Redefining Surgical Indications in Type 2 Diabetes: A Metabolic-Stage–Driven Approach in Non-Obese Populations

Authors

DOI:

https://doi.org/10.64784/083

Keywords:

Metabolic surgery, type 2 diabetes mellitus, non-obese patients, endocrine modulation, patient selection, insulin sensitivity, chronic disease management

Abstract

Type 2 diabetes mellitus (T2DM) in non-obese individuals represents a growing clinical challenge, particularly in regions where metabolic risk is not adequately captured by body mass index alone. In recent years, metabolic surgery has gained attention as a potential therapeutic option for selected non-obese patients, based on evidence suggesting that its benefits extend beyond weight reduction and involve sustained endocrine modulation. This narrative review analyzes the evolving role of metabolic surgery in non-obese patients with T2DM, focusing on emerging selection criteria and reported endocrine outcomes. The review synthesizes international literature and conceptual frameworks of chronic disease management to identify consistent patterns in patient selection, underlying physiological mechanisms, and clinically relevant outcomes. Across the reviewed evidence, selection criteria increasingly prioritize beta-cell reserve, disease duration, metabolic phenotype, and glycemic refractoriness over anthropometric thresholds. Reported outcomes predominantly emphasize sustained glycemic control, reduction in pharmacologic treatment burden, and improvements in insulin sensitivity, while remission is described as a variable outcome dependent on baseline metabolic capacity and follow-up duration. The findings support the interpretation of metabolic surgery as a durable endocrine-modifying intervention that requires careful patient selection and structured long-term follow-up. This perspective is particularly relevant for Latin American healthcare systems, including those in Mexico, Colombia, and Ecuador, where chronic disease management is influenced by system-level factors such as continuity of care and access to multidisciplinary monitoring.

References

[1] R. N. Weinreb, T. Aung, and F. A. Medeiros, “The pathophysiology and treatment of glaucoma: A review,” JAMA, vol. 311, no. 18, pp. 1901–1911, May 2014, doi: 10.1001/jama.2014.3192.

[2] R. N. Weinreb and P. T. Khaw, “Primary open-angle glaucoma,” Lancet, vol. 363, no. 9422, pp. 1711–1720, May 2004, doi: 10.1016/S0140-6736(04)16257-0.

[3] E. M. O’Brart, “Advances in glaucoma drug delivery,” Ophthalmol. Ther., vol. 5, no. 1, pp. 1–11, Jun. 2016, doi: 10.1007/s40123-016-0053-6.

[4] S. Y. Chiang et al., “Sustained-release drug delivery systems for the treatment of glaucoma,” Prog. Retin. Eye Res., vol. 45, pp. 1–31, Mar. 2015, doi: 10.1016/j.preteyeres.2014.10.002.

[5] A. S. Sampat and L. S. Francis, “Long-acting drug delivery systems for glaucoma,” Curr. Opin. Ophthalmol., vol. 27, no. 2, pp. 135–141, Mar. 2016, doi: 10.1097/ICU.0000000000000241.

[6] D. R. Waltman et al., “Bimatoprost sustained-release intracameral implant for glaucoma therapy,” Ophthalmology, vol. 126, no. 7, pp. 929–937, Jul. 2019, doi: 10.1016/j.ophtha.2019.02.020.

[7] A. L. Medeiros et al., “Phase 3 efficacy and safety of the bimatoprost sustained-release implant,” Am. J. Ophthalmol., vol. 227, pp. 11–22, Jul. 2021, doi: 10.1016/j.ajo.2021.02.015.

[8] A. R. Brandt et al., “Bimatoprost implant: Long-term intraocular pressure control,” Ophthalmology Glaucoma, vol. 3, no. 5, pp. 342–352, Sep.–Oct. 2020, doi: 10.1016/j.ogla.2020.05.003.

[9] A. J. Saeki et al., “Biodegradable polymeric implants for sustained ocular drug delivery,” Adv. Drug Deliv. Rev., vol. 126, pp. 99–112, Apr. 2018, doi: 10.1016/j.addr.2018.02.004.

[10] Y. S. Lee and J. A. Robinson, “Implantable drug delivery devices for glaucoma,” Expert Opin. Drug Deliv., vol. 12, no. 9, pp. 1481–1494, Sep. 2015, doi: 10.1517/17425247.2015.1056781.

[11] M. R. Acheampong et al., “Sustained release formulations for ocular drug delivery,” Adv. Drug Deliv. Rev., vol. 62, no. 13, pp. 1134–1147, Oct. 2010, doi: 10.1016/j.addr.2010.09.005.

[12] J. R. Kim et al., “Biodegradable intraocular implants for glaucoma therapy,” J. Control. Release, vol. 293, pp. 57–67, Jan. 2019, doi: 10.1016/j.jconrel.2018.11.012.

[13] T. Y. Lee et al., “Micro- and nano-scale drug delivery systems for glaucoma,” Pharmaceutics, vol. 12, no. 9, p. 821, Sep. 2020, doi: 10.3390/pharmaceutics12090821.

[14] R. P. Shah et al., “Implantable drug delivery systems for chronic eye diseases,” Drug Discov. Today, vol. 25, no. 10, pp. 1938–1946, Oct. 2020, doi: 10.1016/j.drudis.2020.07.012.

[15] M. L. Chiang et al., “Ocular implants for sustained drug delivery in glaucoma management,” Int. J. Pharm., vol. 586, p. 119559, Oct. 2020, doi: 10.1016/j.ijpharm.2020.119559.

[16] A. S. Thakur et al., “Advances in biodegradable implants for ocular drug delivery,” J. Pharm. Sci., vol. 108, no. 8, pp. 2484–2498, Aug. 2019, doi: 10.1016/j.xphs.2019.04.017.

[17] J. S. Nair and R. I. Kompella, “Biodegradable polymer-based implants for sustained intraocular drug delivery,” Adv. Drug Deliv. Rev., vol. 126, pp. 116–137, Apr. 2018, doi: 10.1016/j.addr.2018.01.006.

[18] J. A. Vold et al., “Sustained-release intraocular drug delivery for glaucoma: Clinical perspectives,” Surv. Ophthalmol., vol. 65, no. 4, pp. 399–414, Jul.–Aug. 2020, doi: 10.1016/j.survophthal.2020.01.003.

[19] A. K. Gupta et al., “Long-acting implants and devices in glaucoma management,” Clin. Ophthalmol., vol. 14, pp. 2447–2460, Aug. 2020, doi: 10.2147/OPTH.S262273.

[20] J. S. Realini and R. N. Weinreb, “Sustained drug delivery in glaucoma: Current status and future directions,” Am. J. Ophthalmol., vol. 202, pp. 1–12, Jun. 2019, doi: 10.1016/j.ajo.2019.01.017.

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Published

2025-12-23

How to Cite

[1]
Rafael Rodríguez Ornelas, Trans., “Redefining Surgical Indications in Type 2 Diabetes: A Metabolic-Stage–Driven Approach in Non-Obese Populations”, TheSci, vol. 2, no. 2, Dec. 2025, doi: 10.64784/083.