Evidence map›Paper›PMID 34120289›Full record

ReviewReviews in endocrine & metabolic disorders2021

Beta-klotho in type 2 diabetes mellitus: From pathophysiology to therapeutic strategies.

Shuang Hua, Qianying Liu, Jufei Li, Mengqi Fan, Kaixuan Yan, Dewei Ye

Abstract readReview
PubMed Publisher
In one paragraph

Review in Reviews in endocrine & metabolic disorders, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 35 citations in OpenAlex.

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  18. Emerging roles of fibroblast growth factor 21 in critical disease.Frontiers in cardiovascular medicine · 2022
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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

6 authors at 1 institution in 2 countries.

Shuang HuaKey Laboratory of Glucolipid Metabolic Diseases of The Ministry of Education, Guangzhou, China.
Qianying LiuKey Laboratory of Glucolipid Metabolic Diseases of The Ministry of Education, Guangzhou, China.
Jufei LiKey Laboratory of Glucolipid Metabolic Diseases of The Ministry of Education, Guangzhou, China.
Mengqi FanKey Laboratory of Glucolipid Metabolic Diseases of The Ministry of Education, Guangzhou, China.
Kaixuan YanKey Laboratory of Glucolipid Metabolic Diseases of The Ministry of Education, Guangzhou, China.
Dewei YeKey Laboratory of Glucolipid Metabolic Diseases of The Ministry of Education, Guangzhou, China. deweiye@gdpu.edu.cn.ORCID 0000-0003-1295-3063
Ministry of Education of the People's Republic of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 2 diabetes mellitus (T2DM) has become a global health problem with no cure. Despite lifestyle modifications and various pharmaceutical options, the achievement of stable and durable glucose control along with effective prevention of T2DM-related cardiovascular complications remains a challenging task in clinical management. With its selective high abundance in metabolic tissues (adipose tissue, liver, and pancreas), β-Klotho is the essential component of fibroblast growth factor (FGF) receptor complexes. It is essential for high-affinity binding of endocrine FGF19 and FGF21 to evoke the signaling cascade actively involved in homeostatic maintenance of glucose metabolism and energy expenditure. In this Review, we discuss the biological function of β-Klotho in the regulation of glucose metabolism and offer mechanistic insights into its involvement in the pathophysiology of T2DM. We review our current understanding of the endocrine axis comprised of β-Klotho and FGFs (FGF19 and FGF21) and its regulatory effects on glucose metabolism under physiological and T2DM conditions. We also highlight advances in the development and preclinical validation of pharmacological compounds that target β-Klotho and/or the β-Klotho-FGFRs complex for the treatment of T2DM. Given the remarkable advances in this field, we also discuss outstanding research questions and the many challenges in the clinical development of β-Klotho-based therapies.

Indexed as

Diabetes Mellitus, Type 2Adipose TissueFibroblast Growth FactorsHomeostasisHumansLiverSignal TransductionFibroblast Growth FactorsDiabetesFGF21HyperglycemiaInsulin resistanceKlotho

Identifiers

PMID34120289
OpenAlexW3168838738

What Socratic holds

Textmetadata
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 Socratic graph.