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Abstract
Whether integrase strand transfer inhibitors (INSTIs) are associated with a higher risk of incident type 2 diabetes mellitus (DM) than other antiretroviral therapies (ART) needs to be established.
MEDLINE, Embase, Web of Science, and ClinicalTrials.gov registries were searched for studies published between 1 January 2000 and 15 June 2022. Eligible studies reported incident DM or mean changes in insulin resistance measured by Homeostatic Model for Insulin Resistance (HOMA-IR) in patients on INSTIs compared with other ARTs. We performed random-effects meta-analyses to obtain pooled relative risks (RRs) with 95% CIs.
A total of 16 studies were pooled: 13 studies meta-analyzed for incident diabetes with a patient population of 72 404 and 3 for changes in HOMA-IR. INSTI therapy was associated with a lower risk of incident diabetes in 13 studies (RR 0.80, 95% CI 0.67 to 0.96, I2=29%), of which 8 randomized controlled trials demonstrated a 22% reduced risk (RR 0.88, 95% CI 0.81 to 0.96, I2=0%). INSTIs had a lower risk compared with non-nucleoside reverse transcriptase inhibitors (RR 0.75, 95% CI 0.63 to 0.89, I2=0%) but similar to protease inhibitor-based therapy (RR 0.78, 95% CI 0.61 to 1.01, I2=27%). The risk was lower in studies with longer follow-up (RR 0.70, 95% CI 0.53 to 0.94, I2=24%) and among ART-naïve patients (RR 0.78, 95% CI 0.65 to 0.94, I2=3%) but increased in African populations (RR 2.99, 95% CI 2.53 to 3.54, I2=0%).
In conclusion, exposure to INSTIs was not associated with increased risk of DM, except in the African population. Stratified analyses suggested reduced risk among ART-naïve patients and studies with longer follow-up.
International Prospective Register of Systematic Reviews (PROSPERO) registration number: CRD42021273040.
- HIV
- Insulin Resistance
- Metabolic Syndrome
- Meta-Analysis
Data availability statement
All data relevant to the study are included in the article or uploaded as supplementary information.
This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
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What is already known on this topic
People living with HIV (PLHIV) have a higher prevalence of metabolic perturbations compared with HIV-negative populations, and integrase strand transfer inhibitors (INSTIs) are currently the preferred first-line and second-line antiretroviral therapy (ART).
Some studies suggested more weight gain among INSTIs users compared with other ART regimens, while others reported accelerated hyperglycemia preceded by weight loss, weeks to a few months after initiating INSTIs.
What this study adds
This systematic review and meta-analysis comprising ~75 000 PLHIV on different ART regimens is the first to examine the risk of insulin resistance and type 2 diabetes mellitus (DM) in INSTIs compared to other ART regimens.
Analyses showed that compared to protease inhibitors and non-nucleoside reverse transcriptase inhibitors, INSTI exposure was not associated with increased risk of insulin resistance and/or DM.
We also identified in multiple analyses that INSTIs might be associated with a reduced risk of type 2 DM in certain subpopulations of PLHIV.
How this study might affect research, practice or policy
Our findings contribute to the evidence of metabolic safety of INSTI therapy, which might implicate the choice of therapy for millions of PLHIV.
We demonstrated that exposure to INSTI therapy did not pose higher risk of insulin resistance and/or DM compared to other ART regimens. Initiating or switching to INSTIs is safe; nevertheless, monitoring is warranted in certain high-risk groups.
