Copyright
©The Author(s) 2019.
World J Diabetes. Feb 15, 2019; 10(2): 114-132
Published online Feb 15, 2019. doi: 10.4239/wjd.v10.i2.114
Published online Feb 15, 2019. doi: 10.4239/wjd.v10.i2.114
Table 1 Literature search strategy
S. No | Search terms |
1 | NAFLD |
2 | Nonalcoholic fatty liver disease |
3 | Non-alcoholic fatty liver disease |
4 | Non alcoholic fatty liver disease |
5 | NASH |
6 | Non-alcoholic steatohepatitis |
7 | Nonalcoholic steatohepatitis |
8 | Non alcoholic steatohepatitis |
9 | Fatty liver |
10 | 1 OR 2 OR 3 OR 4 OR 5 OR 6 OR 7 OR 8 OR 9 |
11 | Type 2 diabetes mellitus |
12 | Type 2 diabetes |
13 | Diabetes mellitus type 2 |
14 | Diabetes type 2 |
15 | 11 OR 12 OR 13 OR 14 |
16 | SGLT-2 inhibitors |
17 | Sodium glucose cotransporter-2 inhibitors |
18 | SGLT-2 |
19 | SGLT2 |
20 | SGLT 2 |
21 | Canagliflozin |
22 | Dapagliflozin |
23 | Empagliflozin |
24 | Ipragliflozin |
25 | Luseogliflozin |
26 | Tofogliflozin |
27 | Sotagliflozin |
28 | Remogliflozin |
29 | Ertugliflozin |
30 | Sergliflozin |
31 | 16 OR 17 OR 18 OR 19 OR 20 OR 21 OR 22 OR 23 OR 24 OR 25 OR 26 OR 27 OR 28 OR 29 OR 30 |
32 | 10 AND 15 AND 31 |
Table 2 Randomised controlled trials
S. No | Ref. | Inclusion criteria | Age (yr) | Male gender | Intervention arm | Control arm | Follow-up duration | Primary outcome |
1 | Kuchay et al[11], 2018 | Age > 20 yr, hepatic steatosis (MRI-PDFF > 6%), HbA1c > 7.0% to < 10.0% | Intervention arm: 50.7 (12.8) | Intervention arm: 16 (64%) | Standard treatment + Empagliflozin 10 mg daily (n = 25) | Standard treatment (n = 25) | 20 wk | Change in liver fat content by MRI-PDFF |
Control arm: 49.1 (10.3) | Control arm: 17 (68%) | |||||||
2 | Ito et al[12], 2017 | Age 20-75 yr, HbA1c 7.0–11.0%, BMI < 45 kg/m2, On diet and exercise therapy alone or with oral hypoglycaemic agents other than SGLT-2 inhibitors and thiazolidinediones and/or insulin, NAFLD, findings suggesting hepatic steatosis and hepatic dysfunction on clinical laboratory tests or on imaging studies (e.g., computed tomography or ultrasound) | Pioglitazone arm: 59.1 (9.8) | Pioglitazone arm: 18 (53%) | Ipragliflozin 50 mg daily (n = 32) | Pioglitazone 15-30 mg daily (n = 34) | 24 wk | Change in L/S attenuation ratio |
Ipragliflozin arm: 57.3 (12.1) | Ipragliflozin arm: 14 (44%) | |||||||
3 | Shibuya et al[13], 2018 | Fatty liver diagnosed on the basis of computed tomography or abdominal sonography, HbA1c 6.0%–10.0%, age 20–70 yr | Luseogliflozin arm: 51 (47-62) | Luseogliflozin arm: 10 (62.5%) | Luseogliflozin 2.5 mg daily (n = 16) | Metformin 1.5 g daily (n = 16) | 24 wk | Change in L/S attenuation ratio |
Metformin arm: 60 (53-66) | Metformin arm: 8 (50%) | |||||||
