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Diverse Strategies for Modulating Insulin Resistance: Causal or Consequential Inference on Metabolic Parameters in Treatment-Naïve Subjects with Type 2 Diabetes.
Kutoh, Eiji; Kuto, Alexandra N; Okada, Rumiko; Akiyama, Midori; Kurihara, Rumi.
Affiliation
  • Kutoh E; Biomedical Center, Tokyo 132-0034, Japan.
  • Kuto AN; Division of Diabetes and Endocrinology, Department of Internal Medicine, Gyoda General Hospital, Saitama 361-0056, Japan.
  • Okada R; Division of Diabetes and METABOLISM, Department of Internal Medicine, Higashitotsuka Memorial Hospital, Yokohama 244-0801, Japan.
  • Akiyama M; Division of Diabetes, Department of Internal Medicine, Kumagaya Surgical Hospital, Kumagaya 360-0023, Japan.
  • Kurihara R; Biomedical Center, Tokyo 132-0034, Japan.
Medicina (Kaunas) ; 60(6)2024 Jun 17.
Article in En | MEDLINE | ID: mdl-38929608
ABSTRACT
Bacground and

Objectives:

The objective of this study is to investigate how different therapies modulating insulin resistance, either causally or consequently, affect metabolic parameters in treatment-naïve subjects with T2DM. Subjects and

Methods:

A total of 212 subjects were assigned to receive either a tight Japanese diet (n = 65), pioglitazone at doses ranging from 15-30 mg/day (n = 70), or canagliflozin at doses ranging from 50-100 mg/day (n = 77) for a duration of three months. Correlations and changes (Δ) in metabolic parameters relative to insulin resistance were investigated.

Results:

Across these distinct therapeutic interventions, ΔHOMA-R exhibited significant correlations with ΔFBG and ΔHOMA-B, while demonstrating a negative correlation with baseline HOMA-R. However, other parameters such as ΔHbA1c, ΔBMI, ΔTC, ΔTG, Δnon-HDL-C, or ΔUA displayed varying patterns depending on the treatment regimens. Participants were stratified into two groups based on the median value of ΔHOMA-R the lower half (X) and upper half (Y). Group X consistently demonstrated more pronounced reductions in FBG compared to Group Y across all treatments, while other parameters including HbA1c, HOMA-B, TC, TG, HDL-C, non-HDL-C, TG/HDL-C ratio, or UA exhibited distinct regulatory responses depending on the treatment administered.

Conclusions:

These findings suggest that (1) regression to the mean is observed in the changes in insulin resistance across these therapies and (2) the modulation of insulin resistance with these therapies, either causally or consequentially, results in differential effects on glycemic parameters, beta-cell function, specific lipids, body weight, or UA.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Insulin Resistance / Diabetes Mellitus, Type 2 / Pioglitazone / Hypoglycemic Agents Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Medicina (Kaunas) Journal subject: MEDICINA Year: 2024 Document type: Article Affiliation country: Japón

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Insulin Resistance / Diabetes Mellitus, Type 2 / Pioglitazone / Hypoglycemic Agents Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Medicina (Kaunas) Journal subject: MEDICINA Year: 2024 Document type: Article Affiliation country: Japón