Introduction
Antiretroviral therapy (ART) has revolutionized HIV treatment and significantly reduced AIDS-associated mortality globally, particularly in sub-Saharan Africa.1 People living with HIV (PLHIV) have more prevalent insulin resistance and diabetes mellitus (DM) than HIV-negative populations due to a combination of demographic and socioeconomic factors, in addition to HIV-related factors.2 3 HIV-associated chronic inflammation and certain forms of ART impair insulin signaling at target organs as well as insulin secretion.4–6 It remains challenging to distinguish to which extent the increased risk of DM is related to the normal aging process, the HIV infection, ART, or a combination of these factors.7–12
In the early ART era, nucleoside reverse transcriptase inhibitors (NRTIs) were coupled in combinations of predominantly stavudine, didanosine, zidovudine, lamivudine and zalcitabine with non-nucleoside reverse transcriptase inhibitors (NNRTIs).13 These drug combinations were linked to a spectrum of metabolic perturbations, including dyslipidaemia, lipodystrophy, and metabolic syndrome, and hence have largely been phased out of use.14 15 Since then, ART has conventionally included NNRTIs, protease inhibitors (PIs), and lately, the preferred integrase strand transfer inhibitors (INSTIs) as anchor agents coupled with largely metabolically safe NRTIs.13 16 17
In 2018, the WHO recommended the use of INSTIs, particularly dolutegravir (DTG) as first-line ART, and since then, the use of INSTIs has largely overtaken NNRTIs and PIs.18 This was after multiple countries reported primary resistance to NNRTIs above the recommended threshold of 10%.19 20 Thereafter, multiple studies demonstrated enhanced efficacy, a higher genetic barrier to resistance, good side effect profiles, and less drug–drug interactions with newer-generation integrase inhibitors.21–25 Despite their favorable side-effect profiles, INSTIs have consistently been associated with weight gain.23 26 Whether the weight gain in PLHIV translates to disorders in glucose metabolism in the long term remains to be demonstrated.27
Multiple case series on ART-experienced patients presenting with diabetic ketoacidosis with preceding weight loss a few weeks to months after starting INSTIs have been published.24 25 28 29 However, large population cohort studies have yielded conflicting results about the risk of diabetes among INSTI users.30
Given the inconsistent literature and to better quantify the risk, we performed a comprehensive literature review and meta-analyses aiming to summarize the current evidence on the association of INSTI therapy with insulin resistance, hyperglycemia, and incident DM versus PIs and NNRTI-based ART. We also explored the effect of other HIV-related factors and potential confounders on this association.
Research design and methods
The protocol for this systematic review is registered on International Prospective Register of Systematic Reviews database (CRD42021273040) and published.31 This study is being reported according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses checklist.32 The link to the study dataset is listed in the online supplemental material (SD).
Supplemental material
Search strategy and selection criteria
We searched PubMed/MEDLINE, Embase, and Web of Science (Clarivate) databases without language or geographical restrictions for randomized controlled trials (RCTs), cohort studies and case–control studies for eligible studies (online supplemental material, Emethods 1). Additionally, we searched Cochrane and clinicaltrials.org registries for eligible RCTs. Our search limit was fixed to the year 2000 to capture phase III clinical trial safety data, given that the first INSTIs, raltegravir, was approved by the Food and Drug Administration in 2007, and the search was last updated on 15 June 2022. We also searched abstracts of HIV conference meetings (International AIDS Society’s Conference on Retroviruses and Opportunistic Infections) for the same themes seeking studies that were eventually published. To identify relevant publications, two authors (FM and HK) independently screened all potential abstracts and reference lists in review articles. For published studies with desired outcomes but without data to calculate relative risk (RR) of diabetes, we reached out to authors for raw data. Studies eligible for full review were agreed on through consensus. A senior investigator (NB) was referred to in case of disagreement between the authors.
Studies were eligible if they reported risk of incident diabetes (or reported the required data to calculate incidence) with or without metabolic syndrome and/or insulin resistance, had exposure to INSTIs for ≥12 weeks, and had comparative arms of either NNRTI or PI anchored ART. Studies with cross-sectional design and studies including pregnant or breastfeeding mothers were excluded. Since we aimed to compare INSTIs versus PIs and/or NNRTIs as anchor agents, we also excluded studies where INSTIs were administered with PIs or NNRTIs in the same regimen. For studies with multiple publications, we included the publication with the most extended follow-up.
