Loading

JSM Atherosclerosis

Nailfold Capillaroscopy a Non-Invasive Tool for Direct Observation of Microvascular Damage in Diabetes Mellitus : Review

Review Article | Open Access

  • 1. Department of Rheumatology, Universidad Espíritu Santo, Ecuador
  • 2. Department of Rheumatology, Centro de Reumatología y Rehabilitación, Ecuador
+ Show More - Show Less
Corresponding Authors
Maldonado G, Department of Rheumatology, Universidad Espíritu Santo La Puntilla, Km. 2.5 Vía a Samborodón. Guayas, Ecuador, Tel: 593-4-2835630.
Abstract

Capillaroscopy is a non-invasive method for the observation of capillary microvasculature. In recent years, it has gained recognition in the field of diseases that affect microcirculation, especially in rheumatic diseases. However, studies published in the last decade have demonstrated the importance of this innovative technique in non-rheumatic diseases such as diabetes mellitus. The purpose of this review is to describe the technique of capillaroscopy and to emphasize its usefulness in the evaluation of vascular micro architecture in patients with diabetes mellitus and its relation to its complications.

Citation

Maldonado G, Paredes C, Roberto G, Ríos C (2017) Nailfold Capillaroscopy a Non-Invasive Tool for Direct Observation of Microvascular Damage in Diabetes Mellitus: Review. JSM Atheroscler 2(4): 1037.

Keywords

•    Diabetes mellitus
•    Capillaroscopy
•    Patterns
•    Microcirculation

INTRODUCTION

Diabetes Mellitus (DM) is defined as a chronic hyperglycemic state with the development of vascular structure alterations. It is currently considered a chronic disease with a high mortality rate due to its long-term cardiovascular, renal and neurological complications [1,2]. Because of the importance of vascular involvement in diabetes mellitus, direct observation tools such as ophthalmoscopes, magnifying lenses, and among them capillaroscopy [3-6], have been used to evaluate microvasculature. Capillaroscopy is a non-invasive method for the observation of capillary microvasculature [7]; in recent years it has gained recognition in the study of diseases that affect the microcirculation, especially in rheumatic diseases [8,9]. However, studies published have demonstrated the importance of this innovative technique in non-rheumatic diseases such as diabetes mellitus [5,9-11]. These studies conclude that capillaroscopy provides key data for the determination of vascular damage in diabetic patients and thus, allows the evaluation of the progression of the disease [9], making this technique a potential future utility in the microvascular disease evaluation. The purpose of this review is to describe the technique of capillaroscopy and to emphasize its usefulness in the evaluation of vascular micro architecture in patients with diabetes mellitus and the relation to it’s complications such as retinopathy, neuropathy and vascular involvement.

Capillaroscopy

Nailfold capillaroscopy is a simple and useful procedure in the evaluation of the spectrum of sclerodermic diseases, especially those associated with vascular damage presenting alterations of the blood vessels that may have diagnostic and prognostic value.

Indications for capillaroscopy are [11,12]:

  1. Evaluation of patients with Raynaud’s Phenomenon
  2. Differential diagnosis of collagenopathies
  3. Primary diagnosis of Scleroderma
  4. Diseases that compromise the capillary microarchitecture, like diabetes mellitus

 Recommendations prior to a videocapilaroscopy [13]:

  • Nails should not have substances that reduce the visibility of the nail fold such as: nail polish, acrylics, gel, etc.
  • Do not have manicure performed for at least of two weeks prior to the study
  • Avoid onychophagia

 A drop of dipping oil should be placed over the nailfold of the four fingers of the hand, the patient should be seated with his hands at the level of the heart and be at an ambient temperature of 20-22o C for at least 15-20 minutes before the test [14,15].

The study should be performed on the nail fold of all fingers, except the thumb. Even though the 4 fingers have to be examined, it has been described that the observation of the fourth and fifth fingers allows the obtainment of better images due to the greater transparency of the skin in these fingers [16,17].

When performing the study, the operator should avoid exerting too much pressure on the nail surface as it may interrupt the blood flow and render images difficult to interpret[17,18]. When placing the camera on the nailfold, the first row of capillaries should be located.

Equipment

Research methods of the capillaries have varied through the years, from the use of stereomicroscopes with magnification of 10-100x for the visualization of the entire nailfold area [15] to new semiautomatic methods for the visualization of the capillaries with an innovative television system called “Capi Shape” [19]. Other optical methods such as ophthalmoscopes and dermatoscopes were also used.

