Evidence map›Paper›PMID 41854531›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2026

Systemic Sonic Hedgehog Signaling Links Intestinal Nutrient Sensing With Sex-Specific Type 2 Diabetes Progression.

Johannes Alfredsson, Nayere Taebnia, Najat Dzaki, Stefan A Ljunggren, Ingela Helmfrid, Emilia C Johansson, Jibbe Keulen, Olov Rolandsson, Ingvar Bergdahl, Volker M Lauschke and 2 more

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Johannes AlfredssonDepartment of Microbiology and Immunology, Gothenburg University, Gothenburg, Sweden.
Nayere TaebniaDepartment of Physiology and Pharmacology and Center for Molecular Medicine, Karolinska Institutet and University Hospital, Stockholm, Sweden.
Najat DzakiDepartment of Molecular Biology, Umeå University, Umeå, Sweden.
Stefan A LjunggrenDepartment of Health, Medicine and Caring Sciences, Linköping University, Linköping, Sweden.
Ingela HelmfridDepartment of Health, Medicine and Caring Sciences, Linköping University, Linköping, Sweden.
Emilia C JohanssonDepartment of Molecular Biology, Umeå University, Umeå, Sweden.
Jibbe KeulenDepartment of Physiology and Pharmacology and Center for Molecular Medicine, Karolinska Institutet and University Hospital, Stockholm, Sweden.
Olov RolandssonDepartment of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden.
Ingvar BergdahlDepartment of Epidemiology and Global Health, Umeå University, Umeå, Sweden.
Volker M LauschkeDepartment of Physiology and Pharmacology and Center for Molecular Medicine, Karolinska Institutet and University Hospital, Stockholm, Sweden.ORCID https://orcid.org/0000-0002-1140-6204
Helen KarlssonDepartment of Health, Medicine and Caring Sciences, Linköping University, Linköping, Sweden.
Mattias AleniusDepartment of Health, Medicine and Caring Sciences, Linköping University, Linköping, Sweden.ORCID https://orcid.org/0000-0001-9795-2099

Funding

ERC Consolidator 101170408Kempe Foundation JCK-3158Kempe Foundation SMK-1764Novo Nordisk Foundation NNF23OC0084420Novo Nordisk Foundation NNF23OC0085944Robert Bosch FoundationSwedish Research Council 2016-05208Swedish Research Council 2021-02801Swedish Research Council 2023-03015Swedish Research Council 2023-04964Swedish Research Council 2024-03401the SciLifeLab and Wallenberg National Program for Data-Driven Life Science WASPDDLS22:006
6 · The paper itself

Abstract

Systemic Sonic Hedgehog (Shh) signaling is increasingly recognized as a potential regulator of adult metabolic homeostasis, yet its role in human disease remains poorly defined. In this study, we measured plasma Shh levels in two large Swedish cohorts to assess their associations with common non-communicable diseases, with a particular focus on type 2 diabetes mellitus (T2DM) and metabolic dysfunction. A population-based screen of 735 individuals revealed substantial inter-individual variability in Shh levels, with elevated levels associated with T2DM and hypertension in females but not in males. These findings were validated in a nested case-control study, where Shh levels were significantly higher in T2DM females compared to matched controls. Correlation analyses showed that Shh levels were associated with insulin resistance in both sexes but reflected different disease states with early compensatory insulin secretion in males and late β-cell dysfunction in females. Mechanistic studies using human intestinal organoids demonstrated that Shh secretion is induced by the combination of glucose and insulin, suggesting the intestine as a nutrient-responsive source of the systemic Shh. Together, these results identify Shh as a sexually dimorphic marker of metabolic dysfunction and support its functional role in glycemic control and metabolic disease.

Indexed as

Diabetes Mellitus, Type 2Hedgehog ProteinsNutrientsSignal TransductionAgedCase-Control StudiesDisease ProgressionFemaleHumansInsulinInsulin ResistanceMaleMiddle AgedSex FactorsHedgehog ProteinsInsulinSHH protein, humancirculationfemaleinsulin resistanceorganoidsplasmaprediabetessex differencessmall intestineSonic Hedgehogtype 2 diabetes

Identifiers

PMID41854531
PMCPMC13001814

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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.