1
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Evaluating serum CXCL12, sCD22, Lp-PLA2 levels and ratios as biomarkers for diagnosis of Alzheimer's disease

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          BACKGROUND

          Grasping the underlying mechanisms of Alzheimer's disease (AD) is still a work in progress, and existing diagnostic techniques encounter various obstacles. Therefore, the discovery of dependable biomarkers is essential for early detection, tracking the disease's advancement, and steering treatment strategies.

          AIM

          To explore the diagnostic potential of serum CXCL12, sCD22, Lp-PLA2, and their ratios in AD, aiming to enhance early detection and inform targeted treatment strategies.

          METHODS

          The study was conducted in Dongying people's Hospital from January 2021 to December 2022. Participants included 60 AD patients (AD group) and 60 healthy people (control group). Using a prospective case-control design, the levels of CXCL12, sCD22 and Lp-PLA2 and their ratios were detected by enzyme-linked immunosorbent assay kit in the diagnosis of AD. The differences between the two groups were analyzed by statistical methods, and the corresponding ratio was constructed to improve the specificity and sensitivity of diagnosis.

          RESULTS

          Serum CXCL12 levels were higher in the AD group (47.2 ± 8.5 ng/mL) than the control group (32.8 ± 5.7 ng/mL, P < 0.001), while sCD22 levels were lower (14.3 ± 2.1 ng/mL vs 18.9 ± 3.4 ng/mL, P < 0.01). Lp-PLA2 levels were also higher in the AD group (112.5 ± 20.6 ng/mL vs 89.7 ± 15.2 ng/mL, P < 0.05). Significant differences were noted in CXCL12/sCD22 (3.3 vs 1.7, P < 0.001) and Lp-PLA2/sCD22 ratios (8.0 vs 5.2, P < 0.05) between the groups. Receiver operating characteristic analysis confirmed high sensitivity and specificity of these markers and their ratios in distinguishing AD, with area under the curves ranging from 0.568 to 0.787.

          CONCLUSION

          Serum CXCL12 and Lp-PLA2 levels were significantly increased, while sCD22 were significantly decreased, as well as increases in the ratios of CXCL12/sCD22 and Lp-PLA2/sCD22, are closely related to the onset of AD. These biomarkers and their ratios can be used as potential diagnostic indicators for AD, providing an important clinical reference for early intervention and treatment.

          Related collections

          Most cited references29

          • Record: found
          • Abstract: found
          • Article: not found

          Alzheimer's disease

          In this Seminar, we highlight the main developments in the field of Alzheimer's disease. The most recent data indicate that, by 2050, the prevalence of dementia will double in Europe and triple worldwide, and that estimate is 3 times higher when based on a biological (rather than clinical) definition of Alzheimer's disease. The earliest phase of Alzheimer's disease (cellular phase) happens in parallel with accumulating amyloid β, inducing the spread of tau pathology. The risk of Alzheimer's disease is 60-80% dependent on heritable factors, with more than 40 Alzheimer's disease-associated genetic risk loci already identified, of which the APOE alleles have the strongest association with the disease. Novel biomarkers include PET scans and plasma assays for amyloid β and phosphorylated tau, which show great promise for clinical and research use. Multidomain lifestyle-based prevention trials suggest cognitive benefits in participants with increased risk of dementia. Lifestyle factors do not directly affect Alzheimer's disease pathology, but can still contribute to a positive outcome in individuals with Alzheimer's disease. Promising pharmacological treatments are poised at advanced stages of clinical trials and include anti-amyloid β, anti-tau, and anti-inflammatory strategies.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: found
            Is Open Access

            Aducanumab for Alzheimer’s disease?

            Patients and families need hope, not false hope
              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              CD22: A Regulator of Innate and Adaptive B Cell Responses and Autoimmunity

              CD22 (Siglec 2) is a receptor predominantly restricted to B cells. It was initially characterized over 30 years ago and named “CD22” in 1984 at the 2nd International workshop in Boston (1). Several excellent reviews have detailed CD22 functions, CD22-regulated signaling pathways and B cell subsets regulated by CD22 or Siglec G (2–4). This review is an attempt to highlight recent and possibly forgotten findings. We also describe the role of CD22 in autoimmunity and the great potential for CD22-based immunotherapeutics for the treatment of autoimmune diseases such as systemic lupus erythematosus (SLE).
                Bookmark

                Author and article information

                Contributors
                Journal
                World J Psychiatry
                WJP
                World Journal of Psychiatry
                Baishideng Publishing Group Inc
                2220-3206
                19 March 2024
                19 March 2024
                : 14
                : 3
                : 380-387
                Affiliations
                Department of Neurology, Dongying People's Hospital, Dongying 257000, Shandong Province, China
                Department of Neurology, Dongying People's Hospital, Dongying 257000, Shandong Province, China
                Department of Neurology, Dongying People's Hospital, Dongying 257000, Shandong Province, China
                Department of Neurology, Dongying People's Hospital, Dongying 257000, Shandong Province, China
                Department of Neurology, Dongying People's Hospital, Dongying 257000, Shandong Province, China. huifangzhang2@ 123456163.com
                Author notes

                Co-first authors: Zeng-Ling Liu and Fei-Fei Hua.

                Author contributions: Liu ZL, Hua FF and Zhang HF conceived and designed the study; Qu L and Yan N provided clinical advice; Liu ZL and Hua FF analyzed the data; Liu ZL and Hua FF prepared the manuscript; all authors have read and approved the final version of the manuscript. Liu ZL and Hua FF made the same contribution to this work and should share the first authorship. The involvement of Liu ZL and Hua FF in the research was equally significant. Their joint appointment as co-first authors serve to acknowledge their equal contributions and underscores the spirit of cooperation and teamwork inherent in our study. Conclusively, it is our belief that naming Liu ZL and Hua FF as co-first authors suitably reflect the essence of our team's collaborative efforts, equal input, and varied strengths.

                Corresponding author: Hui-Fang Zhang, MMed, Staff Physician, Department of Neurology, Dongying People's Hospital, No. 317 Dongcheng South 1st Road, Dongying District, Dongying 257000, Shandong Province, China. huifangzhang2@ 123456163.com

                Article
                jWJP.v14.i3.pg380 90856
                10.5498/wjp.v14.i3.380
                11008386
                0672a9ec-a2ec-4db6-b531-63a00a16bd8a
                ©The Author(s) 2024. Published by Baishideng Publishing Group Inc. All rights reserved.

                This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.

                History
                : 17 December 2023
                : 15 January 2024
                : 4 February 2024
                Categories
                Case Control Study

                alzheimer's disease,biomarkers,cxcl12,scd22,lp-pla2
                alzheimer's disease, biomarkers, cxcl12, scd22, lp-pla2

                Comments

                Comment on this article