Currently, the gold standard for the observation of capillaries is the video capilaroscopy that consists of a combination of a microscope and a digital camcorder that provides a magnification of 50-100x and allows precise measurements like diameter and length through a software.

Capillaroscopy parameters

The dermal papillae are located perpendicularly to the cutaneous surface. The capillary arrangement at the nailfold level is located in a parallel or oblique way in relation to the cutaneous plane, in two or three layers, on a usually visible subpapillary venous network or plexus. This plexus is situated below the dermal papillae without following a defined pattern.

The capillary loop consists of an arterial or afferent branch and a venous or efferent branch. The main parameters to be evaluated are: length, diameter, density, venous plexus and morphological abnormalities. These elements should be evaluated in the distal row or near the nailfold. The normal number of capillaries per millimeter is from seven to twelve arranged in an inverted U-shape (Figure 1).

The evaluated parameters during capillaroscopy are the following (Figure 2):

  • Capillary diameter: according to Maricq descriptions the normal range is 25-50μm. Ectasias are capillaries with arterial or venous branches that measure >15-20μm [20], and giant capillaries are those that surpass the normal range of 4-10 times the width of the apical loop [21-23], and the determination of a capillary mean that is the result of an average of 3 measurements [16,24]. The capillary diameter consider for evaluation is the total width of the apical loop.
  • Cross-linked capillaries: similar to branches that intersect like a number eight and tortuous like capillaries with branches in an undulating, sinuous or twisted arrangement [16-24].
  • Ramified capillaries: they were described as those capillaries that adopt the shape similar to a tree [16].
  • Avascular zones: they were defined as the absence of capillaries in a tract superior to 500 μm [16].
  • Haemorrhages: as the hemosiderin deposit, caused by the rupture of one or more capillaries [20].
  • Dominant morphology: finding that predominates in more than 20%, whether it’s open, tortuous or crosslinked [13,25].
  • Visibility of the subpapillar venous plexus: a network of larger vessels with respect to the capillaries. The presence of the parameter was determined according to the Kabasakal et al., by [26]:

 0: not visible

1: doubtful or limited visibility

2: Plexus visible in certain areas

3: Fully visible in large areas

  • Cuticulitis: inflammation of the insertion of the cuticle at the periungual folds [27].
  • Scleroderma Pattern (SD) pattern: is presence of giant capillaries, avascular zones, haemorrhages and ramified capillaries all together [20].

 Diabetes Mellitus and capillaroscopic changes: Pattern description

Nailfold capillaroscopy is a noninvasive method for the observation of the capillary microvasculature. Maldonado et al. demonstrated that the use of capillaroscopy in patients with diabetes allows the identification of capillaroscopic abnormalities, possibly including a characteristic pattern in this group of patients consisting of tortuous, cross-linked capillaries, avascular zones and ectasias [3] (Figure 3). Similarly, Kuriliszyn-Moskal et. al, studied the microvascular changes with capillaroscopy in type I diabetes, and its association with systemic compromise, disease duration impact, and capillary architecture changes with metabolic control. They reported that patients with type I diabetes presented important capillary changes such as dilated capillaries, tortuosities and capillary density reduction, when compared to the control group (which presented no capillaroscopic abnormalities). Moderate to severe capillary changes were shown in patients with signs of systemic involvement, and severe capillary changes in patients with poor metabolic control [28]. Meyer et al. also reported morphological capillaroscopic changes in the nailfold on diabetic patients. Findings included an increased capillary diameter, tortuosities, and a capillary density decrease; and were shown to be associated with ischemic vascular reactivity [29].

On the other hand, Barchetta studied the possible relationship of microangiopathic lesions detected in retinal vessels and capillary changes in patients with type I and type II diabetes [30]. It was observed that these patients had a greater capillary diameter, ectasias and nailfold edema, in contrast with healthy subjects. Patients with type I DM had more capillaroscopic alterations than patients with type II DM including: abnormal capillary morphology reduced capillary density, ectasic loops, hemorrhages, abnormal flux and edema/exudates. Also, capillaroscopy was able to identify alterations in almost 50% of patients with DM without retinopathy, demonstrating an early microangiopathic alteration [30].

Similar parameters were evaluated by Pazos-Moura and they found that patients with type I and type II diabetes present capillary tortuosities, as well as an increase in capillary diameter and a capillary density decrease. In the same study, it was shown that patients with type II diabetes had more capillaroscopic alterations than patients with type I diabetes. Thus, an association between capillary findings and metabolic control was established [11].