4 | Eriksson et al[14], 2018 | Age 40–75 yr, treated with a stable dose of metformin or sulfonylurea alone or in combination for at least 3 mo, MRI-PDFF > 5.5%, BMI 25–40 kg/m2 | Dapagliflozin arm: 65 (6.5) | Dapagliflozin arm: 16 (76.2%) | Dapagliflozin 10 mg daily (n = 21) or Omega 3-carboxylic acid 4 g daily (n = 20) or Combination (n = 22) | Placebo (n = 21) | 12 wk | Change in liver fat content by MRI-PDFF |
Omega 3-carboxylic acid arm: 66.2 (5.9) | Omega 3-carboxylic acid arm: 11 (55%) | |||||||
O + D arm: 65(5.4) | O + D arm: 15 (68.2%) | |||||||
Placebo arm: 65.6 (6.1) | Placebo arm: 17 (81%) |
Table 3 Observational studies
S. No | Ref. | Design | Inclusion criteria | Age (yr) | Male gender | Sample size | SGLT-2 inhibitor | Follow-up duration |
1 | Ohki et al[15], 2016 | Prospective study | Type 2 diabetes with NAFLD treated with GLP-1 analogues or DPP-4 inhibitors and failed to normalise serum ALT levels | 54.2 (49.3-60.1) | 19 (79.2%) | 24 | Ipragliflozin 25-50 mg daily | 320 d (302-329) |
2 | Seko et al[16], 2016 | Retrospective cohort study | Type 2 diabetes with NAFLD | SGLT-2 inhibitor arm: 60.3 (1.8) | SGLT-2 inhibitor arm: 9 (37.5%) | 24 (SGLT-2 inhibitor); 21 (Sitagliptin ) | Canagliflozin 100 mg (n = 18) or Ipragliflozin 50 mg daily (n = 6) | 24 wk |
Sitagliptin arm: 59.4 (3.7) | Sitagliptin arm: 8 (38.1%) | |||||||
3 | Gautam et al[17], 2018 | Prospective study | Type 2 diabetes with NAFLD | - | - | 32 | Canagliflozin 100 mg daily | 24 wk |
4 | Sumida et al[18], 2018 | Prospective study | Age > 20 yr, HbA1c > 6.5% to < 8.5%, NAFLD | 55.4 (13.6) | 28 (70%) | 40 | Luseogliflozin 2.5 mg daily | 24 wk |
Table 4 Assessment of study quality of randomised controlled trials
Study | Criteria | Risk of bias | Study quality |
Kuchay et al[11] | Random sequence generation | Low risk | Good quality |
Allocation concealment | Low risk | ||
Selective reporting | Low risk | ||
Other bias | Low risk | ||
Blinding of participants and personnel | Low risk | ||
Blinding of outcome assessment | Low risk | ||
Incomplete outcome data | Low risk | ||
Ito et al[12] | Random sequence generation | Low risk | Fair quality |
Allocation concealment | Unclear risk | ||
Selective reporting | Low risk | ||
Other bias | Low risk | ||
Blinding of participants and personnel | Low risk | ||
Blinding of outcome assessment | Low risk | ||
Incomplete outcome data | Low risk | ||
Shibuya et al[13] | Random sequence generation | Unclear risk | Fair quality |
Allocation concealment | Unclear risk | ||
Selective reporting | Low risk | ||
Other bias | Low risk | ||
Blinding of participants and personnel | Low risk | ||
Blinding of outcome assessment | Low risk | ||
Incomplete outcome data | Low risk | ||
Eriksson et al[14] | Random sequence generation | Low risk | Good quality |
Allocation concealment | Low risk | ||
