Evidence map›Paper›PMID 38740694›Full record

SynthesisEndocrine2024

iGlarLixi for type 2 diabetes: a systematic review and meta-analysis.

Yang Liu, Congxin Li, Xuejing Li, Jie Yang, Yingying Zheng, Fan Li, Xianying Wang

Abstract readSystematic ReviewMeta-Analysis
PubMed Publisher
In one paragraph

Synthesis in Endocrine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. 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

7 authors.

Yang LiuDepartment of Pharmacy, Hebei Medical University Third Hospital, Shijiazhuang, China.
Congxin LiDepartment of Pharmacy, Hebei Medical University Third Hospital, Shijiazhuang, China.
Xuejing LiDepartment of Pharmacy, Hebei Medical University Third Hospital, Shijiazhuang, China.
Jie YangDepartment of Pharmacy, Hebei Medical University Third Hospital, Shijiazhuang, China.
Yingying ZhengDepartment of Pharmacy, Hebei Medical University Third Hospital, Shijiazhuang, China.
Fan LiDepartment of Pharmacy, Hebei Medical University Third Hospital, Shijiazhuang, China.
Xianying WangDepartment of Pharmacy, Hebei Medical University Third Hospital, Shijiazhuang, China. 1316076234@qq.com.

Funding

Hebei Provincial Medical Science Research Project Plan in 2024 No. 20241798
6 · The paper itself

Abstract

objectivesTo assess the efficacy and tolerability of iGlarLixi-a novel, fixed-ratio, soluble combination of insulin glargine and lixisenatide-for the treatment of type 2 diabetes (T2D).

methodsThe PubMed, Embase, Cochrane Library and ClinicalTrials.gov databases were searched from inception to November 15, 2023 to identify randomized controlled trials (RCTs) comparing iGlarLixi with a placebo or any other antidiabetic agent in adults with T2D. Risk ratios (RRs) and mean differences (MDs) with 95% confidence intervals (CIs) were calculated to evaluate the outcomes.

resultsA total of 10 trials enrolling 6071 T2D patients were included. Compared with placebos or other antidiabetic agents, iGlarLixi exerted beneficial effects on changes in HbA1c, the percentage of patients who achieved an HbA1c < 7%, the percentage of patients who achieved an HbA1c < 6.5%, the percentage of patients who achieved an HbA1c < 7.0% without weight gain and/or without severe or blood glucose-confirmed hypoglycemic episodes, changes in fasting plasma glucose, and changes in self-measured plasma glucose. Regarding safety, iGlarLixi did not increase the incidence of severe hypoglycemia or serious adverse events but did increase the incidence of gastrointestinal adverse events, symptomatic hypoglycemia, and adverse events (e.g., nausea, vomiting, diarrhea).

conclusionsiGlarLixi showed improved efficacy and safety in patients with T2D. Additional large, multicenter RCTs are warranted to obtain deeper insights into the efficacy and safety of iGlarLixi, thereby providing guidance for clinical treatment decisions.

Indexed as

Diabetes Mellitus, Type 2Hypoglycemic AgentsInsulin GlarginePeptidesBlood GlucoseDrug CombinationsGlucagon-Like Peptide-2 ReceptorGlycated HemoglobinHumansRandomized Controlled Trials as TopicTreatment OutcomeBlood GlucoseDrug CombinationsGlucagon-Like Peptide-2 ReceptorGlycated HemoglobinHypoglycemic AgentsInsulin GlarginelixisenatidePeptidesEfficacyiGlarLixiMeta-analysisRandomized controlled trialsSafetyType 2 diabetes

Identifiers

PMID38740694

What OpenQuestion holds

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Registered trials

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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.