Furthermore, Romano et al., described the advantages of the use of capillaroscopy in diabetic patients, such as highlighting that this is a non-invasive method of evaluation of the capillary microarchitecture, and also a predictor of extent, severity and disease evolution. This author argued that capillaroscopy is indicated in all pathologies with anatomical and functional abnormalities on the microcirculation, and it is an useful tool for diagnosis and prognosis of diabetic microangiopathy [31].

Studies in a pediatric population and in adolescents with type I diabetes have also being published. Hosking et al. used capillaroscopy to detect microvascular changes and found that the most frequent microvascular alterations found were microhemorrhages and avascular zones. Microhemorrhages were associated with elevated HbA1c levels, and avascular zones with diabetic complications, concluding that capillaroscopy is a method that can detect microvascular damage [32].

Other studies such as the one published by Rajaei et al., showed that capillaroscopic changes in diabetic patients (presence of ramified and tortuous capillaries) were more frequent in these patients than in the control group [4]. Moreover, KaminskaWinciorek et al., identified an increase in cross-linked capillaries in patients with diabetes mellitus [33]. Finally, Cicco et al., found a decrease in total capillary density in diabetic patients by 28% [34].

Complications, evolution of disease and capillaroscopy

Vascular disease is the most common morbidity and mortality cause in diabetic patients.

In chronic hyperglicemia, as in diabetes, capillary endotheliais severely altered. This generates microvascular architecture changes [35], which can be evidenced by the use of capillaroscopy.

Several studies have shown that these structural changes progress and are related to prolonged states of hyperglycemia [31,36].

Kuryliszyn et al., found an escalating appearance of ramified capillaries in diabetic patients with a prolonged evolution time (of more than 10 years) [9].

Bollinger et al., showed similar data, in which they described more capillaroscopic alterations in diabetic patients with a disease evolution of over 10 years [15].

Capillary density is an important parameter when evaluating microcirculation because it is a marker of disease severity [19,24,37-40].

Several studies have demonstrated that high capillary density is indicative of microvascular damage. The capillaroscopic alterations observed and analyzed were independent of age, sex and duration of disease. Arboric and tortuous capillaries, avascular zones, cuticulitis and capillary density scores were directly correlated with nephropathy, arteriopathy, central and peripheral vascular disease, hearing loss, neuropathy and ulcers [16,20,40].

These findings overall report the importance on the evaluation of vascular damage in diabetic patients, such as loss of capillary density that is compensated with the appearance of ramifications and capillary dilation.

Diabetic retinopathy and capillaroscopy

Retinopathy is a common vascular complication in patients with diabetes mellitus and is caused by capillary degeneration and development of avascular areas which reduced perfusion and leads to tissue hypoxia [41].

The first changes observed in diabetic retinopathy are: microaneurysms, leukocyte adhesion and apoptosis of vascular and neuronal cells. The compensatory mechanism of this progression is the formation of capillary neovascularization [42,43].

In most cases, the appearance of symptoms suggestive of diabetic retinopathy represents advanced and degenerative changes. Direct observation tools, such as funduscopic examination, are currently used to evaluate retinopathy [6,44]. However, these traditional methods do not detect complications until they are established.

A recent study showed an association between microangiopathies seen at the ophtalmoscopy and the presence of ramified capillaries and avascular zones seen at the nailfold level [3]. Chang et al., also found a correlation between diabetic retinopathy and the presence of tortuous, ramified capillaries and capillary dilatation, in addition to confirming that these alterations are increased with the severity of diabetic retinopathy [5].

Kaminska-Winciorek studied the microcirculation in children with type I DM and observed the presence of dilated capillaries and megacapillaries accompanied by a change of coloration in the bottom of the nailbed (intense red) indicating a possible angiogenesis, in addition, patients with elevated levels of HbA1c presented greater capillary dilation and decreased capillary number [33]. Hosking found that avascular areas are more frequent in patients with type I DM with complications and that elevated levels of HbA1c were associated with the presence of microhemorrhages [32].

Uyar et al., studied a population of patients diagnosed with diabetes mellitus and evidenced large capillaroscopic changes such as: tortuous capillaries, ramified, increased capillary diameter, compared to the control group. In addition, in patients with diabetic retinopathy, these alterations were increased [45].

These patterns demonstrate that a microvascular component exists in the pathophysiology of diabetic retinopathy and capillaroscopy is a tool that can accurately detect capillaroscopic changes and relate them to systemic vascular complications.