Data analysis
We evaluated two outcomes: incident hyperglycemia and type 2 DM (new cases) as a discrete outcome or as part of metabolic syndrome (online supplemental table S1). A separate analysis was performed for mean changes in insulin resistance measured by the Homeostatic Model for Insulin Resistance (HOMA-IR) index, a factor of fasting blood glucose and insulin. We extracted variable study and population characteristics into excel forms (online supplemental table S3). Adjusted effect estimates were sought whenever reported; otherwise, raw data were retrieved.
The quality of the studies was assessed using the Newcastle-Ottawa Scale for cohort or case–control studies33 and the Revised Cochrane Risk-of-Bias tool for randomized trials34 (online supplemental tables S4 and S5).
Statistical analysis was done using meta-R package V.4.0.5 with R package Metaphor and Stata V.15 to generate forest plots of pooled effects with 95% CIs. We performed a random-effects meta-analysis adjusting for in-between-study heterogeneity to pool the risk (new cases/overall population at risk) of DM with or without metabolic syndrome (as discrete outcomes). The populations of interest were HIV patients exposed to INSTIs compared with patients on NNRTI or PI-based ART regimens. We assessed in-between study heterogeneity using the I2 statistic with DerSimonian and Laird’s method, using values <50%, 51%–74%, and ≥75% to represent low, moderate, and high heterogeneity, respectively.35 We sought evidence for publication bias by applying Egger’s test and visually inspecting funnel plots for asymmetry (if ≥10 studies).36 We also performed several subgroup analyses to explore if the risk of DM was affected by longevity on INSTIs, particular types of INSTIs, geographical region of study participants, and past exposure to ART, as some ART drugs were associated with abnormal glucose metabolism.14 To further explore sources of heterogeneity, we also carried out subanalyses by study design, type of caring facility, and type of non-INSTIs in the control group to compare pooled effects and heterogeneity. A p value of <0.1 was considered a statistically significant subgroup effect. We considered sensitivity analyses to test the robustness of our findings by including only studies reporting adjusted risk estimates, excluding studies with comorbidities like viral hepatitis B and C, studies where primary outcome was a metabolic endpoint and studies with no apparent conflict of interest. Studies reporting changes in mean HOMA-IR were separately analyzed to pool mean changes (on a continuous scale) of HOMA-IR pre-INSTI and post-INSTIs exposure compared with PIs and/or NNRTIs. Additionally, we performed a univariable metaregression to explore the effect of the following variables on the outcome: the effect of year of publication, follow-up duration, average age, CD4 count, body mass index (BMI) of participants and the proportion of male participants if at least 10 studies reported sufficient data. In this systematic review and meta-analysis, sex was defined as biological sex at birth.
Results
Literature search and study selection
Out of the 124 studies identified for full-text review, 16 studies were deemed eligible for inclusion in the meta-analysis,27 30 37–50 and 3 studies included in the systematic review could not be pooled in the quantitative synthesis51–53 (figure 1). Excluded studies and reasons for exclusion are presented in online supplemental table S6.
PRISMA flowchart for study selection. INSTI, integrase strand transfer inhibitor; NNRTI, non-nucleoside reverse transcriptase inhibitor; PI, protease inhibitor; PRISMA, Preferred Reporting Items for Systematic Reviews and Meta-Analyses.
Study characteristics
The 19 studies included in the systematic review (n=74 827) included 13 RCTs37–42 45 46 48 49 51–53 and 6 cohort studies27 30 43 44 47 50 (table 1). In the meta-analysis for incident DM, 13 of these studies, including 8 RCTs37–42 45 46 48 49 51–53 and 5 cohort studies,27 30 43 44 47 50 with a patient population of 72 404 were included. To analyze for the effect of INSTIs on insulin resistance, three studies including two RCTs37–42 45 46 48 49 51–53 and one cohort27 30 43 44 47 50 study with a patient population of 766 were pooled. Publications spanned from 201051 to 2022,50 with patients’ enrolment from 2007 to 2018. Studies included cohorts from North America (six studies),30 37 41 42 47 50 Europe (five studies),27 43 44 52 53 Africa (two studies),46 48 and multinational (six studies).38–40 45 47 51 No studies originated from Asia.
