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Powdered black cumin seeds strongly improves serum lipids, atherogenic index of plasma and modulates anthropometric features in patients with Hashimoto’s thyroiditis



Hashimoto’s thyroiditis is associated with serious alterations in serum lipids and glucose homeostasis. The aims of the current study were to evaluate the effect of powdered Nigella sativa on serum lipids, glucose homeostasis and anthropometric variables in patients with Hashimoto’s thyroiditis.


Forty patients with Hashimoto’s thyroiditis, aged between 22 and 50 years old, participated in the trial and were randomly allocated into two groups of intervention and control receiving powdered Nigella sativa or placebo daily for 8 weeks. Serum lipids, glucose homeostasis, and anthropometric variables were evaluated at baseline and after intervention.


Treatment with Nigella sativa significantly reduced body weight and body mass index (BMI). Serum concentrations of low density lipoprotein cholesterol (LDL) and triglyceride (TG) also decreased in Nigella sativa-treated group after 8 weeks; while serum high density lipoprotein cholesterol (HDL) significantly increased after treatment with Nigella sativa (P < 0.05). None of these changes had been observed in placebo treated group. Serum Nesfatin-1 concentrations was in inverse relationship with serum triglyceride (TG) (r = − 0.31, P = 0.04).


Giving attention to the potent beneficial effects of powdered black cumin seeds in improving serum lipid profile and anthropometric features in patients with Hashimoto’s thyroiditis, this medicinal plant could be considered as a beneficial herbal supplement alongside with the disease- specific medications including Levothyroxine in management of Hashimoto’s thyroiditis- related metabolic abnormalities.

Trial registration

Iranian registry of clinical trials (registration number IRCT2014090819082N2- Registered 2014-09-29).


Hashimoto’s thyroiditis (HT) is one of the most common human autoimmune diseases and an organ-specific T-cell mediated disease that affects the thyroid glands [1, 2]. The disease is ten times more prevalent in women than in men and affects 2% of general population [3, 4]. A significant proportion of patients have asymptomatic chronic autoimmune thyroiditis and 8% of woman (10% of woman over 55 years of age) and 3% of men have subclinical hypothyroidism [5]. Hashimoto’s thyroiditis is associated with serious alterations in composition and the transport of lipoproteins; Hypothyroidism is characterized by hyper-cholesterolaemia and a marked increase in low-density lipoproteins (LDL) and apo-lipoprotein B (apo B) because of reduced fractional clearance of LDL by a reduced number of LDL receptors in the liver [6, 7]. Dyslipidemia occurred in thyroid abnormalities is a potent risk factor of cardiovascular events and myocardial infarction among patients with abnormal thyroid function. Numerous studies revealed that hypothyroidism is an independent risk factor of mortality from cardiovascular disease and all-cause mortality [8, 9]. Moreover, Hashimoto’s thyroiditis is a risk factor of non-insulin dependent diabetes mellitus (NIDDM) and more often these two diseases are in co-existence with each other [10]. Up to 38% of patients with NIDDM have also Hashimoto’s thyroiditis [11].

Considering these metabolic abnormalities in Hashimoto’s thyroiditis, therapeutic approaches in treatment of the disease will be important. Levothyroxine sodium is the treatment of choice for Hashimoto’s thyroiditis however its chronic use is related with cardiac dysfunction, left ventricular hypertrophy [12, 13] and rapid bone loss [14].There are limited data evaluating the effects of vitamins or herbal medications in treatment of thyroid abnormalities [15] and no study was available evaluating the effects of herbal medications in treatment of Hashimoto’s thyroiditis in human. Nigella sativais an amazing herb with a rich historical and religious background; it is one of the medicinal plants and belongs to the Ranunculaceae family [16]. The seeds of the Nigella sativa are the source of the active ingredients of this plants; it has considerable health promoting effects including its antioxidant, anti-inflammatory and immune-modulatory properties [16]. Numerous studies have extensively studied therapeutic actions of Nigella sativa in treating the disease especially in animal models; while human studies in this filed are scarce [17,18,19]. Lipid- lowering effects of Nigella sativa had been studied in several human diseases including hypercholesterolemia [20], type two diabetes mellitus [21] and coronary artery disease [22]. However, to our review of literature, the effect of this herbal medicine on dyslipidemia or glycemic status and thyroid function among patients with Hashimoto’s thyroiditis has not been evaluated before; therefore in the current study we aimed to test these hypotheses.