Nailfold capillaroscopy of diabetic toes

Diabetic neuropathy is a common complication of the disease; however, capillaroscopy is not frequently used for evaluation of the microvasculature of the feet. Delcourt et al., designed a study protocol for the direct observation of the capillaries in the feet of healthy subjects withvideocapillaroscopy, the same capilaroscopic changes in the feet and hands were evidenced, however, the examination of the capillaries could only be performed in 87 % of the cases [46].

Fragrell et al., used capillaroscopy to evaluate the microangiopathy of patients with diabetes mellitus, they observed an irregular pattern composed of avascular zones and dilated capillaries, these changes were compared with healthy subjects who did not present alterations, however more studies are needed that can support the importance of Use of capillaroscopy in the evaluation of the microvasculature of the feet [47].

Healthy population and capillaroscopy

It is important to highlight the fact that a healthy population will present capillaroscopic alterations, but with no capillary damage or clinical expression.

A study carried out by Ríos et al. showed that approximately 86% of the healthy subjects that were studied had capillary findings such as tortuous, cross-linked and ramified capillaries [25]. These results are similar to the study by Hoerth et al. [48], in which it was shown that 85% of the subjects had capillaroscopic findings such as: tortuous, cross-linked and ramified capillaries. Coehlo Andrade studied a more extensive cohort and approximately 81% of the subjects presented capillary findings including ramified and tortuous capillaries [39].

CONCLUSION

Capillaroscopy is a non-invasive tool, reproducible, and trustworthy for a qualitative, quantitative, and precise evaluation of pathologies that affect the peripheral microvasculature. The main limitation remains in the small number of articles focusing on the qualitative findings and relationship with markers of disease progression yet to be established. However, the capillaroscopy is a potential future utility in the microvascular diseases since it has been of great contribution for the evaluation of vascular damage in rheumatic diseases.

REFERENCES

1. Cowie C, Rust K, Ford E, Eberhardt M, Byrd-Hlot D, Li C, et al. Screening for type 2 diabetes mellitus. Diabetes Care. 2009; 32: 287-294.

2. Chamberlain J, Rhinehart A, Shaefer CJ, Neuman A. Diagnosis and Management of Diabetes: Synopsis of the 2016 American Diabetes Association Standards of Medical Care in Diabetes. Ann Intern Med. 2016; 164: 542-552.

3. Maldonado G, Guerrero R, Paredes C, Ríos C. Nailfold capillaroscopy in diabetes mellitus. Microvasc Res. 2017; 6: 41-46.

4. Rajaei A, Dehghan P, Farahani Z. Nailfold Capillaroscopy Findings in Diabetic Patients (A Pilot Cross-Sectional Study ). Open J Pathol. 2015; 5: 65-72.

5. Chang CH, Tsai RK, Wu WC, Kuo SL, Yu HS. Use of dynamic capillaroscopy for studying cutaneous microcirculation in patients with diabetes mellitus. Microvasc Res. 1997; 53: 121-127.

6. Chhablani J, Kaja S, Shah V. Smartphones in ophtalmology. Indian J Ophtalmol. 2012; 60: 127-131.

7. Ríos C, Maldonado G. Manual de Capilaroscopia [Internet]. Primera Ed. Guayaquil: Centro de Reumatología y Rehabilitación. 2016; 103.

8. Maldonado G, Ríos C. Utilidad de la capilaroscopia en esclerodermia. Rev Arg Reum. 2016; 27: 40-46.

9. Kuryliszyn−Moskal A, Dubicki A, Zaezycki W, Zonnenberg A, Gorska M. A study on microvascular abnormalities in capillaroscopy in patients with type 1 diabetes mellitus. Diabetol Dosw i Klin. 2006; 6: 98-103.

10. Maldonado G, Ferro C, Ríos C, Ríos K. Capillaroscopic Patterns in Healthy Subjects. Arthritis Rheumatol [Internet]. 2015; 67: 2721- 2722.

11. Pazos-Moura C, Moura E, Bouskela E, Torres-Filho I, Breitenbach M. Nailfold capillaroscopy in diabetes mellitus morphological abnormalities and relationship with microangiopathy. Braz J Med Biol Res. 1987; 20: 777–780.

12. Souza E, Kayser C. Nailfold capillaroscopy: relevance to the practice of rheumatology. Rev Bras Reum. 2015; 55: 264-271.

13. Restrepo JP, R MG, Angelis R De, Grassi W. El papel de la capilaroscopia del lecho ungueal en reumatología. 2008; 15: 187-195.

14. Bergman R, Sharony L, Schapira D, Nahir M, Balbir-Gurman A. The handheld dermatoscope as a nailfold capillaroscopic instrument. Arch Dermatol. 2003; 139: 1027-1030.

