Diabetes increases mortality in patients with pancreatic and colorectal cancer by promoting cachexia and its associated inflammatory status

被引:10
|
作者
Chovsepian, Alexandra [1 ,2 ,3 ]
Prokopchuk, Olga [4 ]
Petrova, Gabriela [4 ]
Kuzi, Hanna [4 ,5 ]
Heisz, Simone [4 ,6 ,7 ]
Martignoni, Marc E. [4 ]
Friess, Helmut [4 ]
Hauner, Hans [6 ,7 ]
Rohm, Maria [1 ,2 ,3 ]
机构
[1] Helmholtz Ctr Munich, Inst Diabet & Canc IDC, German Res Ctr Environm Hlth, Ingolstadter Landstr 1, D-85764 Neuherberg, Germany
[2] Heidelberg Univ Hosp, Joint Heidelberg IDC Translat Diabet Program, Heidelberg, Germany
[3] German Ctr Diabet Res DZD, Neuherberg, Germany
[4] Tech Univ Munich, Sch Med, Dept Surg, Klinikum Rechts Isar, Munich, Germany
[5] Tech Univ Munich, Inst Expt Oncol & Therapy Res, Sch Med, Munich, Germany
[6] Tech Univ Munich, Inst Nutr Med, Sch Med, Munich, Germany
[7] Tech Univ Munich, ZIEL Inst Food & Hlth, Else Kroner Fresenius Ctr Nutr Med, Freising Weihenstephan, Germany
来源
MOLECULAR METABOLISM | 2023年 / 73卷
基金
欧洲研究理事会;
关键词
Type; 2; diabetes; Cancer cachexia; Body weight; Inflammation; Pancreatic cancer; Colorectal cancer; MELLITUS SECONDARY; SURVIVAL; RESISTANCE; OBESITY; SCORE; 3C;
D O I
10.1016/j.molmet.2023.101729
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Cancer is considered an emerging diabetes complication, with higher incidence and worse prognosis in patients with diabetes. Cancer is frequently associated with cachexia, a systemic metabolic disease causing wasting. It is currently unclear how diabetes affects the development and progression of cachexia.Methods: We investigated the interplay between diabetes and cancer cachexia retrospectively in a cohort of 345 patients with colorectal and pancreatic cancer. We recorded body weight, fat mass, muscle mass, clinical serum values, and survival of these patients. Patients were grouped either into diabetic/non-diabetic groups based on previous diagnosis, or into obese/non-obese groups based on body mass index (BMI >30 kg/m2 was considered obese).Results: The pre-existence of type 2 diabetes, but not obesity, in patients with cancer led to increased cachexia incidence (80%, compared to 61% without diabetes, p < 0.05), higher weight loss (8.9% vs. 6.0%, p < 0.001), and reduced survival probability (median survival days: 689 vs. 538, Chi square = 4.96, p < 0.05) irrespective of the initial body weight or tumor progression. Patients with diabetes and cancer showed higher serum levels of C-reactive protein (0.919 mu g/mL vs. 0.551 mu g/mL, p < 0.01) and interleukin 6 (5.98 pg/mL vs. 3.75 pg/mL, p < 0.05) as well as lower serum albumin levels (3.98 g/dL vs. 4.18 g/dL, p < 0.05) than patients with cancer without diabetes. In a sub-analysis of patients with pancreatic cancer, pre-existing diabetes worsened weight loss (9.95% vs. 6.93%, p < 0.01), and increased the duration of hospitalization (24.41 days vs. 15.85 days, p < 0.001). Further, diabetes aggravated clinical manifestations of cachexia, as changes in the aforementioned biomarkers were more pronounced in patients with diabetes and cachexia co-existence, compared to cachectic patients without diabetes (C-reactive protein: Conclusions: We show for the first time that pre-existing diabetes aggravates cachexia development in patients with colorectal and pancreatic cancer. This is important when considering cachexia biomarkers and weight management in patients with co-existing diabetes and cancer. m 2023 The Author(s). Published by Elsevier GmbH. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页数:10
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