Selective reporting | Low risk | ||
Other bias | Low risk | ||
Blinding of participants and personnel | Low risk | ||
Blinding of outcome assessment | Low risk | ||
Incomplete outcome data | Low risk |
Table 5 Assessment of study quality of observational studies
S. No | Criteria | Ohki et al[15] | Seko et al[16] | Gautam et al[17] | Sumida et al[18] |
1 | A clearly stated aim | 2 | 2 | 2 | 2 |
2 | Inclusion of consecutive patients | 0 | 2 | 2 | 1 |
3 | Prospective collection of data | 2 | 0 | 2 | 2 |
4 | Endpoints appropriate to the aim of the study | 2 | 2 | 2 | 2 |
5 | Unbiased assessment of the study endpoint | 0 | 0 | 0 | 0 |
6 | Follow-up period appropriate to the aim of the study | 2 | 2 | 2 | 2 |
7 | Loss to follow up less than 5% | 2 | 2 | 2 | 2 |
8 | Prospective calculation of the study size | 0 | 0 | 0 | 0 |
9 | An adequate control group | NA | 0 | NA | NA |
10 | Contemporary groups | NA | 2 | NA | NA |
11 | Baseline equivalence of groups | NA | 2 | NA | NA |
12 | Adequate statistical analyses | NA | 2 | NA | NA |
13 | Total score | 10/16 | 16/24 | 12/16 | 11/16 |
Table 6 Change in serum alanine aminotransferase levels in individual studies
Study | Serum ALT level (IU/L) | P value | P value between groups | ||
Group | Baseline | Study completion | |||
Kuchay et al[11] | Empagliflozin | 64.3 (20.2) | 49.7 (25.8) | 0.001 | 0.005 |
Control | 65.3 (40.3) | 61.6 (38.4) | 0.422 | ||
Ito et al[12] | Ipragliflozin | 57.4 (27.3) | 38.2 (20.5) | < 0.05 | 0.642 |
Pioglitazone | 53.1 (26.6) | 36.8 (15.1) | < 0.05 | ||
Shibuya et al[13] | Luseogliflozin | 49.5 (31.0, 70.0) | 31 (26.0, 55.0) | 0.057 | 0.064 |
Metformin | 39 (23.0, 56.0) | 39 (27.0, 51.0) | 0.518 | ||
Eriksson et al[14] | Placebo | 33.53 (12.4) | -0.2 (8.8)1 | - | - |
Omega-3 CA | 37.65 (14.7) | +5.9 (16.5)1 | - | Non-significant2 | |
Dapagliflozin | 39.41 (14.7) | -8.2 (8.2)1 | - | < 0.052 | |
O + D | 35.88 (17.1) | +0.1 (12.9)1 | - | Non-significant2 | |
Ohki et al[15] | Ipragliflozin | 62 (43.0-75.0) | 38.0 (31.0-65.0) | 0.01 | - |
Seko et al[16] | SGLT-2 inhibitor | 70.8 (8.1) | 48.8 (5.5) | 0.002 | 0.039 |
Sitagliptin | 92.4 (11.2) | 71.1 (10.0) | 0.012 | ||
Gautam et al[17] | Canagliflozin | 96 (18.7) | 60.0 (17.6) | < 0.00001 | - |
Sumida et al[18] | Luseogliflozin | 54.7 (28.2) | 42.4 (26.5) | < 0.001 | - |
Table 7 Change in serum aspartate aminotransferase levels in individual studies
Study | Serum AST levels (IU/L) | P value | P value between groups | ||
Group | Baseline | Study completion | |||
Kuchay et al[11] | Empagliflozin | 44.6 (23.5) | 36.2 (9.0) | 0.04 | 0.212 |
Control | 45.3 (24.3) | 44.6 (23.8) | 0.931 | ||
Ito et al[12] | Ipragliflozin | 39.7 (16.7) | 27.3 (8.9) | < 0.05 | 0.802 |
Pioglitazone | 43.3 (20.5) | 32.4 (15.4) | < 0.05 | ||
