Evidence map›Paper›PMID 41170467›Full record

ArticleFrontiers in oncology2025

Global burden of early-onset pancreatic cancer attributable to metabolic risks from 1990 to 2021, and projections to 2030.

Yingjin Fang, Yile Xu, Faliang Xing, Weixin Zhang, Chen Liang, Qingcai Meng, Jialin Li, Jin Xu, Wei Wang, Yi Qin and 2 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2025. 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
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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

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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.

Yingjin Fang *Department of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Yile Xu *Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangdong Provincial Key Laboratory of Research in Structural Birth Defect Disease, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangdong Provincial Clinical Research Center for Child Health, Guangzhou, Guangdong, China.
Faliang Xing *Department of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Weixin Zhang *Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangdong Provincial Key Laboratory of Research in Structural Birth Defect Disease, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangdong Provincial Clinical Research Center for Child Health, Guangzhou, Guangdong, China.
Chen LiangDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Qingcai MengDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Jialin LiDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Jin XuDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Wei WangDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Yi QinDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Xianjun YuDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Bo ZhangDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study, based on the Global Burden of Disease (GBD) 2021 data, systematically analyzed the changes in the disease burden of early-onset pancreatic cancer (EOPC) attributable to high fasting plasma glucose (HFPG) and high body mass index (HBMI) among the global population aged 15-49 years from 1990 to 2021 and predicted the mortality trends up to 2030. The results show that metabolic risk factors have a significant impact on EOPC: In 2021, the global deaths from EOPC attributable to HFPG reached 3,334 cases, 2.3 times higher than in 1990 with the age-standardized mortality rate (ASMR) and age-standardized disability rate (ASDR) had average annual growth rates of 1.50% and 1.47%. The ASMR and ASDR growth rates attributable to HBMI were even higher (1.69% and 1.76%). The steepest ASMR increases occurred in low-middle socio-demographic index (SDI) regions with an average annual growth of 2.86%), while the highest absolute burdens were observed in East Asia, high-income North America, and Western Europe. Bayesian age-period-cohort (BAPC) model predictions indicate that by 2030, the ASMR related to HBMI will continue to rise in both sexes (from 0.90 to 1.65 per 100,000 in males and from 1.43 to 1.93 per 100,000 in females), and the HBMI may exert a greater impact on females than HFPG. The study reveals the "double burden" phenomenon of metabolic risks: high-SDI regions have a high absolute burden due to the accumulation of long-term metabolic diseases, while low-middle SDI regions experience significant growth rates due to rapid urbanization and a lack of medical resources. Gender difference analysis shows that males generally have a higher ASMR than females, but the upward trend of metabolic-related mortality rates in females is more severe. The interaction between behavioral pattern changes in young people and metabolic abnormalities further exacerbates the risk. This study provides temporospatial evidence for the prevention and control of global EOPC, emphasizing the need to strengthen interventions for metabolic diseases in middle-and low-income regions, optimize the allocation of medical resources, and prioritize gender- and youth-specific interventions to curb the global spread of this aggressive cancer.

Indexed as

age-standardized disability rateage-standardized mortality rateBayesian age-period-cohortdisease burdenearly-onset pancreatic cancer

Identifiers

PMID41170467
PMCPMC12569605

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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.