摩洛哥东部人口的单克隆丙种球蛋白病特征:大学医院的研究结果。

Q2 Medicine Electronic Journal of the International Federation of Clinical Chemistry and Laboratory Medicine Pub Date : 2024-10-30 eCollection Date: 2024-10-01
Oussama Grari, Kaoutar Benaissa, Nisma Douzi, Imad-Eddine Elkhamlichi, Amina Himri, Dounia Elmoujtahide, El-Houcine Sebbar, Mohammed Choukri
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引用次数: 0

摘要

背景:单克隆丙种球蛋白病(MG)很常见,尤其是在老年人中。本研究旨在确定摩洛哥穆罕默德六世大学医院生化科七年来发现的 MG 的特征和病因:研究时间为 2016 年 1 月 1 日至 2023 年 9 月 1 日,涉及居住在摩洛哥东部的 224 名患者。通过毛细管区带电泳对 MG 进行诊断,然后通过免疫固定法进行确诊:研究共纳入 224 名患者,确诊时的平均年龄为 65.91 岁。男性 122 人(54.46%),女性 102 人(45.54%),性别比为 1.19。就免疫球蛋白异型而言,IgG 是最常见的单克隆蛋白(59.82%),其次是 IgA(19.64%)和 IgM(6.71%)。此外,11.6%的病例仅有游离轻链(FLC)分泌,2.23%的病例有双克隆抗体病。我们研究中的诊断分布包括多发性骨髓瘤(MM)(78.57%)、淋巴瘤(5.35%)、浆细胞白血病(4.02%)、瓦尔登斯特伦巨球蛋白血症(WM)(3.57%)和 MGUS(1.79%):我们的研究发现,MM的发病率高于MGUS。结论:我们的研究表明,MM 的发病率高于 MGUS。导致这一发病率的因素可能有多种,包括医疗服务的可及性、人口统计学特征以及其他值得进一步研究的潜在因素。
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Characterizing Monoclonal Gammopathies in an East Moroccan Population: University Hospital Findings.

Background: Monoclonal gammopathies (MG) are frequent, especially among older people. This study aims to establish the features and etiologies of MG detected over seven years in the Biochemistry department of Mohammed VI University Hospital in Morocco.

Methods: The study was performed from Jan 1, 2016, to Sept 1, 2023, and involved 224 patients residing in east Morocco. The diagnosis of MG was conducted through capillary zone electrophoresis, followed by confirmation through immunofixation.

Results: The study included 224 patients, with an average age at diagnosis of 65.91 years. There were 122 (54.46%) males and 102 (45.54%) females, for a sex ratio of 1.19. In terms of immunoglobulin isotypes, IgG was found to be the most common monoclonal protein (59.82%), followed by IgA (19.64%) and IgM (6.71%). Furthermore, 11.6% of cases had exclusive free light chain (FLC) secretion, and 2.23% had biclonal gammopathy. The distribution of diagnoses in our study included multiple myeloma (MM) (78.57%), lymphoma (5.35%), plasma cell leukemia (4.02%), Waldenström macroglobulinemia (WM) (3.57%), and MGUS (1.79%).

Conclusions: Our study noted the high frequency of MM over MGUS. Several factors could contribute to this prevalence, including variations in healthcare access, demographic characteristics, and potentially other elements that warrant further investigation.

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