In the current double-blinded placebo-controlled trial, forty patients with Hashimoto’s thyroiditis were enrolled (Fig. 1). Subjects were recruited from outpatient endocrinology and metabolism clinics of Isfahan University of Medical Sciences. Inclusion criteria were as follows: age between 20 and 50 years, having Hashimoto’s thyroiditis according to physician diagnosis based on laboratory analysis of thyroid stimulating hormone (TSH), T3, T4 and anti-thyroid peroxidase concentrations. Exclusion criteria were as follows: taking any nutritional supplements for at least 3 months prior participation or during the trial, any history of autoimmune disease, cardiovascular events, other thyroid abnormalities including Grave’s disease, being pregnant or lactating, any history of thyroid surgeries and being on any dietary regimens during and 3 months before recruitment in the trial.

Fig. 1
figure 1

Flow diagram of subject recruitment

Study design

From one hundred recruited subjects, fifty three participants were excluded because of not meeting the inclusion criteria or decline to participate. Among forty seven patients random permuted block procedure was performed and participants were randomly allocated into Nigella sativa-treated (n = 24) or placebo-treated (n = 23) groups.

Patients in the intervention group received a daily dose of 2 g Nigella sativa powder per day and placebo group received 2 g starches per day for 8 weeks. The mature Nigella sativa seeds were obtained from a local market and were milled in a grinder. Both Nigella sativa powder and placebo were identically packaged to have similar appearance. Subjects were advised to receive the supplement or placebo packages in two divided dosages with lunch and dinner. Randomization procedure was performed by a third investigator with no clinical involvement in the trial for ensure in blinding. A follow-up procedure was done with weekly telephone contacts to ensure that subjects consumed the supplements regularly.

Written informed consent was obtained from all of the participants before participation in the trial and the study protocol was approved by the ethics committee of Tabriz University of Medical Sciences (Project number: 93173). The current trial was also registered in the Iranian Registry of Clinical Trials (Identifier: IRCT2014090819082N2) [23, 24].

Anthropometric and nutritional assessments

Body weight and height were measured with a calibrated digital scale and stadiometer respectively. BMI was calculated as weight (kg) divided by height (m) squared [25]. Waist circumference (WC) was measured in horizontal plane, midway between the lowest rib and the iliac crest with a measuring tape in centimeter. Waist to hip ratio (WHR) was calculated by WC divided by hip circumference (HC) [26]. The dietary assessments were performed using a 3-day food record, covering two weekdays and one weekend day, to estimate total energy, carbohydrate, protein, fat and vitamins consumption. Nutrient analysis of the 3-day food record was performed using the Nutritionist IV software (N-squared Computing, Salem, OR, USA).

Physical activity level

Physical activity was obtained by the questionnaire with nine different metabolic equivalent (MET) scales ranging from sleep/rest (0.9 METs) to high-intensity physical activities (> 6 METs). For each activity level, the MET value was multiplied by the time spent at that particular level. The MET-time at each level was added to obtain a total over 24 h MET-time, representing the physical activity level on an average weekday. Physical activities of different intensities were categorized to sedentary (< 3 METs), moderate (3–6 METs) and vigorous (> 6 METs) respectively [27].

Biochemical assays

Fasting blood samples were obtained from all of the participants at the beginning and end of the trail. The serum and plasma samples were separated by centrifugation at 2500 rpm for 10 min (Beckman Avanti J-25; Beckman Coulter, Brea, CA, USA) at room temperature. The serum samples were stored at − 70 °C immediately after centrifugation until their assays.Serum total cholesterol (TC), fasting serum glucose (FSG), triglyceride (TG), high density lipoprotein cholesterol (HDL-C) and low density lipoprotein cholesterol (LDL-C) were analyzed by enzymatic colorimetric method (Pars – Azmoon, Tehran – Iran). Serum insulin was analyzed with enzyme linked immunosorbent assay method (ELISA- Monobind Insulin AccuBind, CA 92630, USA). The Sensitivity of this assay was 0.75 μIU/ml and mean inter and intra assay coefficient of variations (CV) were < 9.8% and < 8% respectively. Atherogenic index of plasma (AIP) was calculated as log TG divided by HDL-C [28]. Assessment of insulin sensitivity was performed by the homeostasis model assessment of insulin resistance (HOMA-IR) based on fasting glucose and insulin measurements as follows: HOMA-IR: (glucose (mg/dl) × insulin (mU/l)) / 405. High HOMA-IR scores denote high insulin resistance [29]. Serum Nesfatin-1 concentration was also assessed by ELISA method (Hangzhou Eastbiopharm Co, USA). This assay had a sensitivity of 0.15 ng/ml.

