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Update on Diabetes Diagnosis: A Historical Review of the Dilemma of the Diagnostic Utility of Glycohemoglobin A1c and a Proposal for a Combined Glucose-A1c Diagnostic Method

2012; King Faisal Specialist Hospital and Research Centre; Volume: 32; Issue: 3 Linguagem: Inglês

10.5144/0256-4947.2012.229

0975-4466

Saleh Aldasouqi, Ved V. Gossain,

Diabetes, Cardiovascular Risks, and Lipoproteins

reviewUpdate on Diabetes Diagnosis: A Historical Review of the Dilemma of the Diagnostic Utility of Glycohemoglobin A1c and a Proposal for a Combined Glucose-A1c Diagnostic Method Saleh A. Aldasouqi and Ved V. Gossain Saleh A. Aldasouqi Search for more papers by this author and Ved V. Gossain Search for more papers by this author Published Online:7 Jun 2012https://doi.org/10.5144/0256-4947.2012.229SectionsPDF ToolsAdd to favoritesDownload citationTrack citations ShareShare onFacebookTwitterLinked InRedditEmail AboutAbstractThe role of glycohemoglobin A1c (A1c) for the diagnosis of diabetes has been debated for over three decades. Recently, the American Diabetes Association (ADA) has recommended adding A1c as an additional criterion for diabetes diagnosis. In view of the continued debate about the diagnostic utility of A1c, and in view of the unabated burden of undiagnosed diabetes, the search for alternative diagnostic methods is discussed. A historical literature review is provided, in view of the new ADA diagnostic guidelines, and a proposal is provided for combining A1c and a glucose measurement as a diagnostic alternative/adjunct to the use of a single criterion. This proposal is based on the non-overlapping of the advantages and disadvantages of these individual tests. The cost-effectiveness of this method remains to be tested.IntroductionThe American Diabetes Association (ADA) has now acknowledged glycohemoglobin A1c (A1c) as a diagnostic criterion for diabetes mellitus,1 for the first time since the publication of the ADA’s first diagnostic guidelines in July of 1997.2 Thus, the current (revised) ADA’s criteria for diabetes diagnosis and screening, as of January of 2010, are:A1c ≥6.5%; orFasting plasma glucose (FPG) ≥126 mg/dL (fasting at least 8 hours); or2-hour glucose per 75 g oral glucose tolerance test (OGTT) ≥200 mg/dL, according to the World Health Organization (WHO) protocol; orRandom glucose (with hyperglycemic symptoms/crisis) ≥200 mg/dL.In the absence of unequivocal hyperglycemia, criteria 1–3 require retesting for confirmation. The guidelines emphasized that A1c assays be standardized to the Diabetes Complications and Control Trial’s (DCCT) A1c assay, and certified by the National Glycohemoglobin Standardization Program (NGSP). Screening criteria for diabetes remained unchanged: In the presence of high risk factor(s), screening should be done at any age, and in the absence thereof, screening should begin at age 45 years, and then every 3 years.Furthermore, the new ADA guidelines1 also added a new category of intermediate dysglycemia, called the “increased-risk” group, to describe individuals with the currently used term “prediabetes”; this high-risk group, while not meeting the diagnostic criteria for diabetes require close attention and monitoring. As is known, prediabetes refers to impaired fasting glucose (IFG), and impaired glucose tolerance (IGT). The change of (the wording) did not affect the glycemic thresholds for IFG or IGT, with the guidelines maintaining the same cut-offs of (≥100–125 mg/dL, and ≥140–199 mg/dL, respectively), and recommending an A1c range of ≥5.7%–6.4% to identify this group of people. Finally, these new ADA guidelines were limited to revisions to the diagnosis of type 2 diabetes mellitus (T2DM), and they made no new recommendations regarding gestational diabetes mellitus (GDM), deferring such recommendations to the then forthcoming recommendations of the International Association of Diabetes and Pregnancy Study Groups (IADPSG).The ADA’s new guidelines endorsing A1c as a diagnostic test for diabetes were based on the recommendations3 of the International Expert Committee (IEC). The IEC is a consensus panel of international experts convened by the ADA, the International Diabetes Federation (IDF) and the European Association for the Study of Diabetes (EASD). The rationale for endorsing A1c for diabetes diagnosis (and the cut-off recommended), according to the IEC’s report,3 is that the risk of diabetes microvascular complications (mainly retinopathy) sharply increases in the same way and at a comparable threshold, as compared to FPG and OGTT. In its first diagnostic guidelines in 1997,2 the ADA had recommended that FPG be the preferred diagnostic test, acknowledging that OGTT might not be appropriate for routine use. The ADA had also recommended (specifically) that A1c not be used for diabetes diagnosis,2 and has since maintained these recommendations in its subsequent annual guidelines that are published every January as a supplement to its journal, Diabetes Care, through the 2009 edition.4Prior to these new ADA guidelines,1 and over the last two to three decades, several publications by various investigators from around the world, including many large epidemiological studies, had advocated the utility of