Background: Microcirculation is affected in diabetes mellitus and Microvascular abnormalities cause persistent diabetic complications. The aim of this study was nailfold capillaroscopic assessment to describe the pathological changes (morphological and structural) in capillary of a large series of patients with type 1 and 2 diabetes. Methods: A cross-sectional study was carried out in a Nailfold Capillaroscopy Center (Tehran-Iran) between 2011 and 2014. The study included 235 types 1, 2 diabetic patients. All patients underwent 10 nailfolds capillaroscopy examinations. Microvascular architecture, disturbances capillary distribution, capillary morphology, capillary density, efferent/afferent limb ratio, subpapillary venular plexus, and morphological abnormalities were evaluated. Conclusions were stated as normalor scleroderma pattern. Results of patients’ capillaroscopic images were recorded and analyzed quantitatively and qualitatively. P value < 0.05 was considered as statistical significance. Results: of all participants with mean age 59.91 ± 12.39, 183 cases (77.9%) were female and 52 (22.1%) were male. Tortuosity of capillaries was more often observed in our subjects (235 cases) followed by angiogenesis (171 cases). Normal and early scleroderma patterns were observed in 195 (83.0%) and 40 cases (17.0%). Based on P values, altered micro vascular architecture, capillary distribution and capillary morphology were more frequent in patients with scleroderma pattern in comparison to patients with normal pattern (P value < 0.05). Morphological abnormalities except from neo formation capillary and mega capillary were also significantly more common in patients with scleroderma pattern than patients in counterpart group (P value < 0.05). Conclusion: Nailfold capillaroscopy as a non-invasive, diagnostic and prognostic method may potentially affect on diabetes outcome and control.
Type 1, 2 diabetes is a worldwide disease with high risk of morbidity and early mortality. Persistent diabetic complications are mainly due to early stage in the pathogenesis of angiopathy and endothelial dysfunction. Both macro and microvasculature are affected in this disease by altered capillary flow, permeability associated with basement membrane thickening and blood cell velocity. Vascular damage, finally leads to eventual capillary obliteration. Morphological and functional changes in capillary microscopy have been reported in relation to vascular reactivity after induced ischemia [
Some techniques like nailfold capillaroscopy, laser Doppler flowmetry, retinal vessel analysis and 24-hour ambulatory blood pressure monitoring (24-hr ABPM) detect cardiovascular system damage once Type 1 or 2 diabetes is well established [
Nailfold capillaroscopy (NC) is a non-invasive, easy to perform, painless, and sensitive technique for evaluat- ing microvascular involvement, mainly in Raynaud’s phenomenon (RP), systemic sclerosis and connective tissue patients [
Several capillary alterations have been explained in diabetes with poor metabolic control. In previous studies correlation between the severities of microvasculature changes and metabolic control of diabetes has also been reported [
A cross-sectional, observational study of adolescent and adult with diabetes, aged 13 - 86 years old between October 2011 and October 2014 was carried out in Nailfold Capillaroscopy Center of Tehran Resalat Hospital, a private General Hospital in Tehran, Iran. The study included 240 patients suffering from diabetes based on their medical records and laboratory examinations for at least one year. Informed consent was obtained from each par- ticipant.
The inclusion criteria were patients with diabetes, without symptoms of diabetes decompensation or acute infection and with satisfactory clinical control. The exclusion criteria were any evidence of clinical cardiovascular and microvascular disease, vascular coexistent disorders, hypertension, hepatopathy, collagen vascular disease, skin diseases, smoking, infection, vascular effective drug use and missing data.
The study was approved by the Research and Ethics Committee of Tehran Resalat Hospital.
All patients underwent a nailfold capillaroscopy examination using a videocapillaroscope.
Videocap D1 (DS Medica, Sr1, Milano, Italy, 2011). The optical microscope was connected to a digital cam- era and computer.
Participants were studied in the morning between 9 - 12 am. We asked them to abstain from caffeine and smoking for 12 hours before the examination. The procedure was explained for patients. The patient was placed in a semi-supine position for 15 minutes in a comfortable ambient temperature of 22˚C to 25˚C with their hands at heart level.
As there may be a high variability in morphology in diabetic patients per nailfold, we evaluated every 10 nailfold in a patient. A drop of immersion oil was placed on the nail fold of finger to maximize the translucency.
For each image the following capillaroscopic parameters were assessed by an expert rheumatologist: Microvascular architecture, capillary distribution (morphology together the numbers), capillary density (the total num- ber of erythrocyte-perfused capillaries per square millimeter of skin), efferent/afferent limb ratio, sub-papillary venular plexus (define according to Wertheimer’s criteria, modified by Terreri et al.), and morphological abnormalities (bushy capillaries, Raynaud loops, megacapillaries) [
Conclusions were stated as normal, non-specific morphological abnormalities, and scleroderma pattern.
