Evidence map›Paper›PMID 37065608›Full record

ArticleKidney diseases (Basel, Switzerland)2023

Intra-Brain and Plasma Levels of L-Serine Are Associated with Cognitive Status in Patients with Chronic Kidney Disease.

Yasunori Iwata, Yusuke Nakade, Masashi Kinoshita, Hemragul Sabit, Riho Nakajima, Kengo Furuichi, Masashi Mita, Maiko Nakane, Norihiko Sakai, Shinji Kitajima and 12 more

Open access · goldAbstract read
In one paragraph

Article in Kidney diseases (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
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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

22 authors at 4 institutions in 1 country.

Yasunori IwataDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Yusuke NakadeDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Masashi KinoshitaDepartment of Neurosurgery, Kanazawa University, Kanazawa, Japan.
Hemragul SabitDepartment of Neurosurgery, Kanazawa University, Kanazawa, Japan.
Riho NakajimaDepartment of Occupational Therapy, Kanazawa University, Kanazawa, Japan.
Kengo FuruichiDivision of Nephrology, Kanazawa Medical University School of Medicine, Kanazawa, Japan.
Masashi MitaKAGAMI Inc., Ibaraki, Japan.
Maiko NakaneKAGAMI Inc., Ibaraki, Japan.
Norihiko SakaiDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Shinji KitajimaDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Tadashi ToyamaDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Taro MiyagawaDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Akinori HaraDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Miho ShimizuDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Kouichi SatoDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Megumi OshimaDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Shiori NakagawaDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Yuta YamamuraDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Hisayuki OguraDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Yoshitaka KoshinoDepartment of Internal Medicine, Mizuho Hospital, Kahoku, Japan.
Mitsutoshi NakadaDepartment of Neurosurgery, Kanazawa University, Kanazawa, Japan.
Takashi WadaDepartment of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.
Kanazawa University · JPKagami Crystal (Japan) · JPKanazawa Medical University · JPSapporo Toho Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The number of patients with chronic kidney disease (CKD) is increasing worldwide. Cognitive impairment is one of the comorbidities of CKD. With the increased number of aged population, novel biomarkers of impaired cognitive function are required. Intra-body profile of amino acid (AA) is reportedly altered in patients with CKD. Although some AAs act as neurotransmitters in the brain, it is not clear whether altered AA profile are associated with cognitive function in patients with CKD. Therefore, intra-brain and plasma levels of AAs are evaluated with respect to cognitive function in patients with CKD. Methods: Plasma levels of AAs were compared between 14 patients with CKD, including 8 patients with diabetic kidney disease, and 12 healthy controls to identify the alteration of specific AAs in CKD. Then, these AAs were evaluated in the brains of 42 patients with brain tumor using non-tumor lesion of the resected brain. Cognitive function is analyzed with respect to intra-brain levels of AAs and kidney function. Moreover, plasma AAs were analyzed in 32 hemodialyzed patients with/without dementia. Results: In patients with CKD, plasma levels of asparagine (Asn), serine (Ser), alanine (Ala), and proline (Pro) were increased as compared to patients without CKD. Among these AAs, L-Ser, L-Ala, and D-Ser show higher levels than the other AAs in the brain. Intra-brain levels of L-Ser was correlated with cognitive function and kidney function. The number of D-amino acid oxidase or serine racemase-positive cells was not correlated with kidney function. Moreover, the plasma levels of L-Ser are also decreased in patients with declined cognitive function who are treated with chronic hemodialysis. Conclusion: The decreased levels of L-Ser are associated with impaired cognitive function in CKD patients. Especially, plasma L-Ser levels may have a potential for novel biomarker of impaired cognitive function in patients with hemodialysis.

Indexed as

Chronic kidney diseaseCognitive impairmentL-Serine

Identifiers

PMID37065608
PMCPMC10090982
OpenAlexW4316022106

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LicenceCC BY-NC
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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.