15. Bollinger A, Fagrell B. Clinical capillaroscopy - a guide to its use in clinical research and practice. Toronto: Hogrefe & Huber Publishers. 1990. 1-123.

16. Grassi W, Del Medico P. Atlas of Capillaroscopy. Milan: Edra Medical Publishing & New Media. 2004.

17. Cutolo M, Grassi W, Cerinic MM. Raynaud’s Phenomenon and the Role of Capillaroscopy. Arthritis Rheum. 2003; 48: 3023-3030.

18. Grassi W, De Angelis R. Capillaroscopy: questions and answers. Clin Rheumatol. 2007; 26: 2009-2016.

19. Hu Q, Mahler F. New system for image analysis in nailfold capillaroscopy. Microcirculation. 1999; 6: 227-235.

20. Maricq H. Widefield capillary microscopy technique and Rating Scale for abnormalities seen in Scleroderma and Related Disorders. Arthritis Rheum. 1981; 9: 1159-1165.

21. Lefford F, Edwards J. Nailfold capillary microscopy in connective tissue disease: quantitative morphological analysis. Ann Rheum Dis. 1986; 45: 741-749.

22. Hofstee H, Serné E, Roberts C. A multicentre study on the reliability of qualitative and quantitative nail-fold videocapillaroscopy assessment. Rheumatology. 2012; 51: 749-755.

23. Hou M, Huang S, Wang C, Tseng L Lo, Chen Y. A computerized system of nail-fold capillaroscopy for dry eye disease diagnosis. Multidimens Syst Signal Process. 2012; 23: 512-524.

24. Cutolo M, Pizzorni C, Sulli A. Capillaroscopy. Best Pr Res Clin Rheumatol. 2005; 3: 437-452.

25. Ríos C, Maldonado G, Ferro C, Ríos K. Estudio de patrones capilaroscópicos en población sana. Rev Arg Reum. 2016; 27: 27-31.

26. Kabasakal Y, Elvins D, Ring E, McHugh N. Quantitative nailfold capillaroscopy findings in a population with connective tissue disease and in normal healthy controls. Ann Rheum Dis. 1996; 55: 507-512.

27. Andrade L, Gabriel A, Assad R, Ferrari A, Atra E. Panoramic nailfold capillaroscopy: a new reading method and normal range. Semin Arthritis Rheum. 1999; 20: 21-31.

28. Kuryliszyn-Moskal A, Dubicki A, Zarzycki W, Zonnenberg A, Górska M. Microvascular abnormalities in capillaroscopy correlate with higher serum IL-18 and sE-selectin levels in patients with type 1 diabetes complicated by microangiopathy. Folia Histochem Cytobiol. 2011; 49: 104-110.

29. Meyer M, Pfhol M, Schatz H. Asssesment of diabetic alterations of microcirculation by means of capillaroscopy and laser-Doppler anemometry. Med Klin. 2011; 15: 71-77.

30. Barchetta I, Riccieri V, Vasile M, Stefanantoni K, Comberiati P, Taverniti L, et al. High prevalence of capillary abnormalities in patients with diabetes and association with retinopathy. Diabet Med. 2011; 28: 1039-1044.

31. Romano C, Costa M, Messina M, Bertini M. Videocapillaroscopy in Diabetes. Diabetes Res Open J. 2015; 2: 3-6.

32. Hosking S, Bhatia R, Crock P, Wright I, Squance M, Reeves G. Noninvasive detection of microvascular changes in a paediatric and adolescent population with type 1 diabetes: a pilot cross-sectional study. BMC Endocr Disord. 2013; 13: 1-9.

33. Kaminska-Winciorek G, Deja G, Polan?ska J, Jarosz-Chobot P. Diabetic microangiopathy in capillaroscopic examination of juveniles with diabetes type 1. Postep Hig Med Dosw. 2012; 66: 51-59.

34. Cicco G, Cicco S. Hemorheology and microcirculation in some pathologies of internal medicine. Minerva Med. 2007; 98: 625-631.

35. American Diabetes Association. Standards of medical care in diabetes-2015. Diabetes Care. 2015; 38: 1-93.

36. Kuryliszyn-Moscal A, Dubicki A, Zarzycki W, Zonnenberg A, Gorska M. Microvascular abnormalities sE-Selectine levels in patiesns with type I diabetes complicated by microangiopathy. Folia Histochem Citobiol. 2011; 49: 104-110.

