Journal of Laboratory and Precision Medicine实验室与精准医学杂志

Journal of Laboratory and Precision Medicine(英文缩写 J LAB PRECIS MED),ISSN 2519-9005,eISSN 2519-9005,中文译名:实验室与精准医学杂志 是一本学术期刊。本页汇总该期刊的最新影响因子、分区信息以及最新收录于 PubMed 的文献,帮助您快速了解期刊全貌。

2026 年数据 · 影响因子
1.800
JCR 分区
Q3
CAS 分区
-
近一年发文量
0
本站 PubMed 收录统计

发文量统计区间:2025-11-01 至 2026-10-31,按本站收录文献的发表日期统计。

ISSN: 2519-9005 · eISSN: 2519-9005 · 缩写: J LAB PRECIS MED ·中文: 实验室与精准医学杂志

期刊介绍

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期刊简介

Journal of Laboratory and Precision Medicine 是一本聚焦检验医学与精准医学交叉领域的开放获取期刊,关注实验室检测技术、生物标志物、个体化诊疗及临床决策支持。内容涵盖分子诊断、质谱分析、临床生化与免疫检测等方向,读者群包括检验科医师、临床研究者、实验室科学家及从事精准医疗转化的专业人员。

研究方向

主要发表检验医学与精准医学相关的研究,包括新型检测方法开发与验证、生物标志物发现、实验室质量管理、分子与基因组诊断、治疗药物监测及临床检验结果向个体化医疗的转化。论文类型以原创研究、综述、方法学报告和短篇通讯为主。

期刊特色

研究取向强调实验室技术与临床应用的衔接,重视分析性能验证和临床效用评估。论文通常要求方法描述清晰、数据完整,并讨论对精准诊疗的实际意义。适合检验医学、临床化学、分子诊断领域的研究者、研究生及希望了解检测技术临床转化的临床医生阅读参考。

投稿难度

投稿难度中等,期刊对方法学严谨性和临床相关性有一定要求,但整体门槛低于顶级检验医学刊物。建议准备时突出检测方法的创新点或临床验证数据,明确研究在精准医疗场景中的定位,并注意统计分析与伦理声明的完整性,避免仅报告分析性能而缺乏临床意义讨论。

历年影响因子趋势

JCR 数据年份影响因子JCR 分区
20241.400Q3
20251.800Q3

Journal of Laboratory and Precision Medicine 最新收录文献

  1. JCR分区: Q3 CAS分区: N/A 影响因子: 1.8

    1. Impact of trimethylamine N-oxide (TMAO) metaorganismal pathway on cardiovascular disease.

    1. 氧化三甲胺(TMAO)元生物通路对心血管疾病的影响
    作者:
    Yongzhong Zhao, Zeneng Wang
    日期:
    2020-04-20

    Host-microbes interaction plays a crucial role in cardiovascular disease (CVD) pathogenesis, mechanistically via metaorganismal pathways. The trimethylamine N-oxide (TMAO) metaorganismal pathway is the most deeply investigated one, which comprises trimethylamine precursors, such as choline, trimethylamine lyase, trimethylamine, host liver FMO3, TMAO, and downstream effectors involving unfolded protein response (UPR), NF-κB and NLRP3 inflammasome. Accumulating data from clinical investigations of CVD patient cohorts and rodent models have supported the critical role of this metaorganismal pathway in the pathogenesis of CVD. We summarize an array of significant animal studies especially for arthrosclerosis with an emphasis on downstream molecular effectors of this metaorganismal pathway. We highlight clinical investigations of the prognostic value of plasma TMAO levels in predicting prospective risk for future major adverse cardiac events (MACE) indicated by composite end points of myocardial infarction (MI), stroke, heart failure (HF), other ischemic cardiovascular events, or death. Further, we discuss the latest advances of preclinical models targeting the gut microbiota trimethylamine lyase of the TMAO metaorganismal pathway for CVD intervention, as well as the catalog of gut microbiota TMA lyase genes and microbes in the human gut as the prerequisite for potential clinical intervention. In-depth characterization of TMAO metaorganismal pathway holds great promise for CVD clinical metagenomics, diagnostics and therapeutics.

