PMID- 36086712 OWN - NLM STAT- MEDLINE DCOM- 20220913 LR - 20240331 IS - 1536-5964 (Electronic) IS - 0025-7974 (Print) IS - 0025-7974 (Linking) VI - 101 IP - 36 DP - 2022 Sep 9 TI - Association between homocysteinemia and mortality in CKD: A propensity-score matched analysis using NHANES-National Death Index. PG - e30334 LID - 10.1097/MD.0000000000030334 [doi] LID - e30334 AB - Hyperhomocysteinemia (HHcy) is considered a risk factor for cardiovascular disease (CVD), including chronic kidney disease (CKD). In this study, we investigated the association between levels of serum homocysteine (Hcy) and mortality, inferred from the presence of CKD. Our study included data of 9895 participants from the 1999 to 2016 National Health and Nutrition Examination Surveys (NHANES). Multivariable-adjusted Cox proportional hazard models using propensity-score, were used to examine dose-response associations between Hcy level and mortality. A total of 9895 participants, 1025 (10.3%) participants were diagnosed with CKD. In a multivariate Cox regression analysis including all participants, Hcy level was significantly associated with all-cause mortality in the nonCKD group, compared to the 1st quartile in the fully adjusted model (2nd quartile: hazard ratio (HR) 1.75, 95% confidence interval (CI) 1.348-2.274, P < .001; 3rd quartile: HR 2.22, 95% CI 1.726-2.855, P < .001; 4th quartile: HR 3.77, 95% CI 2.952-4.830, P < .001). However, this finding was not observed in the CKD group. The observed pattern was similar after propensity score matching. In the nonCKD group, overall mortality increased in proportion to Hcy concentration (2nd quartile: HR 2.19, 95% CI 1.299-3.709, P = .003; 3rd quartile: HR 2.60, 95% CI 1.570-4.332, P < .001; 4th quartile: HR 3.72, 95% CI 2.254-6.139, P < .001). However, the risk of all-cause mortality according to the quartile of Hcy level, did not increase in the CKD group. This study found a correlation between the Hcy level and mortality rate only in the nonCKD group. These altered risk factor patterns may be attributed to protein-energy wasting or chronic inflammation status, that is accompanied by CKD. CI - Copyright (c) 2022 the Author(s). Published by Wolters Kluwer Health, Inc. FAU - Song, Je Hun AU - Song JH AD - Department of Internal Medicine, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, South Korea. FAU - Huh, Hyuk AU - Huh H AD - Department of Internal Medicine, Pusan Paik Hospital, Inje University College of Medicine, Busan, South Korea. FAU - Bae, Eunjin AU - Bae E AD - Department of Internal Medicine, Gyeongsang National University Changwon Hospital, Changwon, South Korea. FAU - Lee, Jeonghwan AU - Lee J AD - Department of Internal Medicine, Seoul National University Boramae Medical Center, Seoul, South Korea. AD - Department of Internal Medicine, Seoul National University College of Medicine, Seoul, South Korea. FAU - Lee, Jung Pyo AU - Lee JP AD - Department of Internal Medicine, Seoul National University Boramae Medical Center, Seoul, South Korea. AD - Department of Internal Medicine, Seoul National University College of Medicine, Seoul, South Korea. FAU - Lee, Jong Soo AU - Lee JS AD - Department of Internal Medicine, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, South Korea. FAU - Kim, Gwang Sil AU - Kim GS AD - Department of Internal Medicine, Sanggye Paik Hospital, Inje University College of Medicine, Seoul, South Korea. FAU - Yoo, Kyung Don AU - Yoo KD AUID- ORCID: 0000-0001-6545-6517 AD - Department of Internal Medicine, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, South Korea. LA - eng PT - Journal Article PL - United States TA - Medicine (Baltimore) JT - Medicine JID - 2985248R RN - Homocysteinemia SB - IM MH - Humans MH - *Hyperhomocysteinemia/complications/epidemiology MH - Nutrition Surveys MH - Propensity Score MH - *Renal Insufficiency, Chronic PMC - PMC10980502 COIS- The authors have no funding and conflict of interests to declare. EDAT- 2022/09/11 06:00 MHDA- 2022/09/14 06:00 PMCR- 2022/09/09 CRDT- 2022/09/10 01:08 PHST- 2022/09/10 01:08 [entrez] PHST- 2022/09/11 06:00 [pubmed] PHST- 2022/09/14 06:00 [medline] PHST- 2022/09/09 00:00 [pmc-release] AID - 00005792-202209090-00040 [pii] AID - 10.1097/MD.0000000000030334 [doi] PST - ppublish SO - Medicine (Baltimore). 2022 Sep 9;101(36):e30334. doi: 10.1097/MD.0000000000030334.