37. Smith B, Peterson K, Fu R. Drugs for fibromyalgia. Final Orginal Rep. 2011.

38. Sulli A, Sechi M, Pizzorni C, Cutolo M. Scoring the nailfold microvascular changes during the capillaroscopic analysis in systemic sclerosis patients. Ann Rheum Dis. 2008; 67: 885-8857.

39. Cutolo M, Sulli A, Smith V. How to perform and interpret capillaroscopy. Best Pract Res Clin Rheumatol. 2013; 27: 237-248.

40. Cutolo M, Sulli A, Pizzorni C, Accardo S. Nailfold videocapillaroscopy assessment of microvascular damage in systemic sclerosis. J Rheumatol. 2000; 27: 155-160.

41. Al-Shabrawey M, Zhang W, Mc Donald D. Diabetic retinopathy: mechanism, diagnosis, prevention, and treatment. Biomed Res Int. 2015; 2.

42. Howangyin K, Silvestre J. Diabetes mellitus and ischemic diseases: molecular mechanisms of vascular repair dysfunction. Arterioscler Thromb Vasc Biol. 2014; 34: 1126-2014.

43. Chakrabarti R, Harper A, Keeffe J. Diabetic retinopathy management guidelines. Expert Rev Ophtalmol. 2012; 7: 417-439.

44. American Academy of Ophthalmology Retina/Vitreous Panel. Preferred Practice Pattern® Guidelines. Diabetic Retinopathy. Amer Acad Opht. San Francisco, CA; 2016. 63.

45. Uyar S, Balkarl J A, Kazum Erol M, Yesil B, Tokuc? A, Durmaz D, et al. Assessment of the Relationship between Diabetic Retinopathy and Nailfold Capillaries in Type 2 Diabetics with a Noninvasive Method: Nailfold Videocapillaroscopy. J Diabetes Res. 2016; 2016: 7.

46. Noy-Delcourt D, Thébaut P. Periungual capillaroscopy of the toes. Criteria for norms. J Mal Vasc. 1986; 11: 288-294.

47. Fagrell B, Hermansson I, Karlander S, Ostergren J. Vital capillary microscopy for assessment of skin viability and microangiopathy in patients with diabetes mellitus. Acta Med Scand Suppl. 1984; 687: 25- 28.

48. Hoerth C, Kundi M, Katzenschlager R, Hirschl M. Qualitative and quantitative as- sessment of nailfold capillaries by capillaroscopy in healthy volunteers. Vasa. Vasa. 2012; 41: 19-26.

Maldonado G, Paredes C, Roberto G, Ríos C (2017) Nailfold Capillaroscopy a Non-Invasive Tool for Direct Observation of Microvascular Damage in Diabetes Mellitus: Review. JSM Atheroscler 2(4): 1037.