  2. JCR分区: Q3 CAS分区: N/A 影响因子: 1.8

    2. GlycA: A New Biomarker for Systemic Inflammation and Cardiovascular Disease (CVD) Risk Assessment.

    2. GlycA:系统性炎症和心血管疾病(CVD)风险评估的新生物标志物
    作者:
    Rami A Ballout, Alan T Remaley
    日期:
    2020-04-20

    The GlycA test is a recently developed proton nuclear magnetic resonance (H-NMR) spectroscopy-based assay that has been gaining increased interest as a serum biomarker for systemic inflammation, and consequently, as a potential biomarker for cardiovascular disease (CVD) risk assessment. The test has undergone investigation in several large cohort studies, since its development, to assess its predictive value for incident CVD events, CVD-associated mortality, and all-cause mortality. Despite variation in the generated estimates by these studies, they have all consistently demonstrated moderate-strength positive correlations between baseline GlycA levels, and incident CVD event rates and associated mortality. These correlations withheld testing even after adjusting for several other established CVD risk factors, including notable inflammatory biomarkers such as high-sensitivity C-reactive protein (hsCRP) and interleukin-6 (IL-6). Compared with hsCRP, which is a well-known inflammatory biomarker for CVD risk assessment, GlycA has a comparable predictive value for future CVD-related events. However, the indications to pursue GlycA testing, and its clinical utility in patient care management, are yet to be determined. In this review, we define the GlycA test and what it "measures", and provide a brief summary of the findings of studies showing its association with incident CVD rates, and CVD-related mortality, as well as its correlation with other inflammatory biomarkers, namely hsCRP. Finally, we highlight the analytical advantages of the GlycA test, compared with "traditional" inflammatory biomarkers, while also mentioning its current limitations.

  3. JCR分区: Q3 CAS分区: N/A 影响因子: 1.8

    3. Prognostic value of Sjögren's syndrome autoantibodies.

    3. 干燥综合征自身抗体的预后价值
    作者:
    R Hal Scofield, Anum Fayyaz, Biji T Kurien, Kristi A Koelsch
    日期:
    2018-10-30

    Sjögren's syndrome is in part considered an autoimmune disease because patient sera contain antibodies binding self-structures. In fact, in addition to anti-Ro (or SSA) and anti-La (or SSB), which are included in the classification criteria, there are a wide variety of autoantibodies found among these patients. We reviewed English-language MEDLINE sources. Anti-Ro and anti-La found among healthy individuals, including mothers giving birth to infants with neonatal lupus, predicts future connective tissue disease. Those with Sjögren's syndrome can be divided into two groups; patients with only exocrine gland involvement and those with systemic disease. The presence of anti-Ro/La is associated with systemic, extraglandular disease. Rheumatoid factor is also associated with extraglandular disease while anti-cyclic citrullinated peptide (CCP) is likely associated with inflammatory arthritis and progression to rheumatoid arthritis. Anti-mitochondrial antibodies are uncommon but predict progression to primary biliary cirrhosis. Cryoglobulinemia is found in excess among those with non-Hodgkin's lymphoma. Determination of autoantibodies on the sera of Sjögren's syndrome patients has prognostic implications for Sjögren's syndrome itself as well as associated diseases.

  4. JCR分区: Q3 CAS分区: N/A 影响因子: 1.8
  5. JCR分区: Q3 CAS分区: N/A 影响因子: 1.8

    5. Is Keratin-18 only a Marker of Cell Death in Acute-On-Chronic Liver Failure?

    5. 角蛋白-18仅仅是慢加急性肝衰竭中细胞死亡的标志物吗?
    作者:
    Benjamin L Woolbright, Hartmut Jaeschke
    日期:
    2018-03-20

    该文献暂无摘要。

  6. JCR分区: Q3 CAS分区: N/A 影响因子: 1.8

    6. CD4:CD8 ratio and CD8+ cell count for prognosticating mortality in HIV-infected patients on antiretroviral therapy.

    6. CD4:CD8比值和CD8+细胞计数对接受抗逆转录病毒治疗的HIV感染者死亡率的预后预测
    作者:
    Jeffrey Daniel Jenks, Martin Hoenigl
    日期:
    2018-02-02

    该文献暂无摘要。

  7. JCR分区: Q3 CAS分区: N/A 影响因子: 1.8
  8. JCR分区: Q3 CAS分区: N/A 影响因子: 1.8
  9. JCR分区: Q3 CAS分区: N/A 影响因子: 1.8

    9. Cardiorenal biomarkers: one step closer.

    作者:
    Xiao-Jun Chen, Amir Lerman, Lilach O Lerman
    日期:
    2017-05

    该文献暂无摘要。

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指标接近的期刊