain crises or other SCD related complications that required hospitalization. Significant differences in most domains existed between well-nourished and undernourished SCD patients. Protein-energy and micronutrient deficiencies were independent predictors of severe SCD and mortality. Correction of undernutrition and hydroxyurea therapy improved SCD severity scores and HRQoL.

CONCLUSIONS

Patients with sickle cell disease have various degrees of macro and micro deficiencies, which increase SCD severity and hospitalizations and reduce the health-related quality of life. Early diagnosis and prompt correction of macro and micronutrient deficiencies need to be incorporated in the standard of care of SCD patients to improve the disease outcomes.

摘要

背景与目的

镰状细胞病(SCD)是一种由突变的血红蛋白S(HbS)导致的遗传性疾病,在全球范围内均有分布,可导致儿童和成人出现显著的发病率和死亡率。很少有研究探讨成人SCD严重程度的决定因素;因此,我们调查了营养对成年SCD患者的结局及健康相关生活质量(HRQoL)的影响。

方法

在这项纵向研究中,我们招募了62名成年SCD患者(年龄≥18岁)并对其进行前瞻性随访,中位随访时间为93个月。在入组和随访时,患者提供了病史和饮食史,接受了体格检查和人体测量,评估了蛋白质能量摄入、微量营养素水平测定、SCD严重程度评分估计以及HRQoL(SF-26v2)测定。研究结局是因SCD危象或死亡导致的住院综合情况。

结果

在基线时,42名(67.74%)患者存在宏量和/或微量营养素缺乏(A组),20名(32.26%)营养状况良好(B组)。与对照受试者相比,SCD患者的BMI和大多数人体测量指标显著更低。70%的SCD患者存在维生素D、维生素B12和锌缺乏。36名营养不良患者(86%)患有胃肠道疾病。在随访期间,46名患者(74.19%)发生了一次或多次血管闭塞性疼痛危象或其他与SCD相关的并发症,需要住院治疗。营养良好和营养不良的SCD患者在大多数领域存在显著差异。蛋白质能量和微量营养素缺乏是严重SCD和死亡率的独立预测因素。纠正营养不良和羟基脲治疗可改善SCD严重程度评分和HRQoL。

结论

镰状细胞病患者存在不同程度的宏量和微量营养素缺乏,这会增加SCD的严重程度和住院率,并降低健康相关生活质量。需要将宏量和微量营养素缺乏的早期诊断和及时纠正纳入SCD患者的标准治疗中,以改善疾病结局。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b4f/7813275/d18a8e55236c/mjhid-13-1-e2021007f1.jpg

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