Received : 20 Apr 2017
Accepted : 14 Jun 2017
Published : 16 Jun 2017
Journals
Annals of Otolaryngology and Rhinology
ISSN : 2379-948X
Launched : 2014
JSM Schizophrenia
Launched : 2016
Journal of Nausea
Launched : 2020
JSM Internal Medicine
Launched : 2016
JSM Hepatitis
Launched : 2016
JSM Oro Facial Surgeries
ISSN : 2578-3211
Launched : 2016
Journal of Human Nutrition and Food Science
ISSN : 2333-6706
Launched : 2013
JSM Regenerative Medicine and Bioengineering
ISSN : 2379-0490
Launched : 2013
JSM Spine
ISSN : 2578-3181
Launched : 2016
Archives of Palliative Care
ISSN : 2573-1165
Launched : 2016
JSM Nutritional Disorders
ISSN : 2578-3203
Launched : 2017
Annals of Neurodegenerative Disorders
ISSN : 2476-2032
Launched : 2016
Journal of Fever
ISSN : 2641-7782
Launched : 2017
JSM Bone Marrow Research
ISSN : 2578-3351
Launched : 2016
JSM Mathematics and Statistics
ISSN : 2578-3173
Launched : 2014
Journal of Autoimmunity and Research
ISSN : 2573-1173
Launched : 2014
JSM Arthritis
ISSN : 2475-9155
Launched : 2016
JSM Head and Neck Cancer-Cases and Reviews
ISSN : 2573-1610
Launched : 2016
JSM General Surgery Cases and Images
ISSN : 2573-1564
Launched : 2016
JSM Anatomy and Physiology
ISSN : 2573-1262
Launched : 2016
JSM Dental Surgery
ISSN : 2573-1548
Launched : 2016
Annals of Emergency Surgery
ISSN : 2573-1017
Launched : 2016
Annals of Mens Health and Wellness
ISSN : 2641-7707
Launched : 2017
Journal of Preventive Medicine and Health Care
ISSN : 2576-0084
Launched : 2018
Journal of Chronic Diseases and Management
ISSN : 2573-1300
Launched : 2016
Annals of Vaccines and Immunization
ISSN : 2378-9379
Launched : 2014
JSM Heart Surgery Cases and Images
ISSN : 2578-3157
Launched : 2016
Annals of Reproductive Medicine and Treatment
ISSN : 2573-1092
Launched : 2016
JSM Brain Science
ISSN : 2573-1289
Launched : 2016
JSM Biomarkers
ISSN : 2578-3815
Launched : 2014
JSM Biology
ISSN : 2475-9392
Launched : 2016
Archives of Stem Cell and Research
ISSN : 2578-3580
Launched : 2014
Annals of Clinical and Medical Microbiology
ISSN : 2578-3629
Launched : 2014
JSM Pediatric Surgery
ISSN : 2578-3149
Launched : 2017
Journal of Memory Disorder and Rehabilitation
ISSN : 2578-319X
Launched : 2016
JSM Tropical Medicine and Research
ISSN : 2578-3165
Launched : 2016
JSM Head and Face Medicine
ISSN : 2578-3793
Launched : 2016
JSM Cardiothoracic Surgery
ISSN : 2573-1297
Launched : 2016
JSM Bone and Joint Diseases
ISSN : 2578-3351
Launched : 2017
JSM Bioavailability and Bioequivalence
ISSN : 2641-7812
Launched : 2017
Journal of Genitourinary Disorders
ISSN : 2641-7790
Launched : 2017
Journal of Fractures and Sprains
ISSN : 2578-3831
Launched : 2016
Journal of Autism and Epilepsy
ISSN : 2641-7774
Launched : 2016
Annals of Marine Biology and Research
ISSN : 2573-105X
Launched : 2014
JSM Health Education & Primary Health Care
ISSN : 2578-3777
Launched : 2016
JSM Communication Disorders
ISSN : 2578-3807
Launched : 2016
Annals of Musculoskeletal Disorders
ISSN : 2578-3599
Launched : 2016
Annals of Virology and Research
ISSN : 2573-1122
Launched : 2014
JSM Renal Medicine
ISSN : 2573-1637
Launched : 2016
Journal of Muscle Health
ISSN : 2578-3823
Launched : 2016
JSM Genetics and Genomics
ISSN : 2334-1823
Launched : 2013
JSM Anxiety and Depression
ISSN : 2475-9139
Launched : 2016
Clinical Journal of Heart Diseases
ISSN : 2641-7766
Launched : 2016
Annals of Medicinal Chemistry and Research
ISSN : 2378-9336
Launched : 2014
JSM Pain and Management
ISSN : 2578-3378
Launched : 2016
JSM Women's Health
ISSN : 2578-3696
Launched : 2016
Clinical Research in HIV or AIDS
ISSN : 2374-0094
Launched : 2013
Journal of Endocrinology, Diabetes and Obesity
ISSN : 2333-6692
Launched : 2013
Journal of Substance Abuse and Alcoholism
ISSN : 2373-9363
Launched : 2013
JSM Neurosurgery and Spine
ISSN : 2373-9479
Launched : 2013
Journal of Liver and Clinical Research
ISSN : 2379-0830
Launched : 2014
Journal of Drug Design and Research
ISSN : 2379-089X
Launched : 2014
JSM Clinical Oncology and Research
ISSN : 2373-938X
Launched : 2013
JSM Bioinformatics, Genomics and Proteomics
ISSN : 2576-1102
Launched : 2014
JSM Chemistry
ISSN : 2334-1831
