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On-line version ISSN 1414-431X
Braz J Med Biol Res vol. 32 n. 1 Ribeirão Preto Jan. 1999
Braz J Med Biol Res, January 1999, Volume 32(1) 67-72
Specific insulin and proinsulin in normal glucose tolerant first-degree relatives of NIDDM patients
Disciplina de Endocrinologia, Universidade Federal de São Paulo, Escola Paulista de Medicina, São Paulo, SP, Brasil
Subjects and Methods
Correspondence and Footnotes
In order to identify early abnormalities in non-insulin-dependent diabetes mellitus (NIDDM) we determined insulin (using an assay that does not cross-react with proinsulin) and proinsulin concentrations. The proinsulin/insulin ratio was used as an indicator of abnormal ß-cell function. The ratio of the first 30-min increase in insulin to glucose concentrations following the oral glucose tolerance test (OGTT; I30-0/G30-0) was taken as an indicator of insulin secretion. Insulin resistance (R) was evaluated by the homeostasis model assessment (HOMA) method. True insulin and proinsulin were measured during a 75-g OGTT in 35 individuals: 20 with normal glucose tolerance (NGT) and without diabetes among their first-degree relatives (FDR) served as controls, and 15 with NGT who were FDR of patients with NIDDM. The FDR group presented higher insulin (414 pmol/l vs 195 pmol/l; P = 0.04) and proinsulin levels (19.6 pmol/l vs 12.3 pmol/l; P = 0.03) post-glucose load than the control group. When these groups were stratified according to BMI, the obese FDR (N = 8) showed higher fasting and post-glucose insulin levels than the obese NGT (N = 9) (fasting: 64.8 pmol/l vs 7.8 pmol/l; P = 0.04, and 60 min post-glucose: 480.6 pmol/l vs 192 pmol/l; P = 0.01). Also, values for HOMA (R) were higher in the obese FDR compared to obese NGT (2.53 vs 0.30; P = 0.075). These results show that FDR of NIDDM patients have true hyperinsulinemia (which is not a consequence of cross-reactivity with proinsulin) and hyperproinsulinemia and no dysfunction of a qualitative nature in ß-cells.
Key words: insulin, NIDDM, proinsulin, first-degree relatives
Non-insulin-dependent diabetes mellitus (NIDDM) is a heterogeneous disorder characterized by insulin resistance, decreased insulin secretion and increased hepatic glucose production. The role of these abnormalities as the earliest or primary causative factors of NIDDM is controversial. However, studies on individuals at high risk to develop the disease, such as offspring of patients with NIDDM and certain population groups, have provided important information. A decrease in insulin sensitivity has been found to precede and to predict the development of NIDDM, possibly occurring 15 to 25 years before the clinical onset of the disease in genetically predisposed individuals (1-3).
In the present study we determined concentrations of proinsulin and insulin (using an assay that does not cross-react with proinsulin) in response to an oral glucose load in individuals with normal glucose tolerance (NGT) who were relatives of NIDDM patients and in control individuals with no family history of diabetes mellitus.
Twenty-seven non-diabetic first-degree relatives (FDR) of NIDDM and 21 non-diabetic subjects with no family history of diabetes were studied. All subjects underwent a standard 75-g oral glucose tolerance test (OGTT) and were classified as having NGT, impaired glucose tolerance (IGT) or diabetes mellitus (DM) on the basis of the World Health Organization criteria (4). Only the subjects with NGT were included in the study, while 12 relatives (4 with NIDDM and 8 with IGT) and 1 control with NIDDM were excluded. Therefore, the study population comprised 35 individuals: 20 subjects with normal glucose tolerance and without diabetes among their FDR (NGT group, 8 men and 12 women) served as normal controls, and 15 with normal glucose tolerance and FDR of patients with NIDDM (FDR group, 5 men and 10 women). There were no differences in age, sex distribution and body mass index (BMI) between groups. NGT and FDR groups were further divided into obese (OB) with a BMI ³25 kg/m2 for women and ³27 kg/m2 for men, and nonobese (L). The clinical characteristics of the study population are given in Table 1.
After a 12-h fast, blood for the determination of glycemia, insulinemia and proinsulinemia was withdrawn from each subject at 0, 30, 60, 90, 120 and 180 min after the ingestion of 75 g glucose.
Plasma glucose was measured by the glucose oxidase method (5). Proinsulin was determined by an immunofluorimetric assay using monoclonal antibodies as previously described (6). Plasma insulin was also measured by a previously reported immunofluorimetric method (7). In this assay, two monoclonal antibodies against insulin were produced: one was used for capture and the other, labelled with europium, was used as tracer antibody. The assay showed no cross-reactivity with intact human proinsulin, des 31-32 proinsulin, split 32-33 (both produced during proinsulin processing) and C-peptide. The area under the glucose, insulin and proinsulin curves was calculated as the sum of half the fasting value plus the sum of the values obtained at 30, 60, 90 and 120 min and half the values obtained at 180 min (8).
The proinsulin/insulin molar ratio (PI/I) was determined under fasting conditions. Insulin secretion was measured as the ratio of the increase in insulin to the increase of glucose concentration at 30 min of the oral glucose tolerance test (I30-0/G30-0) (9). Insulin resistance (R) was evaluated using the
homeostasis model assessment, HOMA
The Mann-Whitney and Fisher exact tests were used to compare two independent groups not normally distributed. A P value <0.05 was considered statistically significant in all tests.
First-degree relatives of NIDDM patients had a higher prevalence of IGT or NIDDM diagnosed by the OGTT compared to the control group (12/27 vs 1/21; P = 0.02).