Study characteristics of the 13 studies included in the meta-analyses for incident type 2 DM and the three studies for insulin resistance
The majority of studies (n=15)27 30 38 39 41 42 45–53 involved multiple centers, while four studies were single centers.37 43 44 50 Eight studies38–41 45 46 48 49 reported virological primary outcomes, mentioning hyperglycemia among the safety data, while 11 studies had metabolic endpoints.27 30 37 42–44 47 50–53 In 14 studies,27 30 38–41 43–49 51 crude numbers of DM were retrieved, while 5 studies37 42 43 52 53 reported mean changes in HOMA-IR. Four studies27 30 47 50 provided adjusted estimates for incidence of DM, 4 studies46–48 50 reported weight changes with INSTI exposure. None of the studies reported DM as part of metabolic syndrome as an outcome.
Overall, the quality of the studies was rated as high (online supplemental table S4 and S5). Common to most RCTs was a lack of blinding in the assessment of the outcome.
Study population characteristics
A total of 74 827 participants were included in the systematic review. The sample size ranged from 3037 to 22 88430 patients. Overall, 37.8% (n=28 289) of patients used INSTIs, particularly Elvitegravir (n=10 218), DTG (n=9783) and raltegravir (n=4478).
Non-INSTI users constituted 62.2% (n=46 538) with 21 391 receiving PIs27 30 39 41 47 51 54 and 17 842 receiving NNRTIs.27 30 38 40 45 46 48 The mean follow-up duration was 21.2 months, ranging from 5.637 to 108.0 months.44 In INSTI populations, the mean age was 38.7 (IQR 27–54) years, similar to 38.4 (IQR 27.0–54.6) years in non-INSTI populations. Two studies included populations <18 years.47 48
In the INSTI group, 82.1% (n=23 231) was male, contrasted to 68.8% (n=32 037) in non-INSTI groups. One study enrolled only female participants.53
All studies reported HIV RNA levels at baseline, with 12 studies27 30 38–43 45 46 48 50 enrolling ART-naïve participants, 5 studies37 49 51–53 enrolling ART-experienced patients and 2 studies enrolling both ART-naïve and ART-experienced patients.27 30 39 41 47 51 54
Risk of incident DM and hyperglycemia with exposure to INSTIs
In the 13 pooled studies27 30 38–41 43–49 (n=72 404), INSTI exposure carried a lower risk of incident DM as compared with any other ART (n=13, RR 0.80, 95% CI 0.67 to 0.96, I2=29%; figure 2). Particularly the risk was lower when compared with NNRTIs27 30 38 40 45 46 48 (n=7, RR 0.75, 95% CI 0.63 to 0.89, I2=0%) and borderline when compared with PIs27 30 39 41 43 47 (n=6, RR 0.78, 95% CI 0.61 to 1.01, I2=27%). There was minimal heterogeneity in both the aforementioned subanalyses (online supplemental figure S1). The test for subgroup difference indicated no statistically significant subgroup effect (p=0.74), suggesting that use of either PI or NNRTIS did not modify the lower risk in INSTIs group.
Forest plot of the association of INSTI exposure to incident hyperglycemia and diabetes mellitus compared with other art regimens. The crude numbers of events are based on the longest follow-up reported in the studies. INSTI, integrase strand transfer inhibitor; RR, relative risk.
