Introduction

Procoagulant and fibrinolytic markers have been proposed as risk factors for the development of type 2 diabetes1. Plasminogen activator inhibitor-1 (PAI-1), a serine-protease inhibitor secreted primarily by adipocytes, endothelial cells and hepatocytes, acts as a key negative regulator of fibrinolysis through its role as the primary inhibitor of tissue plasminogen activator (tPA). Experimental studies in mice homozygous for the PAI-1 null allele have found favourable effects on insulin and glycaemic measures2 and protective effects against the development of obesity and insulin resistance when fed a high-fat/high-carbohydrate diet3, as compared with wild-type mice. Likewise, early cross-sectional studies in humans have reported associations of elevated PAI-1 concentrations with measures of obesity4,5, insulin resistance4,6, impaired glucose tolerance (IGT)4,6 and T2D7,8. These findings have been extended to a prospective context by investigators of the Insulin Resistance Atherosclerosis Study (IRAS) who reported that elevated PAI-1 levels were an independent risk factor for the development of T2D in healthy subjects, after 5.2 years of follow-up9.

Since the publication of these initial studies, a considerable number of additional observational studies have been published, with many, but not all, reporting associations of PAI-1 with T2D10,11,12,13,14,15,16,17. To our knowledge, however, no attempt has been made to consolidate and synthesize the available epidemiological literature on this topic in the form of a systematic review and meta-analysis. Thus, in light of the heterogeneity of findings and the need to quantify the relationship of PAI-1 with diabetes, we performed a systematic review and meta-analysis of observational studies examining the association between plasminogen activator inhibitor-1 and type 2 diabetes.

Methods

Literature Search

We conducted a comprehensive literature search of the bibliographic databases EMBASE, PubMed, Web of Science and the Cochrane Library for all relevant studies, published from 1945 to October 2014. Medical subject headings (MeSH) or equivalent and text word terms were utilised. Search strategies were individualised to specific databases and are presented for each database in Supplementary Data 1. The study protocol is registered with the PROSPERO database of systematic reviews (http://www.crd.york.ac.uk;registrationnumberCRD42014014009).

Titles and abstracts were screened by two independent reviewers (JY,NBB) for inclusion according to pre-specified criteria (see below). If an abstract was not available for a study, the full article was obtained and screened. If an article appeared to be potentially eligible for inclusion based on title and/or abstract, the full article was obtained and formally screened for inclusion, otherwise it was excluded. When duplicate analyses appeared to be presented across more than one publication, we included only the first publication. Reference lists for included studies were screened for additional relevant studies. Lastly, corresponding authors were contacted for additional information pertinent to study inclusion if necessary.

Inclusion and exclusion criteria

Included studies had to meet all of the following inclusion criteria: 1) prospective or retrospective cohort, case-cohort, case-control, or cross-sectional study; 2) Measurement of plasma PAI-1 (antigen concentrations or activity levels); 3) Assessment of T2D (self-reported physician diagnosis and/or medication usage and/or laboratory diagnosed); 4) Adult study population (≥18 years) at baseline; 5) Article was reported in English. In epidemiological studies of the association of plasma PAI-1 with T2D, PAI-1 is typically measured using either an assay that is sensitive to free PAI-1 antigen (both active and latent forms) that is not complexed to plasminogen activators or an assay that detects activity level (active free PAI-1). Both free PAI-1 antigen and activity levels have been shown to strongly correlate with each other17. Thus, studies that examined plasma PAI-1 as antigen or as activity level were both included in this review and pooled in the meta-analysis of prospective studies. We excluded all animal studies, case reports and editorials. Studies were further excluded if they provided outcome data solely on gestational diabetes or type 1 diabetes.

