Evidence map›Paper›PMID 38500057›Full record

ArticleBMC neurology2024

Investigating the causal relationship between immune cell and Alzheimer's disease: a mendelian randomization analysis.

Min Shen, Linlin Zhang, Chen Chen, Xiaocen Wei, Yuning Ma, Yuxia Ma

Open access · goldAbstract read
In one paragraph

Article in BMC neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Interleukin-6, CD8Frontiers in aging neuroscience · 2026
    Review
  6. [Exploring the Causal Relationship Between Circulating Immune Cells and Autoimmune Hepatitis Through Mendelian Randomization Analysis].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2025
    Article
  7. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Min ShenShandong University of Traditional Chinese Medicine, Jinan, Shandong Province, China.
Linlin ZhangShandong University of Traditional Chinese Medicine, Jinan, Shandong Province, China.
Chen ChenShandong University of Traditional Chinese Medicine, Jinan, Shandong Province, China.
Xiaocen WeiShandong University of Traditional Chinese Medicine, Jinan, Shandong Province, China.
Yuning MaShandong University of Traditional Chinese Medicine, Jinan, Shandong Province, China. myning0405@163.com.
Yuxia MaShandong University of Traditional Chinese Medicine, Jinan, Shandong Province, China. phdmayuxia@126.com.
Shandong University of Traditional Chinese Medicine · CN

Funding

Jinan "GaoXiao 20 Tiao" Funding Project Contract 2020GXRC005No. 3, NATCM's Project of High-level Construction of Key TCM Disciplines zyyzdxk-2023116The general program of Shandong Natural Science Foundation ZR2021MH373The Joint Fund of Natural Science Foundation of Shandong Province ZR2021LZY044
6 · The paper itself

Abstract

backgroundComplex interactions between the immune system and the brain may affect neural development, survival, and function, with etiological and therapeutic implications for neurodegenerative diseases. However, previous studies investigating the association between immune inflammation and Alzheimer's disease (AD) have yielded inconsistent results.

methodsWe applied Mendelian randomization (MR) to examine the causal relationship between immune cell traits and AD risk using genetic variants as instrumental variables. MR is an epidemiological study design based on genetic information that reduces the effects of confounding and reverse causation. We analyzed the causal associations between 731 immune cell traits and AD risk based on publicly available genetic data.

resultsWe observed that 5 immune cell traits conferred protection against AD, while 7 immune cell traits increased the risk of AD. These immune cell traits mainly involved T cell regulation, monocyte activation and B cell differentiation. Our findings suggest that immune regulation may influence the development of AD and provide new insights into potential targets for AD prevention and treatment. We also conducted various sensitivity analyses to test the validity and robustness of our results, which revealed no evidence of pleiotropy or heterogeneity.

conclusionOur research shows that immune regulation is important for AD and provides new information on potential targets for AD prevention and treatment. However, this study has limitations, including the possibility of reverse causality, lack of validation in independent cohorts, and potential confounding by population stratification. Further research is needed to validate and amplify these results and to elucidate the potential mechanisms of the immune cell-AD association.

Indexed as

Alzheimer DiseaseBrainCausalityGenome-Wide Association StudyHumansInflammationMendelian Randomization AnalysisAlzheimer’s diseaseBrainCausal inferenceImmune cellMR analysisSensitivity

Identifiers

PMID38500057
PMCPMC10946133
OpenAlexW4392919711

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.