Eriksson et al[14] | Placebo | 29.4 (13.2) | -1.2 (7.2)1 | - | - |
Omega-3 CA | 30.6 (10.2) | +4.8 (9.0)1 | - | Non-significant2 | |
Dapagliflozin | 31.2 (11.4) | -4.2 (5.4)1 | - | < 0.052 | |
O + D | 30 (10.2) | +1.2 (5.4)1 | - | Non-significant2 | |
Ohki et al[15] | Ipragliflozin | 37 (29.0-52.0) | 28 (23.0-31.0) | 0.03 | - |
Seko et al[16] | SGLT-2 inhibitor | 54.4 (5.6) | 38 (3.1) | 0.001 | - |
Sitagliptin | 67 (7.7) | 52.5 (7.7) | 0.016 | ||
Gautam et al[17] | Canagliflozin | 72 (16.7) | 53 (10.3) | < 0.00001 | - |
Sumida et al[18] | Luseogliflozin | 40.7 (22.2) | 31.9 (18.2) | < 0.001 | - |
Table 8 Change in serum gamma-glutamyl transferase levels in individual studies
Study | Serum GGT (IU/L ) | P value | P value between groups | ||
Group | Baseline | Study completion | |||
Kuchay et al[11] | Empagliflozin | 65.8 (36.1) | 50.9 (24.6) | 0.002 | 0.057 |
Control | 63.9 (45.3) | 60.0 (39.0) | 0.421 | ||
Ito et al[12] | Ipragliflozin | 62.8 (58.3) | 44.0 (38.3) | < 0.05 | 0.642 |
Pioglitazone | 71.6 (54.1) | 48.8 (61.2) | < 0.05 | ||
Eriksson et al[14] | Placebo | 32.4 (17.4) | +2.4 (9.6)1 | - | - |
Omega-3 CA | 54.0 (57.6) | +2.4 (12.0)1 | - | Non-significant2 | |
Dapagliflozin | 58.2 (43.2) | -4.8 (13.8)1 | - | < 0.052 | |
O + D | 40.2 (14.4) | -0.6 (13.8)1 | - | Non-significant2 | |
Ohki et al[15] | Ipragliflozin | 75.0 (47.0-105.0) | 60.0 (40.0-101.0) | 0.03 | - |
Seko et al[16] | SGLT-2 inhibitor | 61.7 (9.1) | 58.7 (11.5) | 0.051 | - |
Sitagliptin | 89.2 (11.8) | 82.4 (11.9) | 0.36 | ||
Gautam et al[17] | Canagliflozin | 75.1 (31.8) | 69.2 (26.2) | 0.003 | - |
Sumida et al[18] | Luseogliflozin | 62.4 (77.1) | 48.2 (56.3) | 0.003 | - |
Table 9 Change in hepatic fat in individual studies
Study | Parameter | Group | Baseline | Study completion | P value | P value between groups |
Kuchay et al[11] | MRI-PDFF | Empagliflozin | 16.2 (7) | 11.3 (5.3) | < 0.0001 | < 0.0001 |
Control | 16.4 (7.3) | 15.5 (6.7) | 0.054 | |||
Ito et al[12] | L/S ratio | Ipragliflozin | 0.8 (0.2) | 1.0 (0.2) | < 0.05 | 0.90 |
Pioglitazone | 0.8 (0.3) | 1.0 (0.2) | < 0.05 | |||
Shibuya et al[13] | L/S ratio | Luseogliflozin | 0.9 (0.6-1.0) | 1.0 (0.8-1.2) | 0.0008 | 0.00002 |
Metformin | 1.0 (0.8-1.1) | 0.9 (0.7-1.0) | 0.017 | |||
Eriksson et al[14] | MRI-PDFF | Placebo | 15.1 (6.5) | -0.6 (1.9)1 | - | - |
Omega-3 CA | 22.2 (11.0) | -3.2 (2.9)1 | - | Non-significant2 | ||
Dapagliflozin | 17.3 (9.1) | -2.2 (3.3)1 | - | Non-significant2 | ||
O + D | 17.8 (9.2) | -3.2 (3.5)1 | - | < 0.052 | ||
Sumida et al[18] | MRI-HFF | Luseogliflozin | 21.5 (7.2) | 15.7 (6.8) | < 0.001 | - |
Table 10 Assessment of liver fibrosis in individual studies
Study | Parameter | Group | Baseline | Study completion | P value | P value between groups |
Ito et al[12] | FIB-4 index | Ipragliflozin | 1.44 (0.64) | 1.22 (0.55) | < 0.05 | 0.596 |