Data extraction and Quality Assessment

Using a standardized data extraction form, two independent reviewers (JY,TW) extracted relevant information from each paper and this information was reported in accordance with guidelines established by the Meta-analysis of Observational Studies in Epidemiology (MOOSE) checklist18. Any discrepancies between reviewers were reconciled by consensus. The following information (if available) was extracted from each study: authors, year of publication, country of origin, study design, sample demographic characteristics, number of cases and controls, covariates adjusted or “matched” for, mean or median PAI-1 concentrations of cases and controls for cross-sectional studies and for prospective studies: duration of follow-up, method of incident T2D assessment, assay method, effect estimates with 95% CIs and data pertinent to methodological quality assessment. If sex-specific analyses were presented, numbers of cases and controls and effect estimates from both sexes were extracted. For cross-sectional studies, if PAI-1 values for T2D groups with and without co-morbidities were presented, information from the group with no or minimal co-morbidities was extracted. If a study presented PAI-1 data for both antigen concentration and activity level, only PAI-1 antigen levels were extracted. Authors were contacted for additional information if any required data from a study was missing or unclear. Study quality was independently assessed by two reviewers (JY,NBB) using the Newcastle-Ottawa Quality Assessment Scale (NOS) to examine the selection of participants and study design, comparability of groups and ascertainment of exposure/outcome19. Scores for low (0–3), moderate (4–6) and high-quality studies (7–9) were assigned.

Statistical analyses

For prospective studies, relative risks (RRs) were used to measure the association between PAI-1 levels and incident T2D. Hazard ratios (HRs) and odds ratios (ORs) were assumed to approximate the same measure of RR. In studies where associations between PAI-1 and incident T2D were presented through multiple sequentially-adjusted models, the effect estimate and 95% CIs from the most fully-adjusted model was extracted and used in the meta-analysis. In order to permit comparison of effect between studies that used different categorical or continuous comparisons, a scaling factor was employed to convert reported RRs of seven studies to upper and lower tertile comparisons, using methods previously reported20. These scaling methods assume a log-normal distribution of baseline PAI-1 concentrations and a log-linear association with diabetes risk. Briefly, effect estimates from four studies that employed a 1-SD comparison of baseline PAI-1 were multiplied by a scaling factor of 2.18 (the equivalent of the difference between means in the top and bottom third of the distribution)9,12,21,22, the effect estimate from one study that employed an interquartile range comparison was scaled by 1.61 (2.18/1.35; difference in means between top and bottom third of distribution)23, one study that employed a quartile comparison was scaled by 0.858 (2.18/2.54; difference in means between top and bottom quartile)24 and one study that compared unequal groups was multiplied by a study-specific scaling factor of 2.18/x where x is the difference in mean PAI-1 (in SD units) between the two groups10. Standard errors of the log RRs were calculated using published confidence limits and standardised in the same manner. Studies were weighted by the inverse of the variance of each transformed log RR and then pooled to generate estimates of average effect using random-effects models. The I2 statistic was used to determine the percentage of variability across studies due to heterogeneity beyond chance and its significance tested using the Cochran Q test. For cross-sectional studies, owing to considerable methodological heterogeneity and the lack of standardized PAI-1 measurement protocols, a meta-analysis of the data was not considered appropriate. Consequently, data from cross-sectional studies were summarized in aggregate.

Sources of heterogeneity among prospective studies were examined by comparing analyses stratified by study design (prospective cohort vs. nested case-control), duration of follow-up (median split), baseline glucose tolerance status (normal glucose tolerance vs. glucose intolerance [IFG or IGT]), adjustment for glucose, adjustment for insulin measures (HOMA-IR, fasting insulin, insulin sensitivity index [SI]), adjustment for visceral adiposity (waist-hip ratio [WHR] or waist circumference [WC]) and adjustment for inflammatory markers. Additionally, a meta-regression was performed by modelling duration of follow-up as a continuous variable with T2D risk. Sensitivity analyses were performed by comparing pooled risk estimates to those generated after: iteratively removing one study at a time to confirm that our findings were not driven by any single study, removal of studies with a NOS score <7 and employing a fixed-effects model. The presence of publication bias in the meta-analysis was assessed using tests of asymmetry (Begg’s, Egger) and visual inspection of funnel plots25,26. All statistical tests were two-sided and significance was defined at p< 0.05. Statistical analyses were performed with R version 3.2.1 and Revman 5.2 (Nordic Cochrane Center).

Results

Literature Search

Our search strategy initially identified 6413 articles, which was reduced to 3741 unique citations after removal of duplicate studies. From these studies, 3609 were excluded based on title and/or abstract and 84 were further excluded after retrieval of full-text articles. Screening of reference lists of included studies identified an additional 4 studies for inclusion. Consequently, a total of 52 studies (44 cross-sectional with 47 unique analytical comparisons and 8 prospective) were included in this review [Fig. 1].

Figure 1
figure 1

Modified PRISMA flow diagram through study search and inclusion.

