Evidence map›Paper›PMID 42086614›Full record

Articlenpj aging2026

Modifiable risk factors attenuated longevity genetic predisposition on life expectancy in the oldest old.

Shimin Chen, Ke Han, Shengshu Wang, Shanshan Yang, Yueting Shi, Wenchang Wang, Shengyan Du, Xiaoxin Ye, Yanhao Wan, Jianhua Wang and 2 more

Abstract read
In one paragraph

Article in npj aging, 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.

Shimin ChenMedical School of Chinese People's Liberation Army, Beijing, China.
Ke HanDepartment of Endoscopy, General Hospital of Northern Theater Command, Shenyang, China.
Shengshu WangInstitute of Geriatrics, Beijing Key Laboratory of Geriatric Comorbidity, National Clinical Research Center for Geriatrics Diseases, Second Medical Center, Chinese People's Liberation Army General Hospital, Beijing, China.
Shanshan YangDepartment of Field Internal Medicine, Graduate School, Chinese People's Liberation Army General Hospital, Beijing, China.
Yueting ShiMedical School of Chinese People's Liberation Army, Beijing, China.
Wenchang WangMedical School of Chinese People's Liberation Army, Beijing, China.
Shengyan DuMedical School of Chinese People's Liberation Army, Beijing, China.
Xiaoxin YeMedical School of Chinese People's Liberation Army, Beijing, China.
Yanhao WanMedical School of Chinese People's Liberation Army, Beijing, China.
Jianhua WangInstitute of Geriatrics, Beijing Key Laboratory of Geriatric Comorbidity, National Clinical Research Center for Geriatrics Diseases, Second Medical Center, Chinese People's Liberation Army General Hospital, Beijing, China.
Miao LiuDepartment of Anti-Nuclear, Biological, Chemical Medicine, Graduate School, Chinese People's Liberation Army General Hospital, Beijing, China. liumiaolmbxb@163.com.
Yao HeInstitute of Geriatrics, Beijing Key Laboratory of Geriatric Comorbidity, National Clinical Research Center for Geriatrics Diseases, Second Medical Center, Chinese People's Liberation Army General Hospital, Beijing, China. yhe301@sina.com.

Funding

National Natural Science Foundation of China 82173590
6 · The paper itself

Abstract

In this prospective cohort study of 1545 participants aged 80 years and older from the China Hainan Centenarian Cohort Study, we investigated the independent and joint associations of modifiable risk factors and genetic predisposition with life expectancy. A weighted modifiable risk factor score (MRFS) based on 11 factors and a polygenic risk score (PRS) for longevity were constructed. A favorable modifiable risk factor profile (low MRFS) was associated with a 40.7% lower death risk (HR 0.593, 95%CI 0.505-0.696) compared with high MRFS. Genetic predisposition to longer lifespan (high PRS) conferred a 13.0% lower risk (HR 0.870, 95%CI 0.768-0.986). Participants with both low MRFS and high PRS had the lowest mortality (HR 0.544, 95%CI 0.432-0.686), with a borderline significant multiplicative interaction (P = 0.040). Life expectancy gains from a low MRFS were more pronounced in those with high PRS (6.92 years at age 80) than low PRS (5.35 years). Among the oldest-old Han Chinese, favorable modifiable risk profiles and genetic predisposition independently and jointly contribute to substantially longer life expectancy. Importantly, an unfavorable modifiable profile may largely negate genetic longevity benefits, emphasizing the critical role of managing these factors even in advanced age and irrespective of genetic inheritance.

Identifiers

PMID42086614
PMCPMC13161428

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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.