Evidence map›Paper›PMID 41995132›Full record

ArticleClinical and translational science2026

Incremental Prognostic Value of Heart-Type Fatty Acid Binding Protein in Patients With Light Chain Cardiac Amyloidosis: A Prospective Cohort Study.

Xinqing Li, Anran Xin, Guo Ai, Chengyi Wang, Xuemei Zhao, Yan Huang, Xiaofeng Zhuang, Huihui Liu, Qiong Zhou, Jian Zhang and 1 more

Abstract read
In one paragraph

Article in Clinical and translational science, 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

11 authors.

Xinqing LiHeart Failure Center, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China.ORCID 0009-0008-4768-3079
Anran XinHeart Failure Center, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China.ORCID 0009-0001-0309-7288
Guo AiHeart Failure Center, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China.ORCID 0000-0003-4971-4824
Chengyi WangHeart Failure Center, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China.
Xuemei ZhaoHeart Failure Center, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China.
Yan HuangHeart Failure Center, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China.
Xiaofeng ZhuangHeart Failure Center, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China.
Huihui LiuHeart Failure Center, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China.
Qiong ZhouHeart Failure Center, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China.
Jian ZhangHeart Failure Center, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China.
Yuhui ZhangHeart Failure Center, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China.ORCID 0009-0000-7477-5712

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The utility of heart-type fatty acid binding protein (H-FABP) as a prognostic biomarker in light chain cardiac amyloidosis (AL-CA) patients remains unestablished. Consecutive patients diagnosed with AL-CA in the Heart Failure Center; Fuwai Hospital were enrolled. Baseline H-FABP levels categorized patients as low (≤ 9.5 ng/mL) or high (> 9.5 ng/mL) group. Kaplan-Meier analysis and Cox proportional hazards models were performed. Model performance was assessed using Harrell's C concordance index (C-index), integrated discrimination improvement (IDI) index, and net reclassification improvement (NRI) index. Eighty-four patients were included (mean age 60.12 ± 11.25 years; 32.1% female), with 30 (35.7%) in the high H-FABP group. Overall survival was significantly lower in the high H-FABP group. In multivariable Cox models adjusted for age, eGFR and chemotherapy, H-FABP > 9.5 ng/mL remained independently associated with an increased risk of all-cause mortality when incorporating either the European modified Mayo 2004 stages [adjusted hazard ratio (HR): 2.79, 95% confidence interval (CI): 1.49-5.22; p = 0.001] or the revised Mayo 2012 stages (HR: 2.67, 95% CI: 1.48-4.83; p = 0.001). Adding H-FABP levels significantly improved predictive performance across both baseline staging systems. For the European modified Mayo 2004 stage, the C-index increased from 0.622 to 0.663, accompanied by positive IDI (0.053) and NRI (0.294). Similarly, for the revised Mayo 2012 stage, the C-index increased from 0.611 to 0.660, with positive IDI (0.074) and NRI (0.308). Elevation of H-FABP is associated with an increased risk of all-cause mortality in patients with AL-CA. It provides significant additive prognostic value to the established staging system for prognosis in AL-CA.

Indexed as

CardiomyopathiesFatty Acid Binding Protein 3Fatty Acid-Binding ProteinsImmunoglobulin Light-chain AmyloidosisAgedBiomarkersFemaleHumansKaplan-Meier EstimateMaleMiddle AgedPrognosisProspective StudiesBiomarkersFABP3 protein, humanFatty Acid Binding Protein 3Fatty Acid-Binding ProteinsH‐FABPlight chain cardiac amyloidosisprognosis

Identifiers

PMID41995132
PMCPMC13088332

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.