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Study Characteristics and Statistical Analyses

Cross-Sectional Studies

Descriptive characteristics of the 44 cross-sectional studies are presented in Table 19,10,12,21,22,23,24,27. In brief, 23 studies were conducted in Europe, 12 in Asia, 5 in the U.S.A, 2 in South America, 1 in the Middle East and 1 in Africa. 21 studies reported adjustment for some covariates (mainly age and sex), while 23 did not report adjustment for covariates. 35 studies enrolled both men and women as participants, 4 enrolled exclusively one sex and in 5 studies it was unclear. 30 studies assessed PAI-1 in its antigen form and 14 as activity level.

Overall, 34 out of 47 analytical comparisons (72%) reported statistically significant elevated mean or median PAI-1 (antigen or activity) among T2D cases as compared to controls, 2 (4%) reported statistically significant elevated mean PAI-1 antigen among controls versus cases and 11 (24%) reported no association of PAI-1 with outcome status. 16 of 23 (70%) comparisons that reported some form of statistical adjustment for covariates reported significantly elevated PAI-1 among diabetes cases, as compared to 18 of 24 (75%) that did not report any adjustment. 8 out of 13 (62%) comparisons from Asia reported significant elevated PAI-1 among diabetes cases, whereas 23 out of 30 (77%) from Europe or North America found elevated PAI-1 among cases. 4 out of 5 comparisons exclusively between women reported significantly elevated PAI-1 among cases, whereas 2 out of 5 between men reported elevated PAI-1 among cases.

Prospective Studies

Eight prospective studies, including a total of 9256 participants and 980 incident T2D cases, were included in this review [Table 2]9,10,12,21,22,23,24,27. Five studies were conducted in the U.S.A.9,12,23,24,27, two in Sweden10,22 and one in France21 and all included both men and women as participants. Five studies were prospective cohort analyses9,10,12,23,24 and three were nested case-control studies21,22,27. Six studies examined baseline PAI-1 in its antigen form9,12,22,23,24,27 and two as activity level10,21. Length of follow-up ranged from four to nine years with a median length of 5.7 years. Incident diabetes was ascertained using a combination of fasting glucose ≥7.0 mmol/L (or ≥126 mg/dL) and self-report of diabetes diagnosis or diabetes medication use in five studies10,12,21,22,23,24,27. In two studies, postload glucose ≥11.1 mmol was included as an additional criterion10,22. In one study, diabetes status was ascertained solely with a standard 75-g OGTT9. Most studies reported adjustment in their models for established diabetes risk factors including age, sex, triglyceride levels, BP or hypertension, measures of insulin or insulin resistance and measures of overall or visceral adiposity. Lastly, in quality assessment of these studies, seven were categorised as being of “high” methodological quality (NOS score > 6) and one as “moderate” quality (NOS score =6) 12[Tables 3, 4].

Table 1 Characteristics of cross-sectional studies of plasminogen activator inhibitor-1 and type 2 diabetes.
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Table 2 Baseline characteristics of prospective studies of plasminogen activator inhibitor-1 and incident type 2 diabetes.
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Table 3 Newcastle-Ottawa Quality Assessment Scale – Cohort Studies.
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Table 4 Newcastle-Ottawa Quality Assessment Scale – Case-control studies.
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When the eight prospective studies were pooled in a random-effects meta-analysis, a comparison of the top third vs. bottom third of baseline plasminogen activator inhibitor-1 concentrations generated a summary relative risk of T2D of 1.67 (95% CI 1.28–2.18) [Fig. 2]. There was moderate evidence for heterogeneity across studies (I2=38.2%, p=0.12), mostly accounted for by Stranges et al. which reported a non-significant “protective” association of elevated PAI-1 with diabetes risk (removal of this study from the meta-analysis reduced the I2 statistic to 25% (p=0.24) without materially changing the pooled RR [1.74, 95% CI 1.37–2.22])27.

Figure 2
figure 2

Individual and pooled risk ratios and 95% confidence intervals for random-effects model examining the association between the top vs. bottom third of baseline plasminogen activator inhibitor-1 levels and type 2 diabetes.

