Evidence map›Paper›PMID 42340115›Full record

ArticleInternal medicine journal2026

Triple combination cystic fibrosis transmembrane receptor modulator effects on glycaemia and insulin kinetics in cystic fibrosis with and without diabetes.

Yi W Chen, Rachel Prasad, Peter G Middleton, D Jane Holmes-Walker

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Article in Internal medicine journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Yi W ChenDepartment of Endocrinology, Nepean Hospital, Sydney, New South Wales, Australia.ORCID https://orcid.org/0009-0002-3835-4894
Rachel PrasadDepartment of Respiratory and Sleep Medicine, Westmead Hospital, Sydney, New South Wales, Australia.
Peter G MiddletonDepartment of Respiratory and Sleep Medicine, Westmead Hospital, Sydney, New South Wales, Australia.
D Jane Holmes-WalkerDepartment of Diabetes and Endocrinology, Westmead Hospital, Sydney, New South Wales, Australia.ORCID https://orcid.org/0000-0002-3640-1370

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGreater insight into the effects of cystic fibrosis (CF) transmembrane modulators such as elexacaftor-tezacaftor-ivacaftor (ETI) on glucose metabolism can support a more dynamic and individualised approach to CF-related dysglycaemia.

aimTo assess changes in glycemia, body weight and pulmonary function in adults with CF with and without cystic fibrosis related diabetes (CFRD) following ETI.

methodsThis single-centre retrospective cohort study included adults with at least one F508del mutation (23 with CFRD, 38 without CFRD). Exploratory outcomes were HbA1c and total daily insulin doses in the CFRD group and glucose and insulin profiles (0-120 min oral glucose tolerance test [OGTT]), HOMA2-derived indices of insulin resistance (IR), secretion (%S), and β-cell function (%B) in the non-CFRD group. Pulmonary function and weight were assessed in both groups.

resultsMean age was 33.8 ± 10.0 years (CFRD) and 32.8 ± 8.8 years (non-CFRD), with median ETI exposure of 12.3 and 13.4 months, respectively. In the CFRD cohort, HbA1c decreased non-significantly (6.6% to 6.1%, p = 0.2) with no significant change in insulin dose (0.28 to 0.20 IU/kg/day, p = 0.1). In non-CFRD participants, ETI significantly reduced 1- and 2-hour OGTT glucose levels (9.6 vs. 9.2 mmol/L at 1 h, p < 0.01; 6.1 vs. 4.8 mmol/L at 2 hours, p = 0.01), with 13/38 participants improving OGTT classification; no progression to CFRD occurred. Lung function improved in both groups.

conclusionsAdults with at least one F508del mutation, ETI was associated with a clinically relevant reduction in HbA1c in those with CFRD and improved glucose tolerance in those without, supporting favourable metabolic effects beyond established respiratory benefits.

Indexed as

AminophenolsBenzodioxolesBlood GlucoseCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorDiabetes MellitusIndolesInsulinPyrrolidinesQuinolonesAdultCohort StudiesFemaleGlucose Tolerance TestGlycated HemoglobinHumansAminophenolsBenzodioxolesBlood GlucoseCystic Fibrosis Transmembrane Conductance RegulatorelexacaftorGlycated HemoglobinIndolesInsulinivacaftorPyrazolesPyridinesPyrrolidinesQuinolonestezacaftorCystic fibrosis‐related diabeteselexacaftor‐tezacaftor‐ivacaftorglucose metabolisminsulin kinetics

Identifiers

PMID42340115
PMCPMC13458249

What Socratic holds

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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 Socratic graph.