Additionally, the risk reduction of diabetes was more evident in studies with a longer follow-up (≥12 months) (n=8, RR 0.70 95% CI 0.53 to 0.94, I2=24%)27 30 38 41 43–45 48 (online supplemental figure S2), than studies with less than 1 year follow-up (n=6, RR 0.89 95% CI 0.80 to 0.99, I2=0). The test for subgroup difference was significant (p=0.07), suggesting that longer follow-up influenced INSTI association with the outcome. The association between INSTIs and lower risk of DM was demonstrated in studies enrolling only adults (RR 0.77, 95% CI 0.65 to 0.91, I2=26%)27 30 38–41 43–46 49 and in multicenter studies (RR 0.84, 95% CI 0.77 to 0.93, I2=0%).27 30 38–41 45–49 INSTI use in PLHIV of African origin was associated with a threefold increased risk of DM in two studies with minimal heterogeneity (RR 2.99, 95% CI 2.53 to 3.54, I2=0%),46 48 and a significant subgroup effect was demonstrated by area of origin (p<0.01). Further interpretation of subgroup analyses is reported in table 2.
Subanalysis for the risk of diabetes mellitus with exposure to INSTIs in people living with HIV
Risk of DM and hyperglycemia in treatment naïve or experienced individuals
The risk of DM on exposure to INSTIs was reduced in ART-naïve patients (n=11, RR 0.78, 95% CI 0.65 to 0.94, I2=3%)27 30 38–41 43–46 48 but equal to controls in ART-exposed patients (n=2, RR 0.85, 95% CI 0.43 to 1.62, I2=0%)47 49 (online supplemental figure S4 and table 2).
No differences in the risk of DM were noted in studies per individual types of INSTIs in ART-naïve patients: DTG (n=7, RR 0.94, 95% CI 0.53 to 1.67, I2=43%),30 39 40 45–48 elvitegravir (n=2, RR 0.80, 95% CI 0.01 to 123.82, I2=78%)30 47 and raltegravir (n=4, RR 1.23, 95% CI 0.91 to 1.6, I2=0%).30 38 41 47
The risk of DM was lower in five cohort studies providing adjusted estimates, although not statistically significant (n=5, RR 0.83, 95% CI 0.58 to 1.18).27 30 47 49 50 In RCTs, the risk of developing hyperglycemia and/or DM was lower (n=8, RR 0.88, 95% CI 0.81 to 0.96) with minimal heterogeneity (I2=0%).38–41 45 48 49 A trend toward decreased risk was also observed in cohort studies, yet not statistically significant (n=5, RR 0.69, 95% CI 0.44 to 1.10) and with substantial heterogeneity (I2=60%)27 30 43 44 47 (online supplemental figure S5).
Effect of weight gain
We sought to analyze the effect of baseline weight, weight gain or changes in BMI on the incidence of diabetes in the study populations. Eleven studies27 30 38–41 43–49 provided estimates of weight and/ or BMI at baseline, yet changes were not presented per type of ARTs nor stratified per persons who developed diabetes and/or hyperglycemia, making it difficult to analyze.
Effect of exposure to INSTIs on insulin resistance
In the three included studies (n=976), INSTIs were associated with an insignificant increase in mean HOMA-IR from baseline compared with non-INSTIs (0.78, 95% CI −0.15 to 1.70) with substantial heterogeneity (I2=82.5%).37 42 43 The same results were noted when comparing INSTIs to PIs (0.90, 95% CI −0.90 to 2.69) and to NNRTIs (0.17, 95% CI −0.44 to 0.79) with substantial heterogeneity in both analyses (online supplemental figure S7).
For studies reporting incident insulin resistance and/or diabetes across different meta-analyses when the number of studies was ≥10, no publication bias or small study effect was detected by funnel plot asymmetry and by Egger’s test (online supplemental figure S6).
Metaregression analysis
We further explored the influence of specific study and HIV-related factors on the pooled risk of developing insulin resistance and/or type 2 DM between INSTIs and non-INSTI comparators. Neither the proportions of male, black population, or publication year were associated with the pooled risk in univariable meta-regression analysis. However, studies with longer follow-up duration were significantly associated with lower risk of type 2 DM in INSTIs compared with non-INSTIs (online supplemental table S7 and figure S9).
