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日本糖尿病学会(JDS)共识声明:2型糖尿病患者药物治疗的推荐算法 - 第2版(英文版)

A consensus statement from the Japan Diabetes Society (JDS): a proposed algorithm for pharmacotherapy in people with type 2 diabetes-2nd Edition (English version).

作者信息

Bouchi Ryotaro, Kondo Tatsuya, Ohta Yasuharu, Goto Atsushi, Tanaka Daisuke, Satoh Hiroaki, Yabe Daisuke, Nishimura Rimei, Harada Norio, Kamiya Hideki, Suzuki Ryo, Yamauchi Toshimasa

机构信息

Diabetes and Metabolism Information Center, Diabetes Research Center, National Center for Global Health and Medicine, Tokyo, Japan.

Department of Diabetes, Metabolism and Endocrinology, Kumamoto University Hospital, Kumamoto, Japan.

出版信息

Diabetol Int. 2024 Jul 11;15(3):327-345. doi: 10.1007/s13340-024-00723-8. eCollection 2024 Jul.

Abstract

The Japan Diabetes Society (JDS) adopted a sweeping decision to release consensus statements on relevant issues in diabetes management that require updating from time to time and launched a "JDS Committee on Consensus Statement Development." In March 2020, the committee's first consensus statement on "Medical Nutrition Therapy and Dietary Counseling for People with Diabetes" was published. In September 2022, a second consensus "algorithm for pharmacotherapy in people with type 2 diabetes" was proposed. In developing an algorithm for diabetes pharmacotherapy in people with type 2 diabetes, the working concept was that priority should be given to selecting such medications as would appropriately address the diabetes pathology in each patient while simultaneously weighing the available evidence for these medications and the prescribing patterns in clinical practice in Japan. These consensus statements are intended to present the committee's take on diabetes management in Japan, based on the evidence currently available for each of the issues addressed. It is thus hoped that practicing diabetologists will not fail to consult these statements to provide the best available practice in their respective clinical settings. Given that the persistent dual GIP/GLP-1 receptor agonist tirzepatide was approved in April 2023, these consensus statements have been revised. In this revision, specifically, tirzepatide was added to the end of [likely involving insulin resistance] of "Obese patients" in Step 1: "Select medications to address the diabetes pathology involved" in Fig. 2. While the sentence, "Insulin insufficiency and resistance can be assessed by referring to the various indices listed in the JDS 'Guide to Diabetes Management.' was mentioned in the previous edition as well, "While insulin resistance is analogized based on BMI, abdominal obesity, and visceral fat accumulation, an assessment of indicators (e.g., HOMA-IR) is desirable" was added as information in order to more accurately recognize the pathology. Regarding Step 2: "Give due consideration to safety," "For renal excretion" was added to the "Rule of thumb 2: Avoid glinides in patients with renal impairment." The order of the medications in "rule of thumb 3: Avoid thiazolidinediones and biguanides in patients with heart failure (in whom they are contraindicated)." to thiazolidinediones then biguanides. In the description of the lowest part of Fig. 2, for each patient failing to achieve his/her HbA1c control goal, "while reverting to step 1" was changed to "while reverting to the opening" and "including reassessment if the patient is indicated for insulin therapy" was added. In the separate table, the column for tirzepatides was added, while the two items, "Characteristic side effects" and "Persistence of effect" were added to the area of interest. The revision also carried additional descriptions of the figure and table such as tirzepatides and "Characteristic side effects" in the statement, and while not mentioned in the proposed algorithm figure, nonalcoholic fatty liver disease (NAFLD) is covered from this revision for patients with comorbidities calling for medical attention. Moreover, detailed information was added to the relative/absolute indication for insulin therapy, the Kumamoto Declaration 2013 for glycemic targets, and glycemic targets for older people with diabetes. Again, in this revision, it is hoped that the algorithm presented here will not only contribute to improved diabetes management in Japan, but will continue to evolve into a better algorithm over time, reflecting new evidence as it becomes available.

摘要

日本糖尿病学会(JDS)做出了一项全面决定,发布关于糖尿病管理中相关问题的共识声明,这些问题需要不时更新,并成立了“JDS共识声明制定委员会”。2020年3月,该委员会关于“糖尿病患者的医学营养治疗和饮食咨询”的第一份共识声明发布。2022年9月,提出了第二份共识“2型糖尿病患者的药物治疗算法”。在制定2型糖尿病患者的糖尿病药物治疗算法时,工作理念是优先选择能够适当解决每位患者糖尿病病理问题的药物,同时权衡这些药物的现有证据以及日本临床实践中的处方模式。这些共识声明旨在根据目前针对所涉及的每个问题的现有证据,呈现委员会对日本糖尿病管理的看法。因此,希望执业糖尿病专家务必参考这些声明,以便在各自的临床环境中提供最佳实践。鉴于长效双靶点GIP/GLP-1受体激动剂替尔泊肽于2023年4月获批,这些共识声明已进行修订。在本次修订中,具体而言,在图2步骤1“选择药物以解决所涉及的糖尿病病理问题”中“肥胖患者”的[可能涉及胰岛素抵抗]末尾添加了替尔泊肽。虽然上一版也提到了“胰岛素不足和抵抗可通过参考JDS‘糖尿病管理指南’中列出 的各种指标进行评估”,但为了更准确地认识病理情况,添加了“虽然基于BMI、腹型肥胖和内脏脂肪堆积来类推胰岛素抵抗,但对指标(如HOMA-IR)进行评估是可取的”作为补充信息。关于步骤2“充分考虑安全性”,在“经验法则2:肾功能损害患者避免使用格列奈类药物”中添加了“对于经肾排泄的药物”。在“经验法则3:心力衰竭患者(禁忌使用噻唑烷二酮类和双胍类药物)”中,药物顺序改为先噻唑烷二酮类后双胍类。在图2最下方的描述中,对于每个未达到糖化血红蛋白控制目标的患者,“同时回到步骤1”改为“同时回到开头”,并添加了“如果患者适合胰岛素治疗则包括重新评估”。在单独的表格中,添加了替尔泊肽的列,同时在关注领域添加了“特征性副作用”和“作用持续性”两项。修订还在声明中对图和表进行了额外描述,如替尔泊肽和“特征性副作用”,并且虽然在提议的算法图中未提及,但本次修订涵盖了需要医疗关注的合并症患者的非酒精性脂肪性肝病(NAFLD)。此外,在胰岛素治疗的相对/绝对适应证、2013年熊本宣言的血糖目标以及老年糖尿病患者的血糖目标方面添加了详细信息。同样,在本次修订中,希望这里呈现的算法不仅有助于改善日本的糖尿病管理,而且随着新证据的出现,将随着时间的推移不断演变成更好的算法。

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