Pioglitazone | 1.84 (1.13) | 1.71 (1.19) | Non-significant | |||
Ohki et al[15] | FIB-4 index | Ipragliflozin | 1.75 (0.82-1.93) | 1.39 (0.77-1.99) | 0.04 | - |
Sumida et al[18] | FIB-4 index | Luseogliflozin | 1.63 (1.19) | 1.52 (0.92) | 0.17 | - |
NAFLD fibrosis score | Luseogliflozin | 1.61 (0.71) | 1.62 (0.88) | 0.86 | - |
Table 11 Change in fasting plasma glucose in individual studies
Study | Fasting plasma glucose (mg/dL) | P value | P value between groups | ||
Group | Baseline | Study completion | |||
Kuchay et al[11] | Empagliflozin | 173.0 (44.0) | 124.0 (17.0) | < 0.001 | 0.85 |
Control | 176.0 (57.0) | 120.0 (19.0) | < 0.0001 | ||
Ito et al[12] | Ipragliflozin | 160.1 (38.7) | 136.5 (26.7) | < 0.05 | 0.785 |
Pioglitazone | 169.4 (50.9) | 139.0 (26.6) | < 0.05 | ||
Shibuya et al[13] | Luseogliflozin | 127.0 (116.0, 136.0) | 125.0 (113.0, 138.0) | 0.87 | 0.583 |
Metformin | 147.0 (126.0, 161.0) | 134.0 (122.0, 145.0) | 0.32 | ||
Eriksson et al[14] | Placebo | 169.2 (29.7) | +6.7 (14.8)1 | - | - |
Omega-3 CA | 162.4 (26.6) | +3.8 (19.3)1 | - | Non-significant2 | |
Dapagliflozin | 161.8 (33.3) | -17.6 (26.8)1 | - | < 0.052 | |
O + D | 168.8 (35.5) | -16.4 (36.0)1 | - | < 0.052 | |
Ohki et al[15] | Ipragliflozin | 162.0 (135.0-189.0) | 135.0 (120.0-166.0) | 0.3 | - |
Seko et al[16] | SGLT-2 inhibitor | 125.0 (6.0) | 116.6 (4.2) | 0.07 | Non-significant |
Sitagliptin | 114.6 (7.0) | 134.0 (10.5) | 0.067 | ||
Sumida et al[18] | Luseogliflozin | 142.0 (30.3) | 135.4 (25.6) | 0.04 | - |
Table 12 Change in glycosylated haemoglobin in individual studies
Study | Glycosylated haemoglobin (%) | P value | P value between groups | ||
Group | Baseline | Study completion | |||
Kuchay et al[11] | Empagliflozin | 9.0 (1.0) | 7.2 (0.6) | < 0.001 | 0.88 |
Control | 9.1 (1.4) | 7.1 (0.9) | < 0.0001 | ||
Ito et al[12] | Ipragliflozin | 8.5 (1.5) | 7.6 (1.0) | < 0.05 | 0.522 |
Pioglitazone | 8.3 (1.4) | 7.1 (0.9) | < 0.05 | ||
Shibuya et al[13] | Luseogliflozin | 7.8 (7.2, 7.9) | 6.5 (6.4, 7.0) | 0.002 | 0.023 |
Metformin | 7.4 (6.9, 7.7) | 7.3 (6.7, 7.6) | 0.362 | ||
Eriksson et al[14] | Placebo | 7.4 (0.8) | -0.1 (0.4)1 | - | - |
Omega-3 CA | 7.4 (0.7) | +0.1 (0.4)1 | - | Non-significant2 | |
Dapagliflozin | 7.4 (0.6) | -0.6 (0.7)1 | - | < 0.052 | |
O + D | 7.5 (0.8) | -0.5 (0.5)1 | - | Non-significant2 | |
Ohki et al[15] | Ipragliflozin | 8.4 (7.8-8.9) | 7.6 (6.9-8.2) | < 0.01 | - |
Seko et al[16] | SGLT-2 inhibitor | 6.7 (0.1) | 6.5 (0.1) | 0.055 | Non-significant |
Sitagliptin | 7.0 (0.3) | 6.9 (0.3) | 0.331 | ||
Sumida et al[18] | Luseogliflozin | 7.3 (0.7) | 7.0 (0.7) | 0.002 | - |
Table 13 Change in homeostasis model assessment-estimated insulin resistance in individual studies