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Studies that presented results stratified by baseline glucose tolerance status or limited participants exclusively to those with normal glucose tolerance at baseline suggested an increased risk of diabetes, in relative terms, among participants with normal glucose tolerance at baseline compared to those with glucose intolerance (normal glucose tolerance: RR 2.54, 95% CI 1.78–3.63; glucose intolerance: RR 1.55, 95% CI 1.23–1.95; p=0.02 for sub-group difference), though these analyses were limited to seven comparisons from four studies9,10,22,23 [Fig. 3]. Further, a sensitivity analysis performed by removal of Meigs et al. from both sub-groups attenuated these differences toward non-significance suggesting substantial influence of this study on sub-group differences (normal glucose tolerance: RR 4.00, 95% CI 1.95–8.23; glucose intolerance: RR 2.21, 95% CI 1.14–4.27; p=0.23 for sub-group difference). Additionally, in secondary sub-group analyses comparing studies by adjustment for BMI, which were not specified a priori, we found a stronger association in studies that adjusted for BMI as compared to those that did not (adjustment for BMI: RR 2.18, 95% CI 1.60–2.96; no adjustment for BMI: RR 1.31, 95% CI 1.06–1.93; p-sub-group difference=0.008). However, as in sensitivity analyses performed by baseline glycemia status, removal of Meigs et al. from this sub-group analysis attenuated these differences toward non-significance (adjustment for BMI: RR 2.18, 95% CI 1.60–2.96; no adjustment for BMI: RR 1.29, 95% CI 0.73–2.31; p-sub-group difference=0.12). No significant sub-group differences were found for all other sub-group analyses though statistical power may have been limited to detect any differences present [Fig. 3]. Additionally, we failed to find a significant linear association of duration of follow-up (in years) with T2D risk in a meta-regression (p=0.94). Although it was our intention to look into potential differential associations of PAI-1 with diabetes by sex, the lack of studies reporting stratified analyses by sex prevented this.

Pooled effects were robust to sensitivity analyses performed by removal of one study with “moderate” methodological quality (NOS score: 6) from our pooled analysis, use of the “leave-one-out” method and use of a fixed-effects model. Visual inspection of funnel plots did not reveal substantial asymmetry indicative of small-study bias [Fig. 4]. Results from Begg’s (p=0.46) and Egger’s (p=0.26) tests further suggested absence of publication bias.

Figure 4
figure 4

Funnel plot for 8 prospective studies examining the association of plasminogen activator inhibitor-1 levels with risk of type 2 diabetes.

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Discussion

This systematic review of 52 epidemiological studies supports a link between plasminogen activator inhibitor-1 and type 2 diabetes, thus highlighting a potentially significant yet under-appreciated risk factor for diabetes. While cross-sectional studies were not aggregated in a meta-analysis, most studies reported significantly elevated PAI-1 levels among individuals with T2D, as compared to controls. Pooled analyses of 8 prospective studies revealed a 67% increased risk of T2D (upper vs lower tertiles of baseline PAI-1) at a median follow-up of 5.7 years. Notably, this association was maintained in analyses adjusted for established risk factors for diabetes, including various measures of the metabolic syndrome. In sub-group analyses, greater risk of T2D was reported for participants with normal glucose tolerance at baseline, as compared to those with glucose intolerance, though this difference was no longer statistically significant after removal of the largest study. Sensitivity analyses performed by removal of one “moderate” methodological quality study, use of the “leave-one-out” method and use of fixed-effects models did not substantially modify associations, thus supporting the robustness of our overall pooled effect estimate. Lastly, though relatively few studies contributed to our meta-analysis of prospective studies, we did not find evidence for publication bias.

The primary rationale for performing this systematic review and meta-analysis was to provide the first comprehensive summary of the available epidemiological literature on the association of PAI-1 with T2D, which we consider to be the primary strength of this review. Pooled prospective studies adjusted for a comprehensive panel of established diabetes risk factors, allowing for investigation of independent effects of PAI-1 on diabetes risk, though the presence of residual or unknown confounding from individual studies cannot be ruled out. Finally, in quality assessment of the prospective studies included in our review, seven studies were considered to be of “high” methodological quality with the remaining one being considered “moderate” methodological quality.