Influence analysis
We conducted influence analysis by the leave-one-out method to investigate the individual impact of each study (online supplemental figure S10). There was no significant change in the pooled effect estimates. Baujat plot pointed to one study with the most impact on overall study heterogeneity yet with minimal effect on the pooled effect estimates (online supplemental Figure S11).
Discussion
In this comprehensive systematic review and meta-analysis of approximately 75 000 PLHIV exposed to different ART regimens, INSTI use was associated with a lower risk of incident DM and hyperglycemia compared with NNRTI and PI anchored ART. Particularly, ART-naïve PLHIV and prolonged follow-up studies suggested a lower risk of DM among the INSTI group compared with the non-INSTI group. The association was consistent when pooling eight RCTs in the analysis. By contrast, PLHIV of African origin treated with INSTIs had a threefold increased risk of DM compared with their non-INSTI peers. Analysis per individual type of INSTIs showed similar risk compared with peer non-INSTIs, with raltegravir demonstrating a trend toward a higher risk compared with elvitegravir and DTG. Univariable regression analysis suggested that studies with longer follow-up times showed a lower risk.
Multiple cases of accelerated hyperglycemia in patients starting INSTIs have been reported, particularly on DTG and, in a few cases, raltegravir.25 55 The common presentation was diabetic ketoacidosis preceded by weight loss, weeks to months after initiating therapy, which might represent a typical phenotype of insulin deficiency.25 29 Some of the postulated mechanisms for the accelerated hyperglycemia included intracellular magnesium chelation induced by INSTIs leading to altered hepatic and skeletal muscle insulin signaling, mitochondrial dysfunction from previous exposure to more toxic NRTIs and possible genetic predisposition (online supplemental file 1, ref. 57).56 Interestingly, at the population level, INSTIs particularly DTG have been consistently associated with weight gain (online supplemental file 1, ref. 58). A recent systematic review concluded that INSTIs have a higher risk of DM compared with alternative backbone ART regimens.56 Most of the conclusions in that narrative review were premised on the consistent association of INSTIs with weight gain, a known precursor for metabolic syndrome or DM.56 We could not conclusively ascertain the effects of weight gain on the incidence of diabetes as data were lacking to perform a subanalysis for BMI changes. In the current analysis, studies with follow-up more than 12 months showed a 30% lower risk of type 2 DM among INSTIs versus non-INSTIs. This reduced risk tended to attenuate when restricted to studies with shorter follow-up. We observed a trend toward more insulin resistance (increase in HOMA-IR) rather than overt type 2 DM among INSTIs compared with non-INSTIs (online supplemental figure S7). It is unclear whether this trend is induced by the increased weight accompanying the ‘return-to-health phenomenon’ with possible metabolic perturbations in some susceptible individuals or could lead to overt type 2 DM and metabolic syndrome in the long term (online supplemental file 1, ref. 59). Considering the small sample size of this analysis (three studies with 766 patients) and the heterogeneity of PLHIV populations, long-term follow-up studies are therefore warranted, particularly accounting for sex, the presence of malnutrition, obesity, and/or metabolic syndrome at treatment initiation.
