Diagnostic Dilemma: Clinical and Histological Abnormalities in a Hispanic Patient With Diabetes
Hispanic male died at age 34 years
Diabetes duration 21 years (diagnosed at age 13 years with type 1 diabetes)
BMI 23.5 kg/m2
HLA A*02:06,24:02; DRB1*04:07,14:06; DQA1*03:01,05:01; DQB1*03:01,03:02 not associated with either risk or protection for type 1 diabetes
Type 1 diabetes–associated autoantibodies negative at time of death; HbA1c not available
High C-peptide (3.18 ng/mL) at time of death despite 21-year history of presumed type 1 diabetes (nonfasting C-peptide <0.6 ng/mL suggests absolute insulin deficiency )
Medical comorbidities included hypertension and end-stage renal disease on hemodialysis for 1.5 years prior to death
Social history of occasional alcohol consumption (wine 1/month, liquor 3/month) and cigarette smoking (2 pack-years)
Became unresponsive at home, developed respiratory insufficiency, was intubated, and suffered an intracranial hemorrhage that progressed to brain swelling and death 12 days later
Cause of death: stroke
The review of organ donors’ medical history is often limited to the terminal hospitalization records. This 32-year-old Hispanic patient had a history of type 1 diabetes since age 13 years and was treated with insulin since diagnosis. However, we have reasons to challenge the clinical diagnosis. The HLA region provides the highest contribution to genetic risk for type 1 diabetes (2). Although the HLA profile observed for this patient is not known to be associated with either risk or protection (2,3), there has been a recent rise in type 1 diabetes incidence among patients with HLA considered to confer lower risk for developing the disease (4). The absence of type 1 diabetes–associated autoantibodies (i.e., glutamic acid decarboxylase, insulinoma-associated protein 2, zinc transporter 8) at the time of study may be attributable to autoantibody loss over time; the absence altogether has been reported in type 1 diabetes in a mere 10% of cases at diagnosis (5). Although only 5%–10% of all diabetes is type 1, the vast majority of patients are diagnosed when they are children and young adults. Although there is increasing awareness of latent autoimmune diabetes in adults, it is most often diagnosed as type 2 diabetes (6).
The Network for Pancreatic Organ Donors with Diabetes (nPOD) collects pancreas and other tissues relevant to type 1 diabetes pathogenesis from organ donors. Through this initiative, we have been able to confirm at and near the time of type 1 diabetes diagnosis the characteristic pathology of insulitis defined as the presence of ≥6 CD3+ cells adjacent to or within an islet in ≥3 islets per section (7). These findings are most often associated with the loss of insulin-positive β-cells (pseudoatrophic islets) and reduction in islet number and size (7). In this donor (nPOD case 6263), histological findings include insulin-positive islets of normal size and numbers, along with severe, multifocal amyloidosis, a characteristic seen most often in patients with clinically diagnosed type 2 diabetes (Fig. 1). Although the presence of insulin-containing β-cells is consistent with observed C-peptide production, the finding is unexpected in type 1 diabetes where significant reductions in β-cell mass are a defining feature of the disease (7). Should these histological findings necessarily change the diagnosis, or is there more to the story of histology and etiology potentially affected by factors such as race, ethnicity, sex, or age? Clinical features of type 2 diabetes include obesity, physical features of insulin resistance, and a family history of type 2 diabetes, whereas the most significant factors strongly correlating with type 1 diabetes have been age at diagnosis <35 years and time to insulin of <6 months (8). This donor was diagnosed and treated as having type 1 diabetes since childhood, with no presumed features of type 2 diabetes, yet presents contradictory histological features along with high C-peptide levels and no type 1 diabetes–related autoantibodies.
A monogenic diabetes genetic panel evaluating common and rare forms of maturity-onset diabetes of the young was performed and demonstrated a heterozygous mutation of AKT2 exon 5 of unknown significance. AKT2 plays a role in insulin action through insulin receptor kinase–mediated signaling (9). Activating mutations in AKT2 have been associated with hypoinsulinemic hypoglycemia (10), and loss of AKT2 function results in severe insulin resistance (11,12). Thus, it is possible that this donor possessed a completely unique form of diabetes, not as yet characterized; alternatively, this may be one of many examples of heterogeneity in type 1 diabetes pathogenesis (13). Further studies are required to determine whether this AKT2 polymorphism may have contributed to the dichotomous clinical and histological picture—information that will be critical as we move into individualized and precision medicine.
The clinical information available was not sufficient to initially refute the diagnosis of type 1 diabetes. Whereas type 1 diabetes affects mostly non-Hispanic white people in the U.S., there is still marked heterogeneity among those affected. The SEARCH for Diabetes in Youth (SEARCH) study demonstrated the incidence of type 1 diabetes among 10- to 14-year-old non-Hispanic white youth to be 32.9/100,000 compared with 17.6/100,000 for Hispanic youth (14). Hispanic youth obesity rates in type 1 diabetes were greater than in non-Hispanic white youth and were similar to rates in African American youth (44%) (15). Type 2 diabetes in youth from 10 to 19 years old is more common in the Hispanic group than the non-Hispanic white group; however, the Hispanic group still falls behind the African American, Asian/Pacific Islander, and American Indian groups for incidence of type 2 diabetes in youth (14). Even within this population there is diversity based on geographic location in addition to independent and unique cultural practices and genetic variations (16). Type 2 diabetes is rising, but type 1 diabetes remains more prevalent in youth, even among Hispanic adolescents (16). More importantly, we know that minority youth have poorer diabetes control and are more at risk for deleterious consequences (17).
In sum, although diagnosed with type 1 diabetes, postmortem analysis in this donor revealed histological findings consistent with type 2 diabetes, elevated C-peptide levels suggesting possible type 2 diabetes or maturity-onset diabetes of the young, and a genetic polymorphism in AKT2. Together these findings suggest that an alternative diagnosis may be appropriate. How we move forward with unique cases of conflict between clinical diagnosis and histopathological findings is critical; genetic sequencing may provide the answer, but there is still much we do not know. Each new case adds more information to the growing understanding of all forms of diabetes. There are limitations to data obtained from a single organ donor, but studies of these unusual cases also offer a cornucopia of information, which will hopefully open the door for more effective clinical intervention in the coming age of personalized medicine.
Acknowledgments. The authors acknowledge the nPOD staff members and Organ Procurement Organizations that partner with nPOD to recover organ donors. Additional donor details can be obtained through the JDRF nPOD website (www.jdrfnpod.org). This study used data from the Organ Procurement and Transplantation Network. Donor data sets are available through nPOD DataShare, an online database for collaborative communication organized around the nPOD specimen repository.
Funding. This work was supported by JDRF (25-2013-268, 17-2012-3, and 25-2012-516 to M.C.-T. and D.A.S.).
Duality of Interest. No potential conflicts of interest relevant to this article were reported.
Author Contributions. L.M.J. researched the data and wrote the manuscript. A.L.P. contributed to discussion and reviewed and edited the manuscript. M.C.-T. researched the data and reviewed and edited the manuscript. D.A.S. conceived of the study and reviewed and edited the manuscript. D.A.S. is the guarantor of this work and, as 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.
- Received March 31, 2016.
- Accepted June 8, 2016.
- © 2016 by the American Diabetes Association.
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