Some limitations of this review deserve mention. Firstly, it is important to emphasize the inherent limitation in inferring causal direction of associations from cross-sectional studies. While pooled analyses of prospective studies suggest that heightened levels of PAI-1 can predict development of T2D, we cannot rule out a potential aetiological role of the diabetic state in further influencing PAI-1 levels. Secondly, approximately half of the cross-sectional studies included in our review did not report any adjustment for the presence of possible confounding factors. However, the lack of a substantial difference in the proportion of unadjusted and adjusted cross-sectional studies that reported elevated PAI-1 levels among those with diabetes and the maintenance of an elevated risk of diabetes in pooled adjusted analyses of prospective studies would not appear to suggest a strong role of known confounding influencing these results. Thirdly, while a comprehensive literature search was performed to identify all observational studies examining an association of PAI-1 with T2D, only eight prospective studies were identified and included in our meta-analysis. Consequently, the total number of incident cases in our meta-analysis was relatively small and statistical power was limited in sub-group analyses and tests for publication bias. Additionally, prospective studies were confined to American and European populations, potentially limiting external validity of findings to other genetically-distinct populations. This issue is particularly relevant in light of evidence suggesting significant differences in circulating PAI-1 levels between various ethnic groups28,29,30 in addition to the differences between these groups in both susceptibility to T2D31 and in the relative contribution of established risk factors to diabetes development32. Lastly, we found moderate heterogeneity across studies, although a substantial contribution to this heterogeneity was provided by a single study which reported a “protective” association of elevated PAI-1 with diabetes risk. It is feasible that the relatively small size of this study may have contributed to a chance finding.

That other circulating markers of endothelial dysfunction such as coagulation factor VIII, E-selectin, intercellular adhesion molecule-1 and tPA have also been found to predict T2D10,33,34,35,36,37, also supports a role of PAI-1 in the pathogenesis of T2D. Of particular relevance are three studies that have reported associations of tPA activity and tPA antigen with risk of diabetes10,22,35, as PAI-1 serves as the primary regulator of tPA in the fibrinolytic pathway and the PAI-1/tPA antigens have been shown to be highly correlated38. Further, in a follow-up of their initial analysis in the IRAS, Festa et al. reported that change in PAI-1 over time, in addition to elevated baseline levels, predicted incident diabetes39. Additionally, alleles of various SNPs which elevate plasma PAI-1 have been found to be individually associated with an increased odds of T2D40. Lastly, successful randomised, controlled diabetes prevention trials involving lifestyle and pharmacological interventions have been shown to decrease plasma PAI-1 levels41,42,43.

Various putative mechanisms have been proposed to explain the association of PAI-1 with T2D. Animal models have suggested that PAI-1 may play a causal role in the development of obesity and insulin resistance2,3 and elevated PAI-1 in humans has been shown to predict incident metabolic syndrome in two prospective studies21,44.

The majority of circulating PAI-1 is synthesized by adipose tissue45. Visceral fat has been shown to secrete more PAI-1 than subcutaneous fat tissue in the obese phenotype46,47,48 and WHR has been found to correlate more strongly with PAI-1 than BMI49,50,51. Lifestyle and dietary-mediated weight loss in the moderately overweight and obese has been associated with concomitant reductions in PAI-1 levels, further supporting a causal link between adiposity and PAI-1 expression52,53,54,55. However, in our review, 7 of the prospective studies that adjusted for measures of overall (BMI) or visceral adiposity (WHR or WC) maintained a significant association between PAI-1 and diabetes, though the association was attenuated in some studies. Further, when we stratified our analyses by studies with adjustment for WHR or WC, we failed to find substantial heterogeneity in associations across studies that did and did not control for measures of visceral adiposity.

Adipose tissue is also responsible for the secretion of various pro-inflammatory cytokines, markers of low-grade chronic inflammation that have been linked with development of insulin resistance56. Further, these adipocytokines have all been shown to up-regulate production of PAI-157,58,59,60,61,62. Thus, the association of PAI-1 with incident T2D could simply reflect residual confounding of an association of one or more other inflammatory markers with diabetes. In our meta-analysis, four of the prospective studies that adjusted for C-reactive protein (CRP) did not report strongly attenuated associations after including this inflammatory marker in their models. Further, Kanaya et al. reported the maintenance of an association of PAI-1 with diabetes after adjusting their model for baseline concentrations of leptin and adiponectin, two other adipocytokines involved in regulating inflammatory tone which have been found to modulate T2D risk12,63,64. Likewise, we failed to find evidence of heterogeneous associations of PAI-1 with diabetes across studies stratified by adjustment for any inflammatory markers.