Mean fasting plasma glucose was not significantly different between the FDR group and their controls (NGT group). However, after the oral glucose load, plasma glucose levels showed a larger increase in the FDR than in the controls at 60 min (Figure 1).
Also, the insulin levels at 60 min were higher in the FDR group than in the NGT group (Figure 2A). When these groups were subdivided on the basis of BMI, no significant differences in insulin levels were detected between the nonobese subgroups (Figure 2B). In contrast, in the obese subgroups, the relatives (FDR-OB) showed higher fasting and 60-min post-glucose insulin levels (P<0.05) compared with control (NGT-OB) (Figure 2C). Figure 3A shows the plasma proinsulin response during the OGTT of the relatives and the controls. The FDR group had higher values at 90 min compared to the NGT group. No differences were found between NGT-L and FDR-L (Figure 3B) or between NGT-OB and FDR-OB (Figure 3C). However, when obese and nonobese subjects from the NGT group were compared, the NGT-OB had higher proinsulin at all times along the curve than the NGT-L (P<0.05). In contrast, no difference was found between obese and nonobese subjects in the FDR group.
No differences were found between the NGT and FDR groups with regard to the molar ratio between proinsulin and insulin in the fasting state. Similarly, the I30-0/G30-0 ratio, used as an indicator of insulin secretion, did not differ between the two groups. Insulin resistance assessed by the HOMA method did not differ between the two groups (Table 2). However, a trend to higher values was observed in the FDR-OB subgroup compared to NGT-OB (2.53 vs 0.30; P = 0.075).
|Figure 1 - Plasma glucose levels (mean ± SEM) during the oral glucose tolerance test in control subjects (NGT, N = 20) and first-degree relatives (FDR, N = 15). *P<0.05 compared to control group (Mann-Whitney test).|
In the present study, both plasma insulin and proinsulin levels after oral glucose loading were higher in subjects with normal glucose tolerance and first-degree relatives of patients with NIDDM compared to subjects without a family history of diabetes. When these subjects were subdivided according to BMI, among obese individuals those who were relatives of NIDDM patients presented significantly higher insulin levels under fasting conditions and after glucose loading and a trend to higher values in relative insulin resistance as determined by HOMA. These data indicate that, regardless of obesity, individuals with normal glucose tolerance and a family history of diabetes are more insulin resistant than those without diabetes among their first-degree relatives.
The results of previous studies on insulin and proinsulin levels in relatives of patients with NIDDM have been contradictory. Gelding et al. (11) and Roder et al. (12) reported increased fasting insulin, but not proinsulin, in first degree relatives of patients with NIDDM, while others (13) found that both insulin and proinsulin were increased among the relatives. Kahn et al. (14), in a prospective study on Japanese-American men, a population with a high prevalence of DM, observed that subjects who subsequently developed diabetes had higher proinsulin levels at baseline than those who continued to have NGT or IGT. These data indicate that an increase in proinsulin levels may be a risk factor for the subsequent development of non-insulin-dependent diabetes mellitus.
The importance of insulin resistance and of abnormal insulin secretion as a primary factor in the development of diabetes mellitus is still a controversial matter. Haffner et al. (15) observed that among Mexican-Americans with normal glucose tolerance, both insulin resistance and a decrease in insulin secretion were predictive factors for the development of NIDDM. In the present study, in which insulin secretion was assessed on the basis of the ratio of the increased insulin to increased glucose ratio at 30 min following OGTT, no significant differences were observed among individuals with normal glucose tolerance with or without a family history of diabetes, even when they were subdivided according to body mass index.
An increased proportion of proinsulin to insulin, i.e., an increase in the proinsulin/insulin ratio, is thought to reflect abnormal ß-cell function (16). This alteration may be due to an intrinsic abnormality in the conversion of proinsulin to insulin or may be the result of an increased demand for insulin leading to the release of immature granules rich in proinsulin (17). Several studies have demonstrated a disproportionate increase in proinsulin in patients with NIDDM (18-20); however, few data are available about high-risk subjects with normal glucose tolerance. Haffner et al. (15) have shown that nondiabetic Mexican-Americans with a parental history of diabetes have a disproportionate elevation in proinsulin relative to insulin. In contrast, two other reports concerning Pima Indians (19) and Finnish subjects (20) did not find an increase in the proinsulin/insulin ratio. Similarly, among the individuals evaluated in the present study we did not find a qualitative change in ß-cell function when subjects with normal glucose tolerance with and without a family history of diabetes were compared. One of the possible explanations for this discrepancy may be the ethnic difference of the groups studied. Furthermore, previous reports showed that the increase in the proinsulin/insulin ratio is associated with the severity of hyperglycemia (20) and is reversible by the normalization of glycemia through the diet or with the use of sulfonylurea (21). However, we cannot rule out the possibility of the existence of an intrinsic defect in beta cells among subjects at high risk to develop non-insulin dependent diabetes mellitus that will not manifest overtly while normoglycemia is maintained.
We found that first-degree relatives of patients with NIDDM, who are at high risk to develop the disease, presented high proinsulin and insulin levels in an assay that does not cross-react with proinsulin, reflecting insulin resistance and no dysfunction of a qualitative nature in ß-cells.
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Address for correspondence: R.S. Moisés, Disciplina de Endocrinologia, EPM, UNIFESP, Rua Botucatu, 740, Caixa Postal 20266, 04034-970 São Paulo, SP, Brasil. Fax: +55-11-570-6636. E-mail: email@example.com
Publication supported by FAPESP. Received March 3, 1998. Accepted October 20, 1998.