A1c as a diagnostic tool in diabetes.5–26 Furthermore, preceding these ADA guidelines, different expert panels and diabetes and endocrinology organizations from different countries had already recommended A1c for diabetes diagnosis/screening, including the following major examples:An expert panel8 convened in 2008 by the Endocrine Society (TES) in the United States and published in its journal although TES itself did not explicitly endorse the panel’s recommendations;A report posted in 2007 at the website27 of the United Kingdom National Health Services- National Institute of Health Research ( www.ncchta.org), published by Waugh et al;A report published in 200828 by the US Preventive Services Task Force (USPST), in which the USPSTF did not explicitly recommend A1c for diabetes screening, but vaguely stated that “three tests have been used to screen for diabetes: FPG, OGTT, and A1c”;A recommendation by the Japanese Diabetes Association, published in 1999.29As an explanation for the ADA’s prior reluctance to recommend A1c for diabetes diagnosis, the main concerns expressed by the ADA had to do with test standardization. The ADA’s Expert Committee, the writing group of the guidelines, stated that diverse methods had been used in A1c assays, and that standardization of the test was not achieved at the time, and so identifying a cut-off diagnostic A1c value was difficult to achieve.2 However, shortly thereafter, this obstacle was overcome30 by the development of the National Glycohemoglobin Standardization Program (NGSP). In brief, to be NGSP compliant, any local assay should be made traceable to the assay used by the DCCT. Global compliance of local laboratories with NGSP standardization is difficult to track, but in the United States, a very satisfactory compliance (over 99%) was reported across the nation in 2006.31 Nevertheless, A1c is not a perfect or ideal test; perhaps a perfect/ideal diagnostic test with 100% specificity and sensitivity does not even exist in clinical medicine. Like many other diagnostic tests in clinical medicine, A1c results should be interpreted in the right context, taking into account any interferences that could influence these results.Thus, clinicians should be aware of the potential interferences that have been noticed to influence the A1c measurement, including effects of age, ethnicity, possible variability in glycation rates (hemoglobin glycation index), hemoglobin variants, uremia, iron deficiency anemia, effects of medications such as erythropoietin, and infection with HIV.25,32–36 Certainly clinicians should be vigilant to evaluate their patients individually, and to consider all possible factors before ruling in or ruling out diabetes if only relying on A1c for diagnosis. The issue of population screening is a difficult one to tackle, and it is not clear how A1c will perform in this regard, compared to FPG.It should be emphasized that the pressing impetus for searching for alternative or adjunct diagnostic tools for diabetes is the observation of legitimate concerns regarding FPG and OGTT (Summary of Advantages and Disadvantages). This Appendix lists the advantages and disadvantages of FPG, OGTT and A1c.8,14,17,24,25,32–36 Of the disadvantages of FPG and OGTT, two major issues raise significant concerns, and thus deserve emphasis, as follows:FPG could miss a significant proportion of patients with (overt) diabetes,14,17 a manifestation of inadequate sensitivity stemming largely from the natural course ofT2DM, which is believed to begin often as a post-prandial hyperglycemic state for some time;37 andOGTT is seldom used in routine clinical settings, or population screening,8,15,38,39 and thus has conceivably not contributed to effective screening and diagnosis of diabetes, even though it is considered the gold diagnostic standard.These aforementioned concerns are quite important, and it is believed that these disadvantages of both FPG and OGTT, besides the other disadvantages listed in the Appendix, could be among the major causes of undiagnosed diabetes.23,26 The issue of undiagnosed diabetes is a serious health problem, and this was specifically mentioned in the older ADA guidelines of 1997,2 which stated that in the United States about 50% of people with DM were undiagnosed at the time. At present, and with the use of only FPG and OGTT for diabetes diagnosis/screening, this percentage of undiagnosed diabetes is still significant—20% to 30%.23,26 It logically follows that these tests have been suboptimal.This change in position on the part of the ADA1 is naturally expected to encounter mixed responses in the diabetes community, by both advocates and skeptics of this new recommendation. Prior to this new position, some investigators8 had criticized the ADA for its reluctance about endorsing A1c for diagnosis, stating that this reluctance was “based on old data”. On the other hand, of the strongest criticism of the new ADA recommendations, other investigators32 described this move as “a departure from the long established approach to diagnosing diabetes mellitus”. Besides the concerns about potential pitfalls of A1c diagnostic performance,25,32–36 other concerns have been voiced about test cost and availability in developing countries, as exemplified in a