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©The Author(s) 2024.
World J Diabetes. May 15, 2024; 15(5): 828-852
Published online May 15, 2024. doi: 10.4239/wjd.v15.i5.828
Published online May 15, 2024. doi: 10.4239/wjd.v15.i5.828
Type of insulin | Brand name | Onset of action (min) | Peak time (h) | Duration of action (h) | Ref. | ||
Short acting insulin | |||||||
Human regular insulin | Humulin® R; Novolin® R; Actrapid® | 30-60 | 2-4 | 6-8 | [39] | ||
Ultra-rapid insulin | |||||||
Ultra-rapid aspart | Fiasp® | 2 | 1-3 | 3-5 | [40] | ||
Ultra-rapid lispro | Lyumjev® | 20 | 1-3 | 3-4 | [41] | ||
Rapid-acting insulin | |||||||
Insulin lispro | Humalog® | 20-30 | 1-2 | ≤ 5 | [42] | ||
Insulin aspart | Novolog® | 15 | 1-3 | 3-5 | [43] | ||
Insulin glulisine | Apidra® | 12-30 | 1.5 | Approximately 4 | [44] | ||
Intermediate-acting insulin | |||||||
NPH insulin | Humulin®; Novolin® | 2-4 | 4-10 | Up to 18 | [45] | ||
Long-acting insulin | |||||||
Insulin glargine-100 | Lantus® | N/A | No peak | 24 | [46] | ||
Insulin detemir | Levemir® | N/A | No peak | 14-24 | [47] | ||
Insulin glargine-300 | Toujeo® | N/A | No peak | Up to 36 | [48] | ||
Insulin degludac | Tresiba® | N/A | No peak | > 40 | [49] | ||
Premixed insulins | |||||||
Human insulin mix (70/30) | Mixtard® 30; Novolin® 70/30 | 30 | 2-10 | Up to 24 | [50] | ||
Lispro mix (75/25) Lispro mix (50/50) | Humalog® Mix (75/25); Humalog® Mix (50/50) | 5-20 | 1-2 | Up to 24 | [51] | ||
Aspart mix (70/30) | NovoMix® 30 | 10-20 | 1-4 | Up to 24 | [52] | ||
Degludec/Aspart | Ryzodeg® | 15 | 2-4 | > 24 | [53] |
Effect on QOL | Comparison | PROMs | Result | Ref. |
Negative | Insulin vs non-insulin users at baseline | SF-12v2; ADDQoL | Stable insulin treatment was associated with worse health status and QOL in comparison to non-insulin users | [123] |
Insulin vs non-insulin users at baseline and after 1 year | DHP; Rand-36 | Insulin users had more significant problems in social functioning, pain and mental state than non-insulin users | [166] | |
Insulin vs non-insulin users | SF-36v.2; WHOQOL-BREF | Insulin treated patients were associated with lower mental score than non-insulin users with no significant difference in other domains | [180] | |
Insulin vs non-insulin users | DQOL; Rosser index | Individuals with established insulin therapy showed lower satisfaction and QOL | [123] | |
Insulin vs non-insulin users | EQ5D; DTSQ | Insulin treatment was associated with lower HRQOL and treatment satisfaction scores than non-insulin treatment | [136] | |
Insulin vs non-insulin users | SF-36 | Insulin users had worse vitality and physical function domains than non-insulin users | [125] | |
Insulin vs non-insulin users | EQ-5D | Insulin users had lower HRQOL scores than those not using any therapies | [126] | |
Insulin vs non-insulin users | ADDQOL | Insulin therapy was associated with lower QOL scores | [181] | |
Insulin vs non-insulin users | SF-12 | Insulin was associated with significant lower HRQOL scores (especially mental composite scores) | [174] | |
Insulin vs non-insulin users | SF-36; DHP | Insulin users showed lower scores in six domains of SF-36 questionnaire (physical functioning, social functioning, role physical, mental health, vitality, and general health) and in 2 domains of DHP-1 (barriers to activity and psychological distress) than non-insulin users | [175] | |
Insulin vs non-insulin users | DQOLBCI; PDDT; QOL-VAS | Insulin therapy was associated with lower overall QOL scores (especially pain associated with treatment scale) | [182] | |
Insulin vs non-insulin users | ADDQOL | Insulin use was associated with lower scores of QOL especially in younger patients | [131] | |
Insulin vs non-insulin users | SF-36; HADS | Insulin therapy negatively affected emotional state, bodily pain, and physical state | [176] | |
Insulin vs non-insulin users | ADDQOL-18 | Insulin use was associated with negative impact on QOL | [183] | |