A threefold increased risk of diabetes in African patients was observed in the subanalysis by geographical origin. These two pooled studies46 48 were high-quality RCTs involving ART-naïve adults with primarily virological outcomes. They included ART-naïve patients of mean baseline age 32–38 years with unsuppressed viral loads and mean baseline CD4s of 280 and 336 cells/mm3. The baseline BMI for both studies did not significantly differ from the mean BMI from other meta-analyzed studies with BMI data. Exposure groups had patients on DTG and comparator groups, efavirenz. Estimates of metabolic syndrome prevalence among PLHIV in SSA range from 13% to 58%, with a higher proportion among ART-experienced than among ART-naïve (online supplemental file 1, ref. 60). It is likely that the increased risk of type 2 DM observed is driven by the higher prevalence of metabolic syndrome in this population (online supplemental file 1, ref. 60). On metaregression for age, baseline CD4, and viral load, we found a pattern of an increased risk of diabetes with higher baseline viral loads and low CD4 cell counts (online supplemental file 1, figure S8). This is in tandem with the known literature suggesting that chronically heightened inflammation in patients with high viral loads is a driver of insulin resistance and hence a precursor of type 2 DM (online supplemental file 1, ref. 61). These factors could have been drivers of this risk in this African population with more likely late presentation compared with PLHIV in resource-affluent settings. These results should, however, be interpreted with caution, given there were only two studies meta-analyzed with a small patient population; hence, these findings may not be extrapolated to the general African population. Studies suggested that women living with HIV have higher risk of ART-related weight gain compared with men (online supplemental file 1, ref. 62); moreover, women with HIV have higher odds of type 2 DM compared with women without HIV infection(online supplemental file 1, ref. 63). This might be attributed to higher weight gain, and possibly more prevalent cardiometabolic risk factors in women population with HIV. Whether African women living with HIV have heightened risk for type 2 DM compared with male peers is debated. In a meta-analysis of 20 studies from Africa, the prevalence of type 2 DM was similar in HIV and non-HIV populations regardless of sex, and similar prevalence was noted between treated and untreated PLHIV, though in between-studies heterogeneity was high (online supplemental file 1, ref. 64). In our analysis, sex was not associated with the pooled risk of type 2 DM in metaregression analysis.
INSTI exposure was associated with a low risk of diabetes, noted in ART-naïve populations compared with ART-experienced patients. This is in line with collection of reports on lower prevalence of metabolic syndrome in ART-naïve versus ART-experienced patients (online supplemental file 1, ref. 61). Another potential explanation might be thatbe clinicians tended not to start INSTIs in patients at high risk of diabetes, which could not be applied to ART-exposed patients being switched to INSTIs due to virological failure with less consideration for metabolic risk (online supplemental file 1, ref. 65 and 66).
We encountered certain limitations such as insufficient data on possible factors affecting glucose metabolism, which are potential confounders such as changes in BMI, family history of diabetes, lifestyle, concurrent drugs such as steroids and gender-affirming hormonal therapy in transgender patients. In the ART-experienced populations, we could not adjust for prior exposure to drugs like stavudine, didanosine, and zidovudine, known to cause lipodystrophy, insulin resistance and dyslipidaemia due to lack of patient-level data. There was variation in the criteria used to define diabetes in the different studies, with most retrospective cohort studies using multiple criteria: HBA1C, fasting blood glucose, oral glucose tolerance tests, and prescriptions for diabetes medication, while most RCTs used division of AIDS grading of fasting blood glucose (online supplemental file 1, ref. 67). To partially account for these limitations, we conducted influence and stratified analyses by study design, primary metabolic outcome, and ART status. There was minimal heterogeneity and an absence of publication bias across several subgroups and sensitivity analyses.
Conclusion
In conclusion, this meta-analysis demonstrated that INSTI use was not associated with an increased risk of DM compared with PIs and NNRTIs except in African PLHIV. There is a need for long-term follow-up studies with primarily metabolic outcomes to ascertain these results further and delineate the contribution of weight gain in PLHIV exposed to INSTIs on glucose dysmetabolism. Additionally, the increased risk of DM in African PLHIV merits more targeted research as this population in the meta-analysis was largely under-represented.
Data availability statement
All data relevant to the study are included in the article or uploaded as supplementary information.
Ethics statements
Patient consent for publication
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Not applicable.
References
Supplementary materials
Supplementary Data
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Footnotes
Contributors FM conceptualised the study, wrote the manuscript and was the guarantor of this work and, such, had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. FM, HK and NB wrote the protocol, FM and HK performed data extraction. HK and DMB performed the data analysis. Karolinska Institute librarians GK and NH performed the data search. All authors participated in the critical interpretation of the results and revision of the manuscript.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None declared.
Provenance and peer review Not commissioned; externally peer reviewed.
Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.