Though PAI-1 has been demonstrated to contribute to insulin resistance, insulin has also been shown to stimulate PAI-1 secretion by fat cells, in a pathway that is upregulated in hyperinsulinemia and hyperglycemia65,66, thus suggesting that the relationship between endothelial dysfunction and insulin resistance is bi-directional67. In our review, an initial association of elevated PAI-1 with risk of T2D in Davidson et al. became non-significant upon adjustment for baseline insulin measures24. Similarly, an initial increased risk of T2D with elevated PAI-1 activity in Eliasson et al. was no longer significant after adjustment for fasting insulin, diastolic blood pressure and triglycerides, though this may have led to over-parameterization in their model owing to the limited number of incident diabetes cases in the study (n=15)10. In contrast, the three other prospective studies in our review that adjusted for insulin reported maintenance of their respective associations. When we compared associations of PAI-1 with diabetes across studies adjusting for measures of insulin (fasting insulin, HOMA-IR, SI), we failed to find evidence of differential risk across sub-groups.

Lastly, while elevated PAI-1 levels have been shown to predict incident hyperglycemia, plasma glucose levels may also influence PAI-1 secretion. For example, experimental studies in both animals and humans have shown that glucose up-regulates PAI-1 gene expression in vascular smooth muscle cells, endothelial cells and adipose tissue68,69,70,71. Thus, it could be expected that as glucose levels rise, enhanced PAI-1 gene expression would result in elevated circulating PAI-1 concentrations. However, in sub-group analyses performed on studies stratified by adjustment for glucose we failed to find evidence for heterogeneous associations across studies that did and did not include glucose measures in their models. On the contrary, results from our sub-group analyses of studies stratified by baseline glucose tolerance status of participants suggested a significantly greater risk of T2D with heightened PAI-1 levels among participants with normal, as compared to elevated glucose levels, at baseline, though this difference appeared to be driven primarily by one study.

Recently, a novel explanation for the relationship between PAI-1 and diabetes was provided by Lee et al. who examined the association of a group of inflammatory markers with longitudinal changes in the Metabolic Clearance Rate of Insulin (MCR) in the Insulin Resistance Atherosclerosis Study72. It was reported that among 784 non-diabetic participants, higher baseline levels of plasma PAI-1, but not of CRP, TNF-α, leptin, or fibrinogen, were associated with a decline in the MCR after five years of follow-up. This association remained significant after adjustment for measures of adiposity, fasting blood glucose, insulin sensitivity and CRP.

Taken together, the available literature appears to support a role of PAI-1 as both contributor to and consequence of the metabolic syndrome. However, our meta-analysis of eight prospective studies found an association of PAI-1 with T2D risk in multivariate analyses adjusting for various measures of the metabolic syndrome including central adiposity, insulin resistance and hyperglycemia, in addition to other established risk factors for diabetes. Consequently, this independent association could conceivably support a pathophysiological mechanism distinct from the metabolic syndrome.

Thus, these findings, by furthering the understanding of the causal pathways involved in diabetes pathophysiology, could potentially help shape future prevention strategies including pharmacological interventions. Further, investigation of the addition of PAI-1 to diabetes risk prediction models could provide insight into the clinical utility of inclusion of PAI-1 into diabetes screening tools. Findings from this review additionally extend evidence of a role of elevated PAI-1 in diabetic retinopathy73, diabetic nephropathy74 and coronary heart disease in individuals with type 2 diabetes74, to the risk of incident diabetes, thus identifying a role of PAI-1 in contributing to morbidity across the blood glucose continuum. In light of the relative homogeneity of the sample populations included in the eight prospective studies in our review and the identification of significant heterogeneity between ethnic groups in circulating PAI-1 levels, further prospective examination of the association of PAI-1 with diabetes in non-Caucasian samples is warranted. Additionally, findings from our review suggest the need for investigation of the role of PAI-1 on diabetes risk within cohorts that can permit greater exploration of the potential role of differences in baseline glycaemia, on this association. Our findings also identify a potential role for randomised controlled trials to determine the effectiveness of pharmacological interventions targeting impaired fibrinolysis in order to prevent new cases of T2D. Lastly, with the recent identification of a number of functionally relevant SNPs for circulating PAI-1 concentrations40,75, Mendelian randomisation analyses could provide an additional tool for exploration of a causal effect of PAI-1 on diabetes risk.

Additional Information

How to cite this article: Yarmolinsky, J. et al. Plasminogen activator inhibitor-1 and type 2 diabetes: a systematic review and meta-analysis of observational studies. Sci. Rep. 6, 17714; doi: 10.1038/srep17714 (2016).