recent position article from Mexico, rejecting A1c as a new diagnostic criterion.34It is prudent to point out that while there is a strong case for the utility of A1c for the diagnosis and screening of T2DM, the situation is different for GDM. Pioneered by Pollak et al,40 most studies addressing A1c in GDM diagnosis are old and they included small numbers of subjects and utilized different non-standardized A1c assays.40–47 More recent studies are quite scarce,22,48,49 including a study by our group.22 Conclusions from these old and new studies are conflicting, and thus, it follows that more studies are needed to settle this issue. In this regard, and as alluded to earlier, the new ADA guidelines deferred recommendations regarding GDM to the IADPSG’s report that was anticipated at the time of publication of the ADA’s guidelines. The IADPSG’s report can be referred to regarding new GDM diagnostic guidelines.50 In summary, these guidelines proposed new recommendations in regards to screening strategies and the categorization of glycemia in pregnancy, recommending A1c at the earliest antenatal visit, to distinguish pre-existing overt diabetes as a separate entity.50While A1c was not recommended for GDM screening, the IDADPSG recommended that A1c be performed early in pregnancy (at the time of the first antenatal visit) to exclude pre-existing (overt) diabetes. While neither the ADA nor the IADPSG recommended A1c for GDM screening or diagnosis, our group believes22,24 that there is a promising diagnostic role for A1c in GDM in the future, and that the main obstacle in this regard is the lack of large, prospective epidemiological studies.To conclude this historical overview on A1c, it is prudent to briefly mention the following relevant issues:Since the new ADA guidelines were published,1 other organizations have endorsed A1c for diabetes diagnosis including American Association of Clinical Endocrinologists (AACE)51 and TES,52 with some restrictions and caveats.51,52 Diagnosis by A1c has subsequently been endorsed by WHO, EASD and the IDF (see official websites of organizations).The new ADA guidelines1 recommended that portable A1c devices53 not be used for diabetes diagnosis or screening at present.The issue of deriving a glucose equivalent from A1c assays, the so-called estimated average glucose “eAG”, is debatable.31,54The use of other measurement units for A1c (ie, mmol/mol), and the lowering of the A1c normal range31 would probably create confusion amongst clinicians and patients,25 and therefore, these two suggestions may not be appropriate for use in clinical practice.The recent notion, that in community-based population screening in adults without diabetes, A1c is similarly associated with a future risk of diabetes, and even more strongly with death and cardiovascular disease, than FPG, further supports the ADA’s recommendation of A1c for diabetes diagnosis, and rounds up the case for A1c as a valid diagnostic test.55Finally, it appears that the debate about the diagnostic role of A1c is still ongoing, although it was conceivable that the ADA’s new guidelines1 would have put this three-decade-long debate to rest. The most recent, and strong, example of this ongoing debate was the heated debate session between two nationally renowned diabetes experts, Dr. Bloomgarden (advocating against) and Dr. Bergenstal (advocating for), at the conclusion of the AACE 2010 annual meeting.56Given this argument, and since A1c has disadvantages (but likewise also do FPG and OGTT), it is conceivably appealing to recommend using A1c not as an alternative but as an adjunct to FPG to achieve the best possible sensitivity and specificity. This combination strategy was suggested by a few investigators.14,15 Since the disadvantages of A1c and FPG are generally not overlapping, it is hoped that this combination will be complimentary, and additive, as a powerful diagnostic tool. Manley et al reported a very favorable sensitivity and specificity of combined A1c and FPG, of over 90% in high-risk individuals.14While the debate continues about the diagnostic role of A1c, diabetes has become a global epidemic and it continues to pose human and economic burdens on communities worldwide. A major obstacle in diabetes management is delayed diagnosis, and hence the development of complications, especially cardiovascular complications23,26 at the time of diagnosis. Besides socioeconomic problems such as access to health care, we believe that ineffective diagnostic and screening methods in population and practice settings is another major cause of undiagnosed diabetes.23,26What really matters is not what the best diagnostic test is as recommended by health organizations, but how often and how effectively it is used in clinical practice. In fact this assertion was reported in studies in community-based settings.38,39 Evolega et al,38 and Tabaei et al,39 evaluated the opportunistic screening methods in community-based settings, and found that the recommended diagnostic tests (FPG and OGTT) were not applied effectively in routine clinical screening, and were rarely used for opportunistic screening.It seems that utilizing a combination method (A1c and FPG) for diabetes screening and diagnosis, the accuracy of which has been proven,14 