Insulin vs non-insulin users | EQ-5D-5L; SF-12; EQ-5D-3L | Insulin users experienced more issues in self-care and usual activities, while individuals receiving combination therapy of insulin and oral drugs encountered greater difficulties in mobility, pain/discomfort, and anxiety/depression domains | [184] | |
Insulin vs non-insulin users | SF-36; HADS; COPM; VAS-P; IPAQ | Insulin users exhibited more significant impairments in quality of life, functional capacity, and socialization, while also reporting higher levels of neuropathic pain and symptoms of anxiety and depression compared to non-insulin users | [127] | |
Retrospective comparison | EQ-5D-5L | Longer duration of insulin use was associated with lower scores of QOL | [185] | |
Positive | Baseline vs follow up for 4 years of insulin therapy | SF-12v2; ADDQOL | Initiation of insulin therapy did not significantly affect health status or QOL during 4 years of follow up | [123] |
Baseline vs 4-8 wk short course of intensive insulin therapy | SF-36; DQOL; DSC-R | Early initiation of a short course of intensive insulin Therapy (IIT) associated with increased satisfaction and QOL | [129] | |
Baseline vs one year of insulin treatment | DHP; Rand-36 | Significant improvements in psychological distress and disinhibited eating scores of DHP questionnaire. Also, scores of vitality, physical function, social functioning and health change domain related to Rand-36 showed significant improvements | [166] | |
Insulin vs non-insulin users | SF-36 | Insulin users showed better quality of life in 2 domains (physical and emotional) out of 8 domains compared to non-insulin users | [167] | |
Baseline vs 4 and 12 wk for insulin and non-insulin users | SF-36; DTSQ; GDS; GHQ-28 | Insulin was associated with improvement in QOL, treatment satisfaction and mood reflected in different domains (Mental Health-Vitality-Social functioning-Role emotional and physical) | [133] | |
Baseline vs 6 months of follow up | SF-36; DTSQ; HADS | Significant improvement in health status of Basal/Bolus group over time (7 domains) and in comparison, to oral medication group (vitality, social function, and mental health domains). Also, Basal/Bolus showed improvement in depression scores (first 3 months) and anxiety. Treatment satisfaction improved in all groups | [134] | |
Baseline vs 6 months of follow up | HFS-w; DSC-R; WHO-5; ITAS | Significant improvement of well-being and QOL especially vitality and general mood | [168] | |
Insulin (analog vs human) ± OAD vs OAD alone | DAWN QOL | Insulin users showed higher scores related to diet compliance and 3 subscales related to QOL measurements in comparison to non-insulin users | [169] | |
Baseline vs 18 months of insulin initiation or switching | EQ-VAS; PITQ; EITQ | Improvement of the patients’ satisfaction to insulin and QOL scores in comparison to baseline | [170,171] | |
Baseline vs one year of follow up | SF-36v2; DQOLCTQ | Scores of treatment satisfaction, diabetes impact and worry improved over time for each group with no significant difference between them | [172] | |
Baseline vs 12 vs 24 wk for insulin users and non-insulin-users | DTSQ; ADDQOL | Significant improvement of treatment satisfaction and QOL for insulin group better than oral antidiabetic group | [135] | |
Baseline vs 24 wk after insulin initiation or insulin switching | EQ-5D | Significant improvements in all measured 5 domains (Mobility- Pain/discomfort-Anxiety/depression-Self-Care-Usual activities) related to QOL for both insulin naïve and experienced patients | [164] | |
Baseline vs 24 wk after insulin initiation or insulin switching | EQ-5D | Significant improvement in 3 domains (Mobility-Pain/discomfort-Anxiety/depression) out of 5 domains related to QOL for both insulin naïve and experienced patients | [165] |
Result | Type of insulin therapy | Study design | PROMs | Comment | Ref. |
Favor basal bolus therapy | Glargine + glulisine (BB) vs lispromix or aspartmix (PM) | Comparative 12 wk intervention (crossover) phases | Validated generic and diabetes-specific modules of treatment satisfaction and QOL | The basal-bolus insulin regimen showed better outcomes in terms of treatment satisfaction and quality of life scores compared to premixed insulin regimens | [203] |