Statistical assays

Statistical analysis was performed by SPSS™ statistical software (SPSS Inc., Chicago, IL, USA). Quantitative data were presented as mean ± standard deviation (SD), and qualitative data were demonstrated as frequency and percent. Kolmogorov-Smirnov test was used to assess the normality of data. Between groups comparisons of continuous variables were performed by independent sample t-test. Paired t-test was used for before and after intervention comparisons. Analysis of covariance (ANCOVA) was used to identify any differences between two treatment groups after intervention adjusting for the confounding effects of baseline concentrations of parameter, age and gender.


In the current study 40 patients with Hashimoto’s thyroiditis were enrolled. The demographic and biochemical characteristics of study population are shown in Table 1. Participants in two Nigella-sativa and placebo treated group were similar in their mean age and gender distribution. Baseline values of anthropometric variables were also similar between groups. Whereas, weight and BMI of Nigella-sativa group significantly reduced after 8 weeks intervention period while no changes observed in placebo-treated group. Dietary energy and nutrient intakes before and after intervention are presented in Table 2. Energy and nutrient intakes were similar between groups before intervention and no significant change observed after intervention. Nigella sativa significantly reduced serum LDL, TG and AIP values (P < 0.05). Serum HDL increased after Nigella sativa supplementation. None of these changes were observed in placebo treated group. Serum Nesfatin-1 also did not change after intervention; moreover, serum TSH and anti-TPO concentrations reduced while serum T3 increased in Nigella sativa treated group (P < 0.05). (Table 3). A significant negative relationship was observed between baseline values of Nesfatin-1 and serum triglyceride concentrations (Fig. 2).

Table 1 Demographic characteristics and anthropometric variables in treatment groups before and after intervention
Table 2 Dietary intakes of energy and nutrients in treatment groups before and after intervention
Table 3 Metabolic parameters and thyroid hormones in treatment groups before and after intervention
Fig. 2
figure 2

Relationship between serum Nesfatin-1 and triglyceride concentrations in total participants


Hashimoto’s thyroiditis is accompanied with disturbances in serum lipids and glucose homeostasis. The disease is a known risk factor for hyperlipidemia and diabetes mellitus [6, 10]. The results of the current study provide insight into lipid-lowering effects of Nigella sativa in patients with Hashimoto’s thyroiditis. Moreover Nigella sativa reduced body weight and BMI in these patients. It is the first trial evaluating the effects of Nigella sativa on serum lipids and BMI in patients with Hashimoto’s thyroiditis.

Weight reducing effects of Nigella sativa has been observed in previous studies; Zaoui A [30] reported a significant reduction in body weight in rats after 6 weeks treatment with Nigella sativa fixed oil (P < 0.001). In other study 3 month supplementation with 1.5 g daily powdered Nigella sativa in central obese men significantly reduced body weight [31]. In other study in menopausal women also slight and non-significant reduction in body weight was observed after 2 month treatment with 1 g/ day Nigella sativa [32]. The anti-obesity effects of Nigella might be explained by increasing mean rates of satiety and fullness [33]. Other possible mechanisms includes reduction in lipid absorption, reduced energy intake, increased energy expenditure, decreased pre-adipocyte differentiation and proliferation, or decreased lipogenesis and increased lipolysis [34].

In fact, other health promising effects of Nigella sativa like its hypolipidemic or hypoglycemic effects observed in our study and also previous reports [31, 35] could be explained by these mechanisms; we observed a strong reduction in serum LDL and TG and AIP and increase in serum HDL concentrations (P < 0.001 and P < 0.05 respectively). A mild non-significant reduction in serum FSG was also observed in Nigella sativa treated group. Serum insulin was increased in both groups and comparison of mean difference in serum insulin between groups showed no statistically significant difference.

Although not clear explanation can be attributed to this phenomenon, however, the possible underlying reason can be the direct effects of pro-inflammatory cytokines in the Hashimoto’s thyroiditis against insulin resistance and deteriorating the pancreas’ β-cell function; TSH is a potent stimulator of interleukin (IL)-6, IL-2, C-reactive protein (CRP) and tumor necrosis factor (TNF)-α secretion from adipose tissue in patients with Hashimoto’s thyroiditis [36]. On the other hand, previous studies reporting the beneficial effects of Nigella sativa on glycemic status and insulin resistance used higher doses of Nigella sativa compared with our study [37, 38] or even more prolonged study duration time [39, 40]. Therefore, the beneficial effects of Nigella sativa on glycemic status and insulin resistance in the current dose and the study’s duration have not been observed.

The underlying mechanisms previously suggested for hypolipidemic effects of Nigella sativa included an up-regulation of LDL-C molecules through receptor mediated endocytosis [35], decreased dietary cholesterol absorption, stimulation of primary bile acid synthesis and its fecal losses probably contributed to its dietary soluble fibers and sterols [32] and non-enzymatic lipid peroxidation by antioxidant properties of Nigella sativa making liver cells more efficient to remove LDL-C from blood by increasing LDL-C receptor densities in the liver and binding to apolipoprotein, apo-B [41,42,44].

In the current study serum Nesfatin-1 concentrations did not change after Nigella sativa supplementation. However, its serum concentrations was in inverse relationship with serum triglyceride concentrations (r = − 0.31, P < 0.05). Nesfatin-1 is a new anorexigenic hormone which is expressed from several regions of hypothalamus and peripheral tissues, including the adipose tissue, gastric mucosa, pancreatic beta-cells. Recent studies have demonstrated that Nesfatin-1 is negatively related with obesity and insulin resistance [32, 45]. Our finding also confirmed these results. However no change after Nigella sativa supplementation was observed in serum Nesfatin-1 concentrations. Probably because of the study’s low sample size.


We have demonstrated beneficial effects of powdered black cumin in improving serum lipids and reducing body weight in patients with Hashimoto’s thyroiditis. Considering these health-promoting effects of Nigella sativa, it can be considered as a beneficial herbal supplement alongside with the disease- specific medications including Levothyroxine in management of Hashimoto’s thyroiditis- related metabolic abnormalities.



Body mass index


Hip circumference



T4, Thyroxine:

TG-Ab, thyroglobulin antibody


Thyroid peroxidase antibody


Thyrotropin releasing hormone


Thyroid stimulating hormone, VEGF, vascular endothelial growth factor


Waist circumference; WHR, waist to hip ratio


  1. Chistiakov DA. Immunogenetics of Hashimoto's thyroiditis. J Autoimmune Dis. 2005;2(1):1–21.

    Article  PubMed  PubMed Central  Google Scholar 

  2. Jalilzadeh S, Bahrami A, Eftekhar-Sadat B, Pezeshki Z, Salek Zamani Y, Mobasseri M. Electrodiagnostic changes in patient with subclinical hypothyroidism. Med J Tabriz University of Med Sci Health Serv. 2007;29(1):11–20.

    Google Scholar 

  3. Wang C, Crapo LM. The epidemiology of thyroid disease and implications for screening. Endocrinol Metab Clin N Am. 1997;26:189–218.

    Article  CAS  Google Scholar 

  4. Tunbridge WM, Vanderpump MP. Population screening for autoimmune thyroid disease. Endocrinol Metab Clin N Am. 2000;29:239–53.

    Article  CAS  Google Scholar 

  5. Vanderpump MP, Tunbridge WM, French JM, Appleton D, Bates D, Clark F, et al. The incidence of thyroid disorders in the community: a twenty-year follow-up of the Whickham survey. Clin Endocrinol. 1995;43:55–69.

    Article  CAS  Google Scholar 

  6. Duntas LH. Thyroid disease and lipids. Thyroid. 2002;12(4):287–93.

    Article  CAS  PubMed  Google Scholar 

  7. Farhangi MA, Eshraghian M, Keshavarz SA, Saboor-Yaraghi AA. Thyroid-stimulating hormone, triiodotyronine and thyroxine concentrations and their relationship with metabolic parameters, anthropometric variables and body composition in premenopausal euthyroid obese women. Turk J Endocrinol Metab. 2015;19(1):1–6.

    Article  Google Scholar 

  8. Singh S, Duggal J, Molnar J, Maldonado F, Barsano CP, Arora R. Impact of subclinical thyroid disorders on coronary heart disease, cardiovascular and all-cause mortality: a meta-analysis. Int J Cardiol. 2008;125(1):41–8.

    Article  PubMed  Google Scholar 

  9. Klein I, Danzi S. Thyroid disease and the heart. Circulation. 2007;116(15):1725–35.

    Article  PubMed  Google Scholar 

  10. McCanlies E, O’Leary LA, Foley TP, Kramer MK, Burke JP, Libman A, et al. Hashimoto’s thyroiditis and insulin-dependent diabetes mellitus: differences among individuals with and without abnormal thyroid function. J Clin Endocrinol Metab. 1998;83(5):1548–51.

    CAS  PubMed  Google Scholar 

  11. Kontiainen S, Schlenzka A, Koskimies S, Rilva A, Maenpaa J. Autoantibodies and autoimmune diseases in young diabetics. Diabetes Res. 1990;13:151–6.

    CAS  PubMed  Google Scholar 

  12. Monzani F, Di Bello V, Caraccio N, Bertini A, Giorgi D, Giusti C, et al. Effect of levothyroxine on cardiac function and structure in subclinical hypothyroidism: a double blind, placebo-controlled study. J Endocrinol Metab. 2001;86(3):1110–5.

    Article  CAS  Google Scholar 

  13. Dai DZ, Hu HJ, Yang DM, Hao XM, Zhang GQ, Zhou PA, et al. Chronic levothyroxin treatment is associated with ion channel abnormalities in cardiac and neuronal cells. Clin Exp Pharmacol Physiol. 1999;26(10):819–21.

    Article  CAS  PubMed  Google Scholar 

  14. Panebianco P, Rosso D, Destro G, Scarpinato RA, Tropea S, Rizzo A, et al. Use of disphosphonates in the treatment of osteoporosis in thyroidectomized patients on levothyroxin replacement therapy. Arch Gerontol Geriatr. 1997;25(2):219–25.

    Article  CAS  PubMed  Google Scholar 

  15. Farhangi MA, Keshavarz SA, Eshraghian M, Ostadrahimi A, Saboor-Yaraghi AA. The effect of vitamin a supplementation on thyroid function in premenopausal women. J Am Coll Nutr. 2012;31(4):268–74.

    Article  CAS  PubMed  Google Scholar 

  16. Salem ML. Immunomodulatory and therapeutic properties of the Nigella sativa L. seed. Int Immunopharmacol. 2005;5(13):1749–70.

    Article  CAS  PubMed  Google Scholar 

  17. Kanter M, Coskun O, Korkmaz A, Oter S. Effects of Nigella sativa on oxidative stress and β-cell damage in streptozotocin-induced diabetic rats. Anat Rec A Discov Mol Cell Evol Biol. 2004;279(1):685–91.

    Article  PubMed  Google Scholar 

  18. Kanter M, Coskun O, Budancamanak M. Hepatoprotective effects of Nigella sativa and Urtica dioica on lipid peroxidation, antioxidant enzyme systems and liver enzymes in carbon tetrachloride-treated rats. WJG. 2005;11(42):6684–8.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Abdel-Sater KA. Gastroprotective effects of Nigella sativa oil on the formation of stress gastritis in hypothyroidal rats. Int J Physiol Pathophysiol Pharmacol. 2009;1(2):143–9.

    PubMed  PubMed Central  Google Scholar 

  20. Bhatti IU, Ur Rehman F, Khan MA, Marwat SK. Effect of prophetic medicine kalonji (Nigella sativa L.) on lipid profile of human beings. An in vivo approach. World Appl Sci J. 2009;6(8):1053–7.

    CAS  Google Scholar 

  21. Akash MSH, Rehman K, Rasool F, Sethi A, Abrar MA, Irshad A, et al. Alternate therapy of type 2 diabetes mellitus (T2DM) with Nigella (Ranunculaceae). J Med Plants Res. 2011;5(31):6885–9.

    Google Scholar 

  22. Tasawar Z, Siraj Z, Ahmad N, Lashari MH. The effects of Nigella sativa (Kalonji) on lipid profile in patients with stable coronary artery disease in Multan. Pakistan Pak J Nutr. 2011;10(2):162–7.

    Article  CAS  Google Scholar 

  23. Farhangi MA, Dehghan P, Tajmiri S, Abbasi MM. The effects of Nigella sativa on thyroid function, serum vascular endothelial growth factor (VEGF) – 1, Nesfatin-1 and anthropometric features in patients with Hashimoto’s thyroiditis: a randomized controlled trial. BMC Complement Alternat Med. 2016;16:471–80.

    Article  Google Scholar 

  24. Tajmiri S, Farhangi MA, Dehghan P. Nigella sativa treatment and serum concentrations of thyroid hormones, transforming growth factor β (TGF-b) and interleukin 23 (IL-23) in patients with Hashimoto’s thyroiditis. Eur J Integrat Med. 2016;8:576–80.

    Article  Google Scholar 

  25. Farhangi MA, Keshavarz SA, Eshraghian MR, Ostadrahimi A, Saboor-Yaraghi AA. Vitamin a supplementation, serum lipids, liver enzymes and C-reactive protein concentrations in obese women of reproductive age. Ann Clin Biochem. 2013;50:25–30.

    Article  CAS  PubMed  Google Scholar 

  26. Sharifi N, Mahdavi R, Ebrahimi-Mameghani M. Perceived barriers to weight loss programs for overweight or obese women. Health Prom Perspect. 2013;3(1):11–22.

    Google Scholar 

  27. Kelishadi R, Ardalan G, Gheiratmand R, Gouya MM, Razaghi EM, Delavari A. Association of physical activity and dietary behaviours in relation to the body mass index in a national sample of Iranian children and adolescents: CASPIAN study. Bull World Health Organ. 2007;85:19–26.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Farhangi MA, Keshavarz SA, Eshraghian M, Ostadrahimi A, Saboor-Yaraghi AA. White blood cell count in women: relation to inflammatory biomarkers, haematological profiles, visceral adiposity, and other cardiovascular risk factors. J Health Popul Nutr. 2013;31(1):58–64.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Farhangi MA, Jahangiry L, Mirinazhad MM, Shojaeezade D, Montazeri A, Yaghoubi A. A web-based interactive lifestyle modification program improves lipid profile and serum adiponectin concentrations in patients with metabolic syndrome: the “red ruby” study. Int J Diabetes Dev Ctries. 2017;37(1):21-30.

  30. Zaoui A, Cherrah Y, Alaoui K, Mahassine N, Amarouch H, Hassar M. Effects of Nigella sativa fixed oil on blood homeostasis in rat. J Ethnopharmacol. 2002;79(1):23–6.

    Article  CAS  PubMed  Google Scholar 

  31. Datau EA, Surachmanto EE, Pandelaki K, Langi JA. Efficacy of Nigella sativa on serum free testosterone and metabolic disturbances in central obese male. Acta Med Indones. 2010;42(3):130–4.

    CAS  PubMed  Google Scholar 

  32. Ibrahim RM, Hamdan NS, Ismail M, Saini SM, Abd Rashid SN, Abd Latiff L, et al. Protective effects of Nigella sativa on metabolic syndrome in menopausal women. Adv Pharm Bull. 2014;4(1):29–33.

    PubMed  Google Scholar 

  33. Qidwai W, Hamza HB, Qureshi R, Gilani A. Effectiveness, safety, and tolerability of powdered Nigella sativa [kalonji] seed in capsules on serum lipid levels, blood sugar, blood pressure, and body weight in adults: results of a randomized, double-blind controlled trial. J Altern Complement Med. 2009;15:639–44.

    Article  PubMed  Google Scholar 

  34. Hasani-Ranjbar S, Jouyandeh Z, Abdollahi M. A systematic review of anti-obesity medicinal plants-an update. J Diabetes Metab Disord. 2013;12(1):28–33.

    Article  PubMed  PubMed Central  Google Scholar 

  35. Ibrahim RM, Hamdan NS, Mahmud R, Imam MU, Saini SM, SNA R, et al. A randomised controlled trial on hypolipidemic effects of Nigella sativa seeds powder in menopausal women. J Transl Med. 2014;12:82.

    Article  PubMed  PubMed Central  Google Scholar 

  36. Varim C, Kaya T, Varim P, Nalbant A, Vatan MB, Yaylaci S, Gokosmanoglu F, Tamer A. Insulin resistance in the patients with euthyroid Hashimoto thyroiditis. Biomed Res. 2017;28(4):1543–7.

    CAS  Google Scholar 

  37. Najmi A, Haque SF, Naseeruddin M, Khan RA. Effect of Nigella sativa oil on various clinical and biochemical parameters of insulin resistance syndrome. Int J Diab Metab. 2008;16:85–7.

    Google Scholar 

  38. Najmi A, Nasiruddin M, Ali Khan R, Haque SF. Therapeutic effect of Nigella Sativa oil On different clinical and biochemical parameters In metabolic syndrome. Int J Diabetes Dev Ctries. 2008;28(1):11–4.

    Article  PubMed  PubMed Central  Google Scholar 

  39. Kaatabi H, Bamosa AO, Badar A, Al-Elq A, Abou-Hozaifa B, Lebda F, et al. Nigella sativa improves glycemic control and ameliorates oxidative stress in patients with type 2 diabetes mellitus: placebo controlled participant blinded clinical trial. PLoS One. 2015;10(2):e0113486.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Bamosa AO, Kaatabi H, Lebdaa FM, Elq AM, Al-Sultanb A. Effect of Nigella sativa seeds on the glycemic control of patients with type 2 diabetes mellitus. Indian J Physiol Pharmacol. 2010;54(4):344–54.

    PubMed  Google Scholar 

  41. Al-Naqeeb G, Ismail M, Al-Zubairi AS. Fatty acid profile, α- tocopherol content and total antioxidant activity of oil extracted from N sativa seeds. Int J Pharmacol. 2009;5(244–50):4.

    Google Scholar 

  42. Sokhanvar S, Mazaki R, Mousavinasab N, Golmohammadi Z. The association between serum lipoprotein (a) and other cardiac risk factors with the severity of coronary artery disease. J Cardiovasc Thorac Res. 2011;3(1):35–9.

    Google Scholar 

  43. Sokhanvar S, Khoshi A, Hajiaghaei S, Mousavinasab SN, Golmohammadi Z. Association between Apo lipoprotein B levels at admission of patients and short-term morbidity and mortality after myocardial infarction. J Cardiovas Thoracic Res. 2012;4(3):61–4.

    Google Scholar 

  44. Su Y, Zhang J, Tang Y, Bi F, Liu JN. The novel function of nesfatin-1: anti-hyperglycemia. Biochem Biophys Res Commun. 2010;391:1039–42.

    Article  CAS  PubMed  Google Scholar 

  45. Bashir J, Gholami F, Rahbaran A, Tarmahi V. Effects of single bout of aerobic exercise on serum Nesfatin-1 levels in non-athlete elderly men. Med J Tabriz Uni Med Sci. 2012;34(4):25–30.

    Google Scholar 

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The current research was financially supported by a grant from Tabriz University of Medical Sciences.


This research has been performed by a grant from Tabriz University of Medical Sciences (Project number: 93173).

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MAF conceived and designed the project and wrote the manuscript and performed the statistical analysis, PD was invloved in study design and revision of the manuscritp, ST performed the sampling and data collection. All authors read and approved the final manuscript.

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Correspondence to Mahdieh Abbasalizad Farhangi.

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All participants signed a written informed consent approved by the Institutional Review Board of Tabriz University of Medical Sciences. The study design and protocol was approved by the ethical committee of Tabriz University of Medical Sciences (Project number: 93173). The study has also been registered in Iranian registry of clinical trials (registration number IRCT2014090819082N2- Registered 2014-09-29).

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Farhangi, M.A., Dehghan, P. & Tajmiri, S. Powdered black cumin seeds strongly improves serum lipids, atherogenic index of plasma and modulates anthropometric features in patients with Hashimoto’s thyroiditis. Lipids Health Dis 17, 59 (2018).

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