PMID- 33120814 OWN - NLM STAT- MEDLINE DCOM- 20201231 LR - 20221005 IS - 1536-5964 (Electronic) IS - 0025-7974 (Print) IS - 0025-7974 (Linking) VI - 99 IP - 43 DP - 2020 Oct 23 TI - Factors affecting the Apgar score of offsprings born to mothers suffering from systemic lupus erythematosus. PG - e22843 LID - 10.1097/MD.0000000000022843 [doi] LID - e22843 AB - To reveal which disease activity parameters affect low Apgar scores of newborns, which is considered as a predictive parameter for neurological development.We examined retrospectively the data from 42 newborns who were delivered from systemic lupus erythematosus (SLE) mothers from 2006 to 2019. We evaluated whether the disease activity parameters, such as the achievement ratio of lupus low disease activity state (LLDAS), SLE disease activities index (SLEDAI), complement level, titer of anti-double stranded DNA (anti-dsDNA) antibody, therapeutic agents were related with low Apgar scores of newborns.In 42 newborns, adverse pregnancy outcomes, especially preterm birth (16.7%), low birth weight (31.0%) light-for-date (11.9%) were associated with disease activity parameters or prednisolone dose. Apgar scores at 1 minute were related with unachieved LLDAS and the titer of anti-dsDNA antibody at first and third trimester, SLEDAI score and complement level at third trimester, mean prednisolone dose. Apgar scores at 5 minutes were also associated with the titer of anti-dsDNA antibodies at first and third trimester and mean prednisolone dose. Multivariate analysis showed only high titer of anti-dsDNA antibody was significantly associated with low Apgar score at both one minute and 5 minutes.In our retrospective study, high titer of anti-dsDNA antibodies at first and third trimester was a risk factor for low Apgar scores of newborns born to SLE mothers. We considered that high titer of anti-dsDNA antibody influenced on childrens neurological development, therefore, there is a need for long-term follow-up study of SLE offsprings. FAU - Shimada, Hiromi AU - Shimada H AUID- ORCID: 0000-0001-5792-9919 AD - Department of Internal Medicine, Division of Hematology, Rheumatology and Respiratory Medicine. FAU - Kameda, Tomohiro AU - Kameda T AD - Department of Internal Medicine, Division of Hematology, Rheumatology and Respiratory Medicine. FAU - Kanenishi, Kenji AU - Kanenishi K AD - Department of Perinatology and Gynecology. FAU - Miyatake, Nobuyuki AU - Miyatake N AD - Department of Hygiene, Faculty of Medicine, Kagawa University, Kagawa, Japan. FAU - Nakashima, Shusaku AU - Nakashima S AD - Department of Internal Medicine, Division of Hematology, Rheumatology and Respiratory Medicine. FAU - Wakiya, Risa AU - Wakiya R AD - Department of Internal Medicine, Division of Hematology, Rheumatology and Respiratory Medicine. FAU - Kato, Mikiya AU - Kato M AD - Department of Internal Medicine, Division of Hematology, Rheumatology and Respiratory Medicine. FAU - Miyagi, Taichi AU - Miyagi T AD - Department of Internal Medicine, Division of Hematology, Rheumatology and Respiratory Medicine. FAU - Mansour, Mai Mahmoud Fahmry AU - Mansour MMF AD - Department of Internal Medicine, Division of Hematology, Rheumatology and Respiratory Medicine. FAU - Hata, Toshiyuki AU - Hata T AD - Department of Perinatology and Gynecology. FAU - Kadowaki, Norimitsu AU - Kadowaki N AD - Department of Internal Medicine, Division of Hematology, Rheumatology and Respiratory Medicine. FAU - Dobashi, Hiroaki AU - Dobashi H AD - Department of Internal Medicine, Division of Hematology, Rheumatology and Respiratory Medicine. LA - eng PT - Journal Article PT - Observational Study PL - United States TA - Medicine (Baltimore) JT - Medicine JID - 2985248R RN - 0 (Antibodies, Antinuclear) SB - IM MH - Adult MH - Antibodies, Antinuclear/blood/*immunology MH - *Apgar Score MH - Disease Progression MH - Female MH - Humans MH - Infant, Low Birth Weight MH - Infant, Newborn MH - Lupus Erythematosus, Systemic/complications/genetics/*immunology MH - Pregnancy MH - Pregnancy Complications/genetics/immunology MH - Premature Birth MH - Retrospective Studies PMC - PMC7581183 COIS- The authors report no conflicts of interest. EDAT- 2020/10/31 06:00 MHDA- 2021/01/01 06:00 PMCR- 2020/10/23 CRDT- 2020/10/30 01:01 PHST- 2020/10/30 01:01 [entrez] PHST- 2020/10/31 06:00 [pubmed] PHST- 2021/01/01 06:00 [medline] PHST- 2020/10/23 00:00 [pmc-release] AID - 00005792-202010230-00090 [pii] AID - MD-D-20-04395 [pii] AID - 10.1097/MD.0000000000022843 [doi] PST - ppublish SO - Medicine (Baltimore). 2020 Oct 23;99(43):e22843. doi: 10.1097/MD.0000000000022843.