PMID- 37529333 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20230918 IS - 1759-720X (Print) IS - 1759-7218 (Electronic) IS - 1759-720X (Linking) VI - 15 DP - 2023 TI - A prognostic immune nutritional index can predict all-cause mortality in patients with antineutrophil cytoplasmic antibody-associated vasculitis. PG - 1759720X231188818 LID - 10.1177/1759720X231188818 [doi] LID - 1759720X231188818 AB - BACKGROUND: Studies have proposed that nutritional and immune-related markers are relevant with patient outcomes of various medical conditions and could be a useful indicator of patient prognostication. OBJECTIVES: This study investigated whether a prognostic immune nutritional index (PINI) at diagnosis could predict adverse clinical outcomes in patients with antineutrophil cytoplasmic antibody-associated vasculitis (AAV). DESIGN: A retrospective, single-centre observational cohort analysis of patients with AAV. METHODS: All-cause mortality and end-stage renal disease (ESRD) were investigated outcomes during the observation period. PINI was calculated by serum albumin (g/mL) x 0.9 - monocyte count (/mm(3)) x 0.0007, and the optimal cut-off of PINI was obtained using a Youden index-based bootstrapping method. Cox hazard analyses were performed to identify independent predictors of patient outcomes. RESULTS: Of the 250 eligible patients, the median age of patients was 60.0 years, and 34.0% were men. During the disease course, 33 (13.2%) died and 42 (16.8%) developed ESRD, respectively. The ideal PINI cut-offs for all-cause mortality and ESRD were set as ⩽2.47 and ⩽3.12 (sensitivity and specificity of 75.1% and 60.6% for mortality and 46.2% and 78.6% for ESRD). AAV patients with PINI ⩽2.47 and those with PINI ⩽3.12 exhibited significantly higher rates for all-cause mortality and ESRD compared to those with PINI >2.47 and >3.12. In the multivariable Cox analysis, PINI ⩽2.47 (hazard ratio [HR]: 3.173, 95% confidence interval [CI]: 1.129, 8.916, p = 0.029) was independently associated with all-cause patient mortality; however, PINI ⩽3.12 was not independently associated with ESRD (HR: 1.097, 95% CI: 0.419, 2.870, p = 0.850). CONCLUSION: Findings from this study demonstrated PINI could predict all-cause patient mortality in AAV, and a higher clinical attention is warranted in those with PINI ⩽2.47 at initial diagnosis. CI - (c) The Author(s), 2023. FAU - Ahn, Sung Soo AU - Ahn SS AUID- ORCID: 0000-0002-9002-9880 AD - Division of Rheumatology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea. FAU - Pyo, Jung Yoon AU - Pyo JY AD - Division of Rheumatology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea. FAU - Song, Jason Jungsik AU - Song JJ AD - Division of Rheumatology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea. AD - Institute for Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul, Republic of Korea. FAU - Park, Yong-Beom AU - Park YB AD - Division of Rheumatology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea. AD - Institute for Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul, Republic of Korea. FAU - Lee, Sang-Won AU - Lee SW AUID- ORCID: 0000-0002-8038-3341 AD - Division of Rheumatology, Department of Internal Medicine, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun-gu, Seoul 03722, Republic of Korea. AD - Institute for Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul, Republic of Korea. LA - eng PT - Journal Article DEP - 20230729 PL - England TA - Ther Adv Musculoskelet Dis JT - Therapeutic advances in musculoskeletal disease JID - 101517322 PMC - PMC10387778 OTO - NOTNLM OT - antineutrophil cytoplasmic antibody OT - end-stage renal disease OT - mortality OT - prognostic immune nutritional index OT - vasculitis COIS- The authors declare that there is no conflict of interest. EDAT- 2023/08/02 06:43 MHDA- 2023/08/02 06:44 PMCR- 2023/07/29 CRDT- 2023/08/02 03:54 PHST- 2023/01/25 00:00 [received] PHST- 2023/06/28 00:00 [accepted] PHST- 2023/08/02 06:43 [pubmed] PHST- 2023/08/02 06:44 [medline] PHST- 2023/08/02 03:54 [entrez] PHST- 2023/07/29 00:00 [pmc-release] AID - 10.1177_1759720X231188818 [pii] AID - 10.1177/1759720X231188818 [doi] PST - epublish SO - Ther Adv Musculoskelet Dis. 2023 Jul 29;15:1759720X231188818. doi: 10.1177/1759720X231188818. eCollection 2023.