Non-Sugar Sweeteners and Glycemic Regulation: Controlled Feeding Trials in Middle-Aged and Older Adults with Prediabetes
| dc.contributor.author | Boone, Jordan Thomas | en |
| dc.contributor.committeechair | Hedrick, Valisa Ellen | en |
| dc.contributor.committeemember | Savla, Jyoti Shital | en |
| dc.contributor.committeemember | Davy, Kevin P. | en |
| dc.contributor.committeemember | Davy, Brenda Mueller | en |
| dc.contributor.department | Human Nutrition, Foods and Exercise | en |
| dc.date.accessioned | 2026-05-27T08:02:23Z | en |
| dc.date.available | 2026-05-27T08:02:23Z | en |
| dc.date.issued | 2026-05-26 | en |
| dc.description.abstract | Type 2 diabetes (T2D) and prediabetes represent a major share of the overall metabolic disease burden across the globe. Middle-aged and older adults, who account for over a third of those with T2D, with nearly half having prediabetes, are at increased risk of glucose intolerance and insulin resistance and are among the highest consumers of widely used non-sugar sweeteners (NSS). NSS are often recommended as healthier alternatives to traditional sugar, yet the understanding of their effects remains limited due to mixed results and a lack of rigorous study designs. To overcome the limitations of the currently available research, two separate three-arm randomized controlled feeding trials were conducted to isolate glycemic responses for four distinct NSS types. Adults (≥40 years) with prediabetes followed a standardized eucaloric diet for a 2-week lead-in period, followed by a 4-week randomized intervention period (trial 1: sucralose, aspartame, or control; trial 2: acesulfame potassium [Ace-K], saccharin, or control). NSS doses were individualized to body weight, using 25% of the acceptable daily intake (NSS mg/kg body weight). All intervention arms received identical diets matched to usual U.S. intake, except for NSS dosing, delivered via a study beverage and capsules. Outcomes, including 24-hr glycemic control (continuous glucose monitoring, CGM), glucose tolerance (2-hour oral glucose tolerance test, OGTT), and insulin sensitivity, were assessed pre- and post-intervention. The results from these pilot studies indicate no significant differences in glycemic control or insulin sensitivity among the four NSS types and the control group over the 4-week intervention in middle-aged and older adults with prediabetes. CGM-derived area under the curve (AUC, mg·h/dL) did not differ significantly between sweetener type and control groups in either trial, with no differences observed for aspartame vs control (Δ = +2.12 ± 11.6 vs +1.56 ± 8.0; p = 0.973), sucralose vs control (Δ = +1.62 ± 10.5 vs +1.56 ± 8.0; p = 0.935), Ace-K vs control (Δ = +1.8 ± 10.9 vs +2.3 ± 11.4; p = 0.972), or saccharin vs control (Δ = +1.2 ± 4.6 vs +2.3 ± 11.4; p = 0.870), indicating no effect of NSS consumption on overall glycemic exposure under free-living conditions. Further research is warranted to address longer-term effects, diverse populations, and explore mechanistic pathways to clarify the effects of NSS across settings. | en |
| dc.description.abstractgeneral | Prediabetes affects millions of middle-aged and older adults and increases the risk of developing type 2 diabetes. Many middle-aged and older adults also use artificial sweeteners to reduce sugar intake or are unaware that they are consuming them. Yet, there is ongoing debate about how these sweeteners may affect blood sugar control. Current findings on artificial sweeteners remain mixed because the studies are not robust or well-designed. The present studies evaluated how several commonly consumed artificial sweeteners, compared with not consuming any artificial sweeteners (control), affect blood sugar control in middle-aged and older adults with prediabetes. In two independent six-week controlled feeding pilot studies, individuals aged ≥40 years with prediabetes consumed a typical American diet and were randomized to receive aspartame, sucralose, or a control group (trial 1), or acesulfame-potassium (Ace-K), saccharin, or a control group (trial 2). The sweeteners were provided via study beverages and capsules to carefully control intake. Blood sugar measures (glucose and insulin) were collected before and after the intervention. The studies resulted in no significant differences in blood sugar or insulin control between any of the artificial sweeteners and the control groups. These results help improve understanding of the potential benefits and risks of artificial sweetener use and may inform dietary recommendations for people with prediabetes and for healthcare professionals advising on sugar alternatives. Although these studies suggest no harmful effects of artificial sweeteners on glucose control in middle-aged and older adults with prediabetes, more research is needed to help expand on and overcome limitations so that clear intake recommendations can be provided to the public. | en |
| dc.description.degree | Doctor of Philosophy | en |
| dc.format.medium | ETD | en |
| dc.identifier.other | vt_gsexam:46925 | en |
| dc.identifier.uri | https://hdl.handle.net/10919/143164 | en |
| dc.language.iso | en | en |
| dc.publisher | Virginia Tech | en |
| dc.rights | In Copyright | en |
| dc.rights.uri | http://rightsstatements.org/vocab/InC/1.0/ | en |
| dc.subject | Prediabetes | en |
| dc.subject | Non-Sugar Sweeteners | en |
| dc.subject | Glycemic Control | en |
| dc.subject | Insulin Response | en |
| dc.subject | Controlled Feeding Study | en |
| dc.title | Non-Sugar Sweeteners and Glycemic Regulation: Controlled Feeding Trials in Middle-Aged and Older Adults with Prediabetes | en |
| dc.type | Dissertation | en |
| thesis.degree.discipline | Human Nutrition, Foods, and Exercise | en |
| thesis.degree.grantor | Virginia Polytechnic Institute and State University | en |
| thesis.degree.level | doctoral | en |
| thesis.degree.name | Doctor of Philosophy | en |
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