Premixed vs basal bolus | 6 months observational prospective study | EQ-5D-3L | Basal-bolus regimen showed the most significant potential to increase HRQOL in comparison to other regimens | [204] | |
Glargine + glulisine (BB) vs aspartmix (PM) | BB vs PM after 24 wk of treatment | DTSQ; ITSQ; ADDQOL; EQ-5D | The basal-bolus group showed significantly higher overall satisfaction with treatment, satisfaction with insulin, perceived frequency of hyperglycemia, and overall present quality of life | [137] | |
Glargine + glulisine (BB) vs aspartmix (PM) | Baseline vs 60 wk follow up | PAIS-SR; EQ-5D; HFS; DQOL | The basal-bolus regimen showed superior outcomes compared to the premixed group in terms of QOL. The basal-bolus group experienced significant improvements in psychological adjustment to illness and less fear of hypoglycemia. The premixed group reported significant increases in hypoglycemic worry and a significant decline in general health related QOL | [205] | |
Glargine + lispro (BB) vs lispromix (PM) | Baseline vs 24 wk follow up | DTSQ; EWITQ | No significant difference between the two groups in term of DTSQ and EWITQ scores except that premixed group showed significantly higher perceived frequency of hypoglycemia than basal-bolus group | [138] | |
Favor Premixed therapy | Glargine or NPH based BB regimen vs aspartmix (PM) | 24 wk prospective study after switching to AspartMix | EQ-5D | Switching to AspartMix showed significant improvement in HRQOL | [206] |
Glargine + glulisine (BB) vs aspartmix (PM) | 26 months randomized trial | EQ-5D; DQOL; WPAI | No significant difference of different scales for three questionnaires between two groups except for work missed for health which is significantly lower in BB group | [128] | |
NPH + lispro (BB) vs lispromix (PM) | 12 wk randomized comparative trial | ITR-QOL | The premixed group exhibited significantly higher scores in the total score and daily activities subscale score of ITR-QOL compared to the basal-bolus group | [207] | |
Undetectable difference | Glargine + glulisine (BB) vs lispromix or aspartmix (PM) | Patients switched from PM to BB with follow up for 16 wk | DTSQ | No significant difference in treatment satisfaction between two groups | [139] |
Detemir + aspart (BB) vs aspartmix (PM) | Baseline vs 50 wk of treatment | SF-36; DiabMedSat; DPM; TRIM-D | No statistically significant differences between premixed and basal-bolus group in term of patients’ satisfaction, productivity and quality of life | [130] | |
Premixed vs basal bolus | Baseline vs 6 months Switching to basal bolus regimen | DQOL | No significant difference in satisfaction, impact of diabetes, social concern and concern related to diabetes after initiation of basal-bolus regimen | [101] | |
Glargine + lispro (BB) vs lispromix (PM) | 48 wk open label randomized study | EQ-5D; DHP-18 | No significant difference of different scales for two questionnaires between two groups | [208] | |
Glargine + lispro (BB) vs lispromix (PM) | Baseline vs 24 wk follow up | ITSQ; PAM-D21 | No significant difference between the two groups in terms of ITSQ domain and total scores, and PAM-D21 questionnaires domain scores | [132] | |
Glargine + lispro (BB) vs lispromix (PM) | Baseline vs 48 wk follow up | EQ-5D; DTSQ | No significant difference between the two groups | [140] | |
Glargine + glulisine (BB) vs aspartmix (PM) | Baseline vs 24 wk follow up | DTSQ | No significant difference between the two groups in term of treatment satisfaction | [141] |
- Citation: Emad-Eldin M, Balata GF, Elshorbagy EA, Hamed MS, Attia MS. Insulin therapy in type 2 diabetes: Insights into clinical efficacy, patient-reported outcomes, and adherence challenges. World J Diabetes 2024; 15(5): 828-852
- URL: https://www.wjgnet.com/1948-9358/full/v15/i5/828.htm
- DOI: https://dx.doi.org/10.4239/wjd.v15.i5.828