Although the combination of microvascular alterations in the nailfold and major morphological parameters including giant capillaries, A decreased number of loops (<30 over 5 mm in the distal row of the nailfold), disorganization of the normal distribution of capillaries, budding (bushy) capillaries, the associated micro-haemorr- hages when they start to collapse, the loss of capillaries with a decrease in their density (7 - 10 capillaries/mm as the mean reference value), the neo-vascularisation, and reduced blood flow were detected as early capillaroscopic changes [
¾ Patients with two or more definitely abnormal morphological parameters (at least in two nailfolds) asscleroderma pattern group.
¾ Participants with homogeneous distribution of hairpin-shaped capillaries (comb-like structure), with a density of between 9 and 14 capillaries per mm or existence of just one abnormal parameter (non-specific morpho- logical abnormalities) as normal capillaroscopic pattern.
Finally all gathered data were recorded and analyzed statistically.
Capillaroscopic images from all patients were analyzed quantitatively and qualitatively using SPSS16.0. Data are presented as mean ± standard deviation for continuous variables and n% for categorical variables. Independent-samples T test and chi-square test was used to analyze the relationships between variables. With the proposed sample size of 240, the study had a power of 90%. P value < 0.05 was used as statistical significance.
Among 240 enrolled subjects, 5 cases were ineligible due to poor quality of capillaroscopy images, smoking, infection and missing data. Of all participants with mean age 59.91 ± 12.39, 183 cases (77.9%) were female and 52 (22.1%) were male.
Normal and early scleroderma patterns were observed in 195 (83.0%) and 40 cases (17.0%), respectively.
Visibility of sub-papillary venular plexus in all cases was notable but micro vascular architecture in 27% of all patients was abnormal (
Variables | Total = 235 N (%) | |
---|---|---|
Micro vasculararchitecture | Normal | 170 (71.9) 65 (27.7) |
Altred | ||
Capillary distribution | Regular | 230 (97.9) 5 (2.1) |
Non homogenous | ||
Capillary morphology | Homogenous | 231 (98.3) 4 (1.7) |
Non homogenous | ||
Capillary density | Normal | 231 (98.3) 4 (1.7) |
Reduced | ||
Sub-papillary venular plexus | Visible | 235 (100) 0 |
Non visible | ||
Efferent/Afferent limb ratio | Normal | 233 (99.1) 2 (0.9) |
Increased |
Among 40 patients with scleroderma pattern, 33 of them were female. Tortuous capillaries, angiogenesis and altered micro vascular architecture were the most frequent morphological abnormalities in patients with scleroderma pattern. Based on P values, altered micro vascular architecture, capillary distribution and capillary morphology were more frequent in patients with scleroderma pattern in comparison to patients with normal pattern (P value < 0.05). Morphological abnormalities except from neo formation capillary and mega capillary were also significantly more common in these patients (with scleroderma pattern) than patients in counterpart group (P value < 0.05). Detailed data are demonstrated in
However, mean age in subjects with scleroderma pattern was higher than normal pattern (61 ± 8.81 vs. 59.69 ± 13 years), this difference was not statistically significant (P value = 0.543). No correlation was also found between different patterns (normal or scleroderma) and participants’ gender (P value = 0.439).
We evaluated the frequency of nailfold capillaroscopic abnormalities of 235 patients with Type I and Type II diabetes mellitus and showed a high prevalence of pathological nailfold capillary changes.
According with our findings, morphological changes in diabetics’ micro circulation were notable. This vascular heterogeneity may be related to significant autonomic neuropathy disturbances among population with this disease. Some other reports confirmed our results [
In consistence to other investigations [
Of all participants 17% had different degrees of advanced microcirculation angiopathy (scleroderma pattern) that warned us for more attention against consequence complications.