Launched : 2013
Journal of Trauma and Care
ISSN : 2573-1246
Launched : 2014
JSM Surgical Oncology and Research
ISSN : 2578-3688
Launched : 2016
Annals of Food Processing and Preservation
ISSN : 2573-1033
Launched : 2016
Journal of Radiology and Radiation Therapy
ISSN : 2333-7095
Launched : 2013
JSM Physical Medicine and Rehabilitation
ISSN : 2578-3572
Launched : 2016
Annals of Clinical Pathology
ISSN : 2373-9282
Launched : 2013
Annals of Cardiovascular Diseases
ISSN : 2641-7731
Launched : 2016
Journal of Behavior
ISSN : 2576-0076
Launched : 2016
Annals of Clinical and Experimental Metabolism
ISSN : 2572-2492
Launched : 2016
Clinical Research in Infectious Diseases
ISSN : 2379-0636
Launched : 2013
JSM Microbiology
ISSN : 2333-6455
Launched : 2013
Journal of Urology and Research
ISSN : 2379-951X
Launched : 2014
Journal of Family Medicine and Community Health
ISSN : 2379-0547
Launched : 2013
Annals of Pregnancy and Care
ISSN : 2578-336X
Launched : 2017
JSM Cell and Developmental Biology
ISSN : 2379-061X
Launched : 2013
Annals of Aquaculture and Research
ISSN : 2379-0881
Launched : 2014
Clinical Research in Pulmonology
ISSN : 2333-6625
Launched : 2013
Journal of Immunology and Clinical Research
ISSN : 2333-6714
Launched : 2013
Annals of Forensic Research and Analysis
ISSN : 2378-9476
Launched : 2014
JSM Biochemistry and Molecular Biology
ISSN : 2333-7109
Launched : 2013
Annals of Breast Cancer Research
ISSN : 2641-7685
Launched : 2016
Annals of Gerontology and Geriatric Research
ISSN : 2378-9409
Launched : 2014
Journal of Sleep Medicine and Disorders
ISSN : 2379-0822
Launched : 2014
JSM Burns and Trauma
ISSN : 2475-9406
Launched : 2016
Chemical Engineering and Process Techniques
ISSN : 2333-6633
Launched : 2013
Annals of Clinical Cytology and Pathology
ISSN : 2475-9430
Launched : 2014
JSM Allergy and Asthma
ISSN : 2573-1254
Launched : 2016
Journal of Neurological Disorders and Stroke
ISSN : 2334-2307
Launched : 2013
Annals of Sports Medicine and Research
ISSN : 2379-0571
Launched : 2014
JSM Sexual Medicine
ISSN : 2578-3718
Launched : 2016
Annals of Vascular Medicine and Research
ISSN : 2378-9344
Launched : 2014
JSM Biotechnology and Biomedical Engineering
ISSN : 2333-7117
Launched : 2013
Journal of Hematology and Transfusion
ISSN : 2333-6684
Launched : 2013
JSM Environmental Science and Ecology
ISSN : 2333-7141
Launched : 2013
Journal of Cardiology and Clinical Research
ISSN : 2333-6676
Launched : 2013
JSM Nanotechnology and Nanomedicine
ISSN : 2334-1815
Launched : 2013
Journal of Ear, Nose and Throat Disorders
ISSN : 2475-9473
Launched : 2016
JSM Ophthalmology
ISSN : 2333-6447
Launched : 2013
Journal of Pharmacology and Clinical Toxicology
ISSN : 2333-7079
Launched : 2013
Annals of Psychiatry and Mental Health
ISSN : 2374-0124
Launched : 2013
Medical Journal of Obstetrics and Gynecology
ISSN : 2333-6439
Launched : 2013
Annals of Pediatrics and Child Health
ISSN : 2373-9312
Launched : 2013
JSM Clinical Pharmaceutics
ISSN : 2379-9498
Launched : 2014
JSM Foot and Ankle
ISSN : 2475-9112
Launched : 2016
JSM Alzheimer's Disease and Related Dementia
ISSN : 2378-9565
Launched : 2014
Journal of Addiction Medicine and Therapy
ISSN : 2333-665X
Launched : 2013
Journal of Veterinary Medicine and Research
ISSN : 2378-931X
Launched : 2013
Annals of Public Health and Research
ISSN : 2378-9328
Launched : 2014
Annals of Orthopedics and Rheumatology
ISSN : 2373-9290
Launched : 2013
Journal of Clinical Nephrology and Research
ISSN : 2379-0652
Launched : 2014
Annals of Community Medicine and Practice
ISSN : 2475-9465
Launched : 2014
Annals of Biometrics and Biostatistics
ISSN : 2374-0116
Launched : 2013
JSM Clinical Case Reports
ISSN : 2373-9819
Launched : 2013
Journal of Cancer Biology and Research
ISSN : 2373-9436
Launched : 2013
Journal of Surgery and Transplantation Science
ISSN : 2379-0911
Launched : 2013
Journal of Dermatology and Clinical Research
ISSN : 2373-9371
Launched : 2013
JSM Gastroenterology and Hepatology
ISSN : 2373-9487
Launched : 2013
Annals of Nursing and Practice
ISSN : 2379-9501
Launched : 2014
JSM Dentistry
ISSN : 2333-7133
Launched : 2013
Author Information X