Evidence map›Paper›PMID 42310684›Full record

ArticleBMC research notes2026

Stage-wise variation in serum C-reactive protein and cardiovascular risk in chronic kidney disease of uncertain etiology among Sri Lankans; a preliminary study.

Hansani Niroshika, Harshi Weerakoon, Nalaka Herath, Sujani Premathilake, Prasad Jayasooriya, Kosala Weerakoon

Abstract read
In one paragraph

Article in BMC research notes, 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

6 authors.

Hansani NiroshikaFaculty of Graduate Studies, General Sir John Kotelawala Defense University, Ratmalana, Sri Lanka. hansaniniroshika014@gmail.com.
Harshi WeerakoonDepartment of Biochemistry, Faculty of Medicine and Allied Sciences, Rajarata University of Sri Lanka, Saliyapura, Sri Lanka.
Nalaka HerathColombo North Teaching Hospital, Ragama, Sri Lanka.
Sujani PremathilakeTeaching Hospital, Kurunegala, Sri Lanka.
Prasad JayasooriyaDepartment of Bioprocess Technology, Faculty of Technology, Rajarata University of Sri Lanka, Mihintale, Sri Lanka.
Kosala WeerakoonDepartment of Parasitology, Faculty of Medicine and Allied Sciences, Rajarata University of Sri Lanka, Saliyapura, Sri Lanka. kosalagadw83@gmail.com.ORCID https://orcid.org/0000-0002-4814-6928

Funding

Asian Development Bank R2-RJ4
6 · The paper itself

Abstract

backgroundChronic kidney disease of uncertain etiology (CKDu) is a progressive nephropathy histologically characterized by tubulointerstitial fibrosis with varying degrees of inflammatory infiltrations. C-reactive protein (CRP) is an acute phase protein that serves as a marker of systemic inflammation and cardiovascular disease (CVD) risk. Therefore, this study aimed to evaluate serum CRP levels in patients with CKDu and to assess their association with renal function and CVD risk.

methodsA cross-sectional study was conducted on 40 clinically diagnosed CKDu patients at different severity stages (stage 2 (n = 5, 12.5%), stage 3A (n = 8, 20.0%), stage 3B (n = 10, 25.0%), stage 4 (n = 10, 25.0%), and stage 5 (n = 7, 17.5%). As the control group, age and sex matched 16 apparently healthy individuals (mean age 52.19 ± 10.26 years, 56.2% male) were recruited. CRP concentrations were measured using immunoturbidimetry (range 0-150 mg/L), and CVD risk was categorized based on CDC/AHA guideline. Patients with CRP > 10 mg/L were excluded to minimize confounding from potential underlying infections.

resultsCRP levels across CKDu stages demonstrated a nonlinear trend with significant peak at stage 3A (1.6 mg/L; IQR: 1.08-2.95), compared to their matched control subjects (0.50 mg/L; IQR 0.30-1.73; p = 0.0045), followed by a decline in later stages. No significant association was observed between CRP and eGFR (r = 0.11, 95% CI -0.21 to 0.41, p = 0.49). After classifying the CKDu patients for CVD risk, Stage 3A patients had higher odds of increased CVD risk than controls (odds ratio = 21.0, p = 0.0236) followed by stage 3B (odds ratio = 13.5, p = 0.0352). Further, CVD risk stratification was not confounded by age, sex, and renal function indicators (eGFR and serum creatinine).

conclusionElevated CRP levels and associated CVD risk in CKDu patients appear most pronounced in intermediate disease stages (3A-3B), providing a rationale for a large longitudinal study.

Indexed as

Cardiovascular DiseasesChronic Kidney Diseases of Uncertain EtiologyC-Reactive ProteinRenal Insufficiency, ChronicAdultBiomarkersCase-Control StudiesCross-Sectional StudiesFemaleHeart Disease Risk FactorsHumansMaleMiddle AgedRisk FactorsSri LankaBiomarkersC-Reactive ProteinChronic kidney disease of uncertain etiologyCKDuCRPCVD riskInflammation

Identifiers

PMID42310684
PMCPMC13508195

What OpenQuestion holds

Textmetadata
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.