In accordance with expectations, altered micro vascular architecture, capillary distribution and capillary morphology were seen more frequently in patients with scleroderma pattern in comparison to patients with normal pattern. We suppose that many factors like duration or severity of disease may be involved in micro circulation impairment. Barchettast et al. showed greater alterations of capillary length (P = 0.004), distribution (P = 0.02), and morphology (P = 0.0001) in their subjects with diabetes [
In addition, we saw that Avascular areas and micro bleeding were significantly more frequent in participants with scleroderma pattern. In consistent to our results Hosking et al. indicated more common Avascular areas and
P Value | Scleroderma Pattern N = 40 | Normal Pattern N = 195 | Variables | ||
---|---|---|---|---|---|
0.000 | 16 (40) 24 (60) | 153 (78.5) 41 (21) | Normal | Micro vascular architecture | |
Altered | |||||
0.000 | 35 (87.5) 5 (12.5) | 195 (100) 0 (0) | Regular | Capillary distribution | |
Non homogenous | |||||
0.001 | 36 (90) 4 (10) | 195 (100) 0 (0) | Homogenous | Capillary morphology | |
Non homogenous | |||||
0.135 | 38 (95) 2 (5) | 193 (99) 2 (1) | Normal | Capillary density | |
Reduced | |||||
0.312 | 39 (97.5) 1 (2.5) | 194 (99.5) 1 (0.5) | Normal | Efferent/Afferent limbRatio | |
Increased | |||||
0.534 | 7 (17.5) 33 (82.5) | 45 (23.1) 150 (76.9) | Male | Sex | |
Female | |||||
P Value | Scleroderma Pattern N (%) | Normal Pattern N (%) | Morphological Abnormalities | |
---|---|---|---|---|
0.006 | 36 (90) 4 (10) | 135 (69.2) 60 (30.8) | Yes | Angiogenesis |
No | ||||
0.000 | 40 (100) 0 (0) | 195 (100) 0 | Yes | Tortuosity |
No | ||||
0.000 | 10 (47.5) 21 (52.5) | 8 (4.1) 187 (95.9) | Yes | Isolated enlarged loop |
No | ||||
0.003 | 4 (10) 36 (90) | 1 (0.5) 194 (99.5) | Yes | Isolated microbleeding |
No | ||||
.650 | 0 (0) 40 (100) | 1 (0.5) 194 (99.5) | Yes | Neo formation capillary |
No | ||||
0.000 | 9 (22.5) 31 (77.5) | 5 (2.6) 190 (97.4) | Yes | Irregular enlarged loop |
No | ||||
0.017 | 4 (10) 36 (90) | 3 (1.5) 192 (98.5) | Yes | Architecture derangement |
No | ||||
0.002 | 5 (12.5) 35 (87.5) | 2 (1) 193 (99) | Yes | Micro bleeding |
No | ||||
0.028 | 2 (5) 38 (95) | 0 (0) 195 (100) | Yes | Avascular area |
No | ||||
0.650 | 0 (0) 40 (100) | 1 (0.5) 194 (99.5) | Yes | Mega capillary |
No |
Variables | Women (%) | Men (%) | P Value |
---|---|---|---|
Altered microvascular architecture | 29 | 25 | 0.612 |
Non homogenous capillary distribution | 2.7 | 0 | 0.228 |
Non homogenous capillary morphology | 2.2 | 0 | 0.282 |
Reduced capillary density | 2.2 | 0 | 0.449 |
Increased efferent afferent limb ratio | 1.1 | 0 | 0.439 |
Angiogenesis | 71 | 78.8 | 0.264 |
Toruosity | 100 | 100 | - |
Isolated enlarged loop | 12 | 9.6 | 0.631 |
Isolated microbleeding | 2.2 | 1.9 | 0.908 |
Neo formation capillary | 0.5 | 0 | 0.593 |
Irregular enlarged loop | 7.1 | 1.9 | 0.164 |
Architecture derangement | 3.8 | 0 | 0.152 |
Micro bleeding | 3.3 | 1.9 | 0.612 |
Avascular area | 1.1 | 0 | 0.449 |
Mega capillary | 0.5 | 0 | 0.593 |
microhaemorrhages in participants with diabetes (t = −2.33, P = 0.03). They demonstrated a positive association between recent HbA1c and the number of microhaemorrhages (r = 0.44, P = 0.03) [
We also found that isolated and irregular enlarged loops were seen more frequently in cases with scleroderma pattern. Halfoun et al. highlighted the role of abnormal capillaries adaptation to hypoxia in prolonged vasodilatation and irregular loops enlargement among diabetic patients [
A higher frequency of enlarged capillaries and nodular apical elongation were reported in type 2 diabetic patients with chronic clinical complications by Pazos-Moura et al. [
Despite of sub-papillary venous plexus visibility can be influenced by local conditions including hyperkeratosis, skin pigmentation, injuries and edema [
Ingegnoli et al. reported that reduced capillary density may be detected very early in patients with scleroderma pattern [
We could not find any correlations between microvascular abnormalities and participants’ age and sex. Kaminska-Winciorek et al. and Barchetta et al. depicted that microcirculation alterations revealed by nailfold capillaroscopy was independent from age and sex in patients affected by diabetes [
The main strength of our study was demonstration of capability of nailfold capillaroscopy; a useful method for revealing diabetic microangiopathy. Besides that, such a large sample size study had not been previously carried out in Iran and our results can provide comparable data source to other publications.
We did not evaluate relationships between altered parameters and duration or severity of disease. Some participants’ para clinical data like blood sugar status, HbA1c level, … were not assessed, as well. Furthermore, in this project no control group was entered and studied. The answers to these questions definitely affect on our results interpretation.
Our results demonstrated that the presence of diabetes mellitus significantly influences on microcirculation mor- phology and structure, which may predispose to occurrence of sever late complications. Moreover, nailfold capillaroscopy as a non-invasive and diagnostic method may potentially affect on diabetes outcomes and diabetic control.
The authors declare that there is no conflict of interests.
Dr. Rajaie carried out the design and coordinated the study, participated in most of the experiments. Dr. Dehghan coordinated and carried out all the experiments and participated in manuscript preparation, Mrs. Farahani was responsible for Analysis of data and manuscript review. All authors have read and approved the content of the manuscript.