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Characteristics and clinical course of type 1 diabetes mellitus related to anti-programmed cell death-1 therapy.
Baden, Megu Yamaguchi; Imagawa, Akihisa; Abiru, Norio; Awata, Takuya; Ikegami, Hiroshi; Uchigata, Yasuko; Oikawa, Yoichi; Osawa, Haruhiko; Kajio, Hiroshi; Kawasaki, Eiji; Kawabata, Yumiko; Kozawa, Junji; Shimada, Akira; Takahashi, Kazuma; Tanaka, Shoichiro; Chujo, Daisuke; Fukui, Tomoyasu; Miura, Junnosuke; Yasuda, Kazuki; Yasuda, Hisafumi; Kobayashi, Tetsuro; Hanafusa, Toshiaki.
Afiliação
  • Baden MY; 1Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, Suita, Osaka Japan.
  • Imagawa A; 2Department of Internal Medicine (I), Osaka Medical College, 2-7 Daigakucho, Takatsuki, Osaka 569-8686 Japan.
  • Abiru N; 3Department of Endocrinology and Metabolism, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Awata T; 4Department of Diabetes, Endocrinology and Metabolism, International University of Health and Welfare Hospital, Otawara, Tochigi Japan.
  • Ikegami H; 5Department of Endocrinology, Metabolism and Diabetes, Kindai University Faculty of Medicine, Higashi-osaka, Osaka Japan.
  • Uchigata Y; 6Tokyo Women's Medical University Medical Center East, Tokyo, Japan.
  • Oikawa Y; 7Department of Endocrinology and Diabetes, School of Medicine, Saitama Medical University, Saitama, Japan.
  • Osawa H; 8Department of Laboratory Medicine, Ehime University School of Medicine, Toon, Ehime Japan.
  • Kajio H; 9Department of Diabetes, Endocrinology, and Metabolism, Center Hospital of the National Center for Global Health and Medicine, Tokyo, Japan.
  • Kawasaki E; 10Diabetes Center, Shin-Koga Hospital, Kurume, Fukuoka Japan.
  • Kawabata Y; 5Department of Endocrinology, Metabolism and Diabetes, Kindai University Faculty of Medicine, Higashi-osaka, Osaka Japan.
  • Kozawa J; 1Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, Suita, Osaka Japan.
  • Shimada A; 7Department of Endocrinology and Diabetes, School of Medicine, Saitama Medical University, Saitama, Japan.
  • Takahashi K; 11Faculty of Nursing and Graduate School of Nursing, Iwate Prefectural University, Takizawa, Iwate Japan.
  • Tanaka S; Ai Home Clinic Toshima, Tokyo, Japan.
  • Chujo D; 9Department of Diabetes, Endocrinology, and Metabolism, Center Hospital of the National Center for Global Health and Medicine, Tokyo, Japan.
  • Fukui T; 13Department of Internal Medicine, Division of Diabetes and Endocrinology, Showa University School of Medicine, Tokyo, Japan.
  • Miura J; 14Diabetes Center, Tokyo Women's Medical University School of Medicine, Tokyo, Japan.
  • Yasuda K; 15Department of Metabolic Disorder, Diabetes Research Center, Research Institute, National Center for Global Health and Medicine, Tokyo, Japan.
  • Yasuda H; 16Division of Health Sciences, Department of Community Health Sciences, Kobe University Graduate School of Health Sciences, Kobe, Hyogo Japan.
  • Kobayashi T; 17Okinaka Memorial Institute for Medical Research, Tokyo, Japan.
  • Hanafusa T; Sakai City Medical Center, Sakai, Osaka Japan.
Diabetol Int ; 10(1): 58-66, 2019 Jan.
Article em En | MEDLINE | ID: mdl-30800564
ABSTRACT

AIMS:

We conducted a national survey to clarify the characteristics and clinical course of type 1 diabetes related to anti-programmed cell death-1 therapy.

METHODS:

We analyzed the detailed data of 22 patients that were collected using a Japan Diabetes Society survey and a literature database search.

RESULTS:

Among the 22 patients, 11 (50.0%) met the criteria for fulminant type 1 diabetes and 11 (50.0%) met the criteria for acute-onset type 1 diabetes. The average patient age was 63 years. The mean duration between the date of the first anti-PD-1 antibody injection and development of type 1 diabetes was 155 days and ranged from 13 to 504 days. Flu-like symptoms, abdominal symptoms, and drowsiness were observed in 27.8, 31.6, and 16.7% patients, respectively. Mean ± standard deviation or median (first quartile-third quartile) glucose levels, HbA1c levels, urinary C-peptide immunoreactivity levels, and fasting serum C-peptide immunoreactivity levels were 617 ± 248 mg/dl, 8.1 ± 1.3%, 4.1 (1.4-9.4) µg/day, and 0.46 (0.20-0.70) ng/ml, respectively. Seventeen of 20 patients (85.0%) developed ketosis, and 7 of 18 patients (38.9%) developed diabetic ketoacidosis. Ten of 19 patients (52.6%) showed at least one elevated pancreatic enzyme level at the onset and two of seven patients showed this elevation before diabetes onset. Only one of 21 patients was anti-glutamic acid decarboxylase antibody positive.

CONCLUSIONS:

Anti-programmed cell death-1 antibody-related type 1 diabetes varies from typical fulminant type 1 diabetes to acute-onset type 1 diabetes. However, diabetic ketoacidosis was frequently observed at the onset of diabetes. An appropriate diagnosis and treatment should be provided to avoid life-threatening metabolic alterations.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Diabetol Int Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Diabetol Int Ano de publicação: 2019 Tipo de documento: Article