is an appealing alternative. It is notable that the IEC recommended against such combined A1c-glucose diagnostic approach3 for fear of creating confusion, but in a recently published review article, Herman and Fajans disputed this recommendation, and provided a reasonable combination proposal.57 They concluded that “combining the use of HbA1c and plasma glucose measurements for the diagnosis of diabetes offers the benefits of each test and reduces the risk of systematic bias inherent in HbA1c testing alone”.Whether this is cost-effective remains to be seen. Therefore, we agree with Herman and Fagan’s combination proposal, and we recommend that diabetes organizations, scientists, insurance companies, health industries, and governmental bodies evaluate this proposal. The ultimate goal is to come up with a diagnostic method that is accurate, cost-effective, and convenient for population settings—in an effort to alleviate the burden of undiagnosed diabetes.In conclusion, A1c has just been recommended by the ADA for diabetes diagnosis and screening. This endorsement by the ADA, followed by adoption by other diabetes organizations, may have ended a major portion of a long-standing debate about the utility of A1c for diabetes diagnosis and screening. However, there is still skepticism by some diabetes experts, with concerns about over or under diagnosis of diabetes. Since the disadvantages of FPG, OGTT and A1c are not overlapping, we generally advocate the recently proposed suggestion to use a combination strategy to diagnose diabetes, utilizing A1c with FPG, a strategy that is believed to be promising in achieving the best diagnostic accuracy. However, the efficacy and cost-effectiveness of this strategy remain to be tested.AppendixSummary of the advantages and disadvantages of the old and new diagnostic tests for diabetes originally adapted (with permission) from Kilpatrick et al,35 Additional modifications were compiled from other references.8,14,17,24,25,32–36Fasting Blood GlucoseAdvantages:- is established as the current diagnostic means for diabetes;- is a direct measure of glycemia (which the patients are used to);- is more available than A1c globally;- it has less between-laboratories variability than A1c;- is not affected by non-glycemic factors as is A1cDisadvantages:- is a single time point of glycemia (thus static rather than chronic);- requires fasting (which adds to its inconvenience);- has more within-individual variability than A1c;- has a sub-optimal sensitivity;- requires prompt processing after blood drawing to avoid artifactsOral Glucose Tolerance TestAdvantages:- is established as the current diagnostic means for diabetes;- is a direct glycemic measure;- is more available than A1c globally;- has less between-laboratories variability than A1c;- is not affected by non-glycemic factors as is A1c.Disadvantages:- is a single time point of glycemia;- requires fasting;- has more within-individual variability than A1c;- requires prompt processing after blood drawing to avoid artifacts;- is cumbersome, multi-staged, inconvenient;- the displeasing taste of the concentrated glucose drink; especially for pregnant women;- is unreliable in patients with gastric bypassHemoglobin A1cAdvantages:- is more convenient, since fasting is not required;- has greater pre-analytical stability, and less day-to- day changes that can cause significant excursions in plasma glucose;- is established as a monitoring measure of diabetes control;- is more stable for subsequent measurement.Disadvantages:- can be affected by factors that can affect the lifespan of the erythrocytes (e.g., iron deficiency anemia, blood loss, chronic kidney failure, and erythropoietin therapy as used in renal failure and sometimes in chronic anemia);- can be affected by hemoglobin variants (assay method dependent);- can demonstrate variability due to differences in glycation rates;- can be affected by HIV;- is less available globally than glucose tests.ARTICLE REFERENCES:1. 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Healthcare Professional Homepage (HPV-Live)Available from: http://www.hcplive.com/endocrinology/aace_2010/hemoglobin_test_diabetesLast Accessed on 2010 May 8. Google Scholar57. Herman WH, Fajans SS. "Hemobglobin A1c for the diagnosis of diabetes. Practical considerations" . Pol Arch Med Wewn. 2010; 120:37-40. Google Scholar Next article FiguresReferencesRelatedDetails Volume 32, Issue 3May-June 2012 Metrics History Published online7 June 2012 AcknowledgmentsThe authors would like to acknowledge the following individuals for their valuable assistance in the preparation of this manuscript: Jinie Shirey from the Department of Medicine, Michigan State University College of Human Medicine (East Lansing, Michigan, USA), and the staff of the Sparrow Hospital Medical Library, Lansing, Michigan, USA (Laura Smith, Steve Kalis and Michael Simmon). The authors would also like to thank Dr. Randie Little (University of Missouri, Columbia, Missouri, USA), and Dr. David Marrero (Indiana University and Purdue University at Indianapolis, Indianapolis, Indiana, USA) for their thoughtful reviews of this manuscript.InformationCopyright © 2012, Annals of Saudi MedicineThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.PDF download