The Anti-Nucleocapsid IgG Antibody as a Marker of SARS-CoV-2 Infection for Hemodialysis Patients
<i><b>Background:</b></i> Hemodialysis patients, due to impaired kidney function and compromised immune responses, face increased risks from SARS-CoV-2. Anti-nucleocapsid IgG (anti-IgG N) antibodies are a commonly used marker to assess prior infection in the general population; however, their efficacy for hemodialysis patients remains unclear. <i><b>Methods:</b></i> A retrospective study of 361 hemodialysis patients evaluated anti-IgG N antibodies for detecting prior SARS-CoV-2 infection. Antibody levels were measured using a chemiluminescence immunoassay (CLIA) over the four time points. Boxplots illustrated antibody distribution across sampling stages and infection status. Logistic regression and receiver operating characteristic (ROC) curve analysis determined diagnostic accuracy, sensitivity, specificity, and optimal cutoff values. <i><b>Results:</b></i> Among the 361 hemodialysis patients, 36 (10.0%) had SARS-CoV-2 infection. Sex distribution showed a trend toward significance (<i>p</i> = 0.05). Boxplot analysis showed that anti-IgG N levels remained low in non-infected patients but increased in infected patients, peaking at the third sampling. Anti-IgG N demonstrated high diagnostic accuracy (AUC: 0.973-0.865) but declined over time (<i>p</i> = 0.00525). The optimal cutoff at C1 was 0.01 AU/mL (sensitivity 1.00, specificity 0.94). Adjusted models had lower predictive value. <i><b>Conclusions:</b></i> Anti-IgG N antibodies showed high diagnostic accuracy for detecting prior SARS-CoV-2 infection in hemodialysis patients, though performance declined over time. These findings highlight the need for tailored diagnostic strategies in this vulnerable population.
Authors
- Akihiko Ozaki (ORCID: https://orcid.org/0000-0003-4415-9657)
- Yurie Kobashi (ORCID: https://orcid.org/0000-0002-3442-3779)
- Tianchen Zhao (ORCID: https://orcid.org/0000-0001-8602-6786)
- Chika Yamamoto (ORCID: https://orcid.org/0000-0003-4512-8924)
- Takeshi Kawamura (ORCID: https://orcid.org/0000-0003-1613-6968)
- Masatoshi Wakui (ORCID: https://orcid.org/0000-0002-3953-0872)
- Yudai Kaneko (ORCID: https://orcid.org/0000-0003-0967-782X)
- Akira Sugiyama (ORCID: https://orcid.org/0000-0003-4406-9475)
- Hiroaki Saito (ORCID: https://orcid.org/0000-0002-0824-454X)
- Masaharu Tsubokura (ORCID: https://orcid.org/0000-0001-8027-202X)
- Toyoaki Sawano (ORCID: https://orcid.org/0000-0002-1482-6618)
- Toshiki Abe (ORCID: https://orcid.org/0009-0006-2496-8456)
- Yuki Sonoda (ORCID: https://orcid.org/0000-0002-1729-2295)
- Shun Watanabe (ORCID: https://orcid.org/0000-0002-5529-7791)
- Hiroaki Shimmura
- Aya Nakayama
- A Hara
Institutions
- Tokyo Institute of Technology (JP)
- Fukushima Medical University (JP)
- Keio University (JP)
- Jyoban Hospital of Tokiwa Foundation (JP)
- Medical & Biological Laboratories (Japan) (JP)
- Soma Central Hospital (JP)
- The University of Tokyo (JP)
- Murata (Japan) (JP)
Publication Details
- Journal
- Vaccines
- Published
- 2025-07-13
- DOI
- https://doi.org/10.3390/vaccines13070750
- Primary Topic
- SARS-CoV-2 and COVID-19 Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Japan Agency for Medical Research and Development
- Moderna