Study | HOMA-IR | P value | P value between groups | ||
Group | Baseline | Study completion | |||
Ito et al[12] | Ipragliflozin | 5.2 (2.5) | 4.8 (5.5) | Non-significant | 0.401 |
Pioglitazone | 5.7 (3.4) | 4.5 (2.7) | < 0.05 | ||
Eriksson et al[14] | Placebo | 4.2 (2.4) | -0.2 (1.4)1 | - | - |
Omega 3-CA | 5.4 (2.9) | +0.3 (2.4)1 | - | Non-significant2 | |
Dapagliflozin | 4.3 (1.9) | -1.1 (1.4)1 | - | < 0.052 | |
O + D | 4.4 (1.7) | -0.9 (1.6)1 | - | < 0.052 | |
Seko et al[16] | SGLT-2 inhibitor | 4.5 (0.5) | 7.9 (2.3) | 0.955 | - |
Sitagliptin | 4.4 (0.5) | 6.5 (0.8) | 0.163 |
Table 14 Change in serum triglycerides in individual studies
Study | Serum triglycerides (mg/dL) | P value | P value between groups | ||
Group | Baseline | Study completion | |||
Kuchay et al[11] | Empagliflozin | 201.0 (124.0) | 155.0 (52.0) | 0.01 | 0.678 |
Control | 212.0 (115.0) | 175.0 (43.0) | 0.019 | ||
Ito et al[12] | Ipragliflozin | 166.9 (76.4) | 143.4 (81.4) | < 0.05 | 0.938 |
Pioglitazone | 188.4 (148.8) | 169.3 (131.3) | Non-significant | ||
Eriksson et al[14] | Placebo | 169.2 (84.1) | -11.5 (45.6)1 | - | - |
Omega-3 CA | 186.9 (81.5) | -15.9 (47.4)1 | - | Non-significant2 | |
Dapagliflozin | 178.0 (103.6) | +14.2 (40.5)1 | - | Non-significant2 | |
O + D | 168.3 (72.6) | -25.7 (57.1)1 | - | Non-significant2 | |
Ohki et al[15] | Ipragliflozin | 148.0 (107.0, 222.) | 145.0 (114.0, 172.0) | 0.75 | - |
Seko et al[16] | SGLT-2 inhibitor | 153.8 (15.9) | 137.8 (10.5) | 0.236 | - |
Sitagliptin | 193.4 (25.2) | 191.1 (23.8) | 0.986 | ||
Sumida et al[18] | Luseogliflozin | 158.1 (110.5) | 129.4 (59.5) | 0.062 | - |
Table 15 Change in serum low-density lipoprotein cholesterol in individual studies
Study | Serum low-density lipoprotein cholesterol (mg/dL) | P value | P value between groups | ||
Group | Baseline | Study completion | |||
Kuchay et al[11] | Empagliflozin | 112.0 (35.0) | 95.0 (22.0) | 0.018 | 0.512 |
Control | 114.0 (30.0) | 96.0 (17.0) | 0.001 | ||
Ito et al[12] | Ipragliflozin | 108.3 (36.2) | 110.7 (40.1) | Non-significant | 0.057 |
Pioglitazone | 104.0 (27.9) | 114.6 (29.5) | < 0.05 | ||
Eriksson et al[14] | Placebo | 98.2 (34.4) | +1.6 (15.5)1 | - | - |
Omega-3 CA | 111.8 (34.4) | +2.3 (17.4)1 | - | Non-significant2 | |
Dapagliflozin | 109.4 (34.8) | +7.7 (20.5)1 | - | Non-significant2 | |
O + D | 88.9 (23.2) | +5.8 (21.7)1 | - | Non-significant2 | |
Ohki et al[15] | Ipragliflozin | 113.0 (89.0-142.0) | 103.0 (92.0-122.0) | 0.08 | - |
Seko et al[16] | SGLT-2 inhibitor | 119.2 (5.8) | 119.8 (5.7) | 0.943 | - |
Sitagliptin | 112.9 (4.9) | 127.1 (8.8) | 0.063 | ||
Sumida et al[18] | Luseogliflozin | 101.0 (22.4) | 105.0 (24.4) | 0.11 | - |
Table 16 Change in serum high-density lipoprotein cholesterol in individual studies
Study | Serum high-density lipoprotein cholesterol (mg/dL) | P value | P value between groups | ||
Group | Baseline | Study completion | |||
Kuchay et al[11] | Empagliflozin | 42.0 (12.0) | 45.0 (12.0) | 0.087 | 0.752 |
Control | 45.0 (15.0) | 47.0 (12.0) | 0.097 | ||
Ito et al[12] | Ipragliflozin | 48.9 (9.3) | 54.7 (10.4) | < 0.05 | 0.82 |
Pioglitazone | 47.4 (11.6) | 52.7 (13.5) | < 0.05 | ||
Eriksson et al[14] | Placebo | 51.4 (14.9) | -0.4 (5.0)1 | - | - |
Omega-3 CA | 49.9 (14.1) | +0.4 (3.2)1 | - | Non-significant2 | |
Dapagliflozin | 49.9 (9.5) | +0.4 (4.8)1 | - | Non-significant2 | |
O + D | 51.4 (10.2) | +1.6 (5.0)1 | - | Non-significant2 | |
Ohki et al[15] | Ipragliflozin | 42.0 (40.0-50.0) | 44.0 (42.0-59.0) | 0.01 | - |
Seko et al[16] | SGLT-2 inhibitor | 53.9 (2.5) | 55.4 (2.6) | 0.043 | - |
Sitagliptin | 54.8 (3.3) | 55.6 (2.3) | 0.531 | ||
Sumida et al[18] | Luseogliflozin | 55.6 (11.7) | 57.5 (13.4) | 0.062 | - |
Table 17 Change in body mass index in individual studies
Study | Body mass index (kg/m2) | P value | P value between groups | ||
Group | Baseline | Study completion | |||
Kuchay et al[11] | Empagliflozin | 30.0 (3.8) | 28.7 (3.5) | 0.001 | 0.124 |
Control | 29.4 (3.1) | 28.8 (2.8) | 0.019 | ||
Shibuya et al[13] | Luseogliflozin | 27.9 (26.2, 28.7) | 27.0 (25.6, 28.3) | 0.002 | 0.031 |
Metformin | 27.2 (24.8, 32.1) | 27.3 (24.3, 31.6) | 0.646 | ||
Ohki et al[15] | Ipragliflozin | 30.1 (26.1-31.4) | 27.6 (25.3-30.2) | < 0.01 | - |
Seko et al[16] | SGLT-2 inhibitor | 29.6 (0.7) | 28.3 (0.7) | < 0.001 | - |
Sitagliptin | 29.2 (1.5) | 28.9 (1.4) | 0.295 | ||
Sumida et al[18] | Luseogliflozin | 27.8 (3.6) | 27.2 (1.0) | < 0.001 | - |
Table 18 Adverse effects of sodium glucose cotransporter-2 inhibitors in individual studies
Study | No. of adverse events | No. of patients | Types of adverse events |
Kuchay et al[11] | 3 | 25 | Nonspecific fatigue: 1 |
Arthralgia: 1 | |||
Balanoposthitis: 1 | |||
Ito et al[12] | 9 | 32 | UTI: 3 |
Increased appetite: 2 | |||
Nausea: 1 | |||
Headache: 1 | |||
Diarrhoea: 1 | |||
Vaginal candidiasis: 1 | |||
Eriksson et al[14] | 7 | 21 | - |
Seko et al[16] | 2 | 26 | UTI: 2 |
Gautam et al[17] | 1 | 32 | Recurrent UTI with genital candidiasis: 1 |
Sumida et al[18] | 8 | 40 | Low blood pressure: 3 |
Vaginal itching: 2 | |||
Constipation: 1 | |||
Vertigo: 1 | |||
Dehydration: 1 | |||
Total | 30 | 176 | Most common adverse event: Genitourinary tract infections-10 |
- Citation: Raj H, Durgia H, Palui R, Kamalanathan S, Selvarajan S, Kar SS, Sahoo J. SGLT-2 inhibitors in non-alcoholic fatty liver disease patients with type 2 diabetes mellitus: A systematic review. World J Diabetes 2019; 10(2): 114-132
- URL: https://www.wjgnet.com/1948-9358/full/v10/i2/114.htm
- DOI: https://dx